What is the Treatment for Schizoaffective Disorder?

Many different treatments for schizoaffective disorder exist. Learn about medication and non-medication treatment for schizoaffective disorder on HealthyPlace.

Because schizoaffective disorder is slightly different for each person who lives with it, the treatment varies a bit for everyone, too. The best schizoaffective disorder treatment is individualized, tailored to fit each person and his or her symptoms.

Doctors take into consideration the type of the schizoaffective disorder (schizoaffective disorder bipolar type or schizoaffective disorder depressive type) as well as the severity of symptoms to create an appropriate treatment plan for the best possible outcome.

General Schizoaffective Disorder Treatment Options

In most cases, doctors work with patients and families to create a comprehensive schizoaffective disorder treatment plan. The plan outlines specific, individualized schizoaffective disorder treatment goals and objectives. For some people, the goals might include returning to work and living independently. For others, the goals might involve avoiding hospitalization in a state facility. Goals are established based on the severity of someone’s psychotic and mood symptoms.

General approaches to treating schizoaffective disorder include:

People can be treated in both inpatient and outpatient facilities. In some cases, hospitalization is necessary to provide round-the-clock support, supervision, and medication regulation. In other instances, people can receive schizoaffective disorder treatment through office visits and regular appointments.

There is no single standard for treating this illness. There are, however, schizoaffective disorder treatment guidelines that doctors follow:

  • A combination of the treatment types listed above is preferred over just one, as people respond better to multiple approaches
  • Medication is almost always, if not always, the primary form of treatment for this brain-based illness
  • The individual must be the main factor in making treatment decisions

Let’s take a closer look at schizoaffective disorder treatment options, starting with medication.

Schizoaffective Disorder Treatment: Medication

Once someone is diagnosed with schizoaffective disorder, the first type of treatment given is medication. Many hope that medication is a cure for schizoaffective disorder. Unfortunately, a schizoaffective disorder cure doesn’t exist—at least not at this time. For now, medication is used to soothe and stabilize the brain so that other treatment approaches can work, and someone can function and live well with schizoaffective disorder.

Doctors prescribe many different types of antipsychotics, mood stabilizers, and antidepressants to reduce psychotic symptoms, stabilize mood, and relieve depression. According to the National Institute of Mental Health,

  • 87% of people with schizoaffective disorder are prescribed two or more types of psychotropic medication
  • 93% are prescribed an antipsychotic
  • 48% receive prescription mood stabilizers
  • 42% take an antidepressant

Can schizoaffective disorder be treated without medication? In the vast majority of cases, medication is necessary because it works within the brain, at the root of the disorder.

Once a medication has reduced mania or improved depression and muted psychotic symptoms like hallucinations, the person taking the medication is ready for additional schizoaffective disorder treatments.

Schizoaffective Disorder Treatment: Non-Medication Approaches

Psychoeducation is one of the most important aspects of treatment. When people learn about their illness, they are better able to recognize signs of relapse. Understanding the role of medication and other treatment makes people more likely to comply with their treatment plan and avoid relapse.

Individual, family, and group therapies have also been shown to be effective in treating schizoaffective disorder. Each of these plays a part in helping people make plans and goals, express frustrations, improve close relationships, and improve social skills.

Life skills training and vocational rehabilitation (voc rehab) help people living with schizoaffective disorder to live as independently as possible, manage money, and find and keep jobs.

Doctors, hospitals, and community centers often have resources available to help people find these services. Organizations like the National Alliance on Mental Illness (NAMI) and the Depression and Bipolar Support Alliance (DBSA) often can point people to resources and even offer classes and support groups of their own.

Can Schizoaffective Disorder be Cured?

Can schizoaffective disorder be cured? It can’t at this time. That doesn’t mean, however, that one is doomed to a low-quality life because the prognosis for schizoaffective disorder is good. Treatments are available, and long-term treatment for schizoaffective disorder helps people manage all of their symptoms over time. Getting and complying with proper treatment can even cause the illness to go into remission. It is possible to live a quality life with this disorder.

article references

APA Reference
Peterson, T. (2021, December 27). What is the Treatment for Schizoaffective Disorder? , HealthyPlace. Retrieved on 2025, April 29 from https://www.healthyplace.com/thought-disorders/schizoaffective-disorder-information/what-is-the-treatment-for-schizoaffective-disorder

Last Updated: March 25, 2022

Assessment and Psychological Treatment of Sexual Dysfunctions

Here's a step-by-step guideline of how to diagnose and treat sexual dysfunctions.

Assessment of Sexual Dysfunctions

Often requires medical evaluation

  • By competent, sensitive physician

Psychosocial evaluations

  • Can be complex
  • Multiple etiologies
  • Distinguishing cause, effect, & their interaction
  • Frequently identify co-morbidities
  • Sexual and non-sexual
  • Medical and psychological
  • Within and between partners

Ideally, both partners get interviewed

  • Together and separately
  • Not always possible
  • Could itself be diagnostic
  • Identified patient is sent in to be "fixed"
  • Stories often differ
  • Even about objective data
  • Often about conceptions of the problem
  • Or even if there is a problem

"There are no unaffected partners in sexual dysfunctions" (Bill Masters)

  • Resentment
  • Anger
  • Doubts
  • Does she still love me?
  • Does he still find me attractive, sexy, appealing?
  • Diminished Quality of Life

Sexual dysfunctions vary across several dimensions

  • Nature of presenting complaint
  • Is this really a sexual problem?
  • Length of dysfunction
  • Primary vs. Secondary
  • Has the person always had the dysfunction or was there ever a period of good functioning?

Sexual dysfunctions vary across several dimensions

  • Medical vs. Psychological Etiology
  • Frequently difficult to determine
  • Particularly if the problem is of long duration
  • Locus of the problem?
  • One partner, the other, or both?
  • Do both partners see this the same?
  • Single or multiple dysfunction(s)
  • In one partner or both?
  • Relationship, if any, of multiple dysfunctions?

Important to explore

  • How each partner understands the problem
  • What has the couple has tried to deal with the problem?
  • With what success?
  • Anything make it better/worse?
  • What is the non-sexual relationship like?
  • Non-sexual sources of stress
  • Health problems?
  • Medications?
  • Why are they in treatment now?
  • What does each hope to get from treatment?
  • How willing is each to participate in treatment?
  • Strengths, as well as problems
  • What competes with sex?
  • Time, work, kids
  • A detailed description of what the couple typically does sexually
  • Maladaptive attitudes, beliefs, behaviors, and expectations
  • Each partner's outside sexual experiences
  • Before or during this relationship
  • What's at stake if the problem isn't resolved?
  • Is the problem also a solution?
  • Secrets
  • Fantasies

Sexual History

  • Critical for understanding the problem
  • Always done for symptomatic partner
  • Best when done for both partners
  • Time and detail are variable
  • How far back do you go?
  • How much detail do you need?
  • Certainly, need a detailed history of the problem
  • As far back as it goes
  • Precipitating events?

Sexual history includes

  • Sexual messages received growing up
  • Earliest sexual experience
  • How did it go?
  • Significant sexual experiences
  • Both positive and negative
  • Particularly any abuse (psychological, physical, sexual)
  • History of sexual relationship with current partner

Treatments

Psychological

  • Individual
  • Couple
  • Combination

Medical

  • Rarely includes the partner in assessment or treatment

Combinations

Psychological Treatment

  • Primary goals
  • Support
  • Normalization
  • Permission giving
  • Sex education
  • Stress reduction
  • Symptom removal
  • Improved communication (sexual & other)
  • Attitude change
  • Helping to make sex fun

Most common approaches are cognitive-behavioral, also the most researched and supported

Cognitive: Identifying and challenging irrational or unreasonable beliefs, attitudes, expectations

Behavioral: Sensate focus exercises

Most involve sex education

  • Learning what's "normal"

Improve communication

  • Learn and communicate about each other's desires and fears s

Important to work within the individual's or couple's value system

  • Important to be non-judgmental
  • You must be comfortable talking about sex
  • Any sign of your discomfort will make it more difficult for them to talk
  • How comfortable are you?
  • How do you know?

It will be difficult for many clients to talk about their sexual problems

  • Where were they supposed to learn to be comfortable discussing sex?
  • At home, school, with friends or family?
  • Where did you learn to be comfortable?
  • Admitting to sexual problems is even more difficult
  • Especially for men
  • Gets more difficult the longer the problem has existed

Few seek help for sexual problems

  • 20% of women 10% of men (NHSLS)

Need to identify individual or relationship issues that may cause, maintain, or exacerbate the sexual problem

Individual

Relationship Issues

  • Can be the cause, effect, or both of sexual problems
  • Sexual boredom
  • Dislike of partner
  • Anger, Fear
  • Power differences, control issues
  • Fallen out of love
  • Lack of sexual attraction
  • Infidelity
  • Disappointment
  • Perceived selfishness
  • Money, kids, in-laws
  • Different values or interests
  • Abuse
  • Partner's psychological disturbance

Sensate Focus

  • Developed by Masters and Johnson
  • Guided couple's exercises
  • Both diagnostic and therapeutic
  • In vivo systematic desensitization
  • Early exercises designed to be more sensual than sexual

Designed to

  • Reduce stress, expectations, and spectatoring
  • Increase sexual pleasure

Designed to help couples

  • Identify what pleases them and their partner by focusing on their own and their partner's bodily sensations
  • Improve sexual communication
  • Take time for their sensual pleasure
  • Go back to a place when sex was fun and satisfying

Sensate Focus

  • Done in private
  • Includes prescriptions and proscriptions
  • Is gradual, beginning with non-genital touching
  • Usually precedes more disorder-specific exercises
  • Is individualized to the couples
    • Where they are starting from
    • The nature of their problem(s)
    • Their response to each exercise

Desire Disorder

  • Difficult to treat
  • Prognosis is better when etiology is apparent
  • No empirically validated treatments
  • Approach usually depends on assumed etiology
    • Primary vs. secondary
    • Generalized or partner specific
    • Individual vs. couples' therapy
    • Medical (e.g., estrogen) vs. psychological
  • Often requires lengthy individual and/or couples' therapy

Sexual Aversion

More common in women

  • Prevalence unknown

More serious than desire disorder

  • More often associated with significant individual psychopathology
  • History of abuse, rape or other trauma
  • More often associated with significant relationship problems
  • Severe anger, distrust, infidelity

Difficult to treat

  • Symptomatic partner may have little motivation
  • Almost always requires lengthy individual and/or couples' therapy

Arousal Disorder

  • Medication sometimes helpful
  • Psychological interventions
    • Individual psychotherapy
    • Treat historical issues or Axis I disorders that are etiologically significant
    • Couples' counseling
    • Sensate focus
    • Treat communication and other relationship issues believed to cause or maintain the disorder

Female Sexual Dysfunctions

Vaginismus

  • Good prognosis
  • Dilation
  • Relaxation
  • Kegel exercises
  • Partner involvement

Primary Anorgasmia

  • Good prognosis
  • Directed Masturbation
  • Sensate focus
  • Systematic Desensitization (~)

Secondary Anorgasmia

  • Guarded prognosis
  • Sex education
  • Sexual skills training
  • Communication training
  • Directed masturbation (~)

Dyspareunia/Vaginismus

Treatment:

  • Multidisciplinary
  • Need a physician who understands and treats these problems
  • Cognitive-behavioral therapy:
  • Vaginal dilation (Vaginismus)
  • systematic desensitization
  • couples counseling

Erectile Dysfunction

  • Oral medications
    • PDE-5 Inhibitors
    •  
  • Prostheses
    • Rigid, Semi-rigid, Inflatable
  • Psychological
    • Sensate focus
    • Systematic desensitization
    • Sex education
    • Communication training

Premature Ejaculation

  • Medication
    • E.g., Clomipramine
  • Psychological
    • Sex education
    • Normalizing PE
    • Blueprint alternatives
    • Cognitive-behavioral
    • Squeeze
    • Stop-start
    • Do better in short-term than long-term

APA Reference
Staff, H. (2021, December 27). Assessment and Psychological Treatment of Sexual Dysfunctions, HealthyPlace. Retrieved on 2025, April 29 from https://www.healthyplace.com/sex/main/assessment-and-psychological-treatment-of-sexual-dysfunctions

Last Updated: March 26, 2022

What To Do If You've Been Sexually Assaulted

10 Things Anyone Can Do To Help Prevent Sexual Assault

  1. Be aware of language. Words are very powerful, especially when spoken by people with power over others. When we see women as inferior, it becomes easier to treat them with less respect, disregard their rights, and ignore their well-being.
  2. Communicate. Sexual violence often goes hand in hand with poor communication. Our discomfort with talking honestly and openly about sex dramatically raises the risk of rape. By learning effective sexual communication -- stating your desires clearly, listening to your partner, and asking when the situation is unclear - you can make sex safer for yourself and others.
  3. Speak up. You will probably never see a rape in progress, but you will see and hear attitudes and behaviors that degrade women and promote rape. When your best friend tells a joke about rape, say you don't think it's funny. When you read an article that blames a rape survivor for being assaulted, write a letter to the editor. When laws are proposed that limit women's rights, let politicians know that you won't support them. Do anything but remain silent.
  4. Support survivors of rape. Rape will not be taken seriously until everyone knows how common it is. By learning to sensitively support survivors in their lives, we can help both women and other men feel safer to speak out about being raped and let the world know how serious a problem rape is.
  5. Contribute Your Time and/or Money. Donate your time or money to an organization working to prevent violence against women in our community.
  6. Organize. Join an organization dedicated to stopping violence against women. Men's Anti-Rape groups are powerful in the fight to end sexual violence.
  7. Talk with women... about how the risk of being raped affects their daily lives; about how they want to be supported if it has happened to them; about what they think men can do to prevent sexual violence. If you're willing to listen, you can learn a lot from women about the impact of rape and how to stop it.
  8. Talk with men... about how it feels to be seen as a potential rapist; about the fact that 10-20% of all males will be sexually abused in their lifetimes; about whether they know someone who's been raped. Learn about how sexual violence touches the lives of men and what we can do to stop it.
  9. Work to end ALL oppression. Rape feeds off many other forms of prejudice -- including racism, homophobia, and religious discrimination. By speaking out against any beliefs and behaviors, including rape, that promote one group of people as superior to another and deny other groups their full humanity, you support everyone's equality.
  10. Always make sure it's consensual. If you're going to have sex, make sure that it's consensual. Consensual sex is when both partners are freely and willingly agreeing to whatever sexual activity is occurring. Consent is an active process, you cannot assume you have consent - you need to ask. Consent cannot be given legally when an individual is intoxicated.

What to do if...you are sexually assaulted

The police can take you to the hospital if you need a ride OR call the Rape Crisis Center in your area for an advocate to help you through the process and join you at the hospital.

  1. Find a Safe Place. Get to a safe place - anywhere away from the attacker. Call someone you trust, such as a friend, relative, or police officer to come meet you.
  2. Get Medical Attention Immediately. You may have injuries that aren't yet evident. Even if you have no physical injuries, immediate medical care is important to reduce risks of pregnancy or sexually transmitted disease. You do not have to press charges if you seek medical attention.
  3. Preserve Evidence. You don't have to decide if you want to prosecute right away, but preserving the evidence helps if you decide to prosecute at a later date.
    • Don't bathe or brush your teeth
    • If you have already changed your clothes, place them in a paper bag (NOT plastic) to preserve them.
    • To preserve evidence, ask the hospital to conduct a rape kit exam. If you suspect that you may have been drugged, ask for a urine sample to be collected.
  4. Get Professional Help. Getting help does not mean you have to prosecute. Professionals trained in crisis intervention are available free to UB students (see info below). As you are considering your options, it is vital to remember:
    • It is not your fault
    • Every rape or sexual assault is different
    • It doesn't matter what you did or did not do during the assault
    • Healing from a sexual assault takes time
    • It is never too late to get help, even if the assault happened years ago.
  5. Report the Assault. If or when you are ready, you can report the assault to the police.

Someone you know is sexually assaulted

  1. Believe Them. Listen to them, be there, support them, and don't be judgmental.
  2. Help them understand their options (see above).
  3. Encourage them to seek medical help and contact law enforcement . . . if they permit you to. It is their decision.
  4. Be patient. This will take time for your friend to process and to heal. Encourage them to contact a Rape Crisis Center or the police for assistance.

You have witnessed a sexual assault

  1. Contact the police.
  2. If you have information regarding a crime that took place in the past, you can still contact the police, and even report it anonymously.
  3. Get help, if you need it. Talk to an adult or school counselor.

Frequently Asked Questions

Who needs to know?
You have the right to choose who you tell. You may consider talking to a trusted friend or family member, a trained counselor or the police.

Will my parents be called?
Not without your permission, unless you are under 18 years of age. In the case of a life-threatening emergency, the hospital may call your closest relative.

How can you keep the person who hurt me away?
A report would need to be filed with the police. Orders of protection can be obtained through police and legal system.

Do I have to go to court?
Only if you want to press charges and you don't have to make that decision right away. The police or district attorney's office can explain that in more detail.

Will the person who hurt me know I talked to the police?
Only if you prosecute the person who hurt you.

What if I know someone who has been assaulted?
You can file an anonymous report with the police department

What if I have a pregnancy, HIV/STD or injury concerns?
You can go to any local emergency room for testing, medical care and emergency contraception. Local Planned Parenthood offices can also assist.

APA Reference
Staff, H. (2021, December 27). What To Do If You've Been Sexually Assaulted, HealthyPlace. Retrieved on 2025, April 29 from https://www.healthyplace.com/relationships/teen-relationships/what-to-do-if-you-have-been-sexually-assaulted

Last Updated: March 21, 2022

Vulvodynia

Victoria is a 36-year-old housewife living in Arizona, where her medical nightmare began. By all appearances she is the perfect model of the TV soccer mom, with a boy, 10, a girl, 7, a comfortable house in the suburbs and a 1998 Dodge 7-passenger minivan. Victoria also has a common, but relatively unknown disease, one that consumes her life. It is a disease with no cure - a disease that until recently had no name. It is a malady so personal, that Victoria won't discuss it with her closest friends or relatives, yet one afflicting 20 million or more American woman.

Victoria has "Vulvodynia" - a constant burning and irritation in the mouth of her vagina. She cannot wear pantyhose or jeans. She is extremely uncomfortable sitting or even standing for long periods. Victoria describes it as "'like a particularly painful and irritating yeast infection that never goes away." She's been forced to live with the pain and discomfort for years, because doctors at first misdiagnosed her condition, a too typical occurrence, and then could not find anything to relieve her symptoms. For Victoria, the symptoms of Vulvodynia first appeared in her late twenties, after the birth of her second child. But she thought these might be normal symptoms after giving birth.

Sexual play and intercourse are intolerable. She went to her family physician thinking she had a bladder or yeast infection. However, the doctor who performed the pelvic exam found no abnormalities. She tried her gynecologist, who found red blood cells in her urine and referred her to a urologist. The urologist determined that she had a urinary tract infection, although cultures of the urine showed no bacteria. He started Victoria on antibiotics.

"Because I didn't have an infection the antibiotics didn't help," said Victoria. "I was desperate - and desperately uncomfortable. I couldn't take part in daily living, it seemed." In her desperation, she went to a series of new gynecologists and even tried consulting a psychologist after being convinced by a gynecologist that the whole problem was "in her head."

Finally, she worked her way from one doctor referral to another until she met Dr. James Brown*, a gynecologist recommended by her family doctor. Dr. Brown diagnosed Victoria with "Vulvodynia." In medical terms, it sounded clear cut to Victoria. The doctor told her that Vulvodynia is a female medical syndrome of chronic vulvar discomfort characterized by complaints of burning, stinging, irritation or rawness.

Then he told her what she didn't want to hear -- that there was no known cure. "We've been studying this disease for the past century, but most intensely during the past 25 years. It is still not clear whether this is a neurological, dermatological, gynecological, urological, immunological, metabolic or infectious disease. There is ongoing research into the cause and effective treatments for Vulvodynia in all of these areas.

"There also appears to be some overlap with this disease and some other chronic conditions such as fibromyalgia (which is a painful muscle condition with chronic fatigue and flu-like symptoms), migraine headaches, and the irritable bowel syndrome." He said, "The current treatments include surgery, biofeedback, interferon injections, low oxalate diet, antifungal medications, and chronic pain therapies."

The frequency of Vulvodynia in the U.S. is still unknown, but it is believed to be widespread, possibly affecting one in seven women. It is rarely mentioned in surveys on women's health problems and is not known to many physicians or included in most medical school curricula. In a 1991 report in the American Journal of Obstetrics and Gynecology, Dr. M.F. Goetsch estimated it to be in as high as 15 percent of women. However, the accuracy of such numbers is questionable since it is so often unrecognized or misdiagnosed. Research reports on Vulvodynia are scarce. The National Institutes of Health convened a workshop on the subject in April 1997, and published the proceedings of this forum.

There are two national groups, the National Vulvodynia Association (NVA) and the Vulvar Pain Foundation (VPF), both of which offer peer counseling and support through local chapters. The National Vulvodynia Association, located in Maryland (301-299-0775), also promotes education of the medical community and the public about this disease. Similarly, the Vulvar Pain Foundation located in North Carolina (336-226-0704), supports research and education in the area of vulvar pain.

In searching the Internet, Victoria did discover the National Vulvodynia Association, which she jointed and began attending meets in her area, where she met many women with the same problem and learned that she was not alone with this condition. The also found out about the Vulvar Pain Foundation from her peers and wrote to them for information on the treatment of this condition.

In these support groups as well as with any individual therapy, it is recommended that meetings are held jointly with husbands/partners. The reason is that any sexual dysfunctional condition is disturbing to a marriage and both partners are affected. Sex is equated with love and either consciously or unconsciously men may come to believe that their partners are using this pain as an excuse to avoid sex. Often there is a lack of communication about the problem and they come to avoid discussing it rather than to rock the relationship.

They become frustrated with the failure of medical professionals to provide satisfactory solutions to the problem and both find it a threat to their self-images as a man or woman. Either of both partners may become depressed about their inability to enjoy sexual intercourse. Sex therapists who deal with this problem advise their clients to continually reassure each other that their love remains strong to reinforce these statements with frequent physical contact such as hugging, kissing, massage and oral sex.

Finally, both should continue to aggressively seek answers to this problem. For this demonstrates that their libidos are not declining due to the depressive aspects of this situation.

There are various treatments being tried to cure Vulvodynia - with limited success for some patients. "Vestibular vestibulitis" seems to be a specific sub-group of Vulvodynia, which is a most frequent cause of painful intercourse in premenopausal women. There is pain on touch or vaginal entry; exquisite tenderness to a cotton swab lightly touching the vestibular area (known as the "swab test"); and physical findings confined to vestibular redness. Women with vestibular vestibulitis cannot tolerate insertion of a speculum, manual foreplay or active intercourse. This specific condition is most commonly recognized by physicians and has been treated successfully in some cases with surgical removal of the involved area. However, surgery remains a drastic solution of last resort.


There are a large number of women who do not have localized pain or redness where most physicians search for an infectious cause. These would include candida (a fungus), human papilloma virus, and herpes simplex. Or failing to find any evidence to support this line of investigation, skin conditions would be considered next, such as lichen sclerosis or inflammatory reactions. Finally, nerve damage causes of pain would have to be evaluated including conditions called pudendal neuralgia and reflex sympathetic dystrophy.

Recently, Dr. Clive C. Solomons, Ph.D., a biochemical researcher discovered that oxalate, a substance known to cause irritation and burning in tissue was present in abnormally high amounts in urine and was associated with pain experienced in different parts of the body. Further research led to the development of a non-surgical treatment that was effective in reducing pain in the majority of participants in the study.

Dr. Solomon tests the urine of his patients to determine if it contains an excess of oxalate. Then he uses dietary restriction of oxalate with calcium citrate and Vitamin C to lower the oxalate levels. High oxalate foods include spinach, sweet potatoes, nuts, chocolate, celery, etc. are forbidden. Dr. Solomon stated that the gynecologists who do the excisional surgery on the patients with vulvar vestibulitis do not like his medical therapy because it is taking away business.

Unless a specific cause can be determined, the treatments become trial and error, as in Victoria's case. Thus, the first line of significant treatment is often with antidepressants or anticonvulsants used to treat chronic pain syndromes. These include such drugs as Amitriptyline, Pamelor, Norpramin and Neurontin. It is difficult to determine the success rate in using this type of drug therapy because the number of cases studied is small and some spontaneous cures do occur.

Mindy is another example of the trial and error nature of the cure. She had a different situation. Mindy is a 60-year old post-menopausal female who is the mother of four and who has had problems with repeated yeast infections for the prior ten years before she was told that she had Vulvodynia. Several physicians told her that the problem with pain and burning in the vagina was due to estrogen deficiency.

She was treated with estrogen cream and testosterone creams, but these merely aggravated her problem because they come in an alcohol base which she finds intolerable. She was also giving a cortisone cream in an alcohol base that set her vagina on fire and sent her screaming into a cool tub of water. Currently, she is on hormonal replacement therapy consisting of Premarin and Provera. After taking this for a month her symptoms subsided and she thought that this was the answer, but it was only a temporary reprieve. Next, she tried avoiding chocolate and this too worked only for a brief period. Finally, she went to meetings of the support groups and learned about other treatments the participants had tried. There was a surgical treatment for vulvar vestibulitis with the removal of the diseased area. This had been either partially or completely effective in some women, but not in all and Mindy's condition seem to be more diffuse.

Mindy met several women in the support group who claimed the low oxalate diet and calcium had been effective in controlling their pain. Dr. Solomons reported 80 percent of over 1200 patients respond to the treatment. So Mindy purchased the low oxalate diet booklet produced by the VPF support group and began to religiously adhere to the restrictions on her food intake as well as take supplemental calcium.

After several weeks there was a dramatic improvement in her pain symptoms. However, this lasted only about a month and then the discomfort and pain recurred with no change in the type of diet she was following.

At this point, she decided to investigate other methods of chronic pain control such as biofeedback to relax spastic pelvic muscles. "Biofeedback" is an electronically assisted measurement of physiological processes such as blood pressure, pulse rate, and muscle contraction. With the aid of computers, a specific process is translated into an auditory or visual signal which the patient learns to control by modifying their body's response. For example, a light turns off when the patient relaxes a certain muscle. Dr. Howard Glazer, Ph.D., applied biofeedback techniques to Vulvodynia and vulvar vestibulitis to relieve tension in pelvic muscles. In the first 35 patients treated with this technique, he reported a reduction in pelvic pain in 80 percent. Slightly over 50 percent were pain-free at the end of the treatment and remained pain-free at six-month follow up. Unfortunately, Dr. Glazer works in New York City and Mindy was unable to leave her job in Virginia to travel there for an attempt to test the effectiveness of this technique on her disease.

However, at a later meeting of the support group she learned of a new treatment using magnets inserted in pads which are sewn into the underpants to cover the vulva. Such magnets are used by arthritis patients to relieve joint pain and swelling. Initially, these magnet pads were being supplied free of charge for all who wished to try them But there were so many volunteers, that more pads had to be obtained. But this is not part of a controlled medical study where some get non-magnet pads and others the real thing so that the difference can be compared. This kind of scientific study seems to be in short supply in Vulvodynia treatment.

Dr. Julius Metts described several illustrative cases in his March 1999 article, "Vulvodynia and Vulvar Vestibulitis," in American Family Physician. The first case was a 23-year-old woman treated twice for a suspected urinary tract infection while traveling in Europe. On returning home, she continued to have pain and urgency on urination with vaginal soreness, slight itching and painful intercourse.

Urinalysis and cultures of the urine, vagina and cervix were all normal. During the next two months, the patient went to emergency departments twice and visited four different family physicians. She was treated with numerous antibiotics for presumed cystitis. She was also treated with oral and topical antifungal agents with only temporary relief. During the next two months, she experienced painful intercourse with intermittent vulvar pain and irritation. She subsequently saw four gynecologists, a urologist, and two primary care physicians.

Pelvic exam revealed an area of redness in the back of the vagina and mild tenderness to the swab test. She was treated with an another antibiotic for possible cervicitis. She was then given a diagnosis of Vulvodynia and was prescribed gradually increasing dosages of amitriptyline, along with oral calcium gluconate, and a low-oxalate diet. She was referred to a support group and to a physical therapist specializing in women's health problems for pelvic strengthening, relaxation training and biofeedback training. Over the next three months, she reported a 70 to 90 percent improvement in her symptoms with occasional mild exacerbation.


The second case was a 45-year old woman with a history of one term pregnancy who developed urgency, redness of the vulvar area and irritation at the base of the clitoris that began suddenly after intercourse. Subsequent symptoms included burning, rawness and painful intercourse, which increased with walking and sitting, and also increased one week before menses. The use of an antifungal cream caused further burning and irritation.

Over the next five months, the patient saw a nurse practitioner and two family physicians. She received treatment numerous times for yeast vaginitis and bacterial vaginosis with topical medications. Any improvement was temporary, and symptoms invariably returned. Vaginal cultures grew normal organisms, and no yeast was detected by special exams.

Estrogen vaginal cream gave no significant relief. Over the following two months, the patient saw two gynecologists and was diagnosed with vestibulitis. She was treated with a steroid-antifungal cream for two months and felt improvement in the first week, but later developed further irritation of the vulvar and clitoral area. No biopsies were performed. She was referred to a third gynecologist, who instructed her to stop all topical medications. She began taking calcium citrate, started a low-oxalate diet and was referred to a vulvar pain support group. Over the next year, she was treated with an oral antifungal agent for four months.

She also began biofeedback training and physical therapy for pelvic muscle relaxation and strengthening. The patient underwent a total of two and one-half years of treatment. During her last year of treatment, she experienced a 90 percent improvement in symptoms.

Thus, as these cases illustrate, Vulvodynia is a relatively common disease, which is often misdiagnosed but can often be successfully treated using an array of treatments. It is now well accepted that the pain is real - even when a precise cause cannot be determined. The causes, frequency and search for successful treatment require more investigation and controlled scientific studies, rather than the trial and error methods currently employed. For more information, and/or to find a physician in your area knowledgeable about Vulvodynia, contact either the National Vulvodynia Association or the Vulvar Pain Foundation. A Medline search of the National Library of Medicine will also provide many sources of information and contacts with those studying or suffering from this condition.

TREATMENTS FOR VULVODYNIA

  • Surgery for localized vestibulitis

  • Nerve blocks

  • Injections of Interferon

  • Biofeedback to relax pelvic muscles

  • Tricyclic antidepressants and anticonvulsants for chronic pain

  • Low oxalate diet

  • Estrogen replacement for hormone deficiency

  • Topical anesthetics and steroids

  • Testosterone topically for lichen sclerosis

SUPPORT GROUPS FOR VULVODYNIA

National Vulvodynia Association
P.O. Box 4491
Silver Spring, MD 20914-4491
(301) 299-0775

Vulvar Pain Foundation
P.O. Drawer 177
Graham, NC 27253
1-910-226-704

International Pelvic Pain Society
Women's Medical Plaza Suite 402
2006 Brookwood Medical Center Drive
Birmingham, AL 35209
1-800-624-9676

APA Reference
Staff, H. (2021, December 26). Vulvodynia, HealthyPlace. Retrieved on 2025, April 29 from https://www.healthyplace.com/sex/female-sexual-dysfunction/vulvodynia

Last Updated: March 26, 2022

Vaginismus: Women Who Can't Have Intercourse

Mary, age 25, has been married for one year. While she and her husband are very much in love, they share a secret they have told no one. Despite numerous attempts, they have been unable to have sexual intercourse. She has also never been able to insert a tampon or finger into her vagina.

Betsey, age 32, confides in her gynecologist that while she is able to have a pelvic exam, she and her boyfriend have been unsuccessful in having sexual intercourse. Upon further questioning, her doctor learns that Betsey is still a virgin.

What Mary and Betsey have in common is a condition called vaginismus. Vaginismus is an involuntary spasm of the muscles surrounding the vaginal opening which occurs whenever an attempt is made to penetrate the vagina. For some women, such as Mary, any attempt to insert anything into the vagina is unsuccessful. For other women, such as Betsey, certain types of penetration can occur without pain or discomfort, such as putting in a tampon or undergoing a pelvic exam, however, when intercourse is attempted, penetration is impossible.

What causes this to occur? In most cases, this is not due to a physical deformity or disorder. Instead, it is an emotional condition that occurs because of psychological reasons but manifests itself in a physical response. The majority of women with vaginismus believe that intercourse will be very painful; often thinking that their vagina is too small to accommodate the penis and therefore, their vagina will be ripped or stretched too far. Consequently, they develop a phobic response to the penis; associating it with pain. Other women have indeed experienced some type of trauma to the vagina or genital region, such as rape, sexual abuse, or surgery, which then leads to a fear of intercourse. And, unfortunately, for some women, it is their first pelvic examination that causes them to be fearful. Lack of sensitivity on the physician's part, or neglecting to adequately inform the patient what she can expect, has sometimes contributed to the pelvic exam being a negative experience for women; causing them to fear sexual intercourse.

Sometimes the type of relationship a woman has with her partner or the feelings she has about the relationship interfere with her ability to have intercourse. Women who do not feel physically or emotionally safe with their partner may "shut down" via their bodies. In these cases, vaginismus is not a conscious decision but is a consequence of a desire to protect their bodies and themselves.

Some women who have been brought up to believe that sexual intercourse is wrong to engage in before marriage, or have conflict regarding sexuality and behaving sexually may also find themselves having difficulty with intercourse. Not having intercourse protects these women from doing something they feel wrong doing. For some women, it is the possible consequences of intercourse (pregnancy, childbirth, or sexually transmitted diseases), that make them fearful.

However, in a small number of cases, physical factors (such as the presence of a rigid hymen, or deformities of the vagina) can make penetration of the vagina impossible. Additionally, although physical conditions, such as endometriosis, vaginal infections, or an episiotomy are not directly responsible for a woman experiencing vaginismus, they may, through association, contribute to vaginismus indirectly through conditioning. What this means is if a woman experiences pain upon intercourse, or with a pelvic exam, this may lead to a self-protecting tightening of the vaginal muscles the next time she attempts to have intercourse.

Many women who suffer from vaginismus believe this problem is unique to them. There is a tremendous sense of shame and embarrassment at not being able to do something that is perceived as being simple and natural. A large number of women who eventually seek help admit they have never confided in anyone for fear of being ridiculed and humiliated. In their relationships with their partners, women with vaginismus often experience feelings of guilt and inadequacy. Over time, if they continue to fail in their attempts to have intercourse, many couples eventually decide to stop trying. The inability to be successful and establish a full sexual relationship usually places significant strain on the relationship as a whole.

It is important to know that there is help available for overcoming vaginismus. A key factor, however, is knowing where to get help. Unfortunately, there are still some physicians and gynecologists who may not be very sensitive to a woman's concerns or see the problem as simply one of "needing to relax" or "not worrying." If this is your experience, seek out another physician or gynecologist who understands what vaginismus is. Even if he or she does not treat vaginismus, they should be able to refer you to someone who does, such as a sex therapist. A sex therapist may be a psychologist, social worker, psychiatrist, or nurse who specializes in problems dealing with sexuality and sexual functioning. If your doctor does not know of someone like this, you may want to check with major hospitals and/or medical schools to see if they offer sex therapy services. You can also contact the American Association of Sex Educators, Counselors and Therapists in Chicago at 312-644-0828 for a listing of certified sex therapists in your state.

Treatment for vaginismus consists of a combination of relaxation training and various behavioral exercises in helping the woman overcome her fear of intercourse. The husband or partner's participation in treatment and his emotional support are considered very important to the success of treatment. Sometimes, in addition to the above treatments, individual and/or couples therapy is recommended as well. In the majority of cases, treatment is successful and couples are able to move on to develop and enjoy a sexual relationship that is satisfying to them.

SOURCES: LoPiccolo, Joseph, & Schoen, Mark. Treating Vaginismus. (Videotape). Available through Focus International. (1-800-843-0305). Valins, L. (1992). When A Woman's Body Says No To Sex: Understanding and Overcoming Vaginismus. New York: Penguin.

APA Reference
Staff, H. (2021, December 26). Vaginismus: Women Who Can't Have Intercourse, HealthyPlace. Retrieved on 2025, April 29 from https://www.healthyplace.com/sex/female-sexual-dysfunction/vaginismus-women-who-cant-have-intercourse

Last Updated: March 26, 2022

Enjoying Sex Throughout Your Pregnancy

It all started with making love. But now that you're pregnant, sexual intimacy might not be foremost on your mind: Your belly is ballooning and your mind is busy mulling nursery designs, so it's not unusual for sex to drop a few notches on the priority list.

But putting a little effort into your sex life before the baby arrives is worthwhile, says Laura Berman, Ph.D., a sex therapist and director of the Berman Center, a women's sexual-health center in Chicago. "The challenges of impending parenthood start during pregnancy, so it's a good time to work on maintaining that connection," she says.

And not just for the physical pleasure of it. Sexual intimacy, Berman explains, helps you feel emotionally connected to your partner. "That emotional connection is crucial to a healthy relationship between mother and father, which is the greatest gift you can give your child," she says.

Think of sex during pregnancy as a warm-up for the challenges to come. Once your baby is born, exhaustion, privacy issues and lack of time will be exacerbated, whether it's your first child or your third. And if you abstain from sex, Berman says, it can be tougher to re-establish intimacy later. If keeping that connection isn't enough motivation, consider the immediate benefits that sex offers. "Sex releases endorphins, relaxes muscles and helps you sleep," she says.

Common fears that intercourse could harm the baby aren't warranted in most healthy pregnancies, but certain conditions do require caution, says Jennifer Berman, M.D., Laura Berman's sister and director of the Female Sexual Medicine Center at the University of California, Los Angeles, Medical Center. "Sex is not considered safe when a woman has placenta previa [a condition in which the placenta lies low in the uterus] or an incompetent cervix, or if she is having preterm labor," she says. In these cases, consult your doctor.

On the other hand, a history of miscarriage doesn't necessarily mean sex is out of the question, Jennifer Berman says, but talk with your doctor to be sure. And don't forget that there are other ways to be close, such as cuddling and kissing.

Finally, if the only thing holding you back is that big belly, be creative. One position that works for some pregnant women is lying on one side with their partner "spooned" behind. From there, let your imagination be your guide.

Can sex bring on labor?

In a word: Yes. "However, intercourse will only trigger labor if you are close to or past your due date," says Jennifer Berman, M.D., who is co-host with her sister, Laura, of Berman & Berman, a sexual-advice show on Discovery Health Channel. There are three contributing factors:

* The uterine contractions that accompany orgasm

* Nipple stimulation, which releases oxytocin, a hormone that can trigger contractions

* Semen, which contains prostaglandin, another hormone that can trigger contractions

APA Reference
Staff, H. (2021, December 26). Enjoying Sex Throughout Your Pregnancy, HealthyPlace. Retrieved on 2025, April 29 from https://www.healthyplace.com/sex/women/enjoying-sex-throughout-your-pregnancy

Last Updated: March 26, 2022

Why So Many Women Don't Enjoy Sex

Sex sells. It makes everything--from cars to paper towels--more appealing. This quest for orgasm seems to be a major motivating force, but recent studies suggest that not everyone is oohing and ahhing like actors in shampoo commercials. In fact, studies show that a high rate of sexual dysfunction is wreaking havoc on relationships and that women suffer from it more than men. To help you achieve a healthier, happier sex life, we offer an overview of the latest research on sexuality. In our first installment, we talk to Laura and Jennifer Berman, The Sex Scientists, about why so many women can't enjoy sex. We also take an in-depth look at the where, how and why of one of the major goals-- an orgasm. Future components of SEX TODAY will explore other key factors such as arousal, aging, desire, diet, drugs, and exercise.

YOU KNOW THE CLICHE: A woman is so uninterested in sex that she makes a shopping list while making love. Jennifer and Laura Berman see such women all the time, and it's frustration--not boredom--that brings them to the Bermans' new clinic at UCLA.

"I was talking to a woman earlier today about her low libido, which was a result of the fact that she can't reach orgasm," says psychologist Laura Berman, Ph.D., who with her sister, urologist Jennifer Berman, M.D., is a founder and co-director of the Center for Women's Urology and Sexual Medicine clinic. "Because she can't reach orgasm, sex is frustrating. She feels a hopeless, fatalistic complacency about her sex life. When she's having sex, her partner picks up on that and feels rejected and angry, or notices she's withdrawing. Then intimacy starts to break down. Her partner feels less intimate because there's less sex, and she feels less sexual because there's less intimacy. The whole thing starts to break down."

Acknowledgment of sexual dysfunction in America is booming. But with all the attention on Viagra and prostate problems in men, most people would probably never guess that more women than men suffer from sexual dysfunction. According to an article in the Journal of the American Medical Association, as many as 43 percent of women have some form of difficulty in their sexual function, as opposed to 31 percent of men.

And yet female sexuality has taken a back seat to the penis. Before Viagra, medicine was doing everything from penile injections to wire and balloon implants to raise flagging erections, while female sexual dysfunction was almost exclusively treated as a mental problem. "Women were often told it was all in their head, and they just needed to relax," says Laura.

The Bermans want to change that. They are at the forefront of forging a mind-body perspective of female sexuality. The Bermans want the medical community and the public to recognize that female sexual dysfunction (FSD) is a problem that may have physical as well as emotional components. To spread their message, they have appeared twice on Oprah, have made numerous appearances on Good Morning America and have written a new book, For Women Only.

"Female sexual dysfunction is a problem that can affect your sense of well-being," explains Jennifer. "And for years people have been working in a vacuum in the sex and psychotherapy realms and the medical community. Now we are putting it all together." ;

No single problem makes up female sexual dysfunction. A recent article in the Journal of Urology defined FSD as including such varied troubles as a lack of sexual desire so great that it causes personal distress, an inability of the genitals to become adequately lubricated, difficulty in reaching orgasm even after sufficient stimulation and a persistent genital pain associated with intercourse. "We see women ranging from their early twenties to their mid-seventies with all types of problems," Laura says, "most of which have both medical and emotional bases to them." The physical causes of FSD can range from having too little testosterone or estrogen in the blood to severed nerves as a result of pelvic surgery to taking such medications as antihistamines or serotonin reuptake inhibitors, such as Prozac and Zoloft. The psychological factors, Laura says, can include sexual history issues, relationship problems, and depression.

The Bermans codirected the Women's Sexual Health Clinic at Boston University Medical Center for three years before starting the UCLA clinic this year. At present, they can see only eight patients a day, but each one receives a full consultation the first day. Laura gives an extensive evaluation to assess the psychological component of each woman's sexuality.

"Basically, it's a sex history," Laura says. "We talk about the presenting problem, its history, what she's done to address it in her relationship, how she's coped with it, how it has impacted the way she feels about herself. We also address earlier sexual development, unresolved sexual abuse or trauma, values around sexuality, body image, self-stimulation, whether the problem is situational or across the board, whether it's lifelong or acquired." After the evaluation, Laura recommends possible solutions. "There is some psycho-education in there, where I'll work with her around vibrators or videos or things to try, and talk about addressing sex therapy."

Afterward, the patient is given a physiological evaluation. Different probes are used to determine vaginal pH balance, the degree of clitoral and labial sensation and the amount of vaginal elasticity. "Then we give the patient a pair of 3-D goggles with surround sound and a vibrator and ask them to watch an erotic video and stimulate themselves to measure lubrication and pelvic blood flow," Jennifer says.


The identification of FSD has been called everything from the final frontier of the women's movement to an attempt by the patriarchy to shackle women's sexuality. But given the success that drugs such as Viagra (sildenafil citrate) have had in reversing male sexual dysfunction, the Bermans found an unexpected amount of criticism from their peers. "The resistance we got from the rest of the medical community early on was surprising to us," Laura says, explaining that the urological field, in particular, has been dominated by men.

Clearly, the Bermans will need hard data to win over their critics. Their UCLA facility is enabling the Bermans to conduct some of the first systematic psychological and physiological research on the factors that inhibit female sexual function. One of their first studies suggests that the pharmaco-sexual revolution that helped some men overcome their sexual dysfunction may prove less effective for women. Their initial study of the effects of Viagra on women found that Viagra did increase blood flow to genitalia and thereby facilitate sex, but women who took the drug said it provided little in the way of arousal. In short, subjects' bodies might have been ready, but their minds were not.

"Viagra worked half as often in the women with an unresolved sexual abuse history as in those without it," Laura says. "So it's just not going to work alone. Women experience sexuality in a context, and no amount of medication is going to mask psychologically rooted, or emotionally or relationally rooted sexual problems." Laura believes the results of the Viagra study counter those who contend that FSD is simply a tool of pharmaceutical companies to "medicalize" female sexuality.

"I'm less concerned about it, because I'm aware that it won't work," she says. "And in some respects, pharmaceutical companies are closing the divide between the mind and body camps of FSD. Clinical trials of new drugs for FSD are requiring psychologists to screen participants, and that is an acknowledgement that an accurate assessment of a drug's efficacy requires a consideration of the test subjects' feelings about sex. So these physicians who may not be motivated to bring on a sex therapist are now motivated to participate in a clinical trial, and then that model becomes the norm."

Currently, the sisters are working on MRI studies of the brain's response to sexual arousal, the place where mind and body meet. And although there is a lot more research to be done on FSD, identifying it as a problem has already made a significant impact on how women perceive their sexuality. "Women now feel more comfortable going to their doctors, and they're not taking no for an answer, not being told to just go home and have a glass of wine," explains Laura. "They feel more entitled to their sexual function."

READ MORE ABOUT IT:

For Women Only: A Revolutionary Guide to Overcoming Sexual Dysfunction and Reclaiming Your Sex Life Jennifer Berman, M.D., and Laura Berman, Ph.D. (Henry Holt & Co., 2001)

APA Reference
Staff, H. (2021, December 26). Why So Many Women Don't Enjoy Sex, HealthyPlace. Retrieved on 2025, April 29 from https://www.healthyplace.com/sex/women/why-so-many-women-dont-enjoy-sex

Last Updated: March 26, 2022

Telling Others You Are HIV Positive (Your Employer, Your Child's School)

This is an excerpt from There is Hope: Learning to Live with HIV, 2nd Edition, written by Janice Ferri, with Richard R. Roose and Jill Schwendeman, a publication of The HIV Coalition.

How to Tell Others You Are HIV Positive

There's really no easy way to tell someone close to you that you have a life-threatening illness. Test Positive Aware Network suggests the following approach for breaking the news to the "significant others" in your life (especially your parents):

1) Assess the reasons you want to tell your friends or family. What do you expect from them? What do you hope their reaction will be? What do you expect it to be? What's the worst possible reaction they could have?

2) Prepare yourself. Gather clear, simple, educational brochures, hotline numbers, pamphlets and articles on the disease. Take these with you to leave after your discussion.

3) Set the stage. Call or write and explain clearly that you have to meet with them to discuss something extremely important. This is a once-in-a-lifetime experience for all of you--don't treat it in an offhand or rushed manner.

4) Enlist help. Ask a close friend or family member who knows the situation to come along or write a letter to your folks asking them to try to understand and reminding them that their acceptance and support are vital. Ask your physician or therapist to write a letter to your folks as well. This can be most effective--many parents will believe or listen to a stranger before listening to their own child.

5) Be optimistic. Accept the possibility that your parents are caring and rational adults. Likewise, you need to be as caring and rational; having a chip on your shoulder or selling your parents short is not going to help win the support you need.

6) Let the emotion come through. You are not asking to borrow the family car. The prospects to be considered are as frightening for them as they are for you. Now is not the time to assume false fronts or joke away the more serious implications.

7) Let them know you are in good hands. Explain how you are taking care of yourself, that your physician knows what to do, that a support network exists for you. The single thing you are asking of them is love.

8) Let them accept or deny it in their own fashion. Do not try to change their position right there. Leave them the material and put an end to the discussion if things go very badly. Try not to revisit past discussions about lifestyle.

9) Give them some time to digest the information and adjust to the news. After a reasonable period of time, call them back to assess their reaction.

10) ACCEPT their reaction and move on from there.

Attempt to keep the lines of communication open. Approach the process of telling with the best expectations. Still, with all the preparation possible, there may be surprises. Be willing to pull out, pull back and give them some room. If you're prepared for the worst, the best will be a blessing. adapted from Positively Aware (formerly TPA News), July, 1990. Based on an article by Chris Clason. reprinted with permission.

Telling Your Employer You Are HIV Positive

Deciding if and when to tell your employer about your HIV status is an extremely important decision. Timing is everything. If you haven't had any HIV-related symptoms or illnesses and are not on medication that is affecting your job performance, there's probably no need to open up that particular can of worms.

If, on the other hand, your illness is interfering with your work such that your job might be in jeopardy, it's time to sit down privately with your boss and reveal your situation. Bring a letter from your doctor explaining the current state of your condition and how it might affect your ability to perform your job. (Keep a copy for yourself.) Let your boss know you want to continue to do your job to the best of your ability, but that because of the effects of your illness or medication, there are times when your schedule or workload may have to be adjusted. Because the law regards a person with HIV or AIDS as a disabled person, your employer is required to reasonably accommodate your needs if you are otherwise qualified to perform the essential duties of the job.

Ask your boss to keep your condition confidential, only notifying those people in the company who absolutely have to know. Illinois law requires this of anyone you tell, but many people (employers included) are not aware of their legal obligation. For your own protection, you may want to decide on a non-combative way to make the people you tell aware of this. Again, it's always a good idea to have a few pamphlets or hotline numbers available to help your employer understand your illness and locate resources.

Once you present the facts of your condition to your employer in this manner, you may be protected from job discrimination under the Americans with Disabilities Act (ADA), the Illinois Human Rights Act, and local ordinances. As long as you are able to do the essential functions of your job, your employer cannot legally fire you, demote you, refuse to promote you, or force you to work separately from others on account of your condition. Depending on the state in which you live, your employer may not be able to limit your medical benefits or life insurance coverage. (Remember, it's important to carefully document any communication with your employer or questionable incidents on the job for future reference.)

If you're applying for a job, be aware that under the ADA, prospective employers do not have the right to make inquiries about your health or the existence of a disability prior to a conditional job offer. However, they may inquire if you are aware of any physical limitation that would interfere with your ability to perform the essential job functions.

If you are asked on an employment application or in an interview whether you have HIV, any symptoms of AIDS, or even whether you are associated with anyone else who does, it's best to tell the truth or decline to answer. Although the employer has violated the ADA, you do not want to raise the matter at this time. An employer may not legally refuse to hire you based on your perceived or actual HIV status. If you do not get the job, you may have an easier time proving discrimination if the employer had knowledge of your status. You would also be better protected from on-the-job discrimination if hired.

Employers can request a medical examination only after a conditional offer of employment has been made, and when two other conditions apply: the request can be shown to be job-related, and the same examination is required of all other entering employees of the same classification. All medical information obtained by the employer must be kept confidential.

Keep in mind that you cannot be forced to take an HIV test as a condition for getting or keeping a job. However, many HIV-positive people are also active users of illegal drugs. While the ADA protects you from discrimination based on your HIV status, it does not protect you from discrimination based on drug use. Pre-employment screening for illegal drugs is permitted, and an employer or prospective employer may terminate or refuse to hire you based on drug test results.

After July 26, 1994, all employers with 15 or more employees are subject to the provisions of the ADA. If you feel you have been discriminated against in any employment situation, consult an attorney to determine whether the ADA or any of several anti-discrimination laws apply to your situation.


Telling Your Child's School That Your Child is HIV Positive

You have probably heard horror stories about children who were kicked out of school, taunted or worse when their HIV status became known. Telling others about your child's HIV infection is nothing to rush into. However, it may be in your child's best interest to work with certain professionals from his or her school.

You'll want to schedule a meeting with the school's principal to ensure that the school has a good HIV policy in place, identify those who should be informed, and establish a working relationship between yourself and the school. Then, set up a second meeting with the principal, school nurse, and your child's classroom teacher.

Remind those you meet with that your child's HIV infection is confidential information by law and that improper disclosure could be answered with a lawsuit, which no one wants to see. Ask for an explanation of the school's policy on HIV and obtain a written copy. Find out what education has taken place or is planned to reduce the chances of negative responses in case word gets out there's an HIV-positive student in the school. Ask what steps will be taken to assure your child's confidentiality.

The school nurse should discreetly follow your child's progress, monitor side effects of medications needed during school days, and inform you when there is an outbreak of infectious disease. An informed teacher can reinforce developmental goals established for your child, keep an eye out for medication-related side effects, and observe and report possible physical or emotional problems.

Both you and the school need to be prepared for the possibility that others will learn about your child's HIV. In-service training for school staff and parents, along with age-appropriate education for students will help create a supportive environment. In the Chicago Public School system, the only criteria for exclusion from school are large open sores that can't be covered or aggressive behaviors that have the potential to spread HIV, such as biting. (However, to date, not a single person has been reported to have gotten HIV as a result of biting or having been bitten.) Your child also may be advised to remain out of school temporarily for his or her own protection if there are outbreaks of measles, chicken pox, mumps, or other dangerous infectious diseases. Children excluded from school or unable to attend because of health conditions are entitled to have a teacher assigned in the home.

Some Personal Perspectives on Telling Others You Are HIV Positive

It may also be helpful to know how HIV professionals and men and women who are living with the HIV/AIDS disease have dealt with telling others. Here are some of their perspectives.


As far as telling people goes, that's an individual decision. I personally think your doctor needs to know. If she or he can't handle the diagnosis, then go to a doctor who can.

You should only tell people whom you really know, who'll be on your side and be supportive, not judgmental. But realize there's only so much they can handle. They may be wonderful and loving and caring and open--but they're still going to be flipped out. This isn't movieland, it's the real thing. So you have to respect their need to be flipped out for a while. If you know the news is going to give someone a heart attack, don't tell them.

In terms of how to tell, just be direct. People know when you have something bad to tell them. The minute you say, "Let's talk"--they'll hear it in your voice. It can be a double coming out for a lot of people. I also think it's important to let the person you're telling know how you're handling it. That will give them some clue of how to deal with it.

There's no easy way to tell someone, and there's no such thing as breaking the news gently--because once the point comes across, it hits them like a hammer anyway. If you have to tell someone, just tell them you're HIV-positive, then ask if they have any questions. Then you can just answer yes or no, open up a discussion. That can make it a little easier on you because you don't have to reveal everything all at once. You can just answer questions a little bit at a time.

In the hospital, you can call in a professional, like the immunologist, to talk with the family and give them the straight story. Reassure them that even though you're sick, you are getting good care and will follow doctor's orders. A lot of people tell their families they have cancer, but the families always figure it out after awhile. Lying about this won't help anyone learn to face it any faster.
-- Dr. Harvey Wolf, Clinical Health Psychologist


If someone brings up telling their parents, I always say you'd better plan on supporting them first. They know less about this than you do. It violates the law of nature--kids don't die before their parents. That's what they'll be thinking, and you've just turned their world upside-down. You'd better be able to help them deal with it before you can expect to get any support back.

You'd also better be prepared to answer a lot of questions. I suddenly was faced with the fact that I was going to have to tell my family about my gayness. Now, it's out of your hands--you're "outed." The only control you've got left is when to tell, and how.

People at work have noticed the weight loss and they ask what's going on. I work among a relatively sophisticated, progressive group of people. I'm not afraid for the most part that they would go, "Eww! I can't work with this guy." But there are some people in the company who could react that way. I guess what I'm more concerned about is people treating me weird or talking about me, because as soon as people find out you're positive, they start to speculate: "Is he a junkie or is he gay? He certainly ain't Haitian! Transfusion? Hemophiliac?" I don't want all that hassle and mess. Most people won't pry, but some don't know when to stop.

If someone is being really nosy or prying, the temptation is to just lie and say no. But in most cases, my strategy has been to sidestep. I learned early on, the instant you start lying about things, it gets really complicated and awful. Now you've got to remember your lies, and back them up and embellish them. It's easier just to say, "It's none of your business."

With certain people you can be a little more subtle, because they have a better understanding of things like privacy. If someone were to ask me point blank, "What's the matter, Charlie--do you have AIDS?" I guess at this stage I'd have to say yes. Four years ago, I probably would've said, "What a question!" trying to deflect and make them feel ashamed for asking. Now, depending on who it is, if it's somebody I work with closely, I might say, "Well, sometime we'll talk about that, but it's really not appropriate right now." That's basically a "yes," but it's a "yes" that discourages further discussion then and there. Let them seek me out privately later.
-- Charlie


After my "stoic" period, there was a period of feeling very isolated. It made me want to be around my friends and talk about this a whole lot. At times, I wanted to tell everyone I was HIV-positive--just go to the top of the building and scream it.

Finding out any news like this that is health-related and mortality-related accentuates a lot of what you don't like or what irritates you about your partner. It also accentuates and brings to light a lot of what you don't like about yourself. All the old behaviors, fears, anxieties--attitudes you've been able to keep under control or channel in a slightly different way--that all comes gushing out and there's a lot of garbage that gets dumped on the dinner table. Sometimes, you almost feel like you're starting from scratch. Issues in the relationship you thought were resolved are triggered all over again in a slightly different configuration.
-- "Ralph"


I feel obligated to tell anyone who's interested in me that I'm HIV- positive before they get too interested. If they're going to get real interested in me, it's almost like betting on a three-legged horse. They're not gonna win in the way they might like. They can't have children with me; I'm not going to keep them company in their "golden years." I'm gonna be checkin' out long before then. I just feel like I have to let them know what they're getting into.
-- "Marie"


There are certain people in my life who I'm terrified to tell. I've had some real bad experiences. People who found out I had AIDS wouldn't let their kids play with mine or even come in the house. People have a very poor understanding of how the virus is spread. I figure, the fewer people I have to tell, the less I have to deal with.

Before I decide whether to tell somebody, I try to figure out why am I telling them. What is my reason. Once in a while, it's to get someone to feel sorry for me. Mostly it's to share it with them, or because they're close to me and kind of have a right to know.

People do treat me different once they know. Sometimes they're nicer to me. Not always. It kind of goes from one extreme to the other. Some people will totally stay away from you. They're out of your life for good. Others will try to be very supportive. There aren't too many people in the middle--it's one or the other. I haven't really had anyone come out and try to hurt me or be mean because I have it.

I know it's impossible, but I wish people could kind of disconnect me from my illness. Look at me, and if they want to judge me, fine--but don't keep bringing AIDS into it. Since most people can't separate the two, I really don't volunteer it much. I don't feel it's necessary for everyone to know about my illness.
-- George


You may think that telling would be too stressful, but in truth, the fear of people finding out will haunt you and the secrecy will cause you stress--stress that right now you don't need in your life. For me, to tell was to be set free.

Telling your children, though, that's hard. When I first came out with this, people asked what my sons knew and how they were dealing with it. I told them my sons knew nothing because this is what I thought, or at least what I wanted to believe.

Then one day, my little boy Shane looked up at me, pressed the ambulance button on his play telephone and said, "This is 911. I'll call 911 when you die." My heart broke a thousand times as I realized that he understood my illness all too well.

But now I knew that I could not protect my son from the fearful reality of possibly losing his mother. I was determined to keep Shane, and Tyler, when he gets older, from ever having to deal with the thought that AIDS is something bad people get and something you can't talk about. Shane now goes with me sometimes when I speak to groups about AIDS, and tells everyone there that AIDS is everyone's problem and no one's fault. And in his own way he knows that he is helping, and my heart smiles with love that tells me everything will be okay.
-- Shari


For those who are incarcerated, I would say tell your doctor so that in jail you can receive medical care and have your condition monitored. If you became infected because you've been abused, don't tell anybody other than the doctor. I would tell the doctor an abuse situation happened and identify the abuser. I wouldn't give permission to reveal my name, out of fear that in retaliation I'd lose my life. If telling would mean your life, don't tell. HIV can spread like wildfire in jails. We need to have access to condoms in jails, because there is sex happening. We need bleach, too, because there also are drugs in jail.
-- Annie Martin, Clinical Nurse Specialist, Cook County Women and Children's HIV Program


I was at a TPA meeting a few years back about who, when, and how to tell. The speaker and some other people were advocating that you should tell your parents, and some parents were there advocating that they had a right to know. As far as I'm concerned, nobody has a right to know anything about me that I don't want to tell them. I couldn't understand why everybody was so tied up in saying they had to tell their parents they were gay, or HIV-positive, or anything else. That is up to you. You don't have to tell anybody anything!
-- Steven


At first I thought a lot about, "What are my friends going to say? What is my family going to say?" Now, I just don't care. I know my family and they are with me. If others are my friends, they will stay. If not, they will go.
-- Gail


I still have a lot of fears and resentment about how people would feel about me, how they'd look at me if they knew. I work, and every day I go to work I am fearful: "What if somebody says or finds out something, and they all shun me?" When my daughter found out quite by accident that my partner was positive, she told her boyfriend. He said to her, "Don't you ever take the kids over to your mother's again!" That was even before they knew about me. So the rejection is the biggest fear. But truthfully, most of the close friends I've told have accepted me.
-- "Elizabeth"


In deciding who to tell, consider whether the person is able to keep your confidentiality, is mature, cares about you, is knowledgeable, honest, and open. Helping people learn more is important to me. I feel I was meant to have this disease, to educate people. My husband and I are interracial, and I think we were meant to be that way, too. God has given me this to tackle. We're all here for a purpose, to help each other.
-- Evie


I haven't told the neighbors in my apartment complex yet, because you never know how they'd take it, or how management would take it. It could be like their swimming pool, a big sign: "THIS DAY FOR ADAM ONLY." You never know, so you don't especially want to tell them.

If a stranger came up to me and asked if I had AIDS, I'd say it's none of their business. I'm not going to run around town waving a sign, "I've got AIDS!" It's a private, medical thing. You don't tell just anyone, but you tell the people you're close to.

Telling potential girlfriends is a big ordeal. The third date is about the right time to do it. You start out with the term "hemophilia," then work your way from that to "HIV." You have to start there because the word "AIDS" will send people diving out of third-story windows. You explain that it's a virus that may or may not kill you. You have to say "may or may not," because if you say it's definitely going to kill you, she won't stick around.

It's like the Paris Peace Talks; it's horrible. I dread that whole conversation. How do you say it in a nice way--in a way that will make her not run away? It makes dating a nightmare, because who wants to date if it's never going to lead anywhere? It's a shitty set of circumstances.
-- Adam


Some people have this image that the people they tell will get really hysterical and freak out and stuff, but what is more common is denial. All of a sudden, nobody talks about it. You can't get them to ask how you are. I go two months with no problems and my lover will go, "Are you sure you're sick? Do you think about it often?" And I'll say, "Every five hours, when I take a pill."
-- Jim


I wish I'd had something to help me decide whether to start telling people right away. That was my biggest thing. Right away you feel alone, scared, and then you wonder, "Should I tell my mother and father, should I tell my friends--and what friends shouldn't I tell?" You're afraid to tell your neighbors because they might burn your house down or something. I was very worried about my kids and how they might be teased at school, so I didn't tell them. I didn't tell my neighbors, either, but I figured maybe I should tell my immediate family.

I asked my doctor what she thought I should do. Should I just lie and say I have lung cancer, or should I come right out and tell everybody it's AIDS? She said I had to be the one to make that decision.

I still to this day don't think it's a great idea to run out and tell everyone. You want to share it with people, but then later, some of the aftereffects may not be worth it. I had an incident where my sister told a friend of hers who lives in Wisconsin, and the friend has a brother who lives in Las Vegas, and within a day or so they both knew. The brother just happened to be in town at a garage sale and he blurts out real loud to someone who knew me, "What's this I hear about Sam having AIDS?" It was supposed to be confidential. I had asked my sister to keep it within the family. Taught me a good lesson, I guess.
-- "Sam"

APA Reference
Staff, H. (2021, December 26). Telling Others You Are HIV Positive (Your Employer, Your Child's School), HealthyPlace. Retrieved on 2025, April 29 from https://www.healthyplace.com/sex/diseases/telling-others-you-are-hiv-positive-your-employer-your-childs-school

Last Updated: March 26, 2022

Caring for Someone With AIDS

Providing Emotional Support

You are caring for a person, not just a body; their feelings are important too. Since every person is different, there are no rules about what to do or say, but here are some ideas that may help.

  • Keep them involved in their care. Don't do everything for them or make all their decisions. Nobody likes feeling helpless.

  • Have them help out around the house if they can. Everybody likes to feel useful. They want to be part of the group, contributing what they can.

  • Include them in the household. Make them part of normal talk about books, TV shows, music, what is going on in the world, and so on. Many people will want to feel involved in the things that are happening around them. But you don't always have to talk, just being there is sometimes enough. Just watching TV together or sitting and reading in the same room is often comforting.

  • Talk about things. Sometime they may need to talk about AIDS or talk through their own situation as a way to think out loud. Having AIDS can make a person angry, frustrated, depressed, scared, and lonely, just like any other serious illness. Listening, trying to understand, showing you care, and helping them work through their emotions is a big part of home care. A support group of other people with AIDS can also be a good place for them to talk things out.

  • Invite their friends over to visit. A little socializing can be good for everyone.

  • Touch them. Hug them, kiss them, pat them, hold their hands to show that you care. Some people may not want physical closeness, but if they do, touch is a powerful way of saying you care.

  • Get out together. If they are able, go to social events, shopping, riding around, walking around the block, or just into the park, yard, or porch to sit in the sun and breath fresh air.

Read: Many ways to help someone living with AIDS

APA Reference
Staff, H. (2021, December 26). Caring for Someone With AIDS, HealthyPlace. Retrieved on 2025, April 29 from https://www.healthyplace.com/sex/diseases/caring-for-someone-with-aids

Last Updated: March 26, 2022

Many Doctors Don't Take Treating the Side Effects of Antidepressants Seriously Enough

Like most psychiatrists, I was excited in the late 1980s when drug manufacturers began introducing a new type of antidepressant called selective serotonin reuptake inhibitors (SSRI). These drugs, which include Prozac, and Paxil, offered tremendous relief from the devastating effects of depression with negligible side effects.

Unfortunately like many "wonder drugs," SSRI antidepressants have proven to be a mixed blessing. For the majority of depressed people, these medications offer a desperately needed bridge back from crippling and sometimes suicidal despair. But their record on side effects has not been so good. For some patients they have left daunting roadblocks to full recovery in the form of serious side effects, including physical and mental lethargy, loss of sexual drive and performance and significant weight gain.

These side effects erode the fragile wellness and self-esteem that most patients have been working so hard to rebuild. Faced with such fundamental impediments to their health and happiness, many people taking antidepressants become discouraged and discontinue taking their medication, usually with the result of renewed symptoms.

Sadly, some doctors do not appreciate, or may even dismiss, their patients' complaints about side effects. "You're so much better than you were before you started on medication," patients have been told as they are encouraged to accept their fate as the lesser of two evils. "Every drug has side effects. You'll just have to learn to live with them," they are counselled.

This all-too-common response by physicians not only lacks compassion, it's also bad medicine. By dismissing antidepressants' side effects as something patients must learn to live with, doctors are forfeiting their patients' chances for full recovery. If a primary symptom of depression is an inability to enjoy life, then finding pleasure in relationships and work is the ultimate goal of recovery. Who among us can expect to be desirable to others if we feel undesirable? How can we expect to fully enjoy the pleasures of intimacy without a healthy sex drive, full sexual function or a positive body image? Who can hope to compete on the fast track of life and work with reduced vitality and mental alertness?

These questions are hardly peripheral concerns; they go to the heart of recovery from depression.

For years, I treated patients for depression, with both psychotherapy and drugs, only to find their progress diverted by a new set of obstacles. They gained weight - sometimes so much that they resigned themselves to the sidelines of social life. Their sex drives deserted them - love relationships and marriages foundered amid sexual apathy and dysfunction. Most critically, they lacked the energy to keep up with their jobs and fully engage the everyday challenges of life. Over and over again, patients told me that although their depression was controlled, they could not fully enjoy life.

I began working hard with individual patients, searching for a regimen that offered help. We looked at diet, stress levels, exercise and hormones. Today, more than 300 of my patients - about 80 percent of those who tried the program we developed - have found relief from their depression and the side effects of the medication.

More than 25 million Americans are currently on antidepressant medication to treat depression and a wide range of non-depressive disorders, including: anxiety and panic disorders, obsessive/compulsive disorders, chronic pain syndrome, irritable bowel syndrome, migraine headaches and chronic fatigue.

Yet depending on the survey and the side effects being reported, anywhere from 30 to 80 percent of patients on medication suffer such severe side effects that they are significantly impaired in their ability to function in their jobs or relationships.

(As for the so-called "natural" remedies: A lot has been written recently about St. John's wort. And indeed, this herbal supplement helps many people cope with mild to moderate depression. But it doesn't work for many people with more severe depression. Also, St. John's wort has troublesome side effects of its own - and, unlike SSRIs - has no effect on the non-depressive disorders mentioned above.)

The medical underpinnings of side effects are complex and not fully understood, but this much is clear: Antidepressants are powerful agents that can cause widespread changes in the body's neurochemical and hormonal systems. When one of the body's metabolic systems goes out of balance, it tends to create disequilibrium in others - which is, in part, why so many people suffer from multiple side effects. When imbalance occurs, the body struggles to compensate and to reassert its natural balance and healthy order. This innate drive toward equilibrium is your body's hidden gift.

I believe that no one should resign themselves to half a life simply because they're on antidepressant medication. Everyone recovering from depression should aspire to the happiness and fulfillment that comes with vitality, a positive body image, a healthy sex life and the higher-quality relationships they foster. In the end, it's not enough merely to survive depression.

You can thrive.

Robert J. Hedaya is a clinical professor of psychiatry at Georgetown University. He maintains a private practice in Chevy Chase. This article is adapted from "The Antidepressant Survival Guide : The Clinically Proven Program to Enhance the Benefits and Beat the Side Effects of Your Medication".

APA Reference
Staff, H. (2021, December 26). Many Doctors Don't Take Treating the Side Effects of Antidepressants Seriously Enough, HealthyPlace. Retrieved on 2025, April 29 from https://www.healthyplace.com/sex/medications/many-doctors-dont-take-treating-the-side-effects-of-antidepressants-seriously-enough

Last Updated: March 26, 2022