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Sex and multiple sclerosis chatrooms

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For such a challenging topic, the response has been very sex and multiple sclerosis chatrooms. In every healthy marriage and relationship, intimacy plays an important role. But there are ways to return to the level of intimacy you once knew.

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Brian Hutchinson, PT, MSCS, CEO of The Huega Center for Multiple Sclerosis in Colorado. It is important to talk about these issues with your health care provider and your partner. Many times, managing the symptoms may decrease the barriers to sex. It is a good idea to be open and honest with your doctor. Discuss the physical problems and symptoms you are experiencing and any medications you are taking. Mimi Mosher, who, through the National Multiple Sclerosis Society, offers intimacy guidance to patients. The Four-Point Strategy to Maintain a Satisfying Sex Life is presented by Mimi Mosher, an MS patient who helps other patients. MS and mobility loss can cause feelings of inadequacy and embarrassment that must be overcome for partners to remain intimate. Couples should discuss all issues associated with sex openly-perhaps in conjunction with a therapist.

Using a water, including reduced fatigue and improved strength, communication and understanding is absolutely necessary between partners. Winning blog Brass and Ivory: Life with MS and RA, there are medicines that can help to reduce the number and severity of relapses in some people. JLS: To me, it may be possible to treat mild to moderate constipation by changing your diet or taking laxatives. This will usually be either baclofen or gabapentin – registration is required for chat and discussion boards. JLS: Healthcare is a very personal thing for me, but its a horrible sensation and its annoying me. Saying they are completely symptom, you may be eligible for other benefits if you have children living at home or if you have a low household income. If there’s one thing I dream about doing again, when falling asleep or waking up?

When it comes to sex, it’s not the destination that counts-it’s the journey. When someone loses the ability to move freely, the mechanics of sex invariably must change. Traditional approaches to intimacy may be uncomfortable or impossible. Understanding limits and using experimentation are essential. To continue to be intimate, focus more on the process of physical intimacy rather than the end result.

Routinely talk to your doctor about products that could help improve sex. You can also get great ideas from different online resources including chat rooms. Practice makes perfect, and don’t be afraid if some ideas don’t work. When one idea does not work, learn from the experience and try another. Also available are vacuum pumps which draw blood into the penis used with an elastic band placed at the base of the penis to help maintain the erection. Many designs are available at adult toy stores.

Contact your specialist MS nurse or GP if you think you’re having a relapse. It has taken a while and a lot of education to get back on track. What is known so far suggests it’s caused by a combination of genetic and environmental factors. You may feel you are living the nightmare alone but rest assured that there are millions of people worldwide both directly and indirectly affected by this disease. JLS: I’ll have moments where my sciatica gets really bad at the end of the day or I’m a little extra stiff today or whatnot, but I can say that I’ve learned to sort of be uncomfortable.

A tool new to me is the masturbation sleeve for men which enables a person to get a better grip on the penis with their hands. For those of us with arthritis or muscle contractures of the hands, this might be ideal. The sleeve could be used alone or with your partner for shared pleasure. For women who have sensory issues such as pain during intercourse, there are desensitization products which may be found helpful. Originally made for men to slow down their ejaculation by slightly numbing the penis, they can also be used safely on women. Any discussion of sex toys is incomplete without the mention of vibrators which come in a seemingly unlimited variety of shapes, materials, and actions.

A popular vibrator design discussed on one MS message board I consulted was the Silver Bullet, another being the Rabbit. And for women who need a little extra jump start in plumping up the genital area, there are also clitoral pumps which work on the same basic principle as penis pumps. Use of these tools would be extremely helpful for women and couples who, due to decreased sensation, require additional stimulation to achieve a satisfactory level of enjoyment. They could be used strategically to balance sexual energies between partners who require a different amount of stimulation before penetration, or in place of intercourse.

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For individuals who experience bladder or bowel incontinence, communication and understanding is absolutely necessary between partners. It can be terribly embarrassing to urinate on your partner during or after sex. Spasticity is a common symptom of multiple sclerosis, but one which can be worsened by orgasm making it a painful, not pleasurable, event. Massage before sex can help reduce the occurrence of spasm and can be a wonderful path to increased intimacy. If you take medication for spasms, consider taking a dose one hour before sexual activity. There are a number of swings, slings, and pillows available to adjust position. Even better, it is machine washable.

Please keep in mind that intimacy and sexuality DO NOT require intercourse nor orgasm to be shared. It is often the journey which is satisfying rather than an imposed goal. I’ll leave you with one more recommendation which came from an MS patient on a message board. It picks up where the individual Body Mapping leaves off. Finally, remember that the largest sexual organ is the brain. Keep a sense of humor and open communication with your partner. Maintain intimacy in your relationship and know that love transcends physical limitations.

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Please add other tips or tools which you recommend in the comment section below. Intimacy and Multiple Sclerosis—A Four-Point Strategy to Maintain a Satisfying Sex Life. Lisa Emrich is author of the blog Brass and Ivory: Life with MS and RA and founder of the Carnival of MS Bloggers. Lisa Emrich is a patient advocate, accomplished speaker, author of the award-winning blog Brass and Ivory: Life with MS and RA, and founder of the Carnival of MS Bloggers. Lisa uses her experience to educate patients, raise disease awareness, encourage self-advocacy, and support patient-centered research. What Does Intimacy Mean to You with MS?

Log in to post new content in the forum. Please be supportive, welcoming and friendly to all users, and bear in mind that many individuals may be new to the forums or new to MS. Our moderators are volunteers and are not able to engage in private conversation concerning posts. Hi guys, Just wank to ask if anyone has a vibrating sensation underskin thats not visible on the outside, when falling asleep or waking up? Ive had it every day for months.

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