Just my opinion but it seems to me that you both need to take deep breaths and talk. Not accuse or blame but talk and you both need to listen and hear what the other is saying
June 18
MS can significantly affect intimacy and sexual relationships, and it's more common than many people realize. Up to 72% of women and 91% of men with MS report changes in their sex lives. The good news is that many couples find ways to adapt and maintain meaningful intimacy. MS affects the nervous system, which plays a Show Full Answer
MS can significantly affect intimacy and sexual relationships, and it's more common than many people realize. Up to 72% of women and 91% of men with MS report changes in their sex lives. The good news is that many couples find ways to adapt and maintain meaningful intimacy. MS affects the nervous system, which plays a direct role in sexual function. When nerve pathways are damaged by MS lesions, signals between the brain and sexual organs can be disrupted. This can lead to a range of challenges, including:
- Reduced arousal or difficulty with orgasm
- Decreased sensation or numbness
- Vaginal dryness or pain
- Erectile dysfunction
- Loss of sexual desire
- Spasticity or muscle stiffness interfering with intimacy
- Fatigue making sex feel difficult Emotional factors also play a role. MS can bring stress, changes in body image, and sometimes a shift where a partner moves into a caregiver role — which can blur the line between lover and carer. Some medications used to manage MS symptoms can also lower libido as a side effect, so it's worth discussing this with a neurologist. There are practical ways many people with MS manage these challenges:
- Use lubrication — water-based lubricants can help with dryness or vaginal pain (avoid petroleum-based products like Vaseline)
- Explore sex aids — vibrators and other toys can help with sensation and arousal
- Prioritize foreplay and stimulation — taking more time can make a real difference
- Embrace other forms of intimacy — cuddling, touching, and closeness can keep connection alive
- Plan around energy levels — timing intimacy for when fatigue is lower can help One of the most important things is open communication — both with a partner and with a healthcare provider. As one MyMSTeam member put it, talking openly with a partner about needs and concerns "will do wonders." Many people feel embarrassed raising sexual topics with their neurologist, but they are trained to understand how MS affects the body in every way, including sexually.
Relationships can absolutely remain fulfilling and intimate with MS — they may just look a little different than before, and that's okay.
AI-generated responses are not a substitute for medical advice. These services are not intended to
diagnose, treat, or cure any condition or disease. Always ask your doctor about specific health concerns.
Intimacy and Multiple Sclerosis
June 18
I'm not sure if he's the one with MS? I know I've had MS for a long time and it finally started to affect my sexual organs. I started having numbness, pain, burning and other problems that prevents me from even enjoying any type of intimacy. Me and my husband work on it. They don't have a medication to just fix it either. MS is not fair, seems to slowly chip away at everything on your body.
This is what comes up if you Google it-
Sexual dysfunction affects up to 70-80% of people with Multiple Sclerosis (MS). It is a direct result of central nervous system damage, physical symptoms like fatigue and spasticity, or the psychological toll of the disease.
So it's not really him, it's the process of the disease itself. I hope this helps you.
June 18