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Dealing With Multiple Sclerosis In Your Important Relationships

By June 11, 2010 - 3:26pm

Important relationships take effort and energy — even without the added challenges of MS. While MS does pose some additional challenges, it can also enrich relationships and bring people closer together. The first step in figuring out how to deal with MS in your personal interactions is to recognize that the disease affects all of you — whether you have the disease or care about someone who does. The next step is to decide whom you want to tell about the MS and what you want them to understand about it. And the third step is to look for ways to make room for MS in your personal and professional relationships without giving it more time, attention, and energy than it really needs.

Deciding to Disclose…Or Not:

Telling others about your MS may be the first thing you want to do — or the last. No two people feel exactly the same about disclosing their MS to others. Keeping in mind that once the information is out there, you can’t take it back, the key is figuring out when disclosure is in your best interest and when it is not. Read more about disclosing to family, friends, employers and colleagues, and someone you are dating.

Keeping Balance in One-on-One Relationships:

When one person in a couple is affected by MS, the other person lives with it as well. To keep your relationship healthy and balanced, it’s important to make sure that both of you stay on the giving and receiving end of the relationship, in spite of whatever changes MS may bring. Learn how to manage MS as team and enhance your communication and intimacy.

Parenting When You Have MS:

  • Family Planning Decisions — The good news is that women and men with MS can be successful parents of happy, healthy children. Learn the up-to-date findings about the impact of MS on conception, pregnancy, delivery, and breastfeeding, and the impact of childbearing on MS
  • Talking with Children about MS — Kids tend to worry when they know something’s up — even if Mom or Dad has no visible symptoms.

We value and respect our HERWriters' experiences, but everyone is different. Many of our writers are speaking from personal experience, and what's worked for them may not work for you. Their articles are not a substitute for medical advice, although we hope you can gain knowledge from their insight.

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