Multiple sclerosis is a difficult disease to live with. With no known cure, patients often find the day-to-day struggle very challenging. But they’re not the only ones who live with the disease — friends, family and loved ones also have to learn how to deal.
To help everyone cope better, we’ve put together a list of six tips for patients, families, and loved ones. (source: National MS Society)
1. With or without MS, relationships are not easy.
All relationships require energy and effort to go through up and downs — even without a disease to complicate matters. It is almost inevitable that multiple sclerosis will add to the challenge.
Recognizing that MS affects the whole family is the first step to coping with MS in personal interactions. Many times, learning to live with the disease brings spouses, families, and friends closer together. It is important to never compare families and relationships to your own, under any circumstances.
4. MS patients can become parents, too.
People with multiple sclerosis are often concerned about the future demands that come with wanting and having children. This can bring additional stress to relationships. But rest assured: according to the National MS Society, “women and men with MS can be successful parents of happy, healthy children.” Start by discussing the topic of pregnancy with your physician.
The organization also offers resources for patients regarding conception, pregnancy, delivery, and breastfeeding. Information about the impact of childbearing on MS patients is also available. If you already have children, find out how to discuss the disease with your kids.
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5. Clear any negativity associated with caring.
In most cases, the caregivers of patients with multiple sclerosis are family members. Sometimes, patients may feel guilty or sad about the situation. However, there is no reason for associating caring for a loved one with anything negative. In fact, caring for someone you love who struggles with a chronic disease like MS can be very rewarding.
While understanding all the medical jargon used is difficult, what I did understand was the positive attitude regarding the hope for help for those of s with MS.
I have ppms and just completed the first infusion of Ocrevus a week ago. I’m already feeling some improvements. I stood within 5 days after infusion for the first time in 3 months. Very hopeful for continuing improvement.