Patients living with more than one chronic disease face unique challenges. Unfortunately, comorbidities seem more and more common especially with autoimmune diseases. As someone living with multiple sclerosis and rheumatoid arthritis, I am understandable drawn to other patients who live with the same combination of diseases.
This week is Multiple Sclerosis Awareness Week so I asked a few MS/RA patients to share their stories with us today. Six patients were kind enough to contribute. Diagnosed with RA before MS, patients AH, CL, and Momuv6Boys09 (MB) share their stories below. Stories from patients diagnosed with MS first can be found on MS Central .
When were you diagnosed with MS and when were you diagnosed with RA?
AH: I was diagnosed with RA a few months before my diagnosis of MS in 2008. Having the two diseases together somehow tripped up getting a diagnosis.
MB: I was diagnosed with ...
You've found a great site for multiple sclerosis information and community. We have much to offer to people who having been living with MS for years, to people who have just been diagnosed with MS, as well as those who are in limbo and have not yet been diagnosed. Our community members are extraordinary, providing the type of encouragement and support which is sometimes hard to find on the internet.
We have an extensive archive of Shareposts , contributed by experts and community members, spanning a full range of subjects related to multiple sclerosis. Our community members help each other frequently by asking and answering questions in our Q&A section .
If you are looking for what others have already said related to a specific topic, you can use the search bar found at the top of each page. Just enter a couple words or a phrase related to the desired subject and you will find links to the many Shareposts, Questions, and reference material...
The months or years of mystery have been solved. In many ways, you feel relief at having been given the diagnosis at last. MS...multiple sclerosis...is forevermore part of your life. Now one of your immediate concerns is telling family and friends. Who should you tell? When and how? Your health status is a very personal issue and there is no one correct formula for sharing the news. Naturally, the people most effected...your spouse, children, parents or anyone who shares your home...should be told. It's a good idea to have some knowledge of the basic facts of MS so you can answer their first questions. Encourage them to educate themselves. At the time of my diagnosis, I had three teenaged children. When I gave them the news, the first fact I revealed was that MS is not contagious and they cannot “catch” it. Young children and teenagers need to have those fears addressed at the very start. I assured them that MS is rarely fatal and that I could be expected to live a long...
You should knowAnswers to your question are meant to provide general health information but should not replace medical advice you receive from a doctor. No answers should be viewed as a diagnosis or recommended treatment for a condition. Content posted by community members does not necessarily reflect the views of Remedy Health Media, which also reserves the right to remove material deemed inappropriate.