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Real members of MyMSTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
March 6
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A MyMSTeam Member

All the people I have contacted or have seen are usually very nice. Since I am wheelchair about, they are always willing to open a door for me or help me any other way they can. I feel that I am very lucky to live where I do because people are always nice. I'm sorry you have to put up with people being rude or mean. God bless you.πŸ™‚

March 6
A MyMSTeam Member

I was diagnosed in 1999 and since then I was diagnosed with primary progressive I was not given any medications now I am living the life of a quadriplegic. I have lost the use of my legs and my hands and am totally dependent on my husband for all my daily needs. He is such a blessing. I never in my wildest dreams my MS would really change in my life. My faith keeps me going. God bless all of us battling is terrible disease. The doctors always said it affects everybody differently . I guess he was right. I have learned to live with my disease. I'm still able to enjoy the positive things in my life and can be happy with my family , who are very supportive. Life is good.😊

March 7
A MyMSTeam Member

CherylCrawn2, my heart is with youπŸ’• praying you well πŸ™

March 6
A MyMSTeam Member

I wish I could help you more. Good nite

March 6
A MyMSTeam Member

I have the utmost respect for you. Wow 40 years of dealing with this shit. Dmts don't work very effective as we get older anyway. I have no words for you . In other situations I could be very helpful.Just take care of yourself an don't let outsiders bother you. Let it go in one ear an out the other

March 6

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