Hello everyone,
I wanted to ask you all what it takes to be a MS warrior? Now more than ever it seems we need to draw on all of our resources and wondered what these are? I'm newly diagnosed, new to this site and looking for some inspiration to help me cope over the next few weeks and months. Thanks...
I recently got diagnosed January 2021 after 10 years of symptoms and lost use of my legs. After a lengthy stay at the hospital and many pt appointments I can get around with my cane or walker.
I was diagnosed many years ago and the last 15 years have been really difficult. I continue and I do my share of complaining. But it does help having a place to go with questions. Thank you fellow warriors for your struggles are felt. Stay inside and keep hydrated.
Hello fellow Warriors! I’m one, like many others, who enjoy a variety of autoimmune afflictions; MS, Type 1 Diabetes, Fibromyalgia, Pernicious Anemia, Hypothyroidism and a bout of Autoimmune Gastritis. As a veteran diabetic (33 years) and an MS’r since 2010, I find that these two impact me the most ...
Hopefully many of you have seen my fellow MS team mate (from CPISRA World Champs) and all round inspirational girl Kadeena Cox breaking the World Record at the World Championships in Doha this week in the 100M sprint. Kadeena is an outstanding athlete and a most humble, caring and loving character t...