this is a new day and as a born again believer i will have a new heavenly body with no more pain/suffering. blessings all and prayers daily for all who have ms n chronic diseases. d
Sharing from my blog of a recent hospital experience, (https//:fightingms.uk)
Too close for comfort
Comfort, it’s not really the best word, yes I would love to be content and comfortable, but that certainly hasn’t been the case lately, far from it!
Living with Primary Progressive MS, is not easy a...
Hey everyone.
I'm Sam from Stourbridge in the West Midlands. struggling and feeling very alone, I hope to connect with other MSers who understand.
Big love & prayers for you all x
I am going to try to answer some of your questions about SPMS by explaining a little of my history and hope that will help you understand some things. My MS presented in the mid 90’s but it took several years before I was diagnosed with RRMS. I suffered for years with symptoms and no treatment. I de...
I am wheelchair bound and I have to use a shower chair. Do u think I'm lucky enough to have a wide enough doorway to just simply roll up to the tub and transport from one surface to another? NOOOOOO...so I absolutely have get down in the floor and pull myself up on edge of tub, and then pull myself ...
. MS is a crazy type of disease that can cause so many different symptoms. I have had MS since 1994, and for me and many others its been a long hard road... I currently have MS at bay. I currently have very little to no MS pain. I stopped having exacerbations (attacks) for the last 7-8 years. Let ...
One second wide awake, next thing I know I am literally struggling to open my eyes!! It took a few minutes, I dont know how long, but then I had to struggle to move!! Now it's like nothing happened and I am fine. What the hell is happening to me?! The symptoms go on and on..
Got a call from Neurosc...
Well as you all know I wanted to see my neurologist on Friday and I told him the truth
He kept me on 3mg Klonopin three times a day and he said stop drinking he left all the other medication the same except the Copaxone own he's taking me off of and he wants to try me on tecfidera, I believe that'...
I hope you are all doing well. I'm a freaking nervous wreck.
I finally had my first neurologist appointment on October 13. He listened to my story, and examined me, and said that in his opinion it was really unlikely that I have MS. He said that all of my symptoms could be explained by fibromyalgia...