Transitioning into SPMSHi everybody Guess I just wanted to rant here. I feel very misused by my MS doctors.. I was diagnosed with RRMS in 1998, the only symptom I had was...Reactions 0 reactions Comments8 repliesCoping
Covid-19, Living Alone, and MS?The isolation has been particularly frustrating. Many of my structured activities to connect with others are canceled or online. Too much time online is hard on my fatigue and I...Reactions 0 reactions Comments3 replies
How did you know you had MS?Hello! New to the group, not even sure if this is where I need to be yet. How did you or your doctor know to look for MS? What were...Reactions 0 reactions Comments1 repliesCoping
Numb?It happens every few months ever since I can remember. I try to go to sleep my body felt like paper or sticks and everything I touch seems so small/light...Reactions 0 reactions Comments1 replies
Lazy EyeHi everyone. I was diagnosed in 2017 on my 19th birthday due to an onset of optic neuritis, vertigo and a slew of other things. I lost total vision in...Reactions 0 reactions Comments1 repliesSymptoms
Is it common for your mouth to dry up and you have to swallow to keep talking?Is it common when you have MS, that you can be talking then all the sudden it's like your mouth dries up and you have to swallow to keep talking?...Reactions 0 reactions Comments12 replies
Does anyone use an app to log in their daily symptoms? If so, which would you recommend?Reactions 0 reactions Comments2 replies
Has anyone found a way to manage a manual w’chair after mastectomy?Been managing all regular household tasks - laundry, cooking (including bread making) in my manual w’chair (RGK) but now I need breast surgery - I don’t know how I‘ll cope...Reactions 0 reactions Comments5 replies
Does leg pain hurt when you touch your skin and feel it in your bones?My leg hurts and my foot tingles. When I rubbed my leg it hurt so bad all the way down. Is that normal for me? I am not sure, thank...Reactions 0 reactions Comments2 replies