Looking for
something specific?

I want advice as soon as my daughter learnt that I was ill she doesn't want me around is that normal I'm not sure what to do😋

How do I go about getting a caretaker?

I have had MS for over 24 years. The last 5 have been rough. Lately every virus I encounter leaves me run down and I have a harder and harder time bouncing back. Any advice?

I just need to know I’m not crazy. Yesterday I felt like I had pulled my neck, by the evening it was across my neck and shoulders. Today is my back neck chest, basically everywhere to the top of my thigh. It’s hard to explain but it’s as if I’ve been to the gym and then got sunburn. Everything hurts...

Hey, i don’t know how to start. This is my first time writing a post here so i am a little bit nervous. Few months ago, i had a flare up that was basically pain in my right arm and leg. Since then, this pain stayed as a constant symptom. Sometimes goes but most of the time is present. My doctor ad...

Hello everyone one im so lost right I have to pay a co pay to get my meds now im sure why im unable to work .I can no longer walk right..stand up ....i just cry the pain is pass 10 ...but god did bless 2 weeks ago I was able to go to Wal-Mart with my mom an my 2 lil girls an as we were walk people w...

Morning everyone, can anyone please help me? I was diagnosed 3 years ago, but has symptoms for the last 5-6 years. I am on Tysabri and have done wonders, my last MRI showed nothing, I had a very active MS, lesions seemed shrink, the remaining ones not active anymore. It is just in the last MRI resul...

Hi yesterday I wrote my first post, And I received many messages of supportI wanted to thank you for the love have sent me. ♥️♥️ Many people gave me an idea To write here what I needed.I really thought long before I did it Because I am embarrassed. But I'm going to try : My situation at home is n...

my name is ainhoaI am 23 years old And in 2020 I received the Diagnosis ms. Because of this, I lost my job worked as a cook. It's a tough job with a lot of stress . My family does not support me. They say it's not a disease And that's why I'm looking for help To feel that someone understands me

Do any of you guys have issues with your PBA??

Hello. So i have not been diagnosed with MS but I have a referal appt to see a neurologist due to symptoms i have been having for roughly 18mnths that are progressively getting worse. What were the first signs and symptoms you had ?

I have a very weird symptom: it's a weird sensation of weakness in my neck and back of my head, and my entire body starts to feel weak and disoriented, but it's mostly in my neck, it's not tingles or electricity, just weakness or numbness of some sort and the entire thing feels as if I'm about to pa...

Hello!! I actually do not know whether I have ms but have lost a lot of sensation in my toes and feet very quickly. I am pretty troubled how the sensation is all round the soles of my feet and finding it really difficult to sleep. The doctor I saw said they couldn't do anything about neuropathy whic...

Im newly diganosed(3weeks) an i dont know wot 2 do how long do i have to wait 4 an appointment to get treatment? Im so confussed.

Today is really hard. I have relapse ms and I'm in so much pain. I feel like someone is taking a razor my skin,set on fire,, and sharp pains. Been crying and don't know if I should go to the hospital. Need advice...

Can anyone help with recommendations for a comfortable wheelchair cushion thanks?

I have recently been diagnosed with MS. My neurologist diagnosed me in august during this covid pandemic, im 23 years used to be very active a basketball player it started with facial numbness and blurry eyes also coordinaion and weak left side problems, im taking this infusion called ocrevus its b...

Someone has mentioned to me that you can legally have your infusion treatment day as an off/payed day. Something called ‘disability...’ does anyone know how to go about that? Thanks, Petra

I sleep great in day but cannot sleep at night is this common? I have ppms and other health problems. I seem to clime in tub as my legs and lower back hurts I will go to sleep too

I have just recently being diagnosed with quite a few leisons on my brain and spinal cord and have suffered symptoms of ms for years (although never knew that that's what they were) but my neurologist will not diagnose ms, has anyone else had this problem? At first the neurologist wasn't going to se...