What do people think is ill enough? I am trying to claim PIP and gain reduced hours at work but no request is accepted for either. Is there a situation where you are just not ill enough to require change?

Hi all, I was diagnosed 2001 RRMS tried Avonex for 3 years but could cope with the injections, no further contact with Neurologist and decided just to live life taking LDN. Now back in the system and am SPMS. I use an active manual wheelchair but can't blame the ms entirely for that - I have drop ...

I’m so close to finishing my degree.. My MS causes me so much fatigue that I want to drop everything. I feel like a failure and I do really want to finish but it’s so hard to push through. I’m in a very good school and I don’t want to switch to something online.. commuting is exhausting and also I w...

Hello everyone, I take Fingya, an immunosuppressant medication; I take one pill daily. Because of this, I really can't handle the cold—I get sick very easily. What do you do to support your immune system? Besides eating winter fruits rich in Vitamin C, I also drink turmeric mixed into hot water. I...

I hope to you get to know other patients and understand what others are going through.I am going to do a rough time being in and out of the household with pneumonia and magnesium had to have i had to have magnesium impusion Sunday morning at the hospital. Knowing what I'm going through is understand...

My body isn’t my friend at the moment and I have been experiencing burning sensations on my skin since the beginning of March, particularly in a specific area across my hip, but it has now spread. My GP has been trying to support me with this but so far with little success. I am awaiting a referral ...

Had rrms for 25 years now diagnosed with spms. Due to start mayzent/siponimod after being on Tysabri for 20 years. Anyone gone through something similar? And what’s been your experience?

My nerve-pain injections helped for almost three weeks, but the pain has recently returned even though I was told they might last up to six months. I’ve contacted my neurologist, but I’m worried about needing more medication and repeated treatment costs.

Does anyone take ibuprofen or a pain medication after they have a fall?. I just had a fall 2 hours ago and I know I don’t feel anything but I will probably feel something later on lol.