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Hi everyone. Haven't posted much lately but I felt inclined to share today. So, I hadn't had a brain MRI in 2.5 years, and they finally set me for one last month. I don't see the dr until February so I asked my chiropractor (who also does neuro rehab etc) to get the results for me. We went over th...

I don't know if anyone else feels like this, but over the past couple of months I feel lethargic, down and very teary. It's like everything I do, I hit a brick wall and don't want to continue. I've had suicidal ideation, stopped only by the thought of the impact on my family and my partner. I've cri...

Hi I have RRMS but I've never had optic neuritis but since Monday vision has been blurry in my right eye and I've had a weird headache behind my right eye. The kind thats fine if I keep my head still but if I bend down it really hurts. I've been keeping the headache at bay with paracetamol 3 tim...

Hi everyone, I thought I'd just share this short clip explaining very simply how stress causes inflammation and fuels MS. This is from a documentary called "The Connection", very well worth watching. http://youtu.be/qP1d4tqmSuk

Hi there, Ive had MS (relapse and remittance) for 15 year now. I was just wondering whether anyone has heard of 'Soursop' or have tried the herbs/ drink. If so, How did you find it? The reason why I am asking is because I have heard from a number of people (people who don't know each other) that ...

MS is stressing. We MSers know that first hand. Unfortunately seems that my boyfriend of 6 years is only now realizing that. We have been fighting a lot and he has said very hurtful things to me. Its true that he apologizes when his temper has cooled off but truth is that for the past few months we ...

Hi All I am being put forward to try FAMPYRA to see if it helps with my walking. Today my MS Nurse asked me if I was still taking LDN as she wasn't sure if it would be ok with FAMPYRA. Does anybody have experience or know if it will be ok to take both together.

Hi everyone, hope you are all doing well. :) I am interested to hear about people's experiences with Optic Neuritis, and in particular those who have had a slow recovery from it. My own story - I got an attack of Optic Neuritis in my left eye in June this year. It started off with some mild pain a...

I'm 25 and my mother was DX before I was born. It's been 5 years since she has passed. I feel as I'm having symptoms but not sure. Maybe it's all in my head and I'm just worried for nothing. I've had bad headachs since I was very young. But the last 2 months I've noticed something's. Stiff finger...

I'm 24 and find it hard to cope with M.S.