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Hello everyone! I was recently diagnosed with optic neuritis (and what apparently has been MS for several years now) and after long consideration I finally decided to opt for steroid pulse therapy (5 x 1000 mg methylprednisolone). The first few days were fine, I didn't experience any euphoria, slee...

I would appreciate if someone could discuss with me privately about MS and share own thoughts. If you have been diagnosed recently it is abaolutely fine.

Hi I have recently been diagnosed with Ms and am reluctant to take medication and therefore have been looking into alternative treatments. I feel hopeful about Dr Coimbra's vitamin d protocol which has been backed up by many other doctors such as Dr Berg. I have started taking high doses of vitam...

Hello everyone. I just wanted to say hello and maybe get any useful info from anyone who may have had similar experiences. Firstly I want to point out that I am not suffering badly and am well aware that I am more fortunate than many so really don't want any sympathy, just thought my story might be ...

Hello all, I'd like some thoughts from you knowledgable folk plz. I was diagnosed rrms in September 2017 and have been on tec since March 2019. I have remained stable, however my most recent MRI last month (delayed from March) has shown 4 new areas of inflammation. I have not had a noticable relap...

Hi, If anyone can pass this along, or have a read and share it would be greatly appreciated. Myself I have RRMS - have had an official diagnosis for 1 year, and I am a 27 year old woman. I've had a rough time, I've been on steroids to treat a relapse 3 times in the past year, and I've had 2 separ...

I was diagnosed about 9 months ago. I recently started coming to terms with my diagnosis, though most times i try to ignore it, it somehow stick its head in my business.

Hello, was diagnosed in March after two surgeries. I’m learning everyday of what my body can do and cannot. Each day a lil different. My one leg does not follow”directions “ and quite often “drags” . Wondering if any body can suggest a brand or o line of shoes, that might help. Thank you

Has anyone never had a days rest?. Always something with my MS spasms pain bladder optic nerve inflammation in the nerve so on so forth never-ending since I was diagnosed I was wondering is this common with MS

Hi, just wondered since being diagnosed how people's experiences of going abroad have changed. Does insurance go sky high for example? Love going on holiday and hoping I can still go every now and then. Thanks