shift.ms

Hello to all you lovely people. I used to recieve dla higher rate mobility and care and i a friend of mine suggested i should apply for P.I.P and helped me with filling out the form as well. I went for assessment in end of feb beginning of march i think and the P.I.P got refused cause the assessor …

Hi everyone, I’m Emma. I’m a 37yr old single mum who has had RRMS for 12 years. I have recently retired through ill health as a primary school teacher and am struggling to adjust to life after a career that I loved and gave me enormous fulfilment. I am volunteering at the local hospital…

Finally saw the new Neurologist. She called about my MRIs yesterday. She acknowledged that yes, all the issues I had from June through August were from a new active lesion. She wanted to start me on 5 days of mass steroid infusions. Since it was Friday she wanted to admit me to the hospital for 5 …

I received a copy of the letter that went to my gp from my most recent neurology appt that finally diagnosed RRMS, after 4 months (and 3 years) it actually feels a huge relief to have a formal diagnosis. I can stop saying ‘i probably have’ and start moving forward with managing what I n…

Hi all Have you ever of this treatment Has it been released I read its similar to gilenya Maybe less effectiveness in ppms and leas side effects Or maybe the news are wrong https://www.mstrust.org.uk/a-z/siponimod

An undesirable joined us in the last few hours. “She” has sent out various Friend Requests, which has than be followed by a Personal Message, requesting an email exchange, with the offer of photographs. “She” is a scam artist and has been removed. If you have received her P…

I experienced a delightful hours worth of a full body massage a couple of hours ago, my body feels born again and that my walking and self confidence has risen like I would never of expected. I hope that this feeling is still with me in the morning. 😜

Hi, sorry to be repetitive with my subject but it is a real concern for me and a huge irritation for my wife ( she has MS). Both of our lives have been turned upside down, shook around and then stamped on, my wife has gone from a high level career with the NHS to needing help to eat and general mob…

Hi MSers Just wondering has anyone been diagnosed with ms by MRI only and no lumber puncture. While i officially havent been diagnosed with ms, i have only had mri’s which all say my lesions are consitant with ms.

I have now decided to have a vegetarian diet but I will include salmon as it is the only fish I will eat stop dairy products and have soya milk and soya yogurt. I would appreciate anyone’s comments either good or bad as I am not that experienced with this condition so I wanted by someway tryi…