shift.ms

This is hot off the press and has upset people in the medical profession, as well as UK PPMSers. There’s already a campaign to contest this decision :- https://signup.mssociety.org.uk/page/30088/petition/1  

Hi Guys. Suffering from pins and needles again. Just wanted to have a rant. Soooooo annoying and feeling low mood. Also annoying is people trying to manage my MS. Been asked three times in a conversation if i am going to be tried when arranged to go out. Rant over. LJl.🤹‍♀️

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, So I had an appointment woth my nero a few months back and he refered my to the Urology department. After looking into what the appointment would involve ive decided i wanted to cancel it. During this the lady said do i wish to discharge thinking that this just meant canceling the appointment …

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

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…

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…