Join to explore more

Shift.ms is better if you're logged in

Join the communityOr find out more

By signing in to Shift.ms you agree to our terms of use and privacy policy.

Already have an account?

Sign in

Shift.ms
Donate
Learn about MS
MS symptoms
MS symptomsA guide to MS symptomsWhat are the early signs of MS?Understanding visible and invisible symptoms of MSMS HugMS and optic neuritis
MS diagnosis
MS diagnosisBeing diagnosed with MSWhat is MS?Different types of MSIs MS hereditary?Late onset MS and treatment
MS treatment
MS treatmentGetting treatment for MSCoping with MS fatigueExercising with MSUnderstanding MS relapseHSCT treatment for MS
Living with MS
Living with MSAfter diagnosis: living with MSMultiple sclerosis and mental healthWorking with MSMS, sex and relationshipsA guide to MS benefits in the UK
  • Forum
  • Learn about MS
  • MS symptoms
  • MS diagnosis
  • MS treatment
  • Living with MS
  • Find MSers
  • Buddy Network
  • Films
  • MS Latest
  • Get Involved
  • Volunteer
  • Fundraise
  • Donate
  • About us
  • Contact us
  • House rules
  • Terms of use
  • Privacy policy
  • Cookie policy
Sign in

We are a charity and rely on donations

Charity Number: 1117194 (England and Wales)

Registered Company: 06000961

Registered address:
Shift.ms, Platform, New Station Street, LS1 4JB, United Kingdom

London office:
Shift.ms, Somerset House, Strand, West Goods Entrance, London WC2R 1LA, United Kingdom

©2025 Shift.ms

  • Picked for you
  • Browse topics
  • Find MSers

Topics

  • Diagnosis
  • Symptoms
  • Newly diagnosed
  • Healthy living
  • Research
  • Disclosure
  • MRI
  • Browse all
Sort 98 results by
Recent activityNewest posts

@Luxx89 

1 May 2025 17:19Last reply 3 May 2025 12:18

Luxx89

Discriminated against by Mind charity, pushed into unemployment

Hi all, Hope you’re all doing okay and sorry for the long post 🧡 I’m sharing my experience to raise awareness and hopefully get some support from those who understand what it’s like to live with MS. I’ve been battling multiple sclerosis for a while now, and while it’s hard enough dealing with my ...
London, United Kingdom
20

@Clairemcgowan81 

3 Feb 2025 06:20

Clairemcgowan81

immunosuppressed or immunocompromised?

Hi all, I'm taking kesimpta, does this mean I'm immunosuppressed or immunocompromised. Also, If I've had my childhood measles vaccine will I still have immunity?
Glasgow, UK

@justmelove 

16 Jan 2025 22:58Last reply 17 Jan 2025 02:56

justmelove

Sick (again)

I can never seem to fight off sickness myself, either need antibiotics or steroids or I just continue to get worse. I try to remind myself that I'm on an immunosuppressant and have a medical condition that suppresses my immune system, but I always feel so down and defeated by going to the doctors. ...
1

@Abz671 

14 Jan 2025 21:38Last reply 15 Jan 2025 07:09

Abz671

New lesions so new DMT, advice below?

So I’ve been on Tecfidera and tolerating it very well but I found out today my first MRI on it showed new lesions meaning a change in DMT. The choices I’ve been recommended are Mavenclad or Tysabri. I understand Tysabri is more effective but I’m 24 years old and I don’t want to be in a hospital ever...
First posted on the Shift.ms app
6

@ppraka66 

5 Oct 2024 18:51 EditedLast reply 6 Oct 2024 14:21

ppraka66

Decision to go on medication

Hi , i am 40yrs old and have recently been diagnosed with MS where I had a flare last year, what am confused upon is medication .. how to decide if I really need to be on medication or maintaining a good healthy lifestyle can help me sail through .. very confused and afraid and have no idea how thes...
First posted on the Shift.ms app
25

@radwithms 

22 Sep 2024 22:55 EditedLast reply 26 Sep 2024 15:28

radwithms

about that really long cold…

Regarding to my last post I went to the A&E to get checked out and guess what? It turned out I had Covid 19+ pneumonia and a lower respiratory tract infection😭I genuinely forget I’m immunospurssed sometimes because that combination truly made me laugh out of shock. No wonder I felt so sick AND ou...
First posted on the Shift.ms app
5

@paolalav 

17 Sep 2024 20:39Last reply 21 Sep 2024 02:57

paolalav

RRMS and Psoriasis

Hi - this is a tricky question so not sure how many responses I will get ! Anyone happen to be on a biologic drug for psoriasis or athritis and been prescribed an MS drug that has not conflicted with the biologic ? If so what has worked? I’m newly diagnosed and wish to remain on the biologic but ...
First posted on the Shift.ms app
4

@DominicS 

3 Sep 2024 09:40Last reply 6 Sep 2024 19:11

DominicS

RSV Vaccine

Apparently for pregnant women and older adults only. I'm not an expert, though I wonder why immunosuppressed people are not included like they are for Covid and Flu. Does anyone know? https://www.nhs.uk/vaccinations/rsv-vaccine/
  • Work and play
  • Family and children
  • Travel
  • Coronavirus
  • Healthy living
  • Symptoms
  • Pregnancy
19

@Laura94 

21 Jul 2024 10:43

Laura94

Post-infusion infection - advice needed!

Hey all, I’ve been on Ocrevus for almost five years now with almost no problems - until this year. I had my most recent treatment in February, and since March I’ve been struggling with persistent UTIs, which have spread to my kidneys and uterus, and more recently had to be hospitalised for pelvic in...
London, United Kingdom
  • Treatment
  • Ocrevus
  • Diagnosis
  • Symptoms

@Lottesmith 

18 Jul 2024 17:38

Lottesmith

Two immunosuppressants and a whole lot of illness

I've been diagnosed with MS for 4 years now, first presentation was in 2015 however and it's taken til this year (2024) to find a good treatment. I say good treatment because not only do I have MS but I have other diagnoses too and all other treatments have worsened my symptoms of other conditions. ...
Edinburgh, United Kingdom
  • Treatment
  • Ocrevus
  • Which DMT
  • Newly diagnosed
  • Diagnosis
  • Fun drugs
  • Healthy living
  • Relapsing remitting
  • Work and play
  • Symptoms
PreviousNext page