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 1437 results by
Recent activityNewest posts

@mlw85 

24 May 2022 20:35Last reply 25 May 2022 06:16

mlw85

Some Advice

Hi not been on in a few months, started taking tefidera 6 months ago and had my MRI scan and just got results back and have 2 new lesions on my brain but the neurologist wrote in his letter that he thinks that it might have been the space I had came off tysabri and started tecfidera but I am scared ...
  • Symptoms
  • Relapses
  • Tecfidera
  • MRI
  • Treatment
  • Diagnosis
  • Work and play
  • Mental health
2

@julespickering5 

11 Sep 2021 11:52Last reply 11 Sep 2021 23:26

julespickering5

Changing DMD | Ocrevus

Hello I haven’t actually written anything on here but always gone on for support, information and to understand what other people are going through. I have been on Tefidera for little under 2 years now, which hasn’t helped in anyway as I am still getting lesions on the brain and spine. I’ve now d...
  • Ocrevus
  • Treatment
  • Healthy living
  • Tysabri
  • MRI
1

@betty 

9 Jul 2016 21:04Last reply 10 Jul 2016 19:03

betty

I learn something new here everyday!

Wow, I'm so glad I have this group to turn to, I don't feel that I always get the truth from my doctors and nurses here in Canada, so I am a little frustrated! None of my doctors or nurses have EVER cautioned me about taking ibuprofen while on Tecfidera. I take it frequently for back and neck pain ...
  • Diagnosis
  • Disclosure
  • Symptoms
  • Mental health
  • Pain
  • Treatment
  • Copaxone
  • Tecfidera
3

@Littlemisssunshinedon 

24 Jan 2016 17:38Last reply 25 Jan 2016 17:44

Littlemisssunshinedon

Babies!

Hi everyone :) I was diagnosed with MS aged 27. Since turning 30, I have had the overwhelming urge to try for a baby. Started on Tecfidera six weeks ago but discussed with my neuro about trying and he said to get an mri and then he will see me and if the ms is stable he is happy for me to come off t...
  • Diagnosis
  • Newly diagnosed
  • Symptoms
  • Mental health
  • Relapses
  • Treatment
  • Which DMT
  • Work and play
  • Family and children
  • Positives of MS
6

@Tash41 

4 Nov 2014 17:07Last reply 9 Nov 2014 13:51

Tash41

Tecfidera - advice please

Hi, just looking for some advice please. I know it's only early days but I took my first Tefidera this morning and within two hours I felt terrible. I felt really sick and then began having hot flushes. I know these are common side effects but wasn't expecting to feel so bad. I don't want to give up...
  • Symptoms
  • Hot and cold
  • Mental health
22

@Jeng 

7 Jan 2021 13:02Last reply 15 May 2025 19:04

Jeng

Brabio or Tecfidera🤔🙃

I was diagnosed RRMS in Dec 2020, the neurologist believes I've had it for 11 years. I've had 2 relapses in 2 years and currently have 1 active lesion (great way to end the year!) I have narrowed my choice of DMT down to Brabio 3xweek or Tecfidera, I like that Tecfidera is more effective and a pill ...
  • Treatment
  • Tecfidera
  • Newly diagnosed
  • Diagnosis
  • Research
  • Work and play
  • Which DMT
  • Fun drugs
  • Relapsing remitting
  • Diet
18

@motorhead 

22 Jul 2024 13:26Last reply 26 Apr 2025 20:32

motorhead

Generic Tecfidera

Hi Everyone! Has anyone had any issues since their Tecfidera has been move to the generic version of the medication? I've been on the generic version for around 3 weeks now- since moving to the new medication I've been flushing literally every night, even after taking an antihistamine and aspirin ...
London, United Kingdom
  • Tecfidera
  • Treatment
  • Symptoms
  • Fatigue
  • Diagnosis
  • Work and play
  • Gilenya
10

@Jillianleigh16 

3 Apr 2025 19:30 EditedLast reply 14 Apr 2025 14:43

Jillianleigh16

Tecfidera (dimethyl fumerate)

Has anyone taken this Medication? I took my first dose Last Friday and had a horrible reaction of severe flushing, high BP and HR I was sent to ER from work. Any advice or similar reactions? Update: I have been completely stopped on the Tecfidera. I will be switching neurologists due to mine movin...
First posted on the Shift.ms app
43

@clars64 

24 Mar 2025 20:20Last reply 24 Mar 2025 23:42

clars64

I was diagnosed 17 years ago. Started with Tecfidera then Ocrevus, and now Kesimpta. My question/frustration is as follows. What should i expect from my Dr.? He is a neurologist. I see him 1 time a year which follows an MRi. We meet for 10 minutes and he tells me the MEI showed “ no remarkable changes”. Appointment complete. I get nothing about me and my progressing disability. I feel like a data point and nothing else. Thoughts? Thanks

Suring, United States
First posted on the Shift.ms app
5

@lizzie20 

7 Mar 2025 13:57Last reply 7 Mar 2025 18:44

lizzie20

tecfidera

This may be a silly question but when i was speaking to my ms nurse the day i was starting tecfidera she said im not due for more bloods till may and about a week ago im getting told i need to get bloods done before i go onto the higher dose but the nuse gave me the higher dose i just dont start it ...
First posted on the Shift.ms app
7
PreviousNext page