#fums

7 May 2013 20:43Last reply 10 May 2013 07:54

I've decided that I am going to to get involved with the whole blogging and Twitter thing and finally get out of my head the things that I would like to say to my MS if it were a person. Thinking about this, it has become clear that everything that I would want to say basically fits under the title ...

@FUMS

4 Aug 2018 13:34

Looking for Guests for The FUMS Podcast

Hi! I’m Kathy Reagan Young, founder of FUMSnow.com and the FUMS Podcast Show. I’m interested in interviewing English-speaking MS’ers from several different countries about your diagnosis and treatment experiences in your country. I think it will be really interesting to see the difference in care...

@maljam2002

27 Aug 2024 06:16

Take THAT, MS!

When my #MS says "No" today... fishtank cleaned happily. #FUMS ➽ Thoon & Katia - My Goldfish 🐠 Simple yet keeping me happy → https://rebrand.ly/Thoon ← #Goldfish #Aquarium #Pet

Sydney, Australia

@wxrmthinthesun

28 Feb 2023 14:31 EditedLast reply 2 Mar 2023 18:34

How do you live with your MS?

I'm just sharing some thoughts here and I'm curious about other people's opinions! So, we may all know that Christina Applegate did a red carpet in the past couple days with a cane that had "FUMS" all over it. Which I respect but it's not for me. The "MSWarrior/Fighter" and the " FUMS" mentality isn...

Scotland, UK

@Sheepster

15 May 2022 13:41Last reply 19 Aug 2022 16:28

Any guitar players

I used to play quite badly i must admit lol https://www.youtube.com/channel/UCGvb6zzPd7SqWLeY2wPtxSw trying to learn all over again purely to shove fingers up to the MS FUMS

@wonderwoman

3 Feb 2017 14:02

World ms day

Hey guys, I am just curious: what are you going to plan on world ms day on 31th of may? Are there any cool meet ups or activities you're joining? Hence I live in Germany, I will meet up with my F.U.MS group. I guess we will go out for food, drinks and fun – as usual :) Cheers, Tina

@TracyD

25 Feb 2016 14:55Last reply 7 Mar 2016 15:19

Half time result Lemtrada 1 - MS 0

End of Year 1 MRI - First review results are in. It's bloody awesome news !!!!! NO progression No new lesions Existing damage less conspicuous I swore from the start I would kick this shitty illness in the nuts and teach it who was in charge of my immune system. At half time I'm winning and it'...

@22emkat

13 Jul 2025 20:39Last reply 14 Jul 2025 21:43

Tecfidera to dimethyl fumarate

Has anyone else been changed to generic dimethyl fumarate from Tecfidera? And if so, have you noticed any differences in side effects? I know it is the same thing, but just wondered! Tia!

First posted on the Shift.ms app

@stavy917

10 Jun 2025 19:29Last reply 11 Jun 2025 15:22

Hi just got diagnosed yesterday and was given treatment options I went for the dimethyl fumarate anybody know if it’s any good as I’m completely new to all this and a little worried 🫤

First posted on the Shift.ms app

@Jillianleigh16

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

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

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