#cold - Shift.ms

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7 Dec 2024 20:53Last reply 9 Dec 2024 20:37

Cold

Just whinging because I’m sure there are others who understand. I hate when it’s cold. My fatigue goes through the bloody roof and I end up napping more often than anything. I need to move to country where it stays relatively warm in the winter months 😂 I can’t wait till the weather gets warm b...

First posted on the Shift.ms app

16 Jan 2024 14:48Last reply 8 Aug 2024 13:44

Cold

Hiya quick question, are you in more pain when it’s colder out. I do it’s horrible 🥶😢

Hull, United Kingdom

8 Dec 2023 14:43Last reply 9 Dec 2023 10:05

Cold

Hey everyone, I’ve had a really bad MS week, my worst in a good while and whilst I know the ‘why’ isn’t important, it can help a bit. I just wondered if there’s any chance the cold could make my symptoms worse? My stability was all over the place and I had lots more tingling than usual, but today wh...

Nottingham, UK

@emmastanley123

30 Nov 2023 21:25Last reply 2 Dec 2023 09:27

COLD

Hi all. Any other people with MS really struggle with the cold?? Particularly at night, my muscles spasm and its very painful even when I'm in bed with 5 layers I just can't shift the cold to the bone feeling!! Advice welcome x

19 Jan 2023 23:19Last reply 20 Jan 2023 18:11

Cold

Hi guys how do people cope in the cold it is getting too now 😭

29 May 2022 09:05Last reply 8 Jun 2022 07:41

Cold

Hello hive mind, is feeling cold (even when others say its OK or hot) a thing with MS please?

@Alesia_Poilova_Madni

15 May 2019 07:51Last reply 21 May 2019 00:36

Cold

Hi. My hands are almost always cold...if bit colder outside or in rooms I am shaking like leaf haha. Who knows why?

6 Jul 2025 18:26Last reply 18 Jul 2025 04:49

My hands and fingers have a numbness like they are in icy cold water . Has anyone experienced this ? If so what do you do or take for it ?

First posted on the Shift.ms app

17 Jul 2025 00:50Last reply 17 Jul 2025 23:20

Those on Tysabri, how has it affected your immune system? I’ve got a 3 year old, so colds ect are more prevelant for me.

First posted on the Shift.ms app

30 Jun 2025 04:56 EditedLast reply 30 Jun 2025 23:13

It's been so hard these past couple weeks, last week I was moving something lift it and my back snapped. Its getting better now thank God. Then the heat, I though I was ok because after been diagnosed last winter I realized I had cold sensitivity so I was hoping the summer wouldn't be a problem. Now the heat is here and I'm STRUGGLING. I feel heavy, like I'm walking through wet cement or sand. They say exercise helps with fatigue and we need the sun for vitamin D. I'm so tired...I feel like just crying, I really dont know what to do to help with these feeling. This disease sucks real bad, I'm so tired. What are some things you guys do to help with the fatigue.

First posted on the Shift.ms app