#hair - Shift.ms

5 Jun 2025 22:52

Exercise

Hi everyone, I joined the other day and keep on seeing a repeat question about exercise, we here in England the ms society made a fair few exercise videos and put them on YouTube: channel: m.s society uk. So if your look for light to medium exercises then why not take a look , all the best

First posted on the Shift.ms app

@Yasmin91x

5 Jun 2025 17:06Last reply 5 Jun 2025 18:25

Ms face tickles

Does anyone else get this? I’ve had this all day long since I’ve had a shower washed my hair. Feels like burning

First posted on the Shift.ms app

Unpublished

@WaltSampson

5 Jun 2025 06:36 Edited

Moto X3M: The Ultimate Adrenaline Rush in a Side-Scrolling World

In the ever-growing world of online browser games, few have managed to carve a niche as thrilling and addictive as Moto X3M - https://motox3mfree.io/. Combining elements of physics-based gameplay with high-octane motorcycle stunts, Moto X3M has won the hearts of millions of gamers across the globe. ...

Montreal, Canada

Unpublished

@bukarim

5 Jun 2025 02:46

Ragdoll Archers

Choose from a variety of game modes, including local multiplayer where you and a friend can go head-to-head or AI battles that get progressively harder as you progress. Add diversity and unpredictability to battles with different characters, bows, and power-ups that you unlock as you go. Power-ups l...

New York, NY, USA

@goisgreat87

3 Jun 2025 16:59

Game changer 🚨

If you fall a lot or scared to go outside try this I have one on the way and so excited! https://sairbagpro.com/?fbclid=PAQ0xDSwKsCIBleHRuA2FlbQIxMQABpy04if9SN-P6hjzyex8wLsmeD8omZlwEMiIp3JqKdoSGSVIJrpACJbaDHcd0_aem_mkpfAnRXkONBq4Pf-bmSxQ

First posted on the Shift.ms app

@ChiMum

2 Jun 2025 21:39 EditedLast reply 3 Jun 2025 10:55

Two and a half years through

Hi, I've not been here for ages because it wasn't good for my mental health. I just really needed a safe space to vent. I'm on the maximum dose of Sertraline at the moment but I don't feel that it's helping enough. I was diagnosed with RRMS in December 2022 and my life has completey changed sin...

Sheffield, UK

Unpublished

@Michellejohn35

2 Jun 2025 18:17

ecently had my MRI results and (as I kinda suspected after a rough few months) had new lesions.I'm currently on Plegridy (moved from Tecfidera as I'm JCV positive and my lymphocytes lowered a lot). Tecfidera worked ok for me, but Plegridy obviously hasn't been as effective. Due to the hard few months I've really isolated myself from people (some I'm unsure even how to reach out to again now) and live alone alone some of the time when my four children are at their mum's. Positive news is, they've mentioned Ocrevus and Kesimpta, which are obviously higher efficacy treatments. Could I ask for any advice people have around these DMTs, please? If you've seen me ask on Facebook or Instagram, then feel free to ignore and not repeat yourself.

First posted on the Shift.ms app

@MK24

2 Jun 2025 17:22Last reply 4 Jun 2025 11:34

Ocrevus or Kesimpta

I recently had my MRI results and (as I kinda suspected after a rough few months) had new lesions. I'm currently on Plegridy (moved from Tecfidera as I'm JCV positive and my lymphocytes lowered a lot). Tecfidera worked ok for me, but Plegridy obviously hasn't been as effective. Due to the hard fe...

, United Kingdom

First posted on the Shift.ms app

@KarenMrMoose

2 Jun 2025 08:43Last reply 4 Jun 2025 18:25

Walking

Hi all.. do's anyone else feel let down by their doctors.. My consultant is more bothered about how far I can walk than anything else, I have vision problems but to them it's not a problem to me it's a nightmare and all they keep throwing at me is physio to help my walking... I'm not on DMT as my bo...

First posted on the Shift.ms app

@RoseRivera1214

1 Jun 2025 03:03Last reply 1 Jun 2025 07:24

What to do?? Hi, my name is Rose. I’m new to this app. I was diagnosed with Ms back in 2016. Since than I’ve tried two dmts. Gilenya and mavenclad since than. Gilenya gave me horrible rashes for four years before my neuro switched me to mavenclad. That medication was the absolute worst. I lost about half of my hair and had frequent heart palpitations to where I needed a heart monitor twice. I only did the first year round 1 and never followed up for my second because of fear. I am meeting with my neuro within the next month about starting a new medication. What is some options that he could give me? And what is your personal experience with those DMTS?

First posted on the Shift.ms app

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