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Unpublished

22 Jul 2025 03:48 Edited

Dive Into the Exciting World of Sprunki: The Ultimate Online Challenge

Welcome to Sprunki: Your Next Favorite Online Multiplayer Game Website: https://sprunkii.io Are you ready for a fresh, exhilarating gaming experience that combines speed, strategy, and a splash of colorful fun? Look no further than Sprunki, game that’s captivating the hearts of online gamers worl...

Washington D.C., United States

@wellbelle

21 Jul 2025 14:15Last reply 21 Jul 2025 15:08

Can you help me get over nerves of travelling in London?

Hi I’m super nervous about travelling by London public transport (local trains, overground and underground) with my mobility scooter (and soon to be purchased electric wheelchair) and have avoided it for 4years! I want to travel into London like I use to pre-MS. looking for anyone who I could ha...

First posted on the Shift.ms app

3

@lekasala

21 Jul 2025 00:18Last reply 21 Jul 2025 10:23

Hi, After my first rituximab infusion I got shingles on my face. Has anyone else experienced this?

First posted on the Shift.ms app

5

@FurbabiesMom

20 Jul 2025 04:45Last reply 21 Jul 2025 13:26

Hi

First posted on the Shift.ms app

8

@Jpetridish

20 Jul 2025 02:33 EditedLast reply 21 Jul 2025 01:20

Hello, so I have a question or just want anyone’s opinion or help if possible please. I first had optic neuritis in 2021, was put on steroids and eventually got better but did leave some perminent damage. I had my first baby in 2023 and after I started to slow down breast feeding I started to get some interesting symptoms. Every morning my hands would be extremely itchy not like dry skin, but from the inside it was driving me insane it was every day and then I started getting random pain either on the top of my head like a bad bruise or on my back which I even thought was shingles, cause it was so painful to the lightest touch, but there was nothing there I even went to the doctor and in about a week that pain subsided The hand itching and the pain on my head continued though. In January I had noticed signs of optic neuritis happening again, but in my other eye, I went to the doctors right away and they had sent me to the emergency room. I was put on Iv steroids and got an MRI I was there for about four days. They saw some white matter lesions in my brain, but it wasn’t clear because of movement. They then did a spinal tap which came out clear. I had gone home and had to follow up with a neurologist about a week after I got home? I had horrible symptoms I was holding my child and my knees gave out my hands were hurting. I was twitching all the time I could not sit still it was worse when I was laying down at night my body just would not stop moving and at some point I could not feel my foot I felt like it was in an ice bucket. I was extremely tired, and I would get random goosebumps in blotches on my arms for no apparent reason I started getting some bad headaches too I then woke up one morning and I could not lift my left arm. It was like it was asleep. I would get pins and needles and different parts of my body also but the muscle weakness in my left arm was horrible. I could barely hold anything. It is still like this to this day, but not as bad if anybody came up and touched me without me, knowing my whole body would spaz out almost like my reflexes were on high drive I have seen three different neurologist since the first neurologist is convinced I have MS the other two which I actually liked better and our MS specialists keep saying I may have it. They did a repeat of my MRIs and again had some white manner lesions in my brain, but they were identical and not in the usual spots where MS lesions would be so they am holding off on fully diagnosing me and want to wait and repeat and see if there are new lesions in the following months. I have not been able to work since since I have a physical job I have good days and bad days if I get sunburn the very next day my hands feel like they’re in a vice. The pain is horrible. I want to know what everyone thinks do I have MS are they just trying to cover their butts and wait or what

First posted on the Shift.ms app

9

@ktdolly

18 Jul 2025 17:40Last reply 20 Jul 2025 00:35

Oral surgery question

Hi everyone. I’m new here and am looking at a probable MS diagnosis. I have some additional testing to get done, but everything is pointing in that direction. In addition to that, I am scheduled for a gum grafting procedure next week. My neurologist said it’s fine to have it done, but I’m anxious ...

First posted on the Shift.ms app

11

@WobbilyButWitty

17 Jul 2025 05:20Last reply 19 Jul 2025 02:38

Depression Days

Does anyone else get random days of depression? I’ve had them before I got diagnosed and they’re a little more prevalent now after my relapse in April. Mine I just feel in a slump and can’t get out of it. They usually just hit me with no specific trigger behind them. It lasts one maybe two days an...

First posted on the Shift.ms app

13

Unpublished

@MayaCardwell

17 Jul 2025 00:55

Blast Away Your Boredom: How Block Blast Takes Match-3 to a New Level

Website: https://block-blast.online/ In the ever-expanding universe of online puzzle games, finding one that truly stands out can feel like searching for a needle in a digital haystack. Yet occasionally, a gem emerges that manages to polish a familiar concept to a brilliant shine. Block Blast is pr...

New York, United States

@denglejr

17 Jul 2025 00:44Last reply 18 Jul 2025 00:16

New here

I'm I'm New here wanted i say hi

First posted on the Shift.ms app

17

@Richielehan

16 Jul 2025 23:40Last reply 17 Jul 2025 08:16

Relationships

Hi, I'm new here. Just pondering the with some thoughts. Is it even possible to be get in a relationship after you get diagnosed. I feel like really won't be able to find anyone because I'd be coming with all this baggage from my health and I would hate to leave that with someone else.

First posted on the Shift.ms app

5

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