#funny - Shift.ms

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Funny

Not to brag but I already have a date for New Year’s Eve. It’s December 31st

Sheffield, United Kingdom

Funny

Whoever told me to leave the car at the pub & get the bus home did not realise I could not drive that either.

Leeds, United Kingdom

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FUNNY NEW TURN 🤗😅

My days have been quite painful since summer’s start. As a result I’m asleep soon after and the days now become nights 😅 the fun find is that I’m darn near pain free all night until the sun comes up. So freaking weird! I can tell the sun has come up by the tightening of my leg muscles as well as ...

Newark, United States

First posted on the Shift.ms app

Totally resonated ‘ I get you’ I’ve been going through similar - few loses over the last 2 yrs - I’m so very sorry for your loss- take care of your ALWAYS & remember be patient with yourself however you feel whenever you feeling it is okAnd I very wise person told me to practice stuff with S’s they really help here’s a few to get you started -Sex/relationships/connectionsService - acts of kindness/gratittude/thanks/ helping others etcExerSize ( yep the big S he’s funny too)Singing ( if like me you make dogs & children cry when you do you can do it while alone to music ie sing a long or humming works too)Socialing - try not to withdraw or isolate being around good people is important especially those who get it - grief sadly is a well trodden path and no one is exempt but there’s comfort in not being in it aloneHope this helps in some tiny way 💪🍀🫂🧡🤞😊

First posted on the Shift.ms app

Hi all, just in update from my last post about Adderall and how it makes my teeth and tongue feel funny. I started using children’s Burt’s Bee’s toothpaste with fluoride and my mouth feels better. Not normal before MS and meds but not as bad as it has been. Just st thought I would share. Mind you it’s only been a few days but a win is a win.

First posted on the Shift.ms app

Since I have moved to Florida from Vermont, I have been learning a lot more about MS as it’s whole until I actually found a neurologist that was actually specializing in MS. I did not know that not only is it a nervous system problem, but it is also autoimmune and I did not know That extreme cold and extreme heat can actually make flareups worse and if it is hereditary, it can also make the MS come out quicker. I did not know that I did 13 years making snow at a ski resort in Vermont and then when I moved to Florida, I did Five years underground construction and I always wondered why I felt funny and triple digit heat, but it wasn’t heat stroke, and there were days where if it got below zero or into the negative temperatures, my body would tighten up intense up like I was getting squished by a bow constrictor. I went years until my primary care physician told me to go see a neurologist, and then he gave me the evaluation told me to take an MRI. They did not find anything in my spine, but my brain said a lot is what the neurologist said, and then he started poking and stab in the bottom of my feet with stuff and doing a tuning fork all over my body and when I told him I couldn’t feel it in certain spots and then in other spots, I could just slightly feel it or it just felt like a ant crawling on my leg or on the top of my foot. I’ve never seen anybody that evaluated me for anything get so concerned, looking on their face and then now he wants me to do a spinal tap, which I am doing August 8. I already know it’s not going to be like the movies or television shows where it’s gonna be excruciating painful off the back. It’s going to be the next day. I’m going to have to recuperate. I have several family members with MS as well so they are kind enough to give me peace of mind explaining to me how they felt after all the stuff they had to do and I am pretty much doing the same thing and my neurologist did put me on something. I can’t remember the name of it or pronounce it but my flareup weren’t so bad, but then my colitis started getting worse so he took me off it and now as long as I just stick to easy tasks, I’m not so bad but it hurts sometimes to move. I can relate to how my mom felt towards the end now, she said she was in so much pain, but because her mind was slipping back into a childish state of mind. She had good spirits about her. My dad just turned into a zombie and he said that he only focused on walls or focused on watching a television show because it was the only way he could control the pain. I meditate to help with my pain and I listen to the doctors and follow my prescription regiment, but there are still days where it feels like I got hit by a truck and I just stood up out of bed. The scary days are when I can’t get out of bed altogether. I do not know if anybody else has ever felt like this, but there are days where I wouldn’t wish this on my worst enemy and to get places of business to understand what you’re going through and to explain to them OK if you have me do these tasks then don’t expect me to come to work tomorrow because I won’t be able to move. I have been rejected so many times my wife just finally decided to fill out for disability and now between my attorneys and Social Security I have my doctors not only giving me tests and labs for their peace of mind but now I have them filling out papers and forms for my attorneys and Social Security and it’s been like that for almost 3 years now every time I think we’re getting close I have more papers in the mail for my doctors to fill out or my neurologist there are days where I just wanna give up but then I think about what it would do to my family and then I sit with my son and play video gamesuntil the feeling goes away, and I snapped back into my normal self

First posted on the Shift.ms app

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all most i fall today hahaha was so funny because i didnt fall BUT i dont know if u guys sometimes fell your left or right side for all ur body like u got a lot of weight? thank u 4 read me friends 😉

First posted on the Shift.ms app

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For the first time since being diagnosed in 1991 I have been dealing with a funny feeling in my neck that feels like a surge of electricity that goes down my back has anyone else had this feeling

Alma, United States

First posted on the Shift.ms app

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“The funny thing is, I work as a caregiver, and now I’m on the lookout for MS patients!”

Life is so Funny

First posted on the Shift.ms app

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Hey I was diagnosed with MS last September I had no physical symptoms but had been under the eye hospital for years with inflammation behind both eyes a new doctor sent me for an MRI which lead me to a neurologist and a diagnosis Ive never had physical symptoms but theres been things in my past like belspalsy that they believe was MS episode for the past week I've been woke. In the night with pins and needles in my hands and lower arms I'm not sure if I'm sleeping funny or it's connected to my remmiting and relapsing MS has anyone else experiences this ?

First posted on the Shift.ms app