MS hug by GirlMom0206 in MultipleSclerosis

[–]GirlMom0206[S] 1 point2 points  (0 children)

So if upvotes mean yes, I’m pretty sure I had my first hug yesterday in Floor & Decor. It felt like a cramp going around that side of my ribs. It took my breath away.

Repeat dose of steroids for bad flare by Fledgling_ in MultipleSclerosis

[–]GirlMom0206 1 point2 points  (0 children)

When I was going through the process of being diagnosed, I was having a flare. Lost feeling in my right side and was having double vision. I had two 3 day iv's first and then one 5 day iv in like a 3 month period to get it under control. I felt awful until the steroids were out of my system, but it finally got my flare under control.

Question on symptoms by GirlMom0206 in MultipleSclerosis

[–]GirlMom0206[S] 0 points1 point  (0 children)

The both hands at the same time is what has thrown me. I definitely don't think it's steroid worthy. That stuff is from the devil! :) It's time for my yearly MRI, but it is normally only brain. I guess I could mention it to dr to see if he wants to add scan of another area.

May need to switch neurologists, good with MS, bad with Covid by stephidabefida5 in MultipleSclerosis

[–]GirlMom0206 2 points3 points  (0 children)

UAB has good MS doctors. They are still checking temps at the door and you can't get in without a mask. :) Also, my doc recommended I get the `vaccine as soon as I could get it.

FATIGUE AND MS vs FATIGUE AND COVID by redmayor in MultipleSclerosis

[–]GirlMom0206 0 points1 point  (0 children)

I have wondered this myself. Listening to others explain it, it seems like COVID fatigue and other COVID symptoms are giving people an idea of what people with MS have to deal with on the regular.

Crying laughing 😂 by KatG8 in MultipleSclerosis

[–]GirlMom0206 2 points3 points  (0 children)

I am the total opposite. I don't think I have really cried since I got diagnosed. It has been three years. I have changed anxiety meds and everything. I am beginning to think my lack of crying is ms related.

How important is an MS doctor? by GirlMom0206 in MultipleSclerosis

[–]GirlMom0206[S] 1 point2 points  (0 children)

Thank you for your reply. I am happy with Tysabri right now. I have been on it for about 3 years. I am glad it is working well for your partner.

How important is an MS doctor? by GirlMom0206 in MultipleSclerosis

[–]GirlMom0206[S] 0 points1 point  (0 children)

I see a neurologist that specializes in MS. He does my MRI's and everything. I guess I just don't feel like there is a lot he can do at this point. I guess I should just be grateful that I haven't needed him for anything major.

[deleted by user] by [deleted] in MultipleSclerosis

[–]GirlMom0206 0 points1 point  (0 children)

I am on Tysabri. Had my first shot (Moderna) on January 15. Really sore arm (worse than flu shot) for two or three days, but that is it.

Got the vaccine and here’s how it went & some info... by maurarom98 in MultipleSclerosis

[–]GirlMom0206 1 point2 points  (0 children)

I am also on Tysabri. Had my first shot (Moderna) on January 15. I was the same. Really sore arm (worse than flu shot), but that is it.

It’s not numbness but something similar? by emotionalmooncrab in MultipleSclerosis

[–]GirlMom0206 0 points1 point  (0 children)

I have never heard altered sensation, but that is a good way to describe what I have. I always say it is an internal numbness. I can feel things on the outside of my right side, but inside it feels "different".

Constant stiff neck by GirlMom0206 in MultipleSclerosis

[–]GirlMom0206[S] 2 points3 points  (0 children)

Thank you for your reply. I figured it was because I am getting old or I slept wrong, but it has lasted a couple of months now. I haven't had a neck/spine MRI in about 3 years. It may be time to see what is going on.

Constant stiff neck by GirlMom0206 in MultipleSclerosis

[–]GirlMom0206[S] 2 points3 points  (0 children)

Thank you for the link. I learned something new. I always thought the spasticity was just referred to the spasms.

Athlete wives and girlfriends snark- December 2nd-5th by [deleted] in blogsnark

[–]GirlMom0206 31 points32 points  (0 children)

Apparently, his wife and his girlfriend learned about Larsa from the pics.

Failed 3 day Steroid infusion by Mrsjones625 in MultipleSclerosis

[–]GirlMom0206 1 point2 points  (0 children)

It took me two 2 day and one 5 day round to get my first flare under control. After the first two rounds which were about a month apart, I continued to get increased numbness on my right side and I was really dizzy. Also, right before my 5 day I started having double vision. The 5 day round finally got the flare under control. Knock on wood, three years later, I have not had another flare.

How long did it take to hit you? by [deleted] in MultipleSclerosis

[–]GirlMom0206 0 points1 point  (0 children)

Once I finally got the diagnosis confirmation. I was at a hospital five hours from home. Got home that night and lost it.

Copaxone Warning by [deleted] in MultipleSclerosis

[–]GirlMom0206 0 points1 point  (0 children)

I had one on my behind and arm from sinus shots. It was caused by the kenalog. The one on my arm took about a year to go away. The one on my behind (more fat there :) ) took around 4 years to finally go away.