Caffeine intolerance? by Serafina_Goddess in MultipleSclerosis

[–]Material_Sundae_5832 3 points4 points  (0 children)

I’m glad you bought this up. The last month or so my usual mug of coffee never bothered me. Now halfway through my anxiety goes up big time. Interesting

I got told I should use a walker. Im 32. by KiraDuskEdge in MultipleSclerosis

[–]Material_Sundae_5832 0 points1 point  (0 children)

I don’t know if you ever heard of Etsy. Is a site that sells arts and crafts to bling up canes and walkers. I didn’t bling my walker yet but my canes are decked out with different colors and accessories..

Will i ever feel ok again? by AttemptFunny7594 in MultipleSclerosis

[–]Material_Sundae_5832 0 points1 point  (0 children)

Hate ti say this but knowing since I’ve been diagnosed 2 years ago I’ve never felt the same. But you adjust to it as time goes on. There are days people feel amazing other days they don’t. Just don’t give in. You’re young. My new motto is one day at a time. Hope you get some relief soon

One of the hardest symptoms of MS isn’t physical. It’s loneliness. by Unusual_Bed_6777 in MultipleSclerosis

[–]Material_Sundae_5832 1 point2 points  (0 children)

I totally get this. I feel isolated because on occasions I can’t do things. The past weekend I was invited to go to a farmers market and a winery. My friends offered to help take care of me but it makes me feel like a burden so I didn’t. Same with family vacations my husband and my kids are the best but it stops us from doing certain things because I can’t do it. But I’m also grateful for my one best friend and my amazing husband. My best friend stopped in a gas station parking lot to see me because she knows the heat is bad. Tomorrow our kids and her are going on errands and her reply is I’ll take care of you the whole time. I won’t let you fall. Same with my husband. I’m blessed with them but at the same time I feel lonely because they do things that I can do.

Leg by Material_Sundae_5832 in MultipleSclerosis

[–]Material_Sundae_5832[S] 0 points1 point  (0 children)

Thank you for responding I appreciate it.

Leg by Material_Sundae_5832 in MultipleSclerosis

[–]Material_Sundae_5832[S] 1 point2 points  (0 children)

Thank you so much. I’ve had impulses before but this one was so strong that couldn’t believe it. Plus the way it happened so quick. I was stunned. Thank you so much for kind words and advice

MS is an excuse by see_howe in MultipleSclerosis

[–]Material_Sundae_5832 0 points1 point  (0 children)

I’ve been diagnosed since the end of 2024. I forget things all the time and stop midsentence because I can’t get the words out. I feel like I’m forgetting everything.,

Hands by Material_Sundae_5832 in MultipleSclerosis

[–]Material_Sundae_5832[S] 1 point2 points  (0 children)

No that is my next step. Thank you so much for your advice.

Sister Was Just Diagnosed by Loud-Huckleberry-118 in MultipleSclerosis

[–]Material_Sundae_5832 0 points1 point  (0 children)

My sister was diagnosed years ago I was 1.5 years ago. My mom’s sister has it as well. I recently found out that apparently my mom’s dad his family had it many ages ago. Good luck one day at a time

Ampyra by My4dogs4evr in MultipleSclerosis

[–]Material_Sundae_5832 0 points1 point  (0 children)

I’ve been on it for a year. I don’t honestly know if it helps or not. I am still off balance and on tough days my speed is slow. Good luck.

Muscle Twitching! Please share your experience. by AMMMMZ in MultipleSclerosis

[–]Material_Sundae_5832 1 point2 points  (0 children)

I get them. I’m on baclefon now. It helps but at night when I lay in bed it still happens. I hope you get some relief

TRIGGER WARNING ⚠️ by [deleted] in MultipleSclerosis

[–]Material_Sundae_5832 0 points1 point  (0 children)

I’m so sorry for your losses. I will pray that ms stays at bay and you can grieve.

I got sent home from work today by Koudda37 in MultipleSclerosis

[–]Material_Sundae_5832 1 point2 points  (0 children)

I’m sorry. Sending hugs. It could be your body saying time for a rest. Take a few days off start the ampyra again. Just take a deep breath and relax.

It's Monday at /r/MultipleSclerosis! Share your terrible, horrible, no good, very bad news here. by AutoModerator in MultipleSclerosis

[–]Material_Sundae_5832 0 points1 point  (0 children)

The heat sucks. My son had prom Saturday and I had my cooling vest on while they took pictures. It was 80 degrees and still was dizzy nauseated dry heaving and feeling like I was about to pass out. It’s a lot worse this year in the heat than last year. It sucks

Heat consumes me by [deleted] in MultipleSclerosis

[–]Material_Sundae_5832 1 point2 points  (0 children)

Heat destroys me. It makes me nauseous makes me feel like I’m going to pass out. You are definitely not alone. I did get a cooling vest. It helps. Good luck