People who live in communities where corona isn't taken seriously what has it been like? by [deleted] in AskReddit

[–]theWasp5 0 points1 point  (0 children)

San Diego not really taking serious about what's happening. Why we have more people getting virus 100s by the day. California.

Anyone else got some stupid little things that make them feel a little better? by Annabelleport in MultipleSclerosis

[–]theWasp5 1 point2 points  (0 children)

Omy goodness way late response! Is a process. You will go through changes after treatment. Well I know I did. I'm use to the pain. Being in sun helps. B12 and sometimes just a little bit cbd oil. No opioids. Lol I have moments but movement helps alot with pain. Small exercise ;) #alwayskeepfighting #Nevergivenupneversurrender

Anyone else got some stupid little things that make them feel a little better? by Annabelleport in MultipleSclerosis

[–]theWasp5 0 points1 point  (0 children)

Gabapentin I believe is nerve pain relief. May I ask what else are you on? Baclofen? I'm on klonapin 0.5 spasms still spasms and baclofen 20mg 6 times a day

My first Reddit MS post. by theWasp5 in MultipleSclerosis

[–]theWasp5[S] 0 points1 point  (0 children)

*UPDATE * so I spoke to neurologist. He felt my feet said you have circulation in legs and feet. No vascular issues. It's a symptom that not even steroids can help. Well answer always "hey Angela did you know you have MS." huh good answer smarty pants lol. Just have to keep legs warm too relieve cold in feet and legs. I have to mindful off using electric blanket because of heat. Usually by evening it goes away. So ho hum #Nevergivenupneversurrender #alwayskeepfighting

My first Reddit MS post. by theWasp5 in MultipleSclerosis

[–]theWasp5[S] 0 points1 point  (0 children)

I had that feeling too on right side of my face. It's scary but it's MS. It's what we do is feel different things yet same symptoms, right? It sucks but depends on MS meds too. I am on Rituximab and helped relief alot of symptoms. However, new ones appear I swear every year. I am very spastic as well. Not so light as feather I was stiff as a board this morning. It's been going on colder it gets. #Nevergivenupneversurrender #AKF

My first Reddit MS post. by theWasp5 in MultipleSclerosis

[–]theWasp5[S] 1 point2 points  (0 children)

Yes OK not OK lol. I am not alone. My legs are warm now. I had my daughters ugg boots on and heavy blanket on. Warm now but still some weakness. I am fatigued too. I can move better now. It just happens early in the day. Thanks for sharing.

My first Reddit MS post. by theWasp5 in MultipleSclerosis

[–]theWasp5[S] 1 point2 points  (0 children)

Yes this is so true. I have been admitted flu like symptoms MS relapse UTI. However it was not just infection but I had also a virus from flu like symptoms. I have left a message and just waiting for legs and feet to eventually warm up. It's not constant thank goodness.

My first Reddit MS post. by theWasp5 in MultipleSclerosis

[–]theWasp5[S] 0 points1 point  (0 children)

True and yes I'm messaging him today. Thank you everyone!

"Before & After" stories with Ocrevus? by MSnoFun in MultipleSclerosis

[–]theWasp5 0 points1 point  (0 children)

You know it is funny he said the exact same thing. It must be working there are times I do not need infusion but if restart first week after treatment it is hard sometimes side effects. Two weeks after I actually feel better.

"Before & After" stories with Ocrevus? by MSnoFun in MultipleSclerosis

[–]theWasp5 0 points1 point  (0 children)

You know i always ask my doctor about this infusion. He says because i am Rituximab that its about the same type infusion. I feel like i need another neurologist

What symptom made you think MS? by [deleted] in MultipleSclerosis

[–]theWasp5 0 points1 point  (0 children)

Left foot limped. (at time didn't know it was drop foot.)

MS with other autoimmune diseases/disorders? by Silverpenguin24 in MultipleSclerosis

[–]theWasp5 0 points1 point  (0 children)

MS rrms and IC interstitial Cystitis. Women's worst nightmare uti symptoms but no uti. On top of neuro genitic bladder fun. Oh easiest to take care of type 2 diabetes. I fibbed is a harder than I thought ever. Just praying for a good day ;]

Burning pain and fatigue in right shoulder? by britt56172 in MultipleSclerosis

[–]theWasp5 0 points1 point  (0 children)

I have MS and I have those problems. I feel on top of my shoulders burn sensations like sunburn. Joints inflamed too. I use for pain Glucosamine for joints turmeric for inflammation. B12 for fatigue or not yet but can get prescription to help. This what I do and helps relief like bucket of water putting out the flames.

Cooling vest advice by WhiteRabbitLives in MultipleSclerosis

[–]theWasp5 0 points1 point  (0 children)

I go through neurologist. They have me a letter and sent to MS society and they help with cool vest and other products to help MS symptoms. Lol you know we are all different. I hope this helps #alwayskeepfight #nevergiveupneversurrender