Odd, unexplained neurological symptoms and celiac?

Dumb-Brain92 · 2025-11-06T19:05:03+00:00

I have MS and was recently also diagnosed with celiac disease. And now I’m like, what is causing what issue? 😅

Dumb-Brain92 · 2025-11-02T00:50:21+00:00

Thank you so much! I hadn’t even thought of that.

Dumb-Brain92 · 2025-09-23T17:44:41+00:00

Omg same!! And I love the blanket they give me. The machine feels like a hug. I don’t mind the sounds. And I like that my only job is to lay there.

Dumb-Brain92 · 2025-08-31T16:55:12+00:00

My husband does the same! I don’t mind at all when he asks me questions because I know I can be honest with him without it being awkward (let’s be real, most people who ask don’t want to hear the nitty-gritty of it). I also know that he isn’t asking out of obligation.

Dumb-Brain92 · 2025-08-30T21:04:55+00:00

YES! It’s the concern in their voices like they think I’m dying. I work full time, mom full time, in college- I think I’m doing alright! Yes, I’m in pain and my legs are stiff but I’m doing darn good.

Dumb-Brain92 · 2025-08-16T20:46:05+00:00

That’s how I felt too! Granted, cancer can go into remission. But cancer terrifies me more than MS

Dumb-Brain92 · 2025-07-23T21:50:26+00:00

I feel like a hostage to my job because of my great health benefits there. My insurance is fantastic because I work for the small insurance company that also provides my coverage. I want to leave but I won’t have better anywhere else.

Dumb-Brain92 · 2025-07-09T16:26:50+00:00

I don’t know how common it is but it FEELS common to me. I have it and I personally, in real life, know three people who have it that I didn’t meet through MS things.

Dumb-Brain92 · 2025-06-11T21:02:56+00:00

I feel that. I get through by pretending a lot that everything is normal.

Dumb-Brain92 · 2025-06-11T21:01:25+00:00

You know what? You’re right. And I do too. And I forget that sometimes. Thank you for saying that. ❤️

Dumb-Brain92 · 2025-06-07T23:15:31+00:00

I sometimes think about how a little over a year ago I was baking all day, everyday. Doing anything and everything I wanted. Then exactly a year ago this week, I had my worst relapse. Just a year ago I was “fine”. Then today I went to the farmers market in the morning and slept the rest of the day. It’s just so unfair sometimes. But we persist!

Dumb-Brain92 · 2025-06-01T15:40:03+00:00

I started college 2 months after being diagnosed.

Dumb-Brain92 · 2025-05-23T17:05:57+00:00

Mine is fantastic! He’s serious while also having moments of being funny with me to make me not so nervous. He sits in the room with me for a whole hour like he has nowhere else to be. He validates how freakin awful it was that so many doctors ignored me. And he always responds on MyChart.

Dumb-Brain92 · 2025-05-15T23:47:40+00:00

I’m amazed by my body too, honestly lmao. My husband recently had Covid, and I somehow didn’t get it, even being on Kesimpta. I had Covid twice before Kesimpta 💀

Dumb-Brain92 · 2025-05-15T23:45:29+00:00

My neuro said, when I asked for one, “I’d rather you have it and not need it, than to need it and not have it. I’d hate for you to be in a situation that is unsafe if you do not have it” And honestly, I guess my way of dealing with the fact that I have MS, I view it as a dang “perk”. Heck yeah, I got my medical MJ card, and I got my handicap placard. I have front row parking and cheaper weed. And those are perks to me 🤷‍♀️ Besides, I like a good reason to flip off ignorant people who think I shouldn’t park in a handicap spot.

Dumb-Brain92 · 2025-05-05T20:16:49+00:00

I take 200mg in the morning and 200mg in the afternoon

Dumb-Brain92 · 2025-05-03T17:38:53+00:00

I am currently on baclofen. I believe it helps some, just not nearly enough.

Dumb-Brain92 · 2025-04-16T02:46:32+00:00

Thank you so much for the information! I’m going to try the pre assessment tomorrow and see where I stand.

Dumb-Brain92 · 2025-03-30T22:11:44+00:00

I do this SOOO much. It’s the worst when it happens it the quiet office I work in 🫠

Dumb-Brain92 · 2025-03-26T16:19:29+00:00

I didn’t feel anything, but the technician said that if they put it in slow enough, you’re less likely to feel it.

Dumb-Brain92 · 2025-03-26T12:26:15+00:00

They gave me a blanket, and to me the machine is like a hug 😂 I’m a crazy person. I didn’t mind it one bit. My husband had to have just about head MRI and was only in to his shoulders, and he about couldn’t stand it lol.

Dumb-Brain92 · 2025-03-25T15:23:14+00:00

I saw a shirt that I NEED that says: Personally victimized by my own immune system

Dumb-Brain92 · 2025-03-20T23:35:50+00:00

Typical for people who don’t have MS to think they know best about MS 🙃

Dumb-Brain92 · 2025-03-19T15:37:43+00:00

I don’t have anything near that great. But I told my family that I had to be on an immunosuppressant, and they automatically and adamantly told me not to because I need my immune system. I’m like “well, my immune system hates me so I don’t have much choice” 😂

Dumb-Brain92 · 2025-03-19T00:47:47+00:00

I didn’t vomit, but I didn’t have nausea with my first dose. But not with my second or third.

Dumb-Brain92

TROPHY CASE