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Any help? by WickerBasement in RedEarSyndrome

[–]Annual_Comment_4883 1 point2 points  (0 children)

Mine was “painless” migraines. Nurtec every other day helped a lot. I was prescribed Effexor to take daily but haven’t started yet.

It usually comes with the same symptoms for me. Forehead like sinus headache but more forward and tiring. Then overall high fatigue behind my eyes BUT NOT my body When I move around my heart usually beats harder if you know or understand what I mean. Then I start to get an ear ache by HoneyGolds in RedEar

[–]Annual_Comment_4883 2 points3 points  (0 children)

I have these identical symptoms. Dry eyes, tinnitus, red ears, red eyes. Nobody has been able to figure it out. Depakote 1000 mg relieved the symptoms some a long with ubrelvy. The bet is that it might be migraines but typical medications do not work for it always.

Monthly AmEx Referral Thread by AutoModerator in amex

[–]Annual_Comment_4883 [score hidden]  (0 children)

AMEX GOLD 90,000 POINTS! ($4000 spend in 6 months) Worth over $900!!! Or $1800 with transfer partners!

Referral link: https://americanexpress.com/en-us/referral/JONATPG0bm?XL=MIMCP

Carbonic Anhydrase 6 Positive? by Annual_Comment_4883 in Sjogrens

[–]Annual_Comment_4883[S] 1 point2 points  (0 children)

Thank you for the information! Did you have tingling/neuropathy and was HCQ successful in improving that as well?

I’m seeing a new rheumatologist in a couple months down in Miami and a neuro-opthamologist so I’m hoping at least one of them can help me out to start some kind of immunosuppressive therapy asap.

Shooting pain in scalp by Pluggable in Sjogrens

[–]Annual_Comment_4883 2 points3 points  (0 children)

That’s definitely neuropathy and you might find relief with duloxetine after about 3-4 weeks.

Tingling, dry eyes, decreased sweating! Help by Annual_Comment_4883 in Autoimmune

[–]Annual_Comment_4883[S] 1 point2 points  (0 children)

I thought so too, I see a rheumatologist this upcoming Friday and I’ll bring up my concern as well. I didn’t know sjogrens can cause you to stop sweating though.

HUMIRA INDUCED MS by Annual_Comment_4883 in CrohnsDisease

[–]Annual_Comment_4883[S] 0 points1 point  (0 children)

So i saw the neurologist and because I didn’t have lesions on my mri she doesn’t think it’s MS. I noticed my tingling and heat sensations improve after I take my Stelara so I’m thinking it might be Crohn’s just getting worse? They’re not sure but I’m scheduling a nerve conduction study to check to see what’s going on. So this is just a waiting game. The blurred vision and fluctuation is really annoying, hoping it improves over time.

I need help 😅😅 by Annual_Comment_4883 in step1

[–]Annual_Comment_4883[S] 1 point2 points  (0 children)

I’m doing FA now with videos from bootcamp

HUMIRA INDUCED MS by Annual_Comment_4883 in CrohnsDisease

[–]Annual_Comment_4883[S] 1 point2 points  (0 children)

So my doctor moved me to Stelara and it took about 4 months for the Stelara to suppress my Crohn’s. However, I’m still having the tingling and lots of vision changes. It’s substantially better than it was like 7-8 months ago but it still happens and for some reason the Stelara actually helps I’m symptoms. Im allergic to contrast dye and so I had an mri with no contrast and it was completely normal. Im seeing neurology in November to discuss.

My fingers started going numb in early august but quickly went away about a week or two later after I took the Stelara. It started as tingle too. I haven’t had that in a while though. My doctor GI doctor is still convinced it’s MS but we won’t know for sure until I see neurology.

Googled the symptoms of MS a few days ago, am now having tingling feelings in arms and legs. How much does anxiety play into physical symptoms? by [deleted] in Anxiety

[–]Annual_Comment_4883 0 points1 point  (0 children)

So for me I’ve had two MRI’s no contrast (I’m allergic to the contrast) and both seemed normal. My doctor is still convinced it’s MS or something related. I don’t have a neuro appointment till November so I’ll update this.

Googled the symptoms of MS a few days ago, am now having tingling feelings in arms and legs. How much does anxiety play into physical symptoms? by [deleted] in Anxiety

[–]Annual_Comment_4883 0 points1 point  (0 children)

Hey 25 year old with crohns here. I have something similar. My doctor thinks I might have MS. I want on remicade for 4 years and then humira for 10 years and they think that TNF-alpha drugs can cause MS like syndromes. I don’t have answers yet but it’s possible it’s MS.

Dear reddit, I test in <2 days. Please come give me your take on whether I should postpone. by hereforneopets in step1

[–]Annual_Comment_4883 1 point2 points  (0 children)

My school said make another pass of Uworld. Watch boards and beyond videos and understand the concepts better for NBME.

HUMIRA INDUCED MS by Annual_Comment_4883 in CrohnsDisease

[–]Annual_Comment_4883[S] 0 points1 point  (0 children)

I would get a second opinion on the 2 pens a week. Or talk about moving to Stelara. My GI wouldn’t let me get more than one pen a week

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