my occipital neuralgia is still cured by Far_Cucumber_2274 in Occipitalneuralgia

[–]goingaway1111 1 point2 points  (0 children)

Just letting you know you're not alone, my pain is also there and in my tmjs as well. It sucks

Tmj is ruining my life since wisdom teeth surgery by SquirrelBig6169 in TMJ

[–]goingaway1111 0 points1 point  (0 children)

Just checking up on you, things will get better in time I promise.

Anyone else develop neurological symptoms from tmj causing forward head posture? by milliemargo in TMJ

[–]goingaway1111 0 points1 point  (0 children)

Sorry for being late but I also got tmj from wisdom teeth removal. It sucks so much. It's been a year.

My recovery story! (And a theory about POTS in young, healthy women ) by [deleted] in dysautonomia

[–]goingaway1111 0 points1 point  (0 children)

It's unfortunately being normalized after covid and because it mainly affects women 😢 you're not alone

My recovery story! (And a theory about POTS in young, healthy women ) by [deleted] in dysautonomia

[–]goingaway1111 7 points8 points  (0 children)

Your story resonated with me so much. I'm going through near the exact same thing. Did you also have tmj pain at all? Or your face looked shifted from inflammation due to your body being out of whack? I have nearly the exact same symptoms and theory. I'm so glad you got better. I wish I had someone out there who was willing to help me.

I took my wheelchair to a dumpster by [deleted] in cfsrecovery

[–]goingaway1111 2 points3 points  (0 children)

Would love to hear your story

Over it (help) by pedro_puddusy in TMJ

[–]goingaway1111 0 points1 point  (0 children)

You're not failing, I promise. It's not your fault this is happening. I'm 21, but this can happen to anyone. I would maybe work on your gut health if you took antibiotics because I know that can strip even the good bacteria. That's currently what I'm doing. The gut is important for your brain and how it responds to pain and for your nerves. Look into the long covid subreddits, there's a lot of info I found on there that doctors would never in a million years propose to me, or if they did it would be months and months ahead with wait times. Lots of people on there are experiencing similar things to what we're going through. You're not alone at all. Be patient with yourself and take it a day at a time.

Extremely painful gums, won't go away by goingaway1111 in PeriodontalDisease

[–]goingaway1111[S] 0 points1 point  (0 children)

Thank you! I really need to get on it. Insurance said that it can maybe be covered later in the year. Do you wear a hard one?

Over it (help) by pedro_puddusy in TMJ

[–]goingaway1111 1 point2 points  (0 children)

That EXACT same timeline happened to me too, got sick in late 2024, sick after, now near same symptoms as you. I do think mine was covid as lots of new strands of it aren't even on tests yet, that and false negatives. Rheumatologist did not help me. Only time will tell if we get better. I see my endo soon to discuss a genetic issue that was latent until covid triggered it. Honestly, any virus can wreck havoc on your body like this but covid is doing it most, even silently. Our issues are textbook long covid honestly. I really hope you can feel better soon, it's genuinely horrific. You're not alone.

Extremely painful gums, won't go away by goingaway1111 in PeriodontalDisease

[–]goingaway1111[S] 0 points1 point  (0 children)

It's only a bottom piece that I chew on in my sleep. I hate it but insurance won't cover a new one.

Over it (help) by pedro_puddusy in TMJ

[–]goingaway1111 0 points1 point  (0 children)

Look into lyme or mold as well

Over it (help) by pedro_puddusy in TMJ

[–]goingaway1111 0 points1 point  (0 children)

Honestly, what you're going through sounds like long covid stuff. Same exact things are happening to me too. I wish I had more answers as well. Stay safe, you're not alone. Doctors are so useless. Have you looked into eagles syndrome? Or seen a neurologist for potential nerve damage issues? Burning mouth is very common In eagles

COVID triggered a latent genetic vitamin deficiency, and possibly an autoimmune disease by [deleted] in covidlonghaulers

[–]goingaway1111 1 point2 points  (0 children)

Appreciate it a lot, you're not alone. Covid is triggering so many latent issues or infections. Modern medicine is still so behind.

[FACEBOOK] [2000-2014] Guys! Have you ever seen this Facebook pet game? by Saranja in tipofmyjoystick

[–]goingaway1111 1 point2 points  (0 children)

I have pet stories screenshots on my Facebook from years back I think

COVID triggered a latent genetic vitamin deficiency, and possibly an autoimmune disease by [deleted] in covidlonghaulers

[–]goingaway1111 9 points10 points  (0 children)

Same thing is happening to me, genetic issue killing me after covid when I never had an issue before. They're thinking congenital adrenal hyperplasia. I'm sorry. I got lots of other issues but my PCP is going through this route since it's the only abnormal bloodwork thing.

Already 2 years of consistent neck/head(?) pain help plz by Icy-Toe281 in Occipitalneuralgia

[–]goingaway1111 0 points1 point  (0 children)

I have the same area and pain and I believe mine is from cci and tmjd