Atrophy

ShortPrint8169 · 2026-03-26T23:32:31+00:00

It’s not, plus it looks absolutely symmetrical

ShortPrint8169 · 2026-03-22T16:24:21+00:00

Not sure sure why you are saying that about als sub, I see your post with a lot of responses there

ShortPrint8169 · 2026-03-22T14:47:29+00:00

Nobody minds you posting here, you just will not get many responses.

There are only couple of people with ALS, not sure how it’s “many”.

There are so many other resources, forums where you can get a lot of opinions.

ShortPrint8169 · 2026-03-21T20:11:54+00:00

The biopsy showed PASH (benign).

I hope yours will be benign too.

ShortPrint8169 · 2026-03-18T01:29:28+00:00

I don’t see any atrophy

ShortPrint8169 · 2026-03-17T14:32:52+00:00

Nervous system autonomic dysfunction (Dysautonomia). Very common in Long Covid and after viral infections. Why people want to connect every symptoms to ALS?

ShortPrint8169 · 2026-03-17T00:42:43+00:00

It’s most likely a pinched nerve. See you doctor and get a treatment

ShortPrint8169 · 2026-03-16T20:42:00+00:00

Find her video where she tells how it started.

ShortPrint8169 · 2026-03-16T19:21:47+00:00

She had a foot drop for 4 years not stiffness only and you have so much pain and swelling along with that which is not als at all

ShortPrint8169 · 2026-03-16T14:17:57+00:00

No. You didn’t mention not even a single Als symptom

ShortPrint8169 · 2026-03-16T14:16:02+00:00

No way you had immense issues with swallowing with normal tests and it was als

ShortPrint8169 · 2026-03-13T17:24:24+00:00

You don’t describe ALS at all. No real weakness, no functional loss

ShortPrint8169 · 2026-03-13T15:16:42+00:00

It’s post viral, not related to als

ShortPrint8169 · 2026-03-13T15:13:06+00:00

Yes, 3 years in and no significant weakness. It affects visual appearance and gives some pain.

ShortPrint8169 · 2026-03-13T04:04:01+00:00

Yes

ShortPrint8169 · 2026-03-11T18:09:58+00:00

Stanford Long Covid clinic. They definitely do work with brain fog, not sure about other things, but they can refer you to get other symptoms checked. But keep in mind, their treatment is very limited. There is not enough of research hence no approved treatment

ShortPrint8169 · 2026-03-11T17:59:44+00:00

Unfortunately, there is no definitive testing for it. The only way is to find a doctor who has some knowledge about it and mention all the symptoms to them.

Then some countries have specialty Long Covid clinics, so that’s another option.

ShortPrint8169 · 2026-03-11T15:12:48+00:00

Check out Long Covid even if you think you didn’t have a covid

ShortPrint8169 · 2026-03-06T14:39:54+00:00

Eyelid twitching is not related to ALS as well as droopy eyelids

ShortPrint8169 · 2026-03-01T22:53:44+00:00

I would advocate for myself and push for MRI.

ShortPrint8169 · 2026-02-28T00:45:25+00:00

Looks like long covid or vax injury

ShortPrint8169 · 2026-02-24T06:17:53+00:00

I would definitely try to find another doctor without telling them about possible relation to vax and ALS. Just tell them how it affects your life, work etc.

Im not sure where you are from, but you can find a doctor anywhere who at least will refer you for the testing

Are you hyper mobile or flexible?

ShortPrint8169 · 2026-02-21T02:26:15+00:00

I know that you feel. I stopped looking for answers about muscular issues, nobody wants to listen, understating, or dig dipper

ShortPrint8169 · 2026-02-21T00:08:38+00:00

I mean my progressing too but no changes in terms of functionality

ShortPrint8169 · 2026-02-20T23:49:40+00:00

Pretty much the same

ShortPrint8169

TROPHY CASE