@genxpaula58v2: Christina Applegate #christinaapplegate #misdiagnosis #neurologicaldisease

Genxpaula58v2
Genxpaula58v2
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Tuesday 20 October 2026 21:10:28 GMT
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faerynarcher
FaerynArcher 🧿✨ :
I have Dysautonomia and I agree with everything you shared in this video. It can be so hard to pinpoint neurological conditions, or even to get in to see a neurologist but I suspect my reactivated Epstein -Barr virus is the culprit in my situation.
2026-10-21 00:57:09
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theblackheretic
Shadow King 👑 :
Do you think 🤔 it’s possible to manifest it by being told what it is ?
2026-10-21 06:14:08
0
robertaedwards2
Roberta Dawn :
I too am a neurological patient as well. ehlers danlos and been told I could possibly have ms.
2026-10-21 02:42:19
1
fringe_log
Fringe_Log :
ESR. Ana. RF. All negative but in chronic pain. Doctor wants to blame it on hormones.
2026-10-21 05:21:10
0
laura_ryleighs.rainbows
Ryleigh’s RainBows :
First I’m hearing of it. Thats terrible. We need more research on women, for women. I’m so tired of hearing “we don’t know”.
2026-10-20 22:41:44
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randy.croce
RanD :
Ischemia causes the lesions too. Great info.
2026-10-21 05:56:13
1
notfluffy10
notfluffy :
happened it to me. I have autoimmune gastritis b12 deficiency, iron and D Pernicious anemia mimics MS brain lesions
2026-10-21 01:34:54
2
nohandmaidsavl
NoHandmaidsAVL :
Dealing with this with my neuromuscular disease. They know I have it, but can’t figure out what it is. They can definitely say I have mitochondrial dysfunction, but awaiting more finite genetic tests to learn more.
2026-10-21 05:54:22
1
georgia676767674
Georgia Love ❤️ :
Look for active lesions.
2026-10-21 03:20:30
0
annie8675309
Anne5757 :
I have Neuro Sjogren’s & it looks very similar to MS
2026-10-21 00:38:16
10
elliottsmom2
ElliottsMom :
I am in diagnostic imaging in healthcare. I scan the brains and spines to aid the drs w/ diagnosis. SO many times patients with obvious neurological symptoms have tests that show NOTHING wrong neurologically. What we need is more advanced medical research. Unfortunately, there's no money to be made in research, so as a capitalistic society with a capitalistic run healthcare system we lag behind in knowledge. Sadly, it really is that basic. I am sorry for those that are difficult to diagnose. Maybe seek treatment in another country??
2026-10-21 00:25:33
7
dueces_b
UnSweet Tea :
Neuro is way behind other diseases because it seems like everything is a dx of exclusion! Mom went thru Myasthenia G, PLS, and ALS. She died before they made a real diagnosis.
2026-10-21 02:58:59
4
aksmithfnp
user9159227778460 :
Spinal tap is helpful too
2026-10-20 23:12:29
6
lucy111111118
lucy :
Wow jeez I’m so sorry ur going through this for so long I hope ur post reaches more people bc it’s very very important, thanks for posting sending strength 💯🥰
2026-10-21 04:45:43
1
shannonherrera
Exhausted empty nester :
I love her and didn’t hear this. Absolutely frustrating for her.
2026-10-20 23:19:21
5
beachbumos
BeachBumOS :
women are misdiagnosed more often than not
2026-10-21 03:14:01
2
nancywharton
elvis :
My daughter has ms. It’s a terrible disease.
2026-10-20 22:08:28
5
holsy505
holsy505 :
Covid changes the immune system not for the better in some people as well.
2026-10-21 01:15:24
3
tc5977
Tc :
Sad
2026-10-21 03:09:52
1
irishlasswithclass
Irishlassy :
I went to nursing school and in addition to MRI with and without contrast a spinal tap MUST be done to check for the specific protein that's in the CSF... only then can you be certain you have MS that protein must be present otherwise it's labeled probable MS...in addition ophthalmologists are able to see your optic nerve which will look different from a person without MS...I myself have had MS for over 20yrs medication changes will eventually happen with flares...5 days inpt with IV steroids to calm down the inflammation causing the new symptoms... if they didn't do a spinal tap I'm not sure why they'd be certain she doesn't have it... but like you said many tests are needed but for ANYONE who has been told they have MS and haven't had a spinal tap... find a different neurologist did she say how they found she doesn't? I know the news is reporting on it but what did she say I'll need to listen to her podcast which I normally never do lol... but I'm passing that info on for anyone who is now questioning or confused
2026-10-21 01:15:23
0
arknaturalstatehippie
ARK🌸NaturalStateHippie🌸 :
Thank you for this
2026-10-20 22:58:49
2
georgia676767674
Georgia Love ❤️ :
It happened to me. 🥺
2026-10-21 03:19:56
1
alannarandall3
Lana :
More info
2026-10-21 02:58:48
1
borgdrone1701
John Doe 1701 :
It's probably misdiagnosed Lyme disease.....
2026-10-20 22:12:21
8
beachbumos
BeachBumOS :
How many men have been misdiagnosed????
2026-10-21 03:15:24
1
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