Has anyone been diagnosed with GFAP (glial fibrillary acidic protein)?

Posted by gardrums123 @gardrums123, May 26, 2023

My husband has been diagnosed with a rare autoimmune disease called autoimmune glial fibrillary acidic protein astrocytopathy.
Has anyone been diagnosed with this. Looking to know what we may have ahead of us.

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Hello, Autoimmune Community:

I found a link to a French study of the GFAP condition. It also has some additional links and brain pictures to show people who don't believe it is an actual condition.

20 to 50 percent of patients relapse. It is difficult for people to understand the condition since I look better, weighing 25 lbs less. A good, inexpensive movie to watch on PRIME is Brain on Fire. A young female columnist in New York starts experiencing psychotic episodes. She is initially diagnosed to have bipolar schzophrenia until one of the consulting physician's former professor neurologist takes a closer look! Not the same condition as the GFAP; however, it gives you a better insight into what a brain autoimmune disease can do and the kinds of struggles that can ensue trying to get a correct diagnosis!

I'm sorry. I tried to post a link but was denied! Really? Just look up " GFAP French Study " on Dr. Google! Take Care!

REPLY
@luceman

Hello, Autoimmune Community:

I found a link to a French study of the GFAP condition. It also has some additional links and brain pictures to show people who don't believe it is an actual condition.

20 to 50 percent of patients relapse. It is difficult for people to understand the condition since I look better, weighing 25 lbs less. A good, inexpensive movie to watch on PRIME is Brain on Fire. A young female columnist in New York starts experiencing psychotic episodes. She is initially diagnosed to have bipolar schzophrenia until one of the consulting physician's former professor neurologist takes a closer look! Not the same condition as the GFAP; however, it gives you a better insight into what a brain autoimmune disease can do and the kinds of struggles that can ensue trying to get a correct diagnosis!

I'm sorry. I tried to post a link but was denied! Really? Just look up " GFAP French Study " on Dr. Google! Take Care!

Jump to this post

Hello @luceman, I noticed that you wished to post a URL to an article with your post. You will be able to add URLs to your posts in a few days. There is a brief period where new members can't post links. We do this to deter spammers and keep the community safe. Clearly the link you wanted to post is not spam. Please allow me to post it for you.

"Glial Fibrillary Acidic Protein Autoimmunity: A French Cohort Study"
- https://pubmed.ncbi.nlm.nih.gov/34799461/

REPLY
@JustinMcClanahan

Hello @luceman, I noticed that you wished to post a URL to an article with your post. You will be able to add URLs to your posts in a few days. There is a brief period where new members can't post links. We do this to deter spammers and keep the community safe. Clearly the link you wanted to post is not spam. Please allow me to post it for you.

"Glial Fibrillary Acidic Protein Autoimmunity: A French Cohort Study"
- https://pubmed.ncbi.nlm.nih.gov/34799461/

Jump to this post

Thanks Justin!

Could you please add to my text that you can watch Brain On Fire for Free
by typing it in a web search engine? Last, would you please make sure that
I don't have any duplicate posts! I sure appreciate all your help. The
info on this condition is so rare. 2 years ago, we basically knew nothing
and did not know where to get it. If I hadn't got diagnosed, I possibly
would no longer be living. If this gets posted some how. Please delete!
Thanks

REPLY
@luceman

I posted this same message in: Has anyone been diagnosed with GFAP to share my experience?

Hey, Everyone. It's 430AM PST. I can't sleep! I am a 61-year-old dude!

I aim to share my symptoms experience and hope you see that you are not alone in this extraordinarily rare medical phenomenon!

I was diagnosed with a GFAP issue 2 years ago, and we believe the cat came back! I am waiting for my spinal fluid to get tested by Mayo to confirm. I have inflammation in my body somewhere. A hot spot was located in my brain on an MRI, but it was inconclusive:

Can anyone identify with some of the symptoms that I have had over both episodes?:

Two Years Ago Symptoms:

1. No vision change, but my blood glucose levels surge past 350.
1.5 8 or 9 days of fevers.
2. Throwing up for 2 months, 2 times a day without fail. True !
3. Getting dizzy and falling several times.
4. No appetite.
5. Not being able to pee or defecate without Flomax pills or enemas.
6. Getting dizzy while standing.
7. No appetite and losing 50lbs.
8. Being put on 40 mg a day of steroids for about 8 weeks, making it almost impossible to get more than 4.5 hours of sleep a night.
9. Not sure if it is GFAP, but testosterone levels went below normal.
10. I felt the closest I have ever have been to being in a vegetative state. I had very little willpower to do anything. It was tough. The good news is that I don't remember a lot of it! My friends were shocked when they came to visit me. Often, I was in a trance-like state.

My wife, an ER nurse, is the one who helped with all my appointments. It took 5 months to diagnose. I did at least 75 blood draws (no exaggeration).
I am a school teacher and was on leave for about seven months.

March 2025 Symptoms

1. 18 days of fevers and night cold sweats! Yup! 18 Days!
2. Tiredness before getting back on Prednisone. I am still tired because the Prednisone won't let me take naps.
3. Not being able to pee for a few days. I didn't need Flomax.
After 4 days of tinkling urine, it cleared up on its own before starting on steroids. Crazy! I had about 2.5 weeks of diarrhea.
4. Inflammation in my liver levels, WBC count. Etc.
5. Surges of pain in my lower extremities when walking. No joint pain.
6. Losing 22 lbs in three weeks.
7. I do not feel a loss of appetite but can feel fine without eating.
8. Body aches.
9. Dizziness, but not falling or passing out.
10. I had to start injecting insulin even though I am a mild diabetic.

The second episode of whatever I have now is milder than before. If it is a result of the GFAP issue coming back, I am better off getting treatment five months sooner. I believe the antibody attacking the GFAP protein the first time was killed. Read that 20% of patients can relapse. I am off work for about five weeks. I can't teach kindergarten ( 29 years so far!) because of my lowered immunity while being on steroids. Prednisone will eventually be changed to Cellcept, which is an autoimmune preventative.

If you ever want to talk, ** I'll give you my phone number. Read that 10% of people who catch this disease are children. It's not just an older person's disease!

Take Care,

Luceman

Jump to this post

Can I please have a moderator remove this post and the description of my symptoms above this post. It is redundant. Thanks!

Luceman

REPLY
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