Unknown autoimmune/neurological disorder

Hello Kyle @lquillen1963, Welcome to Connect. Thank you for being a strong advocate for your wife. I know it has to be difficult when no one is able to give you any answers and your wife has so much going on with her health. I did find an article that discusses the condition that may provide a little information.

Medical News Today - What to know about hypercapnia
-- https://www.medicalnewstoday.com/articles/320501

Have you thought about or tried to get a second opinion? Mayo Clinic is very good at diagnosing difficult to diagnose health conditions. If you would like to seek help from Mayo Clinic, contact one of the appointment offices. The contact information for Minnesota, Arizona and Florida can be found here http://mayocl.in/1mtmR63.

John,
Thanks for reaching out and your article is interesting. Yes, we have mentioned to Emory about going to Mayo clinic but until they inform our insurance company that there is nothing more they can do, the insurance co will not pay for us to go. We have 2 appts with Emory over the next couple of months and we plan on pushing them basically to step up or move out of the way. The only time she gets immediate attention is when she is in ICU, but once she is discharged, she just becomes an number and the attention we get at the neuro-clinics is test for this and see you in 4-6 months. She is emotionally and mentally drained on top of the main physical issues and just looking for guidance.

Kyle @lquillen1963, I did a search on Connect and found a discussion with a member who has similar symptoms after inhaling gasoline engine fumes. It might be helpful to join in that discussion to see if anything stands out that might be helpful.

> Groups > Just Want to Talk > Asthma like symptoms after engine fume inhalation
-- https://connect.mayoclinic.org/discussion/asthma/

Are you able to talk to the Insurance company based on your wife's condition and current providers not being able to diagnose the issue? I'm guessing you have already pushed the doctors but maybe you can put more pressure on them.

Kyle @lquillen1963, I have a number of the same symptoms, but that only means one thing: I have a number of the same symptoms! So understand our diseases may be quite different. But Here is my list as possibilities. !. Eosinophils in excess. 2. Some sort of wild type/systemic amyloidosis. I have a form (Gelsolin) which impacts the larynx and every other tissue and liquid in the body. 3. I also have two partners in crime with Gelsolin, RyR2 Cardiac Wall Dystrophy and FKTN (Fukuyama Limb Girdle Muscular dystrophy). My only suggestion would be to contact a place like Ambry Genetics and go through their inexpensive testing, both sides, neuropathy and cardiac.

Has anyone brought up inherited spinocerebellar ataxia? Many genetic variations.

Have the doctors done a spinal tap (lumbar puncture)? If they haven't, I recommend that they do one.

Yes, and like every other test, it came back negative.

@lquillen1963
I'm glad they did the test. I'm sorry that they have not found the cause yet. Perhaps 2nd and 3rd opinions are needed. Hope they will find answers soon. Best wishes! 💜

Hi Kyle, I realized I left an important factor in my journey with my health, and that is this.

I was misdiagnosed, I really had ocular MG when I took off on a long strenuous bike tour. I presented at the ER just like this marathon runner. I feel I could have died back then. This type of incident, I now suffer from psychosis and I'm on disability.
https://www.ncbi.nlm.nih.gov/pubmed/22311063/

I am not a Med doc, and anything I write is free to download if you want it from Onedrive or Facebook/GelsolinVikingDragon. *dX* marks symptoms I share with your wife. I have RYR2 (cardiac wall dystrophy), FKTN (Fukuyama Limb Girdle Muscular Dystrophy) and Gelsolin (Amyloidosis). We believe there is more, but cannot find the proper testing lab yet. Maybe a few cancers, RA, dystroglycanopathy, etc. Those marked *dX* are some of my stuff. I have listed about 200 significant symptoms of mine, of which about 150 have been properly medically recognized by labs, clinics, hospitals, etc.
1. dX difficulty swallowing -started in 2018 but was infrequent and slowly progressing to now being on thicken and loss of weight.
2. dX blurry and double vision
3. dX balance – falling
4. dX Respiratory- rapid breathing ( failed PFT multiple times) currently Must being trilogy machine when she sleeps or has shortness of breath
5. weight loss – no appetite – (also started early) ( I do have periocarditis liquid building around heart and lungs, along with significant organomegaly-enlarged organs, tissues, etc.)
6. sX depression and anxiety
7. inability to cough – uses cough suppression machine 2 times a day for assistance (I sneeze often --Excess eosinophils)
8. dX muscle stiffness from upper torso to jaw line. basically like the tin man.
9. dX slight hand tremors
10. dX sleep abnormalities, she has had the sleep test twice. goes into REM at the beginning.
There is a lot more, but This is a start. You will learn this: The stack of markers continues to grow throughout life, both because science is learning more, and the disease, whatever it is, progresses. I suggest you also take a look at OMIM.gov (NIH) and University of Helsinki Hospital. Each of the labs has a list called something like "gene map" or "% of these symptoms shown by proven cases of ______________). I use the one for Gelsolin, which speaks of a cohort of 6,000 persons. The highest % shown are problems with thyroid, pancreas, uterus. in OMIM, There is also a frequent mention of having FKTN and RyR2 as an adjunct to Amyloidosis.