Connect with others who understand.

  • Learn from expert-reviewed resources
  • Real advice from people who’ve been there
  • People who understand what you’re going through
Sign Up Log In
Powered By
Real members of MyMSTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.

FND

A MyMSTeam Member asked a question 💭

Neurology diagnosed me as FND with continued monitoring, My question is, Has anyone else been diagnosed FND at first and then eventually end up with ms diagnosis later?

May 19
 · 
Reactions
A MyMSTeam Member

I did have the spinal tap back in December of 2025, Came back with elevated protein and glucose, Had an Abnormal Result on a Mutiple Sclerosis Panel 2, An Abnormal Result showing I had the Epstein-Barre virus Past Result. I then had a genetic genome test that did show variants on ALS, MS and Parkinsons I have also had all these symptoms progressing for a year. I read alot of research about genetic testing for neurological health that it is still developing as understanding of those 3 are understood better. Since the FND diagnosis , having spinal lesions, and those tests makes me wonder what anyone else may have gone through diagnosis wise. I really I was able to answer any questions, I am happy to answer any questions you may still have.

May 22
A MyMSTeam Member

It can be so frustrating trying to get a clear diagnosis. Ive had similar experiences when they just brush off what you tell them.
I hope there is somebody on here who has/had FND diagnosis and MS who can share their experiences with you.
Stay strong and keep on advocating for yourself. You are not alone 🤗

May 20
A MyMSTeam Member

MS and FND can co-exist. FND does not explain your thoracic spine lesions - have you been told why you have those @A MyMSTeam Member? 🤗💜

May 19 (edited)
A MyMSTeam Member

Have you had a spinal tap? @A MyMSTeam Member and @A MyMSTeam Member I went many years with different specialist and wasn’t fully diagnosed until I had the spinal tap.

May 21
A MyMSTeam Member

@A MyMSTeam Member They are claiming my lesions as a syrinx but they are continuing to monitor for changes, and a syrinx is 1-8 people in every 100,000 people that have a true syrinx, Also neurosurgeon told me that a syrinx does not explain all of my symptoms, It is why I am curious with the question I asked, I have looked into a lot of things since it seems like doctors do not seem to care anymore about their patients, at least in Pa they don't. I have kept track of each symptom as best I could as they appear, but they skim over it when I show thwm so I figured this would be thw best place to see what others have may had the same experience.

May 20

Related Questions

View All
A MyMSTeam Member asked a question 💭
Edinburgh, UK

A MyMSTeam Member asked a question 💭
Canada, KY

A MyMSTeam Member asked a question 💭
Plymouth, WI