... people with FN(C)D (sometimes known as 'Medically Unexplained Symptoms') and looking into the misdiagnosis stats should, down the line, help to ensure that resources are allocated appropriately. I have sent him some information about clear cases of misdiagnoses, which usually - but not always - occur in people (often women) who have rare or less common conditions. As such I have donated to his crowdfunding and will continue to support him. If anyone here wants to donate and/or spread the word, here's the link:
One of David Tuller's aims is to look... - Functional Neurol...
One of David Tuller's aims is to look into the actual rather than the reported misdiagnosis stats re FND. He is hugely supportive of ...
Written by
210272
To view profiles and participate in discussions please or .
4 Replies
•
thank you for sharing his work.
My pleasure Is it OK if I pass on your thanks to David?
Of course, thank you. I was trying to see how I could follow him and his work but think I will just have to keep checking back in on his website from time to time as I couldn't find a way to subscribe / share my email with him. Unless I may have missed something?
Not what you're looking for?
You may also like...
Newly diagnosed need advice
Hi was just wondering if anyone has a story like my partners who went to see a neurologist and was...
Confused
Hi, It all started with pins and needles down my neck, spine and right side and over time my bones...
Depression & FND
My partner was diagnosed with FND around a month ago. He’s has quite severe depression and FND was...
The Persistent Theme
Hi there, I have noticed that there is a persistent theme when reading other people's stories. The...
Get moving
My son has FND
and he has to be homebound. He was diagnosed Mary 2017 and it has significantly...