If this story moves you, and you have the means, consider donating to CSF Leak research at Stanford. Cerebrospinal Fluid Leaks are something that can completely mimic a large amount of FTD symptoms, and even in the care of utmost professionals, can be near undetectable - and somehow, treatment can be as beautifully simple as a one and done injection... to a hellish guessing game and years of attempts. As Dr. Ian Carr…
How DOES one get diagnosed for this? Is there a test?
Dr. Ian Carroll is arguably the best resource in the world. Starting here is probably a good choice.
https://profiles.stanford.edu/ian-carroll
https://www.mdedge.com/neurology/migraineresourcecenter/arti...
No idea why I currently can't find a non walled version of the first link. It's important - and general googling would be "when to suspect a CSF Leak Ian Carroll"
Secondary to Dr. Carroll
Dr. Wouter Schievink at Cedars-Sinai also has good information... He's actually the pioneer of research IIRC.
Saved a dude from a diagnosis of dementia and spending the rest of his deluded days in a nursing home.
https://www.nytimes.com/2017/11/02/magazine/why-was-their-br...
IIRC - in the end, based on decades of patient history, he just opened this guy up as a last resort and nearly missed - but did find the leak. Near full recovery.
It seems to be that there are some very high risk groups, like those with connective tissue disorders - specifically, Ehlers Danlos. Also, from Carroll's findings, a lot of people diagnosed with POTS are often misdiagnosed and truly have some small CSF Leak. Ehlers Danlos and POTS often go hand in hand as well...