What is the buspirone test: For the... - Myalgic Encephalo...

Myalgic Encephalomyelitis Community

2,086 members651 posts

What is the buspirone test

Welshiegirl profile image
3 Replies

For the last 18mths I've had a variety of tests for different conditions but with no luck.

My Endo said I may now have cfs. So I went to see a different specialist who has now put me forward for a muscle weakness test and today I've received a letter for a buspirone test. As he said this a test they do for cfs. But I forgot to ask what does it entail and what is it for.

Has anyone had this test and could shed any light on things.

Many thanks xxx

Written by
Welshiegirl profile image
Welshiegirl
To view profiles and participate in discussions please or .
Read more about...
3 Replies
Frodo profile image
Frodo

Never heard of it as I thought there were no tests for CFS but found this link: ncbi.nlm.nih.gov/pubmed/893...

Hello Welshiegirl,

I have not heard of a buspirone test. Have you tried searching for the test on the internet? Sorry I cannot help further. Let us know how you get on with this test and whether you receive a diagnosis. Take care,

Lottie x

LadyBarb profile image
LadyBarb

Hi Welshiegirl ... from what's on internet, sounds like a blood test to see reaction to what they've introduced into your blood that day?

I've a very bad reaction to the 5HT's, and I think they're looking for that response? As though how you're feeling and what you've told them isn't enough? :(

When do you have to go? As has been suggested, have you the facility to search the Internet and find out a bit more about this weird test? Thinking of you! B xx

Not what you're looking for?

You may also like...

Is the Perrin Technique '80% self-administered'?

I only ask, as I've been looking into it and, unfortunately, the only registered practitioners near...
DaveT81 profile image

Two important studies link ME/CFS to changes in the gut microbiome

Though not a ME/ CFS patient, I have joined this community in order to post this message about a...

Desperate for help........

Hi everybody. i'm new to this ME forum. like most ppl with ME/CFS, it's a long story. i'll...
Hidihi profile image

So what if I do have ME?

Hi there. This is the first time I've posted on here - I've been visiting the Thyroid site for...
Schenks profile image

ME research of note: Contrasting ME versus CFS or 'CFS/ME' by Leonard A. Jason et al

Hello, Although this study was first published in 2013 i have recently come across it and see it as...
Starbys profile image

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.