← Return to At a loss, multiple consultations still no answer...any idea?

Discussion
Comment receiving replies
@petuniamom567

Have you considered Chronic Faitigue Syndrome now called ME/CFS. The English discovered on various scans that the brain lining was involved. This, however, doesn't mean a cure exists. Since researchers seem to searching in their own particular directions. Also, have you been tested for Herpes Simplex One and Ebstein Barr Syndrome (mono?) Apparently, most of us walk around with titers to this. There are drugs that treat the Herpes group. They must be taken by mouth not rubbed on your mouth. Apparently, they don't always work. And, as has been said, a good rheumatologist is essential as an essential starting point. You might add a good neurologist,too. I must say I'm telling you all this and none of it has helped me. However, it's worth a try. Good luck. BiskitsMomma

Jump to this post


Replies to "Have you considered Chronic Faitigue Syndrome now called ME/CFS. The English discovered on various scans that..."

Thanks for getting in touch. Yeah, the rheumatologist I saw thought it may indeed be CFS but no official diagnosis was given an I haven't been referred to my local department so I'm still waiting on that. Circumstances have been tricky due to covid so testing has stagnated, however I have recently had a FIT stool test which revealed some abnormalities and I've been offered a emg/ncs test which is taking place tomorrow. This will then be followed by an MRI which will hopefully identify what's wrong. I've not heard about either of those, would a routine blood test reveal if you have it?