My Experience with William Weir

[fraser9]

I just thought I'd post my experience with Dr William Weir.

I booked an appointment in 2021. I had already recovered from M.E. for 9 years but for some reason I relapsed. I was recommended him by Prof. Findley who has since retired so I booked an appointment to Dr. Weir in Devon. I sent him an email to give a bit of my background before we met but it wasn't read. when I saw him he examined and then tested me for POTS which I don't have then he went on to explain what ME/CFS is (with slides on a laptop) which I am already well versed in. He didn't order any blood test or any kind for me. He gave me a short list of supplements to take and told me I should recover in time and that was it! He was supposed to send a letter to my GP which never came and he never kept in touch. Considering I have read such good things about this man I was really underwhelmed and felt a let down. I just chalked it down to a waste of time and moved on. I am still on my journey to recovery.

He seemed like a nice man but the level of interest and care I got was really poor.

 

[ninauae]

can you please tell us what supplement he recommend since this doctor never accept new patients now with long waiting Que?

 

[fraser9]

can you please tell us what supplement he recommend since this doctor never accept new patients now with long waiting Que?

I can't remember the full list. one of them was niacin/B3. NAD precursor.
I've tried loads of supplements over the years. I haven't noticed a bit of difference from any of them. I recently tried oxaloacitate but didn't get any benefit from that either.