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    Created in 2008, Phoenix Rising is the largest and oldest forum dedicated to furthering the understanding of, and finding treatments for, complex chronic illnesses such as chronic fatigue syndrome (ME/CFS), fibromyalgia, long COVID, postural orthostatic tachycardia syndrome (POTS), mast cell activation syndrome (MCAS), and allied diseases.

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  1. S

    London/UK doctors

    Hi, Isn't Dr Russell Lane at Charing Cross? I guess that must mean RHH then. Someone said he was good - maybe he's picking up from Dr Jenkins (fingers crossed). S
  2. S

    London/UK doctors

    Thanks everyone. Good to get all these recommendations of who to see, as I really don't need anyone else to tell me I'm depressed or putting it on and that if I pull myself together I'll be fine. Interesting to know biolab etc are a waste of money. Have had some tests done there by my...
  3. S

    London/UK doctors

    Thanks. That's useful info - and unfortunately it's what I feared re the CBT/GET thing. It's really pervasive, isn't it. Will write to my GP now and cross my fingers... S
  4. S

    London/UK doctors

    Thanks Justy. I'll pick that up with my GP. Am still waiting for the medical questionnaire from ESA, so I guess I'll have to work that out when it comes. I have been seeing a nutritionist privately for the past 6 months as I was originally diagnosed with adrenal fatigue and lupus...
  5. S

    London/UK doctors

    NHS doctors Hi, I'm new here and have read through loads of these threads to try and find a good doctor. My GP has asked me to find out where I want her to refer me to. From what I've read, it seems a pretty rubbish situation in the UK, and it seems that what few good ME doctors there are...