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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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Re: the poll.
Does anyone know if Dr Enlander is still practising? No votes on the poll but perhaps he's retired? I think I remember reading that a grateful patient had left him £100000 to set up a ME/cfs unit and he was training up other doctors. Would be wonderful if something similar were to happen to Dr Davis.
I ask because, although in UK, I will be in New York in the autumn. Is it worth trying to set up an appointment? I try to balance my life using what energy / money I have to do what I want to do/ what might benefit my several health conditions ( one perhaps just as difficult as ME, needing controversial treatment in Germany). Cannot bear to spend all my energy searching for treatments but since will be in NYC anyway, it might be worth trying Dr Enlander.
Would be grateful for Any experiences/knowledge.
Somebody voted for Dr. Bieger. Is this the German Dr. Bieger from Munich? I'm surprised he made the list, but would be really interested in experiences. Thanks
I was quite surprised that he has only 2 treatments at his disposal--a probiotic powder he sells to make GCMAF in a yogurt, and the Hepapressin injections. If these do not work, he does not have any other treatment to offer.
He used to offer Ampligen, and was working on a Rituxan trial. I wonder what happened to that
Not sure the background to this but unless people have seen more than one doctor can they really claim or believe one is better than the other ? Even if they have seen 3 or 4 doctors the poll will still be skewed in the direction of the doctors who have been seen by the most people here. ( Is that what you want to know ?)
By all means have a poll but be wary of drawing any conclusions.
Ask me the question for this thread in five to ten years. My dream is at that time I could then give you a very long list of doctors all over the world.There is no BEST doctor for ME/CFS until medical science can figure out what exactly this illness is. All of these doctors are just guessing at treatments and making a lot of money doing so. No one seems to be cured yet or back to living a "normal" life.