Thanks for the info Orion. I was pretty excited when I read the article - it sounds pretty hopeful and I'm also glad that at least some people in the medical community are trying to help people with cfs. There are just so few treatments out there right now and even fewer that seem to work.
I've been wondering about
you and how you have been doing with the treatment you are getting from your new doctor. Let us know when you get a chance.
Thanks again for the information and take care.
Diagnosis: UCTD (lupus) 2006; Raynauds 2006; Sjogren's 2006; lupus symptoms began 2003; CFS 1991; Mono 1985
Meds: Plaquenil 400mg; Prednisone 5-10mg; Tramadol 100mg 3-4x daily;
Amitriptyline 10mg; Neurontin 300mg; Prevacid; Steriod Cream and Mouth Rinse for tongue and mouth ulcers; Hydrocodone 5/500 prn for severe pain; Restasis eye drops
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