Guest guest Posted December 17, 2006 Report Share Posted December 17, 2006 Hi, I was recently diagnosed with CFS and am looking for a doctor in MD. My PCP doesn't seem to believe it exists and I am really stumped about who I should try to go and see. If anyone has any suggestions, I would be grateful for them! Thanks! Tech Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 17, 2006 Report Share Posted December 17, 2006 Dr. Shoemaker? Looking for a CFS Doc in MD Hi, I was recently diagnosed with CFS and am looking for a doctor in MD. My PCP doesn't seem to believe it exists and I am really stumped about who I should try to go and see. If anyone has any suggestions, I would be grateful for them! Thanks! Tech ------------------------------------------------------------------------------ No virus found in this incoming message. Checked by AVG Free Edition. Version: 7.1.409 / Virus Database: 268.15.23/591 - Release Date: 12/17/2006 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 17, 2006 Report Share Posted December 17, 2006 Dr. Shoemaker in Pocomoke City, MD. Also Dr. Gabe Mirkin in the Washington, DC area. Gabe Mirkin http://www.drmirkin.com/ Call 301-942-7900 for an appointment. Mirkin Medical Associates accepts BlueCross/Blue Shield and Medicare > > Dr. Shoemaker? > Looking for a CFS Doc in MD > > > Hi, > > I was recently diagnosed with CFS and am looking for a doctor in MD. > My PCP doesn't seem to believe it exists and I am really stumped about > who I should try to go and see. If anyone has any suggestions, I > would be grateful for them! > > Thanks! > > Tech > > > > > > > -------------------------------------------------------------------- ---------- > > > No virus found in this incoming message. > Checked by AVG Free Edition. > Version: 7.1.409 / Virus Database: 268.15.23/591 - Release Date: 12/17/2006 > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 19, 2006 Report Share Posted December 19, 2006 Hi, My suggestion is to do a search online and find out what CFS support groups are about you or in your state. Then either message them or give them a ring (or go to one of their CFS support meetings and ask people there). Ask them for doctors who specialise in CFS or those they recommended. Its extremely important to find a doctor who has some understanding of this illness or who is willing and eager to work with you, keep up with the research (either you or them) and try out various things as this is no simple, easily dealt with illness. Over time unfortunately one can end up with many more symptoms coming in (There is now 67 different symptoms I get or have had cause of this, try dumping that onto a doctor who dont know me or about CFS), so its good to find a good doctor perferably one who specialises in it, early in the peice who will be there to help and support you. If you find a doctor who believes in it and is willing to take an interest and work with you but has no experience. You should do okay as there is heaps of stuff online with suggestions on how one can go about treating this. I suggest to not only keep an eye on things on message boards like this one, but also check out things like the Zero- Based Protocol http://lassesen.com/cfids/ZeroBasedProtocol.htm for some more ideas (it has a treatment plan), Dr Cheneys (he's a famous CFS doctor) suggestions etc (there are many about the place, just try things till you find things which seem to help) best wishes to you... > > Hi, > > I was recently diagnosed with CFS and am looking for a doctor in MD. > My PCP doesn't seem to believe it exists and I am really stumped about > who I should try to go and see. If anyone has any suggestions, I > would be grateful for them! > > Thanks! > > Tech > Quote Link to comment Share on other sites More sharing options...
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