posted
name says it all...... this has been going on for 20 mos. now.... and still can`t get any drs. to even talk about the possibility i have lyme. nothing to date as far as meds have worked for me.. is there a chat area here to talk with folks that are online. any feedback or anything would be appreciated.. thanks
Posts: 3 | From peterborough nh | Registered: Jul 2010
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posted
welcome to lymenet......this placa has been a lifesaver for me.......very knowledgable people here who have been down the same road.....
post questions youll get answers.....search for topics, support.........
I am sure people will be along soon with a bunch of links for you to go through.......good luck on your journey...........
-------------------- Oct 09 Positive CDC Western Blot Jan 10 Positive Babesia Duncani Jan 10 Cd57 28 Mar 10 EBV, IgM, IgG HHV-6 IgG Posts: 739 | From NC | Registered: Oct 2009
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Tracy9
Frequent Contributor (1K+ posts)
Member # 7521
posted
Join us as well at www.lymefriends.org ; where you can find a live chat and another resource in addition to lymenet. Sorry you have to be part of this "club."
13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
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posted
Welcome to a club that no one wants to be a part of!
I have found a wealth of information here and the outpouring of support... well... great people!
Posts: 238 | From Jackson, TN | Registered: Mar 2010
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posted
Have you contacted support groups in your state? If not, click on support groups line in green menu box on left side of this page, and go to your state.
Posts: 8430 | From Not available | Registered: Oct 2000
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