posted
Waging war on this disease(s) is so tough. Some days it gets me down. On top of that dealing with people that really don't understand anything about the disease(s) itself and the limitations it puts on us and then on top of that the war to find and get effective treatment--some days it's tough.
Thank you LymeNet community for being here. I feel safe here, knowing that you all understand. I can speak without fear. I don't have to explain myself when it comes to the disease. I know you understand. That is precious to me.
-------------------- I'm not there yet but I'm closer than I was yesterday.---- Lyme Band 31,41,58. Being treated for Lyme and Bartonella. Posts: 149 | From Maine | Registered: Oct 2010
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Catgirl
Frequent Contributor (5K+ posts)
Member # 31149
posted
I'm with you Shiela. :) It is comforting to be among others who understand. I think that's why this site draws me back so much. I want to help, learn, and be among others who actually "get it".
-------------------- --Keep an open mind about everything. Also, remember to visit ACTIVISM (we can change things together). Posts: 5418 | From earth | Registered: Mar 2011
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posted
Thank you - I agree! An ongoing conversation for us -
Additionally, there's all the archived posts as well which you can find through the Search function at the top of the page - a record of everyone being helpful through the years -
Posts: 13116 | From San Francisco | Registered: May 2006
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Rivendell
Frequent Contributor (1K+ posts)
Member # 19922
posted
Very, Very glad lymenet is here. Otherwise, I would still be hopelessly treating Chronic Fatigue Syndrome.
As bad it is to have Chronic Lyme, CFS is NO MAN'S LAND.
Posts: 1358 | From Midwest | Registered: Apr 2009
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Jane2904
Frequent Contributor (1K+ posts)
Member # 15917
posted
Me too! I am so glad Lyme net is here.
Lots of help, kindness and support!!!!
Posts: 1357 | From Massachusetts | Registered: Jun 2008
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