posted
I don't know how many times I've read somebody else's post and you've given me a brilliant idea for my own treatment, and/or some guidance to help my daughter who may also have Lyme. I am so appreciative of all the help and advice you've given me! Just to hear from people who are going through what I'm going through -- knowing that I'm not crazy, lazy, stupid, airheaded, a complainer, I sleep too much, and whatever else everyone around me is thinking!
I've had enough of the Lyme rage -- is there such a thing as Lyme warm and fuzzies? If so, I'm feeling it for all of you!
Posts: 39 | From Colorado | Registered: Dec 2009
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Dekrator48
Frequent Contributor (5K+ posts)
Member # 18239
posted
Nellie,
I agree!
I'm glad you are feeling warm and fuzzy here.
This is a great site because of all the wonderful people.
Hope you continue to get lots of good ideas for you and your daughter.
We can never have too much support.
Big hugs!
-------------------- The fibromyalgia I've had for 32 years was an undiagnosed Lyme symptom.
"For I know the plans I have for you", declares the Lord, "plans to prosper you and not to harm you, plans to give you hope and a future". -Jeremiah 29:11 Posts: 6076 | From Pennsylvania, USA | Registered: Nov 2008
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Tincup
Honored Contributor (10K+ posts)
Member # 5829
posted
The family we have here IS beautiful, isn't it.
I appreciate these folks every day.... so very much!
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