News and resources for neurological Lyme disease and co-infections.
This post was sent to me from a courageous woman with two children - not afraid to speak out. I think we all share in her frustration!
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It also seems that many attempts to connect the level of pain to the ability to function socially and professionally which is affected by other symptoms of Lyme disease such as fatigue, swollen joints, and dizziness to name a few; where specialists have yet to satisfactorily untangled the symptoms between normal pain and “neuropathic” pain and even “neuropychiatric” pain.
So many blog posts and articles devoted to Lyme disease deal with treatment protocols, personal experience, political debate, medical debate, insurance disputes, and technical discoveries.
The debate goes around and around about whether or not Lyms disease can be contracted through sexual contact.
Jackson Hole, Wyoming. Like many valley residents, Scotty Button was “living the dream” when he moved to Driggs in 1995. Immersed in the organic food movement and an avid skier, Button was a proponent of healthy living, cultivating organic crops and digging trenches in the Tetons. With his buddy Tye Talt, he formed Mountain Valley [...]
I think that we can all relate to this! A fellow Lyme-sufferer from a Lyme forum allowed me to reprint this very touching essay.
On those bad days… the ones where you feel so alone and so empty…it is so important to reach out to the greater Lyme community through blogs or forums. It really help to have friends (even if they are new friend) who truly understand what you are going through.
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Dr. Stricker is another rare breed of physician – the courageous ones who are willing to take the heat in this tragic medical debate about chronic Lyme disease. The following observations were made in response to the blatantly false suppositions perpetuated by IDSA, and faithfully delivered by Dr. Dan Kinderlehrer on the Today Show, June [...]
