
Lyme Patient Reality
Lyme disease patients are confronted with a complicated version of reality in a number of ways.
A Lyme & Associated Diseases Resource
Lyme disease patients are confronted with a complicated version of reality in a number of ways.
“I would not have been able to write this book if I had not been a reporter at the San Francisco Chronicle, the only daily newspaper in the United States that did not need a movie star to come down with AIDS before it considered the epidemic a legitimate news story deserving thorough coverage.” It’s a striking statement, isn’t it, with the benefit of hindsight?
Unethical journalism may be committed intentionally or by accident, but the resulting disinformation or misinformation can be potentially damaging either way. In the case of public health, the results can be disastrous.
The crux of the Globe’s concern seems to be financial — the cost to medical insurers and to employers to treat late-stage or persistent cases of Lyme disease with antibiotics, when prescribed by knowledgeable and competent physicians based on sound medical research.
The past couple of weeks have seen remarkable progress for Lyme disease from both research and regulatory perspectives.
The red blood cell parasite Babesia is transmitted increasingly in the United States through blood transfusions, yet unlike with HIV, donated blood is never tested for Babesia.
Lyme can cause severe neuropsychiatric symptoms due to neurological damage and inflammation.
Lyme and AIDS have one thing in common: politics.
Tara Geraghty’s husband David was diagnosed with ALS. When he finally tested positive for Lyme, it was too late. “No one wants to talk about it,” she says.
Bravo’s ‘Housewives’ franchise needs to take health more seriously & stop making light of illness.
Bravo’s ‘Housewives’ Makes a Mockery of Lyme