Her parents said Fizz went to see many doctors and specialists, but nobody could find out what was wrong, which they said crushed her spirit.
It was when they visited a clinic in Germany in 2016 that it was confirmed she had Lyme disease and in the April she started treatment. But by this point she was in the chronic late stages of the illness. "
http://www.herefordtimes.com/…/15624454.Parents_of_Lyme_di…/
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TONS more stories of where the ME/CFS or Fibro turned out to be Lyme Disease.
https://www.facebook.com/jack.dupre.5/posts/1444094105620664
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Proof we are in an epidemic/pandemic:
https://www.facebook.com/jack.dupre.5/posts/1635014213195318
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There have been so many Lyme mistruths & fallacies out there by the authorities. They had always been adamant about the reliability of the tests, yet those at the forefront know already that many of us have taken many, many tests before we finally tested positive. Here by 2017 the CDC FINALLY comes out to say the tests are bad, but so are so many other things about Lyme & the treatment of Lyme patients overall. What has gone on is criminal & it is AIDS all over again, where the people had to fight for recognition, a diagnosis & proper care and treatment.
http://abcnews.go.com/…/cdc-advises-multiple-lyme-disease-t…
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The best Lyme disease documentaries here:
https://www.facebook.com/jack.dupre.5/posts/1446698995360175?pnref=story
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The best Lyme disease documentaries here:
https://www.facebook.com/jack.dupre.5/posts/1446698995360175?pnref=story