For 25 years, former model, Lucinda Edwards, from Beenham, struggled with what she was told was ME (Myalgic encephalomyelitis).

From the UK....."For 25 years, former model, Lucinda Edwards, from Beenham, struggled with what she was told was ME (Myalgic encephalomyelitis).
She suffered from overwhelming fatigue, burning muscle pain, memory and sleep problems, headaches, heart palpitations and many other symptoms.
She and her family spent thousands of pounds trying to get her well. She had visited US clinics five times, including the renowned Mayo Hospital in Minnesota, for treatment, and no doctor diagnosed Lyme disease. Three years ago, she sent her blood to a specialist German lab where Lyme disease was diagnosed. She does not know how she caught it and never saw a tick bulls-eye rash.

When she found out that what she had was Lyme disease and not ME, she says: “I was angry – very, very angry! I felt really let down that so many doctors, hospitals and clinics had misdiagnosed me and had dismissed my illness as psychological. I had to begin a major fight to get better from this truly devastating and debilitating Lyme illness.”" https://www.newburytoday.co.uk/…/24792/don-t-get-ticked-off…
Tons more stories of when the ME/CFS/Fibro turned out to be Lyme Disease. All 3 groups have all the same symptoms. Perhaps ME/CFS & Fibro are also infections of various sorts? Infections that create havoc in the human body, but do not necessarily always kill the person right away?
https://www.facebook.com/jack.dupre.5/posts/1444094105620664

 

 

 

newburytoday.co.uk

Don't get ticked off

Angela Knight talks to Beenham resident Lucinda Edwards about the…