What is it like to have a chronic illness? To have a disease which is very difficult to treat and to diagnose which isn't recognised in many quarters of the medical profession? Welcome to the world of Chronic Lyme Disease. A riddle, wrapped in a mystery, inside an enigma.
“You feel different,” says Elizabeth Rice who suffers from Chronic Lyme Disease. “It’s a very odd feeling. You feel as though you’re not quite in the human race sometimes.”
Lyme Disease is caused by the bite of a simple tick, injecting into the bloodstream the bacterium Borrelia and probably numerous other parasites. The incidence of those contracting the disease has been increasing dramatically in recent years and it's known that swift treatment with antibiotics is enough to stop it in its tracks.
What is causing the medical controversy is the course the disease takes if treatment is not so quick. Many say that heavy treatment at any stage is enough to kill the bacteria and that subsequent blood tests prove them right. The reality is far less clear cut.
Years of pain
“Some of the symptoms are so horrendous you can’t explain it to people who haven’t suffered this illness,” says Cecylia Malenchek. “They don’t understand you. You look fine, they say. In fact, you feel dreadful. Your head is bursting. You can’t think straight. Your bones and muscles are aching; you’ve got pins and needles and numbness. It’s just horrendous.”
Cecylia Melanchek has had the disease for 13 years and as with many sufferers of the chronic condition she was not immediately diagnosed. It has led to many years of pain and mental anguish. Her experience with doctors hasn't helped. Her GP told her it was all in her head, offered no treatment and asked her how she got on with her parents. The experience seems to a common one.
History of medicine
The problem with the disease is that it's a relatively new parasite on the scene. The bacterium that causes it was only discovered 30 years ago and so there's still a great deal to be revealed about how it works and how effective treatment is. What is known is that it's a very tough and resistant bacterium and that it's recently been classified as a potential bio-terror agent by the US government because of its incredible abilities to escape our attempts to kill it.
Dr Andrew Wright is an authority on Lyme Disease and he says that the high wall that patients are facing is a phenomenon that goes back many years.
"That's the history of medicine. You look back at the illnesses called psychological, tuberculosis, epilepsy, schizophrenia, all thought to be psychological until the cause was found and I'm sure that in the not too distant future the same will be seen in illnesses like chronic Lyme. Once we understand things they become respectable but in medicine we do this, we have this defence mechanism whereby, if we can't explain something one way of dealing with it is to make the patient the problem. It's their problem then and not ours. And that gives us an easy way out."
Lack of support
This is a view shared by one of the world's leading authorities on Lyme Disease Professor Sam Donta, who's treated thousands of cases from his base in north-eastern United States where the disease was first discovered.
"The physician has been educated to think about Lyme in very crisp, finite terms. And they've been taught that we don't know what it is but that it's not Lyme. So the patient is then left dangling. Probably having Lyme or something like it that we haven't discovered yet and getting emotional support up to a point or the usual which is 'this is stress, you're depressed, take an anti-anxiety pill, see a psychiatrist and goodbye'. I tell the patient sometimes that if you wanted to make this up you could, but then you're making up the same story that hundreds and thousands of patients are also making up."
There are still major and sometimes bruising fights taking place within the medical profession about the nature of the disease. Does Chronic Lyme Disease exist or not? All the evidence suggests it does but as the arguments continue one thing remains the same - the sufferers are left dangling, knowing that something dramatic and debilitating has happened to their health but often unable to get the support and help needed to overcome it.
An Ode to Health and Ignorance was produced by Chris Chambers. It was originally broadcast in September 2006. The program was awarded a Bronze Medal in the category Health/Medicine at the 2007 New York Festivals.



















Greetings from Boston,
Out of the many Lyme Disease articles & posts I try to read daily, “An Ode to Health and Ignorance” truly captures the essence of this nightmare illness. I am seldom energized enough to respond anymore, as I have been fighting for my life from the devastating effects of Lyme & coinfections which have resulted in a multitude of health complications for over 6 years now.
I was misdiagnosed for 1 ½ years by supposedly the best doctors in our medical community. They might as well have tried bloodletting with leeches because that is how advanced my treatment began, allowing me to go from Acute & easily treated with a short course of antibiotics to Chronic & debilitated now.
The thought of this disease beating me hurts more than the daily suffering I endure. This is from where I somehow draw the strength everyday to crawl out of bed & willingly allow myself to be tortured yet again. If I didn’t believe that I would eventually triumph one day, I would not have made it this far & quit long ago.
But I am stubborn, & that would be too easy. If it’s any comfort, you are not alone in this desperate battle that requires us to put one painful foot in front of the other. I sense your despair & hope you would not act in a dangerous way towards yourself. I have certainly considered it time & again, but realize such drastic action goes against every fiber of my being that I have left - which is what keeps me going each day no matter how painful & tedious.
May you find some comfort in my words & know us Lymies are a chosen group of people for whatever crazy reason, even if it is to just forewarn others of the potential plight facing the uninformed. Now I have to stick around to find out how it all ends or die trying on this journey too few people understand or will ever take. Any other option would be karmic cheating!
Please Be Well,
Jim
Its really quite appalling what is happening with Lyme disease, so many people are getting the wrong diagnosis, like MS. ME. ALS. Alziemer, burnout fibromyalgia, just to name a few..
I have fighting this illness for about 10 years now, and when I listend to my intuïtie, thats when things started materializing for me , I really have lost faith in the medical system, and this is sad, there is not a day goes by, that I think about about ending it all, its so terrible to live with!! There is so much ignorance, and I dont know how doctors, and specialists dont wake up, we need someone to listen to us/
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