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When family members dont believe you have Lyme
A father regrets failing to believe his daughter had Lyme disease
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The Lyme disease support group meeting for November  will be held from 6:30-8 p.m. Nov. 28  in the Hillsboro Public Library meeting room, 819 High Ave.

Residents of Juneau, Monroe, Richland, Sauk and Vernon counties afflicted with a tick borne illness such as Lyme disease, or those seeking to increase understanding of tick borne illness, its prevention, and its treatment, are welcome to attend.

The following letter was written in 2007 by a father whose daughter was afflicted by Lyme disease. “Lymedad” expresses his regrets and offers encouragement about what he has learned:

Dear family of a Lyme disease patient,

I am writing this letter to all parents and family members who are witnessing their children, wife, son, father, aunt, uncle, cousin, etc. struggle with Lyme disease. I am one of you. For more than six years my daughter has suffered through this ugly, dark disease.

She has experienced horrible migraines, severe joint and muscle pain, nausea, vomiting, extreme fatigue and loss of her ability to speak or think logically (these are just a few of her symptoms).

She has become unable to work. She has been forced to move back into our home at the age of 23 (she is now 29). She has virtually lost her 20’s, one of the most productive and exciting time of her life.

We have taken her to every known medical specialist in southern California, as well as three different general practitioners.

She has been diagnosed, at differing times, as having chronic fatigue syndrome, chronic pain syndrome, fibromyalgia, lupus, psychosis, and multiple sclerosis (please notice that all of these are either syndromes or descriptions of symptoms; none of them are diseases).

For the first four years of her struggle, I was not a good parent, even though I thought I was. My daughter didn’t have any outward sign of her illness. She looked “normal.” After many, many blood tests, MRIs, CAT scans, x-rays, psychological tests; everything came back “normal.” I was, and still am, one of the world’s biggest cynics and skeptics (I’m originally from Missouri, so “Show-Me.”).

Surely if you are as sick as you say you are, there must be something that will show up in your blood tests or on X-rays. You can’t possibly be this ill and not have something tangible to show for your symptoms. You’re either just faking it or you’re lazy or it’s psychosomatic or you’re trying avoid the real world. Get off your lazy butt and get some exercise or get a real job or face up to life like the rest of us.

That’s the way I approached her illness. It’s time you took control of your illness and will yourself well. I was so far off-base. It took an outstanding Lyme literate medical doctor to show me the error in my approach with my daughter and to show me the reality of this disease.

My daughter and I have both suffered because of my ignorance. (I’m not saying all of you are ignorant, I’m saying I was ignorant. To be ignorant simply means to be uninformed,  not stupid). I am still working to rebuild the closeness we had before Lyme.

Lyme disease is real, the pain is real, the problem with logical thought is real, the lack of energy is real, etc., etc., etc. If your child or family member has been diagnosed with Lyme disease, they are just as sick, if not more, than someone who has a more “traditional” illness, like lupus or multiple sclerosis or cancer.

I’ve done all the study, I’ve been with my daughter at all of the appointments, I’ve watched the misery she’s been through.

Hey, they just can’t help the way this disease treats them. It’s not their fault. We as family members need to be there to support them. They don’t need our pity. They don’t need our skepticism. They don’t need our criticism. They need our understanding.

If you as family members will take the time to study this disease, you’ll see that it is real. The little buggers who have invaded their bodies are real and they are making our loved ones sick. Please spend the time you currently spend trying to figure out why your loved one acts the way they do really studying the disease. There are volumes being written on the internet as well as new books being published everyday on this disease.

We can’t possibly understand the way they feel, not unless we have the same bacteria in our bodies. My daughter has a long way to go before she’s back to where she was six years ago. She has a lot of work and pain to endure before she can get there. She certainly doesn’t need someone who claims to love her causing her any more pain than she has already.

Families, from one who has been in your shoes, please let them know you love them. Let them know you’re there to help them. Let them know that there’s no way you can possibly understand their pain, but that you will try to understand their illness.

I think one of the most important things I’ve come to learn is that my daughter’s disease may be God’s way to teach me a lesson. I’m not saying God gave my daughter Lyme disease, but He may be using this disease to teach me how to love, how to be patient and how to be more understanding.

I wish you all good health and I hope that none of you will ever have to experience what our Lyme disease loved ones are experiencing.

The above was taken with permission from the blog, Touched by Lyme:

For more information, email, call 608-489-2725 (ask for Gary), or write: Gary Cepek, S1468 Cepek Rd., Elroy, Wis. 53929.