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» LymeNet Flash » Questions and Discussion » Medical Questions » LYME AND FIBROSIS

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Author Topic: LYME AND FIBROSIS
Deep in 'tis pear
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Over the year, I have developed fibrosis in various parts of my body, mostly my legs, arms and face. Has anyone experienced this problem with Lyme or any other co-infection? I have been going to various doctors including rhumatologist who insists that I don't have scleroderma. When asked "then what is it?" The answer is (invariably) "I don't know?"
Posts: 123 | From Los Angeles | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
Tincup
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Welcome to Lyme Net!

Have you been diagnosed with Lyme disease? If so.. how long ago did you contract it?

Is the fibrosis situation getting worse?

Are you on antibiotics now.. or were you?

Sorry for all the questions.. but any info you can provide would help us to help you.

[Big Grin]

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Posts: 20353 | From The Moon | Registered: Jun 2004  |  IP: Logged | Report this post to a Moderator
Deep in 'tis pear
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Member # 10427

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quote:
Originally posted by Tincup:
Welcome to Lyme Net!

Have you been diagnosed with Lyme disease? If so.. how long ago did you contract it?

Is the fibrosis situation getting worse?

Are you on antibiotics now.. or were you?

Sorry for all the questions.. but any info you can provide would help us to help you.

[Big Grin]


Posts: 123 | From Los Angeles | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
farah
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A lot of people with Lyme have an unnatural amount of scar tissue formation in different parts of their body.

This is related to a hypercoagulation issue and excess fibrin.

Hypercoagulation basically means our blood is thicker than normal because we produce too much fibrin.

Fibrin is the building block of scar tissue in the body. It seems like one way the disease walls itself off and hides.

Fibrosis can be the result of all of that excess scar tissue formation.

Taking medications or herbs or supplements to reduce the hypercoagulation problem can help a lot.

It helped me.

Farah

Posts: 208 | From New Mexico | Registered: Dec 2005  |  IP: Logged | Report this post to a Moderator
Deep in 'tis pear
LymeNet Contributor
Member # 10427

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quote:
Originally posted by Tincup:
Welcome to Lyme Net!

Have you been diagnosed with Lyme disease? If so.. how long ago did you contract it?

Is the fibrosis situation getting worse?

Are you on antibiotics now.. or were you?

Sorry for all the questions.. but any info you can provide would help us to help you.

[Big Grin]


Posts: 123 | From Los Angeles | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
Deep in 'tis pear
LymeNet Contributor
Member # 10427

Icon 1 posted      Profile for Deep in 'tis pear     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by Tincup:
Welcome to Lyme Net!

Have you been diagnosed with Lyme disease? If so.. how long ago did you contract it?

Is the fibrosis situation getting worse?

Are you on antibiotics now.. or were you?

Sorry for all the questions.. but any info you can provide would help us to help you.

[Big Grin]


Posts: 123 | From Los Angeles | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
Deep in 'tis pear
LymeNet Contributor
Member # 10427

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Dear Tincup,

It's a long, tedious story. I found a bulleye's rash on my leg in June 2000. At the time, I was surrounded by deer. I immediately went to my rhumatologist (I have lupus) and was told that there was no lyme disease in Southern California and I didn't need to worry. Symptoms, (very similar to those of lupus) started setting in. At the time, my lupus was in complete remission. My doctor said the lupus had come back. Two years later, my Lyme test turned positive. In 2002, my legs started getting thicker in some parts, then it was my tongue and my face. It is not swollen, it is thick. The wrinkles on my hands have disappeared. I suspected scleroderma, but according to the experts, I don't have the disease... Last year, I went as far as the Mayo clinic in Rochester tot ry to find out a reason for the fibrosis. There, I was told I don't have lupus, I don't have scleroderma, I don't have Lyme. A tongue biopsy showed epithylial hyperplesia with submucal edema. When asked what it meant, translated into English, the answer was: Swollen tongue... Dahaaa... My problem is that I am allergic to antibiotics, so over the last few years, I have started a treatment and stopped a week or two later. I finally did a mercury detox, and was able to take a combination of Zithromax and bioxin for three months. That's the extent of my antibiotic intake. I haven't taken anything for the last year. I was also told that Lyme would not cause your tongue to swell, nor Lupus for that matter. They want me to have another tongue biopsy. I'd like to avoid this procedure, if I can. At my last visit with my Lyme doc, he prescribed Cipro and Biaxin. What do you think about this combination. I am getting ready to try it.
Thank you for your interest.

Posts: 123 | From Los Angeles | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
   

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