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»	LymeNet Flash » Questions and Discussion » Medical Questions » Does anyone have this?

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Topic: Does anyone have this?

tidegal
Member
Member # 8262

posted

Does anyone have small fiber neuropathy? I just recently found out that I have this as well as autonomic neuropathy. Docs can't figure out the cause but my lyme doc says it's the lyme of course. Just wondering if anyone else has this and if it has gotten better with treatment.

Posts: 44 | From GA | Registered: Nov 2005 | IP: Logged |

bettyg
Unregistered

posted

Tidegal, please edit/PENCIL icon your topic line to read: "Does anyone have small fiber neuropathy?" Now, you will get some readers/replies if they have it.

We have 3-4 FULL screens daily of posts/replies. So the more info you/others will SPECIFY what you will be discussing, the more help you will get from us since we pick & chose due to time limits.

Also, please hit the enter key more often for all of us with neuro lyme keeping paragraphs 6-8 lines of text. Thanks for helping us, help you!

quote:
Originally posted by tidegal:

Does anyone have small fiber neuropathy? I just recently found out that I have this as well as autonomic neuropathy.

Docs can't figure out the cause but my lyme doc says it's the lyme of course. Just wondering if anyone else has this and if it has gotten better with treatment.

Tide, what is fiber neuropathy? thanks for educating us too.

Are you a diabetic also?

IP: Logged |

Cheryl
Frequent Contributor (1K+ posts)
Member # 75

posted

Yes, lotsa Lyme patients have peripheral neuropathy as well as autonomic neuropathy.

http://www.clevelandclinicmeded.com/diseasemanagement/neurology/pneuro/pneuro.htm

http://www.lymeinfo.net/pain.html

http://www.lymeinfo.net/autonomic.html

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Posts: 1547 | From NY | Registered: Oct 2000 | IP: Logged |

trails
Frequent Contributor (1K+ posts)
Member # 1620

posted

I have lots of neuropathies.

My favorite one is RADICULONEUROPATHY. Because it sounds like a spell from a Harry Potter book.

I am not familiar with small fiber neuropathy.

I have a lot of nerve pain and the only real findings tests have shown is EMG showing damage to nerve roots in cranial segment of spine. No idea WHY.

My LLMDs also say it is Lyme.

[hi]

Posts: 1950 | From New Mexico | Registered: Sep 2001 | IP: Logged |

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