Introduction

Mar 12, 2010 10:29

Hey, I'm Kitty. I've had lyme for two years and have been treated for one. It really is hard, since none of my friends are dealing with it, and don't really understand what I'm going through. However, you gotta pull through, right ( Read more... )

under our skin

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Comments 7

willo April 18 2010, 20:04:28 UTC
Hi Kitty, welcome to the group ( ... )

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badninja May 8 2010, 08:21:03 UTC
Lyme epilepsy, can I ask about that? I've had seizures ever since I was bitten, but they call them 'non organic stress seizures'.

I never fully comprehended your list before, Willo. You're now coming across as a braver person than ever before to me.

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willo May 10 2010, 20:47:17 UTC
My neurologist in the University of WA called it Lyme Epilepsy because I never had seizures before exposure to Lyme. An eeg revealed the partial complex seizures and interrupted brainwaves due to Neuroborreliosis. I'm really trying to get a SPECT scan ordered, which shows how the blood flows in the brain.

Thank you for what you said, it brought such a smile to my face. We're all brave to be facing these diseases. We're all heros in my book. :)

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badninja May 8 2010, 08:23:16 UTC
Hi, welcome to the group! This is a silly question, but I ask it of everyone - have you found or been able to show your friends the Spoon Theory? That helped a lot of my friends to understand at least a little.

If you ever need advice or someone to talk to, I'm always around. My email is aitisi @ rocketmail . com

How far into the infection did they catch your lyme?

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livingwithlyme May 14 2010, 22:16:06 UTC
hi, can I ask what the spoon theory is?

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star_lace May 18 2010, 17:32:03 UTC
The Spoon Theory was written by a girl with lupus as a way to help her friends understand what it's like to live with a chronic illness. You can read it here: http://www.butyoudontlooksick.com/articles/personal-essays/the-spoon-theory-written-by-christine-miserandino/

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livingwithlyme May 14 2010, 22:19:12 UTC
Hi! I'm going to join this support group too! Glad to see you here. I understand what you are saying about your friends. I was always very strong and very healthy, and my friends were too. When i became sick, I guess i was too 'weak' to have as a friend anymore. I've been sick for 5 years, diagnosed 2 years ago after begging for a lyme test and on oral antibiotics for it. I started a blog earlier today because I felt like talking about it, but didn't have anyone to talk to. But now I found YOU GUYS! Yeah! Love to talk to you any time. Good luck with everything!

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