Welcome back my friends, to the show that never ends
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The Days and Nights, Slants and Twists, and Wobbly Meanderings of a Woman With Rare and Incurable Neurological Disorders. Similar to Multiple Sclerosis, it attacks your myelin, leading to painful and debilitating side effects. About 33,000 Americans are currently disabled as a result of this rare neurological disorder. Not one person with TM will ever know their prognosis. I happen to be one of them.
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Welcome back my friends, to the show that never endsDESCRIPTION
I39;m so glad you could attend. Come Inside, Come Inside. .Thanks for stopping by to browse my latest gripes, grumblings or even progress that I39;m making with Transverse Myelitis. This blog is my vent to the world about this rare disorder.CONTENT
This web page dealingwithtm.blogspot.com states the following, "Welcome back my friends, to the show that never ends." We saw that the webpage said " Im so glad you could attend." It also said " Come Inside, Come Inside. Thanks for stopping by to browse my latest gripes, grumblings or even progress that Im making with Transverse Myelitis. This blog is my vent to the world about this rare disorder. 1 Transverse Myelitis Folks Facebook TM support group this is a closed group only for those with TM and other caregivers. 2 Kevins Raising Cane website."SEEK SIMILAR DOMAINS
Tuesday, March 12, 2013.
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Do you need help with your credit card debt. Thursday, March 4, 2010. Sunday, May 10, 2009. No more bailouts for the credit card companies. I speak with people everyday who are not asking to walk away from the credit card payments; they are only asking that the credit card companies work with them, so that they can pay off their balances. It has become a nightmare for so many people, that they just want to throw in the towel and leave it all behind. The credit card companies wan.
Dealing with my life with CP. Monday, August 20, 2012. and probably will be there until Friday or Saturday but I will have my iPad so I will try to post an update most I can. If you like this post, please comment on this post or email me at cp. Or anyone can email me about any of my posts. Take care and hope to hear from you soon. Trying to deal with my life with CP.