Please click on the link to view Michelle's video of what it is like to live with an invisible disability. Michelle is one of my very favourite blogger's. Why - Her sense of humour. Vitality. Wit. Intelligence, there is more but my brain is mushy. Living with Bob - her name for her invisible disability which each day brings forth more challenging symptoms is the place I go when I feel sorry for myself. She reminds me that without humour everything is pants. Michelle gave me permission to link. Its me being lazy as well because it means she gets to wear herself out trying to describe what it is like to have an invisible disability. So much of what she says is just how I feel.
(I promised to send Michelle an email and I have clean forgotten what it was I wanted to say - sorry Michelle)
Why do all the best people live so far away?
I can stretch but not this far
image from yahoo search
5 comments:
Thanks for the kind words you left on my blog. Please do visit often and I will do the same.
Sorry to hear of your invisible disease....you seem to cope very bravely.
Thsnk you for the return visit, Lo. I appreciate it.
Achelois--I saw your comment over at Tiffany's blog, and I have EDS as well and am IMMUNE to local anesthetic at the dentist! I had no idea there was any connection between the two--thanks for the tip. Now I can tell my dentist to stop wasting the damned injections on me (I usually get the gas and just try to go to my happy place while he works anyway).
Thanks for your lovely words. And don't worry about the email no stress. Oh, and can I get the title on a laminated card? I'd love to be able to show it to each new doc.
MFA Mama - The joys of EDS eh.
Michelle - laminate away. Its true.
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