Living with Lymphedema in AnnArbor - Anyone else here? - LSN

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Living with Lymphedema in AnnArbor - Anyone else here?

jc22 profile image
jc22
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Hello all - I am new to this site. I was diagnosed at age 10, I am now 22. Am late in finding a community like this, but better now than never. If any new diagnosees have questions, please feel free to contact me - I would LOVE to meet you. We all need support.

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jc22 profile image
jc22
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Lynora profile image
Lynora

Hi jc22 - this site is based in the UK, and now has quite a few overseas visitors. Are you aware of the National Lymphedema Network, which operates on your side of The Pond? lymphnet.org/ - There is also a patient-run group - lymphedemapeople, which was set up many years ago by Patrick O'Connor, who ran it until his untimely death in 2013 lymphedemapeople.com/

Fizz-wig profile image
Fizz-wig

Unfortunately not AnnArbor. It took almost my life so far to be diagnosed with primary lymphoedema (28 years!) they spotted it at birth but still took so long to diagnose!

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