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cosmina cocan
I've written , but nobody put me in mind . Expect some feedbacks !!!!!!!!!!!!!!!!!!!!!!!!!!!!1
December 11, 2011
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Jenny Sterner
Today, we lost someone from our community who meant so much to so many of us, including myself. I will miss Pat terribly, although we never met in person. The below is reposted from the Advocates for Lymphedema Yahoo group; it is truly a very sad day. :(
It is with great sadness that I must send this message.
Pat O'Connor, Founder of Lymphedema People, Huge Advocate for those who have Lymphedema, etc., passed away this morning in his sleep,per a message that I received via the Lymphedema People Facebook Group page per his son.
He leaves behind a huge group of friends and family including daughter - Emily and family, son - Patrick Jr and family as well as several sisters and other family members.
Once I have more information in regards to funeral/memorial I will pass on all
information.
Nessa
August 14, 2013
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Carol Link
I have lived with lymphedema for the past 20 years. I would like the community to be aware of the potential side effect of lymphedema which is cellulitis. I contracted cellulitis about 15 years ago. My Gyn oncologist called it the "flu which settled in my leg"! I did have flu-like symptoms but my right leg was red and painful to the touch. Finally I went to an emergency room where fortunately the correct dx was made. My primary MD "aspirated" the infection which I later learned was probably the worst treatment he could do. Please make sure MD and healthcare workers are thoroughly educated in the treatment of lymphedema. I was very close to losing my leg because of the infection. I am very grateful to the professionals who are aware of the treatment of lymphedema.
August 19, 2013
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