-
Jean Paul BIKORIMANA
Dear friends I would like to invite to visit this website and you will know about non filarial lymphatic (Podoconiosis) caused by prolonged exposure of the feet without in the volcanic irritant soil.
August 27, 2014
-
-
Gregory Dubershtein
Hi Everyone! My name is Gregory and I have congenital Lymphedema in my left leg. I was wondering if there is anyone in Arizona in the east valley /Phoenix area that is interested in gatherings in order to get support and help with the daily struggles with Lymphedema, to share the stories behind the people, or just socialize and be there for one another.
August 29, 2014
-
Joanne Alexander
Hi - my first post. Last year, I was diagnosed with secondary lymphedema in my right leg. It was 9 years after cancer surgery. I am from Canada and I'm looking to connect with other positive people who are intent on staying active despite this new challenge. I am thinking of a marathon next year and looking for an online training partner.
August 29, 2014
-
-
-
-
-
-
-
-
Barbara Pilvin
Anyone going to the conference in DC? By the time I learned about its timing and location I had already registered and paid for the NAMI convention, which happens to be at the same hotel and during at least some of the same days! I hope to see some of you; I'll try and drop by but I'll have to leave Washington (my home town and a place I don't see nearly often enough!) and come back to Philly on the 7th. Two reasons: work the next day and, most delightful of all, the first rehearsal of the fall season of the U. of PA Choral Society, of which I've been a dedicated member since January 1983, and anyone who thinks anything but a major disaster would make me miss that rehearsal may think again!
August 10, 2014
