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RACHEL KARIA
Thank you guys for the warm welcome. Am happy to be part of this community, i live in Tanzania and here there is no information on lymphedema no clinics or therapist, I have primary lymphedema of the right foot for seven years now, diagnosed myself through google search that was after fruitless trips to different doctors. Happy to be here at least i can get information on how to manage it.
May 17, 2016
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Cindy Stanbery
Anyone else have both lymphedema and claustrophobia? Any tips for surviving compression?
May 24, 2016
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Carol G
Does anyone else have a connective tissue disorder such as Ehlors Danlos Syndrome and also lymphedema? If so, how has it affected your lymphedema course?
May 6, 2016
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