Re: Lymphadema

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Posted by Louise ( on October 13, 2003 at 14:12:58:

In Reply to: Re: Lymphadema posted by Lisa Hubbert on August 28, 2003 at 17:05:07:

: My mother has had secondary lymphadema for about ten years, she also has primary in the other leg. Massage and compression bandaging has not helped and she is now in constant pain and wears body stockings. The side effects with other related illnesses are horrendous. I have now found out my infant son has lymphadema in his right foot. There are many web sites dealing with the deatails but no cure. Places such as the Tasmanian Lymphodema clinic in Australia have had success with laser.

: : : : : Has anyone heard of lymphadema? A friend of mine has this and is having trouble finding treatment because it's so rare. Any suggestions??

: : : : I am a physical therapist in PA. I am trained in treatment of Lymphadema. If you still need help, contact me and let me know the region you are in and i will try to help you locate a facility.
: : : : Or, look up the national lymphadema network.

: : Hi my name is sharon and i am 21 years old. i hve primery lymphdema since i was 9 years old.
: : thisi snor so rare and i know more people who have this . there are ways to treat this

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