The
Lymphedema Association of Quebec is a charitable
organization founded in 1999 to provide education,
awareness, and support to those with lymphedema,
and to encourage research leading to effective
treatments and eventually a cure.
A
small group of volunteers ensure that the LAQ
continues to reach its objectives, however the
slope is steep, the challenges numerous. Your
generosity through donations and willingness to
volunteer is needed and greatly appreciated.
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Visit
our events page regularly...
For
information about lymphedema, risk reduction, and management,
download the LAQ patient pamphlet "Living with
Lymphedema" in PDF format
PDF
format (8.5" x 14") ~1009 kb
For a list of suppliers, therapists, download the LAQ
"Resource Guide" in PDF format
PDF format (8.5" x 11") ~324 kb
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DISCLAIMER:
This site is for information and community support only,
and should not be used as a substitute for professional
medical care. Always seek the advice of your physician
with any question about a health problem or medical
condition. This site also includes links to websites
providing information about lymphedema, but the LAQ
cannot be responsible for the content of those sites.
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