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Connecticut Coalition for Lymphedema Legislation (C.C.L.L.)

PostPosted: Tue Jun 20, 2006 7:33 pm
by patoco
Connecticut Coalition for Lymphedema Legislation (C.C.L.L.)

The Connecticut Coalition for Lymphedema Legislation (C.C.L.L.) is a grassroots organization, compromised of professional and motivated individuals working for legislative change for persons suffering from lymphedema. We are proposing legislation that will mandate Connecticut's private insurance companies to have a yearly minimal mandatory expense for coverage of lymphedema bandages and garments.

For information on the bil and how you can help and be involved visit:

http://www.lymphedemacircleofhope.org/legislation.html

and/or

To find out how you can help, contact:
Carolyn Lucey, OTR/L, CLT
Danbury Hospital, Physical Medicine Center of Southbury (203) 262-4230
Email: NcLucey71@aol.com

or

Jeanne B. Tassis
Circle of Hope Lymphedema Foundation Inc. nonprofit 501 (c) (3)
President and Founder
36 Woodcrest Drive
Prospect, CT 06712
tele. 203-758-6138
fax 203-758-6138
email JTLymphedema@@aol.com

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A super thanks to Jeanne and to the Circle of Hope Lymphdema Foundation for all their wonderful work on behalf of lymphdema patients.

Visit Circle of Hope:

http://www.lymphedemacircleofhope.org/

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We support and endorse the Connecticut Coalition

Lymphedema People

http://www.lymphedemapeople.com