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The RAMQ Assistance Program for Compression Garments for the Treatment of Lymphedema provides reimbursement to individuals with a medical diagnosis of lymphedema or lipo-lymphedema.
At this time, lipedema alone is NOT covered under this program. However, the LAQ is actively working to have the condition recognized so that people with lipedema can access support before the disease progresses to lipo-lymphedema.
This is one of the most generous programs of its kind in Canada. It stands out for:
The amount reimbursed depends on age, access to a social support program, the affected limb, and the type of garment or accessory purchased.
The program covers multiple compression garments per year and can also be combined with private insurance.
This practical one-pager includes:
This Reference Card is essential for prescribers and fitters, and an invaluable resource for patients.
Order free of charge at aql@infolympho.ca
The Lymphedema Association of Québec (LAQ) provides support, education, and awareness to individuals living with lymphedema, lipedema, or lipo-lymphedema, as well as to their families, loved ones, and healthcare professionals.
We inform and educate about these chronic conditions – their causes, risks of progression (including how lipedema can develop into lipo-lymphedema), and the available conservative and postoperative treatment options, such as decongestive therapy and compression.
We also actively support scientific research aimed at improving care and advancing knowledge toward a cure.
Lymphedema Association of Québec
Therapeutic Support Program
1 866 979-2463
514 979-2463
Mailing address
648 Lajeunesse Street,
Laval, Quebec, H7X 3K5CP
Telephone
1 866 979-2463 / 514 979-2463
Email
aql@infolympho.ca
Website
www.infolympho.ca
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