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Living with cystic fibrosis

The only provincial organization "by and for" people living with cystic fibrosis, dedicated to their advocacy and support.

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Tomy L. mcGregor

Tax credits: watch your interests!

18 February 2021

For many of you, it is possible to obtain tax credits at both levels of government. In order to take advantage of these credits, however, you must ask your doctor to complete the forms attesting to your impairment provided for this purpose. At the provincial level, this credit is called the “credit for impairment” (Certificate […]

Classified under: Uncategorized

Quebec announces newborn screening for Cystic Fibrosis

12 October 2018

Dr. Larry Lands, Director of Respiratory Medicine at the Montreal Children’s Hospital, is one of many people who welcomed the news that Quebec would be introducing newborn screening for cystic fibrosis (CF) on September 17. “Quebec is the last jurisdiction in North America to start newborn screening for CF,” says Dr. Lands. “It’s an important […]

Classified under: General

Open Letter

10 September 2018

By Tomy-Richard Leboeuf McGregor Executive Director Living with Cystic Fibrosis People living with rare diseases have very specific preoccupations. These preoccupations are seldom the subject of political debate concerning healthcare policies. The current election campaign is no exception. Cystic Fibrosis is the most common rare disease in Quebec with approximately 1500 living with the disease. […]

Classified under: Uncategorized

Elections 2018 – Our Requests

10 September 2018

On October 1, 2018, Quebecers will have to elect those who will form our next government. On this occasion, we would like to make known our demands on three topics that are at the heart of the priorities of people living with Cystic Fibrosis. These demands also reach several thousand Quebecers. We invite you to […]

Classified under: Uncategorized

Aid fund – Accommodation and travel

2 May 2018

Travel and accommodation costs associated with medical appointments can sometimes hurt the wallet. That is why we are presenting one of the aid funds we have set up to help people living with cystic fibrosis in Quebec. To qualify, you must complete an online form, or print it out and send it to us (only […]

Classified under: Uncategorized

Fax charges at the drugstore

13 July 2017

For several months, some pharmacies charge fees to their clients who must send documents to their doctors by fax. This is a common occurrence for people living with cystic fibrosis, for example at the time of renewal of prescriptions. Sometimes the fees charged for such a service can be up to $ 5.00. It is […]

Classified under: Uncategorized

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