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As of this week, the roughly 4,000 CF patients across the country, their families and friends have a new way to connect.

A social network launched by the non-profit Cystic Fibrosis Canada will help them find one another and converse via video-chat, instant message or online forums.“It’s the kind of thing the community really needs,” says Carly Stagg, 31, of Calgary, a CF patient who was actively involved in planning and designing the new portal.

A new online web portal launched by Cystic Fibrosis Canada allows patients and their families to meet virtually.

Cystic fibrosis is known as a devastating disease that causes severe respiratory problems and interferes with digestion because of thick mucous in the lungs.

Find out more Meetings and conferences are places where cross-infection could occur, so even at cystic fibrosis-related events, or events organised by the Cystic Fibrosis Trust, there should only be one person with CF in attendance at a time.

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