CF chat rooms

Daverog

New member
I would like to find a chat room for people with CF, please recommend some. Dave 29 w/cf from Ontario
 

Dea

New member
Hi Dave,I'm 30 with CF and a member of a CF chat. The link is www.groups.msn.com/CysticFibrosis2chat....I'm not trying to take away from this site...this site is great too....but the other has a chat room and lots of great people as well! You are welcome to join us!Dea
 

Dea

New member
Sorry...did the link wronghttp://groups.msn.com/CysticFibrosis2chatTry that one! Let me know!Dea
 

anonymous

New member
Hey DeaI read somewhere else where someone called Dea said that "Awareness" is one of the biggest issues re CF. Was that u and if so, I would love to be a part of making people aware but I need some information on why it needs to be heightened and what kind of things are best to share with others and what people with CF can expect once others are more aware. Do u have any examples of what people with CF or carers etc have used to get the message across and raise awareness.ThanksNene
 

AbsintheSorrow

New member
It needs awareness raised, because though it's not entirely unknown, it's not nearly as well known as cancer, for instance. And the more people that know, the more fund raising we get done, the better medical research we get done. There are a bunch of CF fund raisers done by the CF Foundation. One of which is actually held in May all over the country. Called Great Strides. Look up on the internet, there should be a Great Strides somewhere near you. There's also bike-a-thons, and parties, and blah blah etc.
 

anonymous

New member
I am writing a paper for my nursing class about CF. What as a CF patient would you want A. nurses to know, B. Public. C. What are the challenges, D. How do you cope etc. (Shadowtitan2002@yahoo.com)<img src="i/expressions/sun.gif" border="0">
 
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