Guest guest Posted January 1, 2001 Report Share Posted January 1, 2001 Each week our large newspaper includes a local community section and in yesterdays was an article about a girl in the area who was diagnosed with cf at the age of 17. The doctors thought she had asthma for years before diagnosing her. She played basketball and volleyball throughout highschool. She received a volleyball scholarship to UC Santa Barbara. She is now 20 and doing well. The article took up about 1/2 a page and the title was in very large print with the words cf in it so it was definately noticable. Very positive, encouraging article. yvonne price mom to madi 12 wcf & ariel w/o Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 1, 2001 Report Share Posted January 1, 2001 It is always great to see the public becoming AWARE of CF ...It is great that this young gal is doing so well and remaining active. It appears to be happening more and more.This disease will be conquered !! The more folks that know about it-----the more will be in the researching and also trial participants.Thanks for the info .Best wishes for the young gal. LOVE & HUGS, GrandmomBEV An article in our local paper Each week our large newspaper includes a local community section and in yesterdays was an article about a girl in the area who was diagnosed with cf at the age of 17. The doctors thought she had asthma for years before diagnosing her. She played basketball and volleyball throughout highschool. She received a volleyball scholarship to UC Santa Barbara. She is now 20 and doing well. The article took up about 1/2 a page and the title was in very large print with the words cf in it so it was definately noticable. Very positive, encouraging article. yvonne price mom to madi 12 wcf & ariel w/o *********************** This is a secular list. *********************** PLEASE do not post religious emails to the list. -------------------------------------------------- The opinions and information exchanged on this list should IN NO WAY be construed as medical advice. PLEASE CONSULT YOUR PHYSICIAN BEFORE CHANGING ANY MEDICATIONS OR TREATMENTS. -------------------------------------------------- Our webpage is at http://www.eohio.net/malbright/cfparents.htm _________________________________________________ Post message: cfparentsegroups Subscribe: cfparents-subscribeegroups Unsubscribe: cfparents-unsubscribeegroups List owner: cfparents-owneregroups _________________________________________________ WE HAVE A CHAT PAGE!!! /chat/cfparents _________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 2, 2001 Report Share Posted January 2, 2001 Hi, It is always very encouraging to read snippets on info printed in local and community newspapers regarding cf. We live in South Africa, where the incidence of cf amongs the white population is even lower that the averages stated for the US and Europe - you mention to folks that your daughter has cf and they stare at you as if you are speaking a totally different language - most people are just plain ignorant and assume that one " grows out of it " Remarks such as those are very hurtful and painful and I am just grateful that my daughter is not old enough to understand yet. We had one such article in our local community paper and it really made me thankful that maybe at least 1 more person was educated about cf because of it! Regards, Karolina (Mum to 16 mo w/cf) Quote Link to comment Share on other sites More sharing options...
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