idonotneedanidforyou (November 30, 1999 at 12:00 am)

cool song in the background. Who is it by and what is it called? Thanks

XImPinkX (November 30, 1999 at 12:00 am)

iis this disease genetic? xx sorry to hear about this xx hope they find a cure xxx

qbb01 (November 30, 1999 at 12:00 am)

My sister has this and she is 17 and never been hospitalized or had a transplant for the disease. There are different degrees to this disease, my sister has to take over 12000 pills for it every year, including sprays and taking salt pills which quite often make her sick. You have to be brave to deal with this disease.

anothergirl157 (November 30, 1999 at 12:00 am)

Hi Everyone. Firstly to everyone that has Cystic Fibrosis, you are so brave and I hope you enjoy your life to its fullest. Secondly, I would like to point out that in Ireland we do not have a specific unit for Cystic Fibrosis sufferers in any public hospital in the whole country. This means that when a sufferer must visit the hospital, they are left in waiting rooms with other sick people, which can be potentially deadly and worsen their sickness. Often, some sufferers are left in sleuth rooms.

ilovepetz12345 (November 30, 1999 at 12:00 am)

hi i have cystic fibrosis too and mine is a bad case so i will pray for u may the gods here me i hope they find a cure soon so we both can live a free life best wishes!!! :)

KristheLester (November 30, 1999 at 12:00 am)

A new hope comes from Thailand. They use thai traditional medicine and they have amazing results for many diseases (even genetic) and hopeless cases. You can see many testimonies on you tube searching "vilac plus" and on their web site: vilacplusdoteu. They have clinical trials to prove the efficiency. Regards!

Rob1084815162342 (November 30, 1999 at 12:00 am)

My comment above/below was to XxxPrincessBlondexxX as I felt it was very hurtful.

Rob1084815162342 (November 30, 1999 at 12:00 am)

That was uncalled for. Sure some people can be better then others but that isn't the case most of the time. Be glad to be doing well, Don't come on here and abuse people for trying to raise awareness for the disease. There trying to help find a cure for when your CF isn't doing so well. I have severe CF and breathing through a straw to me makes no difference. Don't ever be mean to people who are trying to help. Be happy that your doing well and don't upset the ones that are not with your comment

stoelby (November 30, 1999 at 12:00 am)

Well hi this is alyssa, i have cystic fibrosis. And if you have it you would know its different for everyone. You might not have a bad case of it. But i do, unfortunately, i am not as lucky as you are...and it doesn't help when you attack me like that. So thanks =]

stoelby (November 30, 1999 at 12:00 am)

I appreciate your concern for accuracy. We do cover the very treatments you are talking about in our Treatment video. You know, when we started raising money for CF, we never dreamed that we would get such negative feedback, especially from those we are trying to help. Despite your dislike for us, we will keep going and won't give up until there is a cure for all CF patients, including you.