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Breath For CF
- Become a member if you or someone who you love or you just know has CF then become a member
- Me, Myself, and I
- THIS PAGE IS MADE FOR PEOPLE WITH CF OR FOR PEOPLE WHO KNOW SOMEONE WITH IT, LETS SUPPORT EACHOTHER.........
For those who do not know CF is a gentic disorder of the lungs and pancras, the patients with it live very normal lives.....
But i have made this page for those CFers who feel lonely and wo feel like they are the only person in the world with this disease and i'm letting you know that your not and that i want to make this oage so you can come to me and have a safe place to come to and feel loved........ i know what i am talking about as i have CF and i lost my best friend from CF and this is for him and for ver other cfer like him........ my name is rebekah and i honestly love helping everyone... so if your a new parent wth CF i can get my mum to talk to you and if ou a tenager young adult, or a litle kid, i'm here for you......... =)
- rock, metal, hip hop, RnB, pop, classic, everything really apart from country can't stand it
- OM where to begin i love all kind of movies, mainly, comady, and action
- bull rush, soccor, badminton, swimming, running, the word cup hehehe
- Scared Of
- being alone, blood tests, CT scans
- Happiest When
- making people laugh and just having fun
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- What is cystic FIbrosis 0 Taken
Just an update on my health, it's ben awhile so there is alot to update on,
Well i have had a bone disnity exam a few weeks ago and i have good bones but my doctor wants me to have vit D tablets but it's like once a month so pffft i can do that and calcuim tablets once a day which i can do also...
A few months ago i had a new port-a-cath put in my other one blocked up which sucks and a pain in the ass but the new one is working like a charm which is awesome, ended up in hospital abit after the op tho i was in so much pain and mum brought codiene and it work but i reacted to it and ended up in the hospital poor mum felt so bad....
Um yeah that's pretty much everything aye, but will keep you updated and i hope you follower cfers and people who know cfers are doing your bit to fight this pain in the ass condition.
0 Comments 193 weeks
Just an opening blog, thanks you to all who have so far becomed apart of this page i just hope more CFers find it i want to help them so much...... if you know anyone with cf please show them this page..
0 Comments 231 weeks