Recent content by Siobhan1985

Hi This is the first time I've posted on here, I'm Siobhan, from England. Am 23 with CF. My partner is just waiting for his appointment to come through to be tested to see if he is a carrier. Once he's been tested (and is ok, hopefully) we want to try for a baby as soon as poss. My FEV1 latest...

Hi This is the first time I've posted on here, I'm Siobhan, from England. Am 23 with CF. My partner is just waiting for his appointment to come through to be tested to see if he is a carrier. Once he's been tested (and is ok, hopefully) we want to try for a baby as soon as poss. My FEV1 latest...

Hi This is the first time I've posted on here, I'm Siobhan, from England. Am 23 with CF. My partner is just waiting for his appointment to come through to be tested to see if he is a carrier. Once he's been tested (and is ok, hopefully) we want to try for a baby as soon as poss. My FEV1 latest...

Hi This is the first time I've posted on here, I'm Siobhan, from England. Am 23 with CF. My partner is just waiting for his appointment to come through to be tested to see if he is a carrier. Once he's been tested (and is ok, hopefully) we want to try for a baby as soon as poss. My FEV1 latest...

Hi This is the first time I've posted on here, I'm Siobhan, from England. Am 23 with CF. My partner is just waiting for his appointment to come through to be tested to see if he is a carrier. Once he's been tested (and is ok, hopefully) we want to try for a baby as soon as poss. My FEV1 latest...

Yep that one is the CF trust one - and you click onto Meeting Point. That one is pretty busy all the time. Another smaller one is <a target=new class=ftalternatingbarlinklarge href="http://groups.msn.com/CysticfibrosisintheUK ">http://groups.msn.com/CysticfibrosisintheUK </a> Started by my...

Hi Guys I just wanted to post a short message re this forum... I live in England, and started popping on this site quite a while ago. However, lately I've been really put off of bothering to have a look - as so many of you have said this is a place for people with CF to come and ask...

i'm from england and my friend has set up a cf site with chat room -pls visit: http--groups.msn.com-Cysticfibrosisintheuk Siobhan <img src="i/expressions/face-icon-small-smile.gif" border="0">

Wow julie - what a gorgeous wedding dress!! absolutely beautiful. i'm getting married next year and looking for the perfect dress!

Hiya I can't answer your question exactly as I don't know aboout the CF Foundation. I know over here it would be difficult to have lots of CF ers working together due to cross infection - it would be no good for anyone as we'd all be getting ill! But we do have patient advocates that work for...

I also would love a 'CF pal'. I'm 19, soon to be 20, female wcf. I wonder if it would be emailpal these days?! email me too at vaunghy@hotmail.co.uk take care

hehe - this is where we also get to see all the 'mikes'!!! if anyone does discover how to put pics online for free let me know and i will also join in!!! ok i think this will take u to a pic of my new puppy but should also find one of me on there too!! <a target=new...

Hiya I posted on here before asking about the whole 'having children' issue. I received lots of advice and would like to say thanks for that, and yes, Holly Catheryns website was really good - you should have a read through. Since my initial thoughts about it I have had a chat with my...

i've had someone think i had M.S. before! Completely different to C.F. but think they just remembered it was initials of something so went with the first illness that came to mind!