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I say if its something YOU really really want then do it. If it were me in that situation I wouldnt. I am very body self consious and have scars and a port. I still like my scars...weird....I thought about trying that cream once to see if it will make them start disappearing but decided against...

purplelungs is my screenname

I think it depends on your state. I have always been told you have to reapply, sometimes the reapplication process is easier because they have your records....but you still have to reapply and they need to see if you qualify. Now if you were working SSi is different than SSDI and after you have...

also i would check and make sure the needle is right in the middle of the port. sometimes they can go in sideways or a little to much to the side and not go into the port right and someitmes causes a leak....when you flush is it harder than normal? does the needle look centered and straight...

usually innies and outties is really how they tied of the umbilical cord when you were born. any one can have an outie. my cousin with no cf has an outie...well here recently its become an innie.

I just saw this post biscuit. I will say that a diet healthy like that is good for you no matter what. Just cutting out the high greassy foods, even caffine like cokes will help loose some weight fast. But it may not be alot. What can hurt you though is trying to loose weight to fast...not...

The question is how much do you weigh now and how tall are you and how old are you. This will determine whats the best way to loose weight. Now if you dont weigh that much but for some reason feel kinda flabby, maybe you are skinny but lets say your stomach has a tiny pooch or you just feel you...

Maybe those who have the negative feelings towards the CFF was because of their local chapter...not the overall foundation. Sometimes it can be a few rude people that ruin the whole for someone. I do know some are wishing the cff could help those desperate for meds...i have heard that some think...

Unfortunatly it will be a very very lucky thing if you do find life insurance. No life insurance will cover someone with cf...pre exsisting thing. Now if you had life insurance before you found out about cf you would have that....like my mom got me life insurance when I was born, and a year...

I have the omron micro air as well. I love it. it even does tobi in half the time...all the tobi med doesnt fit in it at once but you put half in there and then the rest. but you have to replace the mesh cap once a year and they are about $50....not bad for a year use....and do make sure you...

Heres the link for those doing school projects. This will give you all the general info you need. If you notice the grid above that has diabetes, respriatory, symptoms, pancrease, etc...if you click on those it shows how CF affects those aspects or causes those problems...

Heres the link for those doing school projects. This will give you all the general info you need. If you notice the grid above that has diabetes, respriatory, symptoms, pancrease, etc...if you click on those it shows how CF affects those aspects or causes those problems...

Heres the link for those doing school projects. This will give you all the general info you need. If you notice the grid above that has diabetes, respriatory, symptoms, pancrease, etc...if you click on those it shows how CF affects those aspects or causes those problems...

Heres the link for those doing school projects. This will give you all the general info you need. If you notice the grid above that has diabetes, respriatory, symptoms, pancrease, etc...if you click on those it shows how CF affects those aspects or causes those problems...

Actually I wasnt whining. I was trying to help. To many times people come actually asking us what cf is, when you have to go through a page that has info on cf before you get to the forums. I dont mind helping people with school projects. Heck I have helped so many I cant keep count. I have...

Yes its to the school project people who come here wanting us to answer questions for them. If you go to cysticfibrosis.com the very first page that comes up there is alot of links you can go to...one of which is a page dedicated on information to CF.

I feel like being nice today. So here goes. Look at the very first page on the site. On that site there is a link....its called Cystic Fibrosis information...you will find everything you need to know there.....now what that hard? ok good Now if you need something more specific than thats in that...

I feel like being nice today. So here goes. Look at the very first page on the site. On that site there is a link....its called Cystic Fibrosis information...you will find everything you need to know there.....now what that hard? ok good Now if you need something more specific than thats in that...

I feel like being nice today. So here goes. Look at the very first page on the site. On that site there is a link....its called Cystic Fibrosis information...you will find everything you need to know there.....now what that hard? ok good Now if you need something more specific than thats in that...

I will answer this before you get in trouble. ok you got your pen and paper out? this is important....ok here goes.. Do some RESEARCH!!!!!!!!!!!!!!!!!!!!!!!!!!!!!!! You found this site....the front page before you get to the forums has an aboundance of information and other websites to go...