Im new here and a mum

W

welshwitch

Guest
Hi lilytree,

welcome! here you will find many (as i have found) positive role models w/ CF for you and your daughter.

You are welcome to ask me anything! cf kids have extra needs which are often very subtle, and i wish this website had been around for my parents when i was born.

I've done great for 28 years w/ this condition, one that i look at as an extra challege for me, but doable nonetheless. check out my blog for more info!

take care!
 
W

welshwitch

Guest
Hi lilytree,

welcome! here you will find many (as i have found) positive role models w/ CF for you and your daughter.

You are welcome to ask me anything! cf kids have extra needs which are often very subtle, and i wish this website had been around for my parents when i was born.

I've done great for 28 years w/ this condition, one that i look at as an extra challege for me, but doable nonetheless. check out my blog for more info!

take care!
 
W

welshwitch

Guest
Hi lilytree,

welcome! here you will find many (as i have found) positive role models w/ CF for you and your daughter.

You are welcome to ask me anything! cf kids have extra needs which are often very subtle, and i wish this website had been around for my parents when i was born.

I've done great for 28 years w/ this condition, one that i look at as an extra challege for me, but doable nonetheless. check out my blog for more info!

take care!
 
W

welshwitch

Guest
Hi lilytree,

welcome! here you will find many (as i have found) positive role models w/ CF for you and your daughter.

You are welcome to ask me anything! cf kids have extra needs which are often very subtle, and i wish this website had been around for my parents when i was born.

I've done great for 28 years w/ this condition, one that i look at as an extra challege for me, but doable nonetheless. check out my blog for more info!

take care!
 
W

welshwitch

Guest
Hi lilytree,

welcome! here you will find many (as i have found) positive role models w/ CF for you and your daughter.

You are welcome to ask me anything! cf kids have extra needs which are often very subtle, and i wish this website had been around for my parents when i was born.

I've done great for 28 years w/ this condition, one that i look at as an extra challege for me, but doable nonetheless. check out my blog for more info!

take care!
 

JazzysMom

New member
Welcome Aboard! Its a lot to take in so dont overwhelm yourself with everything on here.

As far as physio....most of us agree as do MOST (not all oddly) that preventive treatment is the way to go from the start which includes some type of therapy. For many of us in the US we use the Vest, but many still use the manual clapping. There is also the accapella & the flutter devices.

Some doctors dont believe bronchdialators are needed before therapy, but again most prescribe it.

I am not sure what questions you have, but ask away & you will get answers.

HUGS
 

JazzysMom

New member
Welcome Aboard! Its a lot to take in so dont overwhelm yourself with everything on here.

As far as physio....most of us agree as do MOST (not all oddly) that preventive treatment is the way to go from the start which includes some type of therapy. For many of us in the US we use the Vest, but many still use the manual clapping. There is also the accapella & the flutter devices.

Some doctors dont believe bronchdialators are needed before therapy, but again most prescribe it.

I am not sure what questions you have, but ask away & you will get answers.

HUGS
 

JazzysMom

New member
Welcome Aboard! Its a lot to take in so dont overwhelm yourself with everything on here.

As far as physio....most of us agree as do MOST (not all oddly) that preventive treatment is the way to go from the start which includes some type of therapy. For many of us in the US we use the Vest, but many still use the manual clapping. There is also the accapella & the flutter devices.

Some doctors dont believe bronchdialators are needed before therapy, but again most prescribe it.

I am not sure what questions you have, but ask away & you will get answers.

HUGS
 

JazzysMom

New member
Welcome Aboard! Its a lot to take in so dont overwhelm yourself with everything on here.

As far as physio....most of us agree as do MOST (not all oddly) that preventive treatment is the way to go from the start which includes some type of therapy. For many of us in the US we use the Vest, but many still use the manual clapping. There is also the accapella & the flutter devices.

Some doctors dont believe bronchdialators are needed before therapy, but again most prescribe it.

I am not sure what questions you have, but ask away & you will get answers.

HUGS
 

JazzysMom

New member
Welcome Aboard! Its a lot to take in so dont overwhelm yourself with everything on here.

As far as physio....most of us agree as do MOST (not all oddly) that preventive treatment is the way to go from the start which includes some type of therapy. For many of us in the US we use the Vest, but many still use the manual clapping. There is also the accapella & the flutter devices.

Some doctors dont believe bronchdialators are needed before therapy, but again most prescribe it.

I am not sure what questions you have, but ask away & you will get answers.

HUGS
 

beleache

New member
Hi & Welcome to the site.. It is a great place for support/information.. My name is joni, i'm a 55 soon to be 56 y/o f w c/f.. I have 4 sons and a 2y/o grandson, i live in the New York area .. We are here for each other, so don't be shy or feel funny to post anything.. Take care and God Bless <img src="i/expressions/face-icon-small-smile.gif" border="0"> joni
 

beleache

New member
Hi & Welcome to the site.. It is a great place for support/information.. My name is joni, i'm a 55 soon to be 56 y/o f w c/f.. I have 4 sons and a 2y/o grandson, i live in the New York area .. We are here for each other, so don't be shy or feel funny to post anything.. Take care and God Bless <img src="i/expressions/face-icon-small-smile.gif" border="0"> joni
 

beleache

New member
Hi & Welcome to the site.. It is a great place for support/information.. My name is joni, i'm a 55 soon to be 56 y/o f w c/f.. I have 4 sons and a 2y/o grandson, i live in the New York area .. We are here for each other, so don't be shy or feel funny to post anything.. Take care and God Bless <img src="i/expressions/face-icon-small-smile.gif" border="0"> joni
 

beleache

New member
Hi & Welcome to the site.. It is a great place for support/information.. My name is joni, i'm a 55 soon to be 56 y/o f w c/f.. I have 4 sons and a 2y/o grandson, i live in the New York area .. We are here for each other, so don't be shy or feel funny to post anything.. Take care and God Bless <img src="i/expressions/face-icon-small-smile.gif" border="0"> joni
 

beleache

New member
Hi & Welcome to the site.. It is a great place for support/information.. My name is joni, i'm a 55 soon to be 56 y/o f w c/f.. I have 4 sons and a 2y/o grandson, i live in the New York area .. We are here for each other, so don't be shy or feel funny to post anything.. Take care and God Bless <img src="i/expressions/face-icon-small-smile.gif" border="0"> joni
 
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