CF Telethon?!

ctalbott0609

New member
Hey Everyone!

I'm sorry I haven't been on for a while. I've been around, but I've just been super busy. There's an amazing woman in Florida, by the name of Ellie Miller, who has a 19 year old Grandson with Cystic Fibrosis. I only met her recently, but she is a huge voice in our fight for awareness.

Recently, Ellie created a group called Fighters Against Cystic Fibrosis (F.A.C.F.). She has decided to take a very huge step, and do what's needed to host a nation wide telethon for Cystic Fibrosis. All she needs for this, is 1 million signatures on a petition!

Recently, Ellie had to make a quick decision, and she had surgery for a full hip replacement on Monday. I've been taking over her efforts for her fight to make this telethon happen.

Right now, we're so close to having exactly what we need. However, the push for extra signatures is stronger then ever. I know a lot of you don't have a Facebook account, so I wanted to post this here, and hopefully get your support behind this. This is a real cause, she's a real person, and she won't take no for an answer. I'll post the URL for the site she created here; and if you don't want to visit the site, or don't want to put your names down, you can certainly do so right here on this thread.

If anyone has any questions, please feel free to ask me!!!
 

ctalbott0609

New member
Hey Everyone!

I'm sorry I haven't been on for a while. I've been around, but I've just been super busy. There's an amazing woman in Florida, by the name of Ellie Miller, who has a 19 year old Grandson with Cystic Fibrosis. I only met her recently, but she is a huge voice in our fight for awareness.

Recently, Ellie created a group called Fighters Against Cystic Fibrosis (F.A.C.F.). She has decided to take a very huge step, and do what's needed to host a nation wide telethon for Cystic Fibrosis. All she needs for this, is 1 million signatures on a petition!

Recently, Ellie had to make a quick decision, and she had surgery for a full hip replacement on Monday. I've been taking over her efforts for her fight to make this telethon happen.

Right now, we're so close to having exactly what we need. However, the push for extra signatures is stronger then ever. I know a lot of you don't have a Facebook account, so I wanted to post this here, and hopefully get your support behind this. This is a real cause, she's a real person, and she won't take no for an answer. I'll post the URL for the site she created here; and if you don't want to visit the site, or don't want to put your names down, you can certainly do so right here on this thread.

If anyone has any questions, please feel free to ask me!!!
 

ctalbott0609

New member
Hey Everyone!

I'm sorry I haven't been on for a while. I've been around, but I've just been super busy. There's an amazing woman in Florida, by the name of Ellie Miller, who has a 19 year old Grandson with Cystic Fibrosis. I only met her recently, but she is a huge voice in our fight for awareness.

Recently, Ellie created a group called Fighters Against Cystic Fibrosis (F.A.C.F.). She has decided to take a very huge step, and do what's needed to host a nation wide telethon for Cystic Fibrosis. All she needs for this, is 1 million signatures on a petition!

Recently, Ellie had to make a quick decision, and she had surgery for a full hip replacement on Monday. I've been taking over her efforts for her fight to make this telethon happen.

Right now, we're so close to having exactly what we need. However, the push for extra signatures is stronger then ever. I know a lot of you don't have a Facebook account, so I wanted to post this here, and hopefully get your support behind this. This is a real cause, she's a real person, and she won't take no for an answer. I'll post the URL for the site she created here; and if you don't want to visit the site, or don't want to put your names down, you can certainly do so right here on this thread.

If anyone has any questions, please feel free to ask me!!!
 

ctalbott0609

New member
Hey Everyone!

I'm sorry I haven't been on for a while. I've been around, but I've just been super busy. There's an amazing woman in Florida, by the name of Ellie Miller, who has a 19 year old Grandson with Cystic Fibrosis. I only met her recently, but she is a huge voice in our fight for awareness.

Recently, Ellie created a group called Fighters Against Cystic Fibrosis (F.A.C.F.). She has decided to take a very huge step, and do what's needed to host a nation wide telethon for Cystic Fibrosis. All she needs for this, is 1 million signatures on a petition!

Recently, Ellie had to make a quick decision, and she had surgery for a full hip replacement on Monday. I've been taking over her efforts for her fight to make this telethon happen.

Right now, we're so close to having exactly what we need. However, the push for extra signatures is stronger then ever. I know a lot of you don't have a Facebook account, so I wanted to post this here, and hopefully get your support behind this. This is a real cause, she's a real person, and she won't take no for an answer. I'll post the URL for the site she created here; and if you don't want to visit the site, or don't want to put your names down, you can certainly do so right here on this thread.

If anyone has any questions, please feel free to ask me!!!
 

ctalbott0609

New member
Hey Everyone!
<br />
<br />I'm sorry I haven't been on for a while. I've been around, but I've just been super busy. There's an amazing woman in Florida, by the name of Ellie Miller, who has a 19 year old Grandson with Cystic Fibrosis. I only met her recently, but she is a huge voice in our fight for awareness.
<br />
<br />Recently, Ellie created a group called Fighters Against Cystic Fibrosis (F.A.C.F.). She has decided to take a very huge step, and do what's needed to host a nation wide telethon for Cystic Fibrosis. All she needs for this, is 1 million signatures on a petition!
<br />
<br />Recently, Ellie had to make a quick decision, and she had surgery for a full hip replacement on Monday. I've been taking over her efforts for her fight to make this telethon happen.
<br />
<br />Right now, we're so close to having exactly what we need. However, the push for extra signatures is stronger then ever. I know a lot of you don't have a Facebook account, so I wanted to post this here, and hopefully get your support behind this. This is a real cause, she's a real person, and she won't take no for an answer. I'll post the URL for the site she created here; and if you don't want to visit the site, or don't want to put your names down, you can certainly do so right here on this thread.
<br />
<br />If anyone has any questions, please feel free to ask me!!!
<br />
 

ashmomo

New member
<a target=_blank class=ftalternatingbarlinklarge href="http://www.facebook.com/#/pages/Fighters-Against-Cystic-Fibrosis-FACF/238548087236?ref=ts
">http://www.facebook.com/#/page...F/238548087236?ref=ts
</a>
here is the link...
 

ashmomo

New member
<a target=_blank class=ftalternatingbarlinklarge href="http://www.facebook.com/#/pages/Fighters-Against-Cystic-Fibrosis-FACF/238548087236?ref=ts
">http://www.facebook.com/#/page...F/238548087236?ref=ts
</a>
here is the link...
 

ashmomo

New member
<a target=_blank class=ftalternatingbarlinklarge href="http://www.facebook.com/#/pages/Fighters-Against-Cystic-Fibrosis-FACF/238548087236?ref=ts
">http://www.facebook.com/#/page...F/238548087236?ref=ts
</a>
here is the link...
 

ashmomo

New member
<a target=_blank class=ftalternatingbarlinklarge href="http://www.facebook.com/#/pages/Fighters-Against-Cystic-Fibrosis-FACF/238548087236?ref=ts
">http://www.facebook.com/#/page...F/238548087236?ref=ts
</a>
here is the link...
 

ashmomo

New member
<a target=_blank class=ftalternatingbarlinklarge href="http://www.facebook.com/#/pages/Fighters-Against-Cystic-Fibrosis-FACF/238548087236?ref=ts
">http://www.facebook.com/#/page...F/238548087236?ref=ts
</a><br />
<br />here is the link...
 
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