people who use cf to make money

[2perfectboys]

There's no lawsuit grounds here people. The letter he posted specifically says i"if u have any questions please feel free to contact me", i;m sure they have a release on file from Jason, so if don't go out and purchase anything new just yet, cause u will just have the bill to pay.

Here's what I think, I believe he does have CF, I had sent him a message a while ago on my space, and he never answered. I was willing to offer help and still am to anyone that needs it. I to am guestioning like another member said, what he needs this money for. Yes CF is expensive as we all know, but he is in California and has no reason not to have state insurance which will pay for almost everything. He has money for enzymes, but nothing else. Come on, those r one of the most expensive things. If we didn't have insurance I think they r about 600-900 a month. Plus all those supplements r not cheap and all that partying he is doing can't be cheap or good for him. So if he wants to get all offended that people r questioning him then to bad he should have never asked for help in the first place or been more clear on what it was he needed so people could truly help him. I still offer my assistance to, just tells us what it is u need.

 

[Brad]

I just want to say Thank You To
the folks here that defended Jason and offered Him help
and didn't question weather he had Cf.

He came here for help, not to be judged.

I know a lot people with Cf that don't look
sick. I myself don't really look like I have Cf.
I have had people make me feel like they resent me for that.

To tell the truth, I wish I didn't have Cf, I am sure everybody
on her SHARES that wish.

So go easy on the Guy, He came here for help....

BTW here is my myspace, look at me and the people in my friends list.
75% of them Have CF...........

<a target=_blank class=ftalternatingbarlinklarge href="http://profile.myspace.com/index.cfm?fuseaction=user.viewprofile&friendid=56920916">http://profile.myspace.com/ind...file&friendid=56920916</a>

 

[Brad]

I just want to say Thank You To
the folks here that defended Jason and offered Him help
and didn't question weather he had Cf.

He came here for help, not to be judged.

I know a lot people with Cf that don't look
sick. I myself don't really look like I have Cf.
I have had people make me feel like they resent me for that.

To tell the truth, I wish I didn't have Cf, I am sure everybody
on her SHARES that wish.

So go easy on the Guy, He came here for help....

BTW here is my myspace, look at me and the people in my friends list.
75% of them Have CF...........

<a target=_blank class=ftalternatingbarlinklarge href="http://profile.myspace.com/index.cfm?fuseaction=user.viewprofile&friendid=56920916">http://profile.myspace.com/ind...file&friendid=56920916</a>

 

[Brad]

I just want to say Thank You To
the folks here that defended Jason and offered Him help
and didn't question weather he had Cf.

He came here for help, not to be judged.

I know a lot people with Cf that don't look
sick. I myself don't really look like I have Cf.
I have had people make me feel like they resent me for that.

To tell the truth, I wish I didn't have Cf, I am sure everybody
on her SHARES that wish.

So go easy on the Guy, He came here for help....

BTW here is my myspace, look at me and the people in my friends list.
75% of them Have CF...........

<a target=_blank class=ftalternatingbarlinklarge href="http://profile.myspace.com/index.cfm?fuseaction=user.viewprofile&friendid=56920916">http://profile.myspace.com/ind...file&friendid=56920916</a>

 

[persiadubois]

O.K. folks - you all should listen more carefully to Jason's message. He has been denied Medi-cal, he has been denied SSI disability. He had coverage in the past, but has none now. This should not be the case, but it is.

As for the info given out from the doctor's office in Fort Bragg...whether he was there before or after the HIPPA
business, it is still a breach of patient confidentiality. Unless Jason signed an agreement with that office to give out his information, they should not have given it out.
I would be very surprised if anyone there did give out info over the phone, as they wouldn't have known who was calling. I used to take my daugters to that office, and I always thought they opperated with high integrity. So Bethie, would you please email me directly, to give me more details on that call. I'd like to follow up on this for jason.
thanks
Persia Dubois
persiadubois@yahoo.com

 

[persiadubois]

O.K. folks - you all should listen more carefully to Jason's message. He has been denied Medi-cal, he has been denied SSI disability. He had coverage in the past, but has none now. This should not be the case, but it is.

As for the info given out from the doctor's office in Fort Bragg...whether he was there before or after the HIPPA
business, it is still a breach of patient confidentiality. Unless Jason signed an agreement with that office to give out his information, they should not have given it out.
I would be very surprised if anyone there did give out info over the phone, as they wouldn't have known who was calling. I used to take my daugters to that office, and I always thought they opperated with high integrity. So Bethie, would you please email me directly, to give me more details on that call. I'd like to follow up on this for jason.
thanks
Persia Dubois
persiadubois@yahoo.com

 

[persiadubois]

O.K. folks - you all should listen more carefully to Jason's message. He has been denied Medi-cal, he has been denied SSI disability. He had coverage in the past, but has none now. This should not be the case, but it is.

As for the info given out from the doctor's office in Fort Bragg...whether he was there before or after the HIPPA
business, it is still a breach of patient confidentiality. Unless Jason signed an agreement with that office to give out his information, they should not have given it out.
I would be very surprised if anyone there did give out info over the phone, as they wouldn't have known who was calling. I used to take my daugters to that office, and I always thought they opperated with high integrity. So Bethie, would you please email me directly, to give me more details on that call. I'd like to follow up on this for jason.
thanks
Persia Dubois
persiadubois@yahoo.com

 

[Emily65Roses]

I will repeat myself one more time, then I'm done.

Even if you ignore the fact that he doesn't look like he has CF (because many of you are right, many of us look normal), he seems suspicious. A lot of stuff he's said and changed have been fishy. We have no right to jump up the kid's @ss, but we have EVERY right to question him if things seems off (and in my opinion, as well as others, they do seem off). There is nothing wrong with doing so. I would hope that anyone that reasonably suspects fraud question it.

 

[Emily65Roses]

I will repeat myself one more time, then I'm done.

Even if you ignore the fact that he doesn't look like he has CF (because many of you are right, many of us look normal), he seems suspicious. A lot of stuff he's said and changed have been fishy. We have no right to jump up the kid's @ss, but we have EVERY right to question him if things seems off (and in my opinion, as well as others, they do seem off). There is nothing wrong with doing so. I would hope that anyone that reasonably suspects fraud question it.

 

[Emily65Roses]

I will repeat myself one more time, then I'm done.

Even if you ignore the fact that he doesn't look like he has CF (because many of you are right, many of us look normal), he seems suspicious. A lot of stuff he's said and changed have been fishy. We have no right to jump up the kid's @ss, but we have EVERY right to question him if things seems off (and in my opinion, as well as others, they do seem off). There is nothing wrong with doing so. I would hope that anyone that reasonably suspects fraud question it.

 

[libby25ln]

I wanted to respond to some of the comments that have been made about Jason. I have been in a relationship with him for over five years and can assure you he has Cystic Fibrosis.

I am new to this cite and think it is wonderful that there is something like this for people to talk who have CF. I have often wished that Jason knew more people with CF so he could have more of a support system. I am suprised that a cite like this would be used to bash someone with the disease who is genuinely in need to help. I feel very offended by some of the insulting comments that have been made about Jason.

Many of these issues people have with Jason's cite could have been cleared up with a little research. He was born in 1982, not 1988 if there was a discrepency, that was the doctors fault not his. He has no medical information up because he has not seen a CF specialist for years. Believe it or not, those are real doctors notes, as people who have had adequate health care, you would not believe what hes gone through with doctors who know nothing about CF. Most of the time they sit there in front of him and look up stuff about it.

He has been denied several times for medical and disability and has had to work full time until just recently when he got sicker. By the way, just because he was working full time, as a manager at GNC, does not mean he got benefits. He didn't! He has been healthy for most of the five years we have been together but has been getting worse since he developed diabetes. Without medical insurance of any kind it is impossible for him to even afford diabetes supplies, or enzymes most of the time. If he had health insurace believe me, he would not be asking for help.

Since I have known him Jason has been extreamly shy and ashamed of his illness. He rarely tells people that he has CF and I know he would rather not go public with it. However, a friend of his, from the gym put together the cite for him. Jason knows nothing putting together a foundation or a website so forgive him if between his friend JT and him, there are discrepencies on the site. He was very excited to do the cite because he truely wanted to tell people about the benefits he has felt from working out. He wanted to serve as a mentor to young people with CF and encourage them to be successful despite the disease. He felt hopeless as a young person because everyone told him what Im sure most of you have heard, "you'll always be sick, you'll always be small, and you probably wont live though your twenties." He greatly resents having been brought up with this outlook and wanted to do something to change the lives of other young people. The donation aspect of the website was a bonus. Also what you guys dont know is that him and his friend are trying to get a nonprofit lisence, until they have it, Jason has no access to the donations. What donations have been given I believe are in an account that is only allowed to be used on medical bills. I hope this helps clear some things up. If you have questions for Jason just ask him and please dont attack him, he has been through enough. If you dont believe him, dont donate but dont discourage others from checking into his cite. By the way the reason why he has a myspace that never mentions CF is because he doesn't like his friends to konw he has it. Jason does not have the medical or financial support most people with CF have, he has been struggling to survive, and he doesnt want your money to go to vegas or throw a party, he wants to share helpful information and get support financial or just through friendship. Please stop writing hurtful comments because they are heart breaking. Thank you for reading and thanks for allowing me into your chatroom. <img src="i/expressions/face-icon-small-frown.gif" border="0">

 

[libby25ln]

I wanted to respond to some of the comments that have been made about Jason. I have been in a relationship with him for over five years and can assure you he has Cystic Fibrosis.

I am new to this cite and think it is wonderful that there is something like this for people to talk who have CF. I have often wished that Jason knew more people with CF so he could have more of a support system. I am suprised that a cite like this would be used to bash someone with the disease who is genuinely in need to help. I feel very offended by some of the insulting comments that have been made about Jason.

Many of these issues people have with Jason's cite could have been cleared up with a little research. He was born in 1982, not 1988 if there was a discrepency, that was the doctors fault not his. He has no medical information up because he has not seen a CF specialist for years. Believe it or not, those are real doctors notes, as people who have had adequate health care, you would not believe what hes gone through with doctors who know nothing about CF. Most of the time they sit there in front of him and look up stuff about it.

He has been denied several times for medical and disability and has had to work full time until just recently when he got sicker. By the way, just because he was working full time, as a manager at GNC, does not mean he got benefits. He didn't! He has been healthy for most of the five years we have been together but has been getting worse since he developed diabetes. Without medical insurance of any kind it is impossible for him to even afford diabetes supplies, or enzymes most of the time. If he had health insurace believe me, he would not be asking for help.

Since I have known him Jason has been extreamly shy and ashamed of his illness. He rarely tells people that he has CF and I know he would rather not go public with it. However, a friend of his, from the gym put together the cite for him. Jason knows nothing putting together a foundation or a website so forgive him if between his friend JT and him, there are discrepencies on the site. He was very excited to do the cite because he truely wanted to tell people about the benefits he has felt from working out. He wanted to serve as a mentor to young people with CF and encourage them to be successful despite the disease. He felt hopeless as a young person because everyone told him what Im sure most of you have heard, "you'll always be sick, you'll always be small, and you probably wont live though your twenties." He greatly resents having been brought up with this outlook and wanted to do something to change the lives of other young people. The donation aspect of the website was a bonus. Also what you guys dont know is that him and his friend are trying to get a nonprofit lisence, until they have it, Jason has no access to the donations. What donations have been given I believe are in an account that is only allowed to be used on medical bills. I hope this helps clear some things up. If you have questions for Jason just ask him and please dont attack him, he has been through enough. If you dont believe him, dont donate but dont discourage others from checking into his cite. By the way the reason why he has a myspace that never mentions CF is because he doesn't like his friends to konw he has it. Jason does not have the medical or financial support most people with CF have, he has been struggling to survive, and he doesnt want your money to go to vegas or throw a party, he wants to share helpful information and get support financial or just through friendship. Please stop writing hurtful comments because they are heart breaking. Thank you for reading and thanks for allowing me into your chatroom. <img src="i/expressions/face-icon-small-frown.gif" border="0">

 

[libby25ln]

I wanted to respond to some of the comments that have been made about Jason. I have been in a relationship with him for over five years and can assure you he has Cystic Fibrosis.

I am new to this cite and think it is wonderful that there is something like this for people to talk who have CF. I have often wished that Jason knew more people with CF so he could have more of a support system. I am suprised that a cite like this would be used to bash someone with the disease who is genuinely in need to help. I feel very offended by some of the insulting comments that have been made about Jason.

Many of these issues people have with Jason's cite could have been cleared up with a little research. He was born in 1982, not 1988 if there was a discrepency, that was the doctors fault not his. He has no medical information up because he has not seen a CF specialist for years. Believe it or not, those are real doctors notes, as people who have had adequate health care, you would not believe what hes gone through with doctors who know nothing about CF. Most of the time they sit there in front of him and look up stuff about it.

He has been denied several times for medical and disability and has had to work full time until just recently when he got sicker. By the way, just because he was working full time, as a manager at GNC, does not mean he got benefits. He didn't! He has been healthy for most of the five years we have been together but has been getting worse since he developed diabetes. Without medical insurance of any kind it is impossible for him to even afford diabetes supplies, or enzymes most of the time. If he had health insurace believe me, he would not be asking for help.

Since I have known him Jason has been extreamly shy and ashamed of his illness. He rarely tells people that he has CF and I know he would rather not go public with it. However, a friend of his, from the gym put together the cite for him. Jason knows nothing putting together a foundation or a website so forgive him if between his friend JT and him, there are discrepencies on the site. He was very excited to do the cite because he truely wanted to tell people about the benefits he has felt from working out. He wanted to serve as a mentor to young people with CF and encourage them to be successful despite the disease. He felt hopeless as a young person because everyone told him what Im sure most of you have heard, "you'll always be sick, you'll always be small, and you probably wont live though your twenties." He greatly resents having been brought up with this outlook and wanted to do something to change the lives of other young people. The donation aspect of the website was a bonus. Also what you guys dont know is that him and his friend are trying to get a nonprofit lisence, until they have it, Jason has no access to the donations. What donations have been given I believe are in an account that is only allowed to be used on medical bills. I hope this helps clear some things up. If you have questions for Jason just ask him and please dont attack him, he has been through enough. If you dont believe him, dont donate but dont discourage others from checking into his cite. By the way the reason why he has a myspace that never mentions CF is because he doesn't like his friends to konw he has it. Jason does not have the medical or financial support most people with CF have, he has been struggling to survive, and he doesnt want your money to go to vegas or throw a party, he wants to share helpful information and get support financial or just through friendship. Please stop writing hurtful comments because they are heart breaking. Thank you for reading and thanks for allowing me into your chatroom. <img src="i/expressions/face-icon-small-frown.gif" border="0">

 

[persiadubois]

Also, anhyone who thinks Jason doesn't look sick, probably hasn't watched his video. When I compare how he looks in his photo on the upper right of his website <jasoncoverston.com> with how he looks in the video, I am alarmed at his decline. It has been rapid. I also notice him laboring for his breath, in the video.
So if you really didn't watch the video, I'd say you missed some important stuff.

Persia DuBois

 

[persiadubois]

Also, anhyone who thinks Jason doesn't look sick, probably hasn't watched his video. When I compare how he looks in his photo on the upper right of his website <jasoncoverston.com> with how he looks in the video, I am alarmed at his decline. It has been rapid. I also notice him laboring for his breath, in the video.
So if you really didn't watch the video, I'd say you missed some important stuff.

Persia DuBois

 

[persiadubois]

Also, anhyone who thinks Jason doesn't look sick, probably hasn't watched his video. When I compare how he looks in his photo on the upper right of his website <jasoncoverston.com> with how he looks in the video, I am alarmed at his decline. It has been rapid. I also notice him laboring for his breath, in the video.
So if you really didn't watch the video, I'd say you missed some important stuff.

Persia DuBois

 

[Prussian]

Can you please elaborate on what he mans by "virus"? I think that will clear up most of the confusion. On his myspace page if you read the blog entitled; FINALLY! It says he had an appointment to get his issues straighted out. I believe he has CF but I think most of us don't understand what specifically is wrong with him.

 

[Prussian]

Can you please elaborate on what he mans by "virus"? I think that will clear up most of the confusion. On his myspace page if you read the blog entitled; FINALLY! It says he had an appointment to get his issues straighted out. I believe he has CF but I think most of us don't understand what specifically is wrong with him.

 

[Prussian]

Can you please elaborate on what he mans by "virus"? I think that will clear up most of the confusion. On his myspace page if you read the blog entitled; FINALLY! It says he had an appointment to get his issues straighted out. I believe he has CF but I think most of us don't understand what specifically is wrong with him.

 

[julie]

Persia,

Since Jason's not responding to my offers for help, maybe you will on his behalf. I'd be happy to work with him regarding medical, GHPP and social security. YOu can ask aroudn this site, I've helped 5 other CFers win an SSA case AFTER being denied, WITHOUT the help of a lawyer. I'm FREEEEEEEE, I don't cost a dime. But if he doesn't want this type of help and ONLY wants money.... I'm going to be honest in saying I'm a bit suspicious.

Feel free to email me at division902@hotmail.com