Guest guest Posted January 30, 2009 Report Share Posted January 30, 2009 First, congratulations, You are very brave and a leader amongst us. Second, why not bring a criminal charge against them for attempting to defraud you. That is larceny. And third a civil suit for all the pain and suffering they caused you. Don't all doctors say to relax and not get stressed? Doesn't Big Pharm make millions on pills that relax us? You certainly should be compensated for all the stress you went through. I am surprised that lawyers have not yet contacted you. I think this would set a great example for all big business out there where CEO's watch porn on their government paid for monitors while we sweat out the exhorbitant bills and they steal from Medicare and Medicaid. This should somehow get to the President. He is trying to make an honest nation out of corporate corruption, I hope! Dolores From: DEBBIE GIBSON <Debbullwinkle@...> Subject: rheumatic Update hospital denying tx/Debbie " support group " <rheumatic > Cc: " socjog " <socjog@...>, " Ellen McCool " <ellenmccool@...> Date: Friday, January 30, 2009, 10:49 PM HI all, just got a letter today regarding the battle we have been having with the hospital billing incorrectly and forcing me...defrauding me...by telling me they could not bill Medicare without that form being signed, hospital sent me a letter, telling me that my photopheresis tx for next Mon and Tue, I will need to schedule at another facility. The story will be in this weeks local paper and the tv news reporter that filmed my meeting with the hospital billing dept over a year ago...where they kept insisting I sign that form..or they could not bill Medicare.... .he is running the story on the Monday evening news...I have also let Mr. Ross of 20/20 know that I received the letter....In addition I have been in contact with ARRP the Magazine.... about doing a story, so this will not happen to others.... It is all good, I will find another facility that can hopefully give me this life saving treatment and further, I don't have to go to Indiana on Mon and Tues now....After 3 yrs I am tired...but I know what happens when I don't get it...the SD brings on the lung disease and then I start suffocating. ...ugh...hate that...so I will get to work next week finding another facility to treat me...nice huh...AND this hospital is a non-profit.. .but the DRs have the right to not treat a patient AND the letter expressly stated that the hospital spoke with my Drs and they agreed I should go elsewhere... Hope everyone is doing well....Have a great weekend...stay warm if you live in the Midwest!! Debbie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 30, 2009 Report Share Posted January 30, 2009 Thank you Delores....once the story goes public here and in Indy...I am hopeful that the attys will be more receptive to taking the case on a contingency...since we have so much proof what they put me thru...and the fact that they lied...on camera too!! about the form being needed and then using it to balance bill me....and I have emails that I forwarded to the tv stations...the word is getting out...the DRs, by refusing to treat me now...have opened themselves up....we will see what an atty has to say...I know they are only doing what the hospital made them do...I filed a complaint with the board where the hospital is accredited as well...and with Med and my secondary and with the State of IN AG office....It has been exhausting...I am bound and determined that they will NOT ever be able to do that to another ill patient....fortunately, the God's were looking out for me...when I called the TV reporter in Indy, where I get my chemo, he answered his phone...sent out his cameraman and we have it on tape the very first meeting with the billing dept where I was refusing to sign the form....and with the emails additionally backing me up...saying the same thing...we are pretty well documented...If Mr. Ross does indeed do the story and he has indicated he is interested....it will be National and then 2 good things will happen....1) no provider will hopefully be able to tell a Medicare patient they have to sign that form and then use it to balance bill them...and 2) my photopheresis tx will be on tv and explained as a very viable tx for SD lung disease...I just found out yesterday from Yale...OMG this is big news...I fought my insurance in 2005...fought them for over a year to get the photopheresis for my SD lung disease....Anthem denied and denied....well, they told me yesterday that Yale has 3 SD patients getting photopheresis for their lung disease and GUESS WHAT !!! Anthem gave them approval!!!!!! YAYYYYYYYY!! It is all good Delores....all good....there is a reason why this happened to me...I apparently am supposed to fight this battle....I just am so thankful that I had the presence of mind to call the local TV station and get a cameraman sent out to document and that I refused to sign the form outright, only signing it when they said I had to....they cannot submit a claim to Medicare without it...only signing it with the amended...I am NOT agreeing to pay for anything other than deductible and out of pocket from Anthem...whew... Things happen for a reason...I would prefer to NOT be on National TV but if that is what it takes...so be it! If Mr. Ross does go with the story I will make sure I post on the board... Thanks for writing, always good to hear from you...Debbie rheumatic Update hospital denying tx/Debbie " support group " <rheumatic > Cc: " socjog " <socjog@...>, " Ellen McCool " <ellenmccool@...> Date: Friday, January 30, 2009, 10:49 PM HI all, just got a letter today regarding the battle we have been having with the hospital billing incorrectly and forcing me...defrauding me...by telling me they could not bill Medicare without that form being signed, hospital sent me a letter, telling me that my photopheresis tx for next Mon and Tue, I will need to schedule at another facility. The story will be in this weeks local paper and the tv news reporter that filmed my meeting with the hospital billing dept over a year ago...where they kept insisting I sign that form..or they could not bill Medicare.... .he is running the story on the Monday evening news...I have also let Mr. Ross of 20/20 know that I received the letter....In addition I have been in contact with ARRP the Magazine.... about doing a story, so this will not happen to others.... It is all good, I will find another facility that can hopefully give me this life saving treatment and further, I don't have to go to Indiana on Mon and Tues now....After 3 yrs I am tired...but I know what happens when I don't get it...the SD brings on the lung disease and then I start suffocating. ...ugh...hate that...so I will get to work next week finding another facility to treat me...nice huh...AND this hospital is a non-profit.. .but the DRs have the right to not treat a patient AND the letter expressly stated that the hospital spoke with my Drs and they agreed I should go elsewhere... Hope everyone is doing well....Have a great weekend...stay warm if you live in the Midwest!! Debbie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 31, 2009 Report Share Posted January 31, 2009 Hi Debbie, this is so fantastic! You are doing this for all of us and I feel for your pain and struggle. I can't wait! Let me know when it goes national. I'll have Mike record it. I also will want to put the story into my book, with your permission, of course. This is monumental. I also have pulmonary fibrosis. Last exam was a year ago. I have an appointment next week with a new pulmonologist. ( You know after 12 years in the same spot, we moved twice this year)---Thus the new doc. Last time, it was good news. The fibrosis did not advance and even showed signs of regression. Don't know what will happen this time. Am keeping my fingers crossed. I have been under a lot of stress with the moves and moving my 94 year old mom with Alzheimer's. She forgets she has just eaten and starts giving me hell about an hour after meals saying she is hungry. Then I put food in front of her, she picks a little, leaves the rest and two hours later she is yelling that she hasn't eaten all day. My husband and I are taking turns feeding her every two hours, tidbits of food. She wants complete meals from soup to dessert. And then she picks a bit on everything and won't eat lefovers. It's like having a newborn crying for food every two hours. Well, thank God she sleeps through the night. I hope I will never need photophoresis, but I thank you from the bottom of my heart for paving the way should I ever have to have it. I don't know where you got the strength to fight them. But you go girl! Take them for all you can and then make a movie out of it. We are keeping an eye on you! Hooray, for you, Love to you from all of us, Dolores & Mike From: DEBBIE GIBSON <Debbullwinkle@ fuse.net> Subject: rheumatic Update hospital denying tx/Debbie " support group " <rheumatic@grou ps.com> Cc: " socjog " <socjogoptonline (DOT) net>, " Ellen McCool " <ellenmccool@ bellsouth. net> Date: Friday, January 30, 2009, 10:49 PM HI all, just got a letter today regarding the battle we have been having with the hospital billing incorrectly and forcing me...defrauding me...by telling me they could not bill Medicare without that form being signed, hospital sent me a letter, telling me that my photopheresis tx for next Mon and Tue, I will need to schedule at another facility. The story will be in this weeks local paper and the tv news reporter that filmed my meeting with the hospital billing dept over a year ago...where they kept insisting I sign that form..or they could not bill Medicare.... .he is running the story on the Monday evening news...I have also let Mr. Ross of 20/20 know that I received the letter....In addition I have been in contact with ARRP the Magazine.... about doing a story, so this will not happen to others.... It is all good, I will find another facility that can hopefully give me this life saving treatment and further, I don't have to go to Indiana on Mon and Tues now....After 3 yrs I am tired...but I know what happens when I don't get it...the SD brings on the lung disease and then I start suffocating. ...ugh...hate that...so I will get to work next week finding another facility to treat me...nice huh...AND this hospital is a non-profit.. .but the DRs have the right to not treat a patient AND the letter expressly stated that the hospital spoke with my Drs and they agreed I should go elsewhere... Hope everyone is doing well....Have a great weekend...stay warm if you live in the Midwest!! Debbie Quote Link to comment Share on other sites More sharing options...
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