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Why ?  I was just switched to generic cellcept, with doc's ok.  Please advise what you have heard.Thanks,IPF/NSIP 08

From: Beth <mbmurtha (AT) yahoo (DOT) com>Subject: Re: Cleveland Clinic - Lung Transplant - Med RetirementTo: Breathe-Support@ yahoogroups. comDate: Thursday, June 4, 2009, 2:10 PM

Ellen,

Welcome! Please don't ever hesitate to post for fear of 'showing your ignorance'.  This isn't instinct, we've all had to learn all this stuff. There is a huge learning curve once one is diagnosed with any illness. I certainly wasn't born knowing about pulmonary fibrosis and I doubt anyone else was either. LOL

 

Your story sounds painfully familiar but it does sound like you are getting excellent care.  I'm not familiar with the med retirement process from the DOD or anywhere for that matter. Maybe we've got another lurker who could share their experience with you.

Medicare absolutely pays transplant costs. As long as the facility accepts assignment you should not have problems.  I've been on SSDI now for 2 and a half years and Medicare since last November. Again there is a learning curve for all the rules (I don't think I'll ever master them. Mainly cause the constantly change)

 

Please continue to post and ask questions. I'm hoping someone may be able to supply you with more information.  I'm glad you have joined us! 

Beth

Moderator

Fibrotic NSIP 06/06 Dermatomyositis 11/08

From: polenellen <polenellen (AT) aol (DOT) com>To: Breathe-Support@ yahoogroups. comSent: Thursday, June 4, 2009 11:07:04 AMSubject: Cleveland Clinic - Lung Transplant - Med Retirement

Good Morning to All,

 

Long subject line!

 

You really don't know me but I know most of you through your e-mails.  Like many people I have been lurking for quite awhile reading for info and just not wanting to show my ignorance.  Let me begin with the same story that I have read over and over again:

Ellen – in Sept 2008 seemed to just run out of breath walking to my car after work one day.  Ended up in the ER and after nine days in the hospital and every test that seemed possible/a Bronch and was dx with Sarcoidosis.  I was treated with Pred of course/oxy 24/7.  Seemed to get a little better at first but as soon as they took me down on Pred I went down hill fast and never returned…Ended up with a wonderful pulm from OSU.  Ended up in the OSU ER and Hosp for another two weeks.  After all the testing/biopsies etc it was determined that I have PF and NOT Sarc…They have no idea, after many, many blood tests, what is causing the inflammation and in fact as of three weeks ago I am getting worse.  I am now going to Cleveland Clinic for testing and

interviews for a lung transplant.  They have been in contact with me and gave me some hope, and told me to call my insurance concerning the cost of, lodging, transportation (I live more than one hr away from Cleveland), and post prescriptions.  I did, the answers I received was – no – no – yes.  That all being said or possibly repeated, I apologize if I repeated anything, I have some questions, especially after reading the e-mails concerning the Lung Center in PA.

 

Ø  Is anyone familiar with the Cleveland Clinic?  (I have been to the site and just see general info)

Ø  Does anyone have any idea what a charter flight would cost?  I can only imagine Ø  I see in PA they have places for people to stay before/after transplant – I am assuming Cleveland has that also.

Ø  Is there anyone who has had to put in for medical retirement from the DoD? I am in the process of this as of three weeks ago. Very painful Ø  I am 60 therefore have to go the med retirement and then SS.  Does medicare help w/transplants?

  Of course I may not even make the list.  I hope so. Any suggestions, advice, help, ideas would be greatly appreciated. Ok now I am actually going to send this.....   Best Regards ellen

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patricia

are you pre or post transplant

my pulmonary said that pre transplant generic is ok for me

check with your pulmonary

Pink Joyce (IPF 3/06) IFA 5/09 Pennsylvania

Donate Life Listed 1/09 Inactive 4/09

www.transplantfund.org---

Subject: Re: generic cellceptTo: Breathe-Support Date: Tuesday, June 9, 2009, 5:20 PM

Why ? I was just switched to generic cellcept, with doc's ok. Please advise what you have heard.

Thanks,

IPF/NSIP 08

From: Beth <mbmurtha (AT) yahoo (DOT) com>Subject: Re: Cleveland Clinic - Lung Transplant - Med RetirementTo: Breathe-Support@ yahoogroups. comDate: Thursday, June 4, 2009, 2:10 PM

Ellen,

Welcome! Please don't ever hesitate to post for fear of 'showing your ignorance'. This isn't instinct, we've all had to learn all this stuff. There is a huge learning curve once one is diagnosed with any illness. I certainly wasn't born knowing about pulmonary fibrosis and I doubt anyone else was either. LOL

Your story sounds painfully familiar but it does sound like you are getting excellent care. I'm not familiar with the med retirement process from the DOD or anywhere for that matter. Maybe we've got another lurker who could share their experience with you.

Medicare absolutely pays transplant costs. As long as the facility accepts assignment you should not have problems. I've been on SSDI now for 2 and a half years and Medicare since last November. Again there is a learning curve for all the rules (I don't think I'll ever master them. Mainly cause the constantly change)

Please continue to post and ask questions. I'm hoping someone may be able to supply you with more information. I'm glad you have joined us!

Beth

Moderator

Fibrotic NSIP 06/06 Dermatomyositis 11/08

From: polenellen <polenellen (AT) aol (DOT) com>To: Breathe-Support@ yahoogroups. comSent: Thursday, June 4, 2009 11:07:04 AMSubject: Cleveland Clinic - Lung Transplant - Med Retirement

Good Morning to All,

Long subject line!

You really don't know me but I know most of you through your e-mails. Like many people I have been lurking for quite awhile reading for info and just not wanting to show my ignorance. Let me begin with the same story that I have read over and over again:

Ellen – in Sept 2008 seemed to just run out of breath walking to my car after work one day. Ended up in the ER and after nine days in the hospital and every test that seemed possible/a Bronch and was dx with Sarcoidosis. I was treated with Pred of course/oxy 24/7. Seemed to get a little better at first but as soon as they took me down on Pred I went down hill fast and never returned…Ended up with a wonderful pulm from OSU. Ended up in the OSU ER and Hosp for another two weeks. After all the testing/biopsies etc it was determined that I have PF and NOT Sarc…They have no idea, after many, many blood tests, what is causing the inflammation and in fact as of three weeks ago I am getting worse. I am now going to Cleveland Clinic for testing and

interviews for a lung transplant. They have been in contact with me and gave me some hope, and told me to call my insurance concerning the cost of, lodging, transportation (I live more than one hr away from Cleveland), and post prescriptions. I did, the answers I received was – no – no – yes. That all being said or possibly repeated, I apologize if I repeated anything, I have some questions, especially after reading the e-mails concerning the Lung Center in PA.

Ø Is anyone familiar with the Cleveland Clinic? (I have been to the site and just see general info)

Ø Does anyone have any idea what a charter flight would cost? I can only imagine

Ø I see in PA they have places for people to stay before/after transplant – I am assuming Cleveland has that also.

Ø Is there anyone who has had to put in for medical retirement from the DoD? I am in the process of this as of three weeks ago. Very painful Ø I am 60 therefore have to go the med retirement and then SS. Does medicare help w/transplants?

Of course I may not even make the list. I hope so. Any suggestions, advice, help, ideas would be greatly appreciated. Ok now I am actually going to send this..... Best Regards ellen

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Guest guest

Is this per the docs at the transplant center? If not, then don't

listen. Only they are the ones to make such a determination.

>

>

> From: Beth mbmurtha (AT) yahoo (DOT) com>

> Subject: Re: Cleveland Clinic - Lung Transplant -

Med Retirement

> To: Breathe-Support@ yahoogroups. com

> Date: Thursday, June 4, 2009, 2:10 PM

>

>

>

>

>

>

>

> Ellen,

> Welcome! Please don't ever hesitate to post for fear of 'showing

your ignorance'. This isn't instinct, we've all had to learnÂ

all this stuff. There is a huge learning curve once one is

diagnosed with any illness. I certainly wasn't born knowing about

pulmonary fibrosis and I doubt anyone else was either. LOL

> Â

> Your story sounds painfully familiar but it does sound like you are

getting excellent care. I'm not familiar with the med retirement

process from the DOD or anywhere for that matter. Maybe we've got

another lurker who could share their experience with you.

> Medicare absolutely pays transplant costs. As long as the facility

accepts assignment you should not have problems. I've been on SSDI

now for 2 and a half years and Medicare since last November.

Again there is a learning curve for all the rules (I don't think I'll

ever master them. Mainly cause the constantly change)

> Â

> Please continue to post and ask questions. I'm hoping someone may be

able to supply you with more information. I'm glad you have joined

us!

> Â

> Beth

> Moderator

> Fibrotic NSIP 06/06 Dermatomyositis 11/08

>

>

>

>

>

>

> From: polenellen polenellen (AT) aol (DOT) com>

> To: Breathe-Support@ yahoogroups. com

> Sent: Thursday, June 4, 2009 11:07:04 AM

> Subject: Cleveland Clinic - Lung Transplant - Med

Retirement

>

>

>

>

> Good Morning to All,

> Â

> Long subject line!

> Â

> You really don't know me but I know most of you through your

e-mails. Like many people I have been lurking for quite awhile

reading for info and just not wanting to show my ignorance. Let me

begin with the same story that I have read over and over again:

> Ellen †" in Sept 2008 seemed to just run out of breath walking

to my car after work one day. Ended up in the ER and after nine

days in the hospital and every test that seemed possible/a Bronch and

was dx with Sarcoidosis. I was treated with Pred of course/oxy

24/7. Seemed to get a little better at first but as soon as they

took me down on Pred I went down hill fast and never

returned…Ended up with a wonderful pulm from OSU. Ended up in

the OSU ER and Hosp for another two weeks. After all the

testing/biopsies etc it was determined that I have PF and NOT

Sarc…They have no idea, after many, many blood tests, what is

causing the inflammation and in fact as of three weeks ago I am getting

worse. Â I am now going to Cleveland Clinic for testing and

> interviews for a lung transplant. They have been in contact with

me and gave me some hope, and told me to call my insurance concerning

the cost of, lodging, transportation (I live more than one hr away from

Cleveland), and post prescriptions. I did, the answers I received

was †" no †" no †" yes. That all being said or

possibly repeated, I apologize if I repeated anything, I have some

questions, especially after reading the e-mails concerning the Lung

Center in PA.

> Â

> Ø Is anyone familiar with the Cleveland Clinic? (I have

been to the site and just see general info)

> Ø Does anyone have any idea what a charter flight would

cost? I can only imagine

> Ø I see in PA they have places for people to stay before/after

transplant †" I am assuming Cleveland has that also.

> Ø Is there anyone who has had to put in for medical retirement

from the DoD? I am in the process of this as of three weeks ago. Very

painful

> Ø I am 60 therefore have to go the med retirement and then

SS. Does medicare help w/transplants?

> Â

> Of course I may not even make the list. I hope so.

> Any suggestions, advice, help, ideas would be greatly appreciated. Ok

now I am actually going to send this.....

> Â

> Best Regards

> ellen

>

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