Well, in addition to all of this. My oncologist saw a significant amt of  
protein in my urine test from nephrologist. She ordered a 24 hr urine test 
which  showed microclonal protein. Which warranted a bone marrow biopsy on 
Friday.  They are now looking at possible multiple myeloma. 
In the meantime saw my nephrologist whom said ultrasound showed left kidney 
 at 7.5 cm to which she says it is no longer working at all. I'm living off 
of  21% of my right kidney. She wants a transplant consult but needs to 
wait for  biopsy results as if I show positive for multiple myeloma then I 
can't do  transplant. I discussed disabiltiy continuation with her and she says 
people on  dialysis are not disabled. So she can not state that. Only submit 
current  medical records and state we are managing chronic kidney disease. 
I'm not  looking for a new disability just for the ckd. I am only looking to 
continue  with all my combined issues and limitations. Ugh!!  This seems so 
stressful  and so unfair. How in the heck am I to prove myself to a 
possible employer when  I have appts weekly and tests. Not to mention fatigue 
and 
sleep issues. I just  don't get this whole system. 
 
Thanks for allowing me to vent and please pray for good results from my bmb 
 which I should get this Wednesday!!
 
Terri
 
 
 
In a message dated 7/31/2013 3:34:24 P.M. Eastern Daylight Time,  
[email protected] writes:

Hi I am told that remission only means temporary and it can come back  
anytime. A good doctor knows this.  Your case is  unbelievable. 
Fight back as hard as you can. Sorry you are under so much  stress. 
Many prayers and blessing to you. 
Jeanie

Sent from my iPhone

On Jul 31, 2013, at 1:07 PM, peg <[email protected]_ 
(mailto:[email protected]) > wrote:



Hi Terri,  I have been on and off of social security disability  for many 
years now, but have never lost my Medicare.  Firstly....if you  have a lawyer 
who isn't certain you can win this..FIND A NEW LAWYER!   This a more than a 
win-able case.  Also, be absolutely certain a  re-determination was 
filed...it will almost always be denied at the first  and 2nd levels.  The rare 
exception to that is if you meet personally  with a social security rep in your 
local office who decides to become your  champion...the key to this is LOOK 
DISABLED! And also paint a daily worse  case senerio picture of your life, 
otherwise they don't get it...they  think what they see is what your life is 
like.  (sorry about the  italics...something glitched!)

Please see this Medicare Publication  which explains how persons needing 
dialysis and/or transplant are eligible  for Medicare: 
www.medicare.gov/pubs/pdf/10128.pdf.   However, it appears it only covers the 
dialysis/transplant 
related  treatments and does not kick in until the fourth month of dialysis.  
So  it is not a perfect solution for you.

The better direction for full  Medicare is to show that you are disabled by 
this condition and  reopen your original disability  claim.  But, be 
careful how your doctor files this...if it is filed  as a NEW and separate 
disability you will have a six month wait for  disability and another TWO YEAR 
wait 
for Medicare.  However, if you can  show that the disability is "the same 
or related to" your original  disability, as in kidney failure due to BMT 
related chemo for CML, your  original claim simply reopens and your disability 
and Medicare is effective  immediately.  This is crucial to getting Medicare 
quickly!  You  are still well within the window of time to reopen your 
disability without  having to start it as a new claim!  See this article...it 
explains all  of this: 
http://www.disabilitysecrets.com/resources/disability/reopening-a-social-sec
urity-disability-claim.h  

Another, but less desirable, option that will buy you a bit of time  if you 
are well enough, is to go back to work...even a little work...people  on 
disability related Medicare, who remain disabled but go back to work, can  
keep free PART A Medicare for 93 months...after that you have the option of  
paying for it ($243 a month) indefinately.  Those who are eligible for  Part A 
may also pay for PART B (the part everyone pays for) and are eligible  for 
PART D.  Once you stop working you are allowed to keep paying for  your 
Medicare, and if you refile for disability and everything in the  previous 
paragraph still applies.  But again...not a perfect  solution...much better to 
file to re-open due to "complications" as  described in the paragraph above.  

The fight here is to prove  that you remain disabled, working or not, in 
order to retain benefits.   My feeling is that you want a lawyer and doctor 
who will fight for  that...rather than the idea that you were unfairly target 
and cancelled due  to cost of medication/treatment.  The latter is a much 
longer and  riskier battle.  Talk to several lawyers...they almost all do free 
 consultation.  Tell them you don't want to die fighting this battle and  
pick the one that you feel will best champion your cause. 

On a more  personal note, there is life while on dialysis.  My mother lived 
a full  active life on dialysis for seven years before succumbing to 
complications  from another illness. Her personal choice was to take the very 
early morning  treatments, so she could nap for a couple of hours after and 
still have her  whole day available.  She even took a cruise that offered 
onboard  treatments.  

Be strong...fight on!
peg       

On Tuesday, July 30, 2013 6:24:59 AM UTC-7, terri wrote:  
 
Hello,
 
I was diagnosed in May of 2000. Started on interferon and arac. Moved  on 
to experimental drugs, Gleevec, Sprycel, Tasigna. in and out of  remission 
until 2011. Everything quit working and I had to go with  transplant at Johns 
Hopkins. They were terrific. I was put on disability.  So now I am two years 
out and just became eligible for Medicare on June 1.  I called to get drug 
coverage and they calculated the cost. Two days later  I received a 
cessation of benefits, stating cml is in remission. I should  be able to get a 
sedentary stress free job. 
 
In the meantime starting Feb, I developed headaches and high blood       
pressure. Creatinine went up. I was referred to a nephrologist with a gfr  of 
40%. I had a kidney biopsy showing glomulersclerosis. 65% of my kidneys  are 
dead and dried up, this damage as I understand is irreversible. Since  then 
I have dropped twice to 11%&  gfr and currently am at 21% which  puts me at 
stage 4 chronic kidney disease. Severe function loss. 
 
Has anyone else dealt with this? I'm looking at poss transplant which  they 
don't even know if I qualify as I am only 2 yrs remission from cml. I  
still take 800 mg tasigna daily to prevent it from coming back. So my  other 
option is to prepare for dialysis. I am only 45 yrs old.
 
Had to hire a lawyer to help with ssd, no guarantees he says. Just a  lot 
to deal with all of a sudden. Would love to speak with someone who has  gone 
through this or knows of anyone.
 
Thanks,
Theresa Migut
Johnstown, Pa


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