maria, I take cranberry capsules everyday to help kidneys. Seems to help. I 
drink what I call cranwater throughout the day, to flush my body of extra 
toxins..1 ounce of straight unsweetened cranberry juice mixed with 7 ounces or 
more of water. I do this several times a day. It is tart, but diluted, it's not 
bad. Some people add a little stevia to unsweeted cranberry juice and that can 
help as well. Good luch with this. I use knudson's brand. Sp? unsure of 
spelling. I think that is it...


take good care, 18's Beth


-----Original Message-----
From: 'Susan Zimmerman' via CMLHope <[email protected]>
To: cmlhope <[email protected]>
Sent: Mon, Feb 23, 2015 11:00 pm
Subject: Re: [CMLHope] Re: Kidney Transplant


Maria,


I would buy cranberry capsules if I was you, as they work better in my book. I 
am diabetic also and can't stand the taste of non-sugared cranberry juice, 
(Lakewood brand).  That's the only one without added sugar.

18's,
Susan





-----Original Message-----
From: Marty Gartenberg <[email protected]>
To: cmlhope <[email protected]>
Sent: Fri, Feb 20, 2015 7:30 pm
Subject: Re: [CMLHope] Re: Kidney Transplant


Hi Maria, 


 Light and diet cranberry juice does have the same effect on your kidneys. Just 
be sure that it is pure cranberry juice and not mixed with other fruit juices 
like grape juice.



18's,


Marty



On Fri, Feb 20, 2015 at 7:01 PM, Maria Cashion <[email protected]> wrote:

Dear Jennie, no matter what, I always count my blessings!!!! I have the 
medication and will start it tomorrow morning  after breakfast.


BMA went OK, Results will be available in two weeks...


Marty, I am diabetic.  I drink light and diet cranbery juice.  I don't know if 
it has the same effect...


Must rest.  Take care you all!!!!! 


Maria



On Fri, Feb 20, 2015 at 8:31 AM, 'Icandoallttc' via CMLHope 
<[email protected]> wrote:


What good news Maria!!!
It sounds like you had an awful insurance experience!!
My team at Moffitt took care if getting my ponatinib and I think that is why it 
was approved so quickly.   I was really worried as I had no idea they would 
approve it that quick. It was a good thing too as my platelets were in the 
millions and my WBC dangerously high. 
After only 22 days on ponatinib the blood counts are back to normal.  I think 
the reason they start on a high dose is to get you back in remission as soon as 
possible. Then they can lower the dose if needed, at least that is always 
happened in my case.  
I have high blood pressure and heart problems and they went ahead and put me on 
ponatinib even though they know the risk. And you are right.  They don't 
listen.  
Are you blood counts out if whack?   They can test you for the mutant for 
sprycel.  I had it.  
So happy you got your meds. That is always a hurdle to jump. 


Prayers & Blessings Jeanie . 18,s

On Feb 19, 2015, at 4:19 PM, Maria Cashion <[email protected]> wrote:



Jeannie, they never put you to sleep here. They use a little anethesia for the 
skin and muscles where they will introduce the needle, but that' all.  So far I 
have had 8 done since I was diagnosed and all I get is local anesthesia.  Out 
of 8, seven have been OK, but my last one was done on Feb 14, 2014 and it was a 
bad one.  The Dr. was not all there either, she had a bad cold. You can't 
imagene how happy I was last November when they told me I could have a PCR/FISH 
instead.


This is happening because in my last CBC done at the Hospital my white blood 
count was a little elevated. ( no, for them infections don't count...patient 
needs another hole in the hip<4F4.gif>) Immediately she has assumed that I have 
lost remission because I have been off Sprycel since November...It all goes 
back to my infamous "Blast Crisis".  God knows that I have outgrown it, but my 
doctors haven't... They care so much that at times they can hurt you!


I also went to the nephrologist today.  I fear the dose of Bosulif that the DR. 
wants me to start:  500mg.  My kidneys are small, apparently my GFR is 59% 
according to my nephrologist and that is near normal.  It's the near that 
bothers me!!!  According to him, there are no indications as to adminstering a 
lower dose of this medication.


If you guys check Phizer's page for Bosulif, it suggests a lower dose of 
300-400 mcg for patients with renal disfuntion or with the possibility of renal 
disfunction or impairment.  Bosulif is toxic to the kidneys...<320.gif>


My sonogram showed both kidneys were small in size and recommended additional 
exams like an abdominal sonogram, etc.  I will have to ask my GP to do that for 
me.  What really bothers me is that they don't listen to you.  It's that 
feeling that you get of being catalogued as "stupid patient" when you leave 
your doctor's office...<4F4.gif><4F4.gif><4F4.gif>


Also, i found out today that insurance approved my Bosulif...that is some good 
news, the problem that I have with it is the dose, but we will see what 
happens.  I will get the first prescription tomorrow.  This time it only took 2 
weeks to get it.  I believe that I got results because I took matters into my 
own hands, called the pharmacy, med rejected initially.  Called the insurance, 
called back the pharmacy, they resubmitted.  Told the pharmacy what to do.  
Called over and over the insurance company, letting them know, of cvourse that 
my life was at stake...Also mentioned that since the Insurance carrier for my 
zone was changing in April, that they might be stretching approval of the 
medication...<1B2.gif>Called today when I got home and the med was approved, 
called the pharmacy and med will be dispensed tomorrow.  I will pick it up 
after the porcedure mannana..


I know this is a long one.  I have been away for a while, trying to get some 
personal matters finished.  You never know what can happen and I dont really 
want to leave my family with any loose ends.


I think of you guya everyday, WE ARE TRUE WARRIORS, struggling againt a 
threacharous disease, unkind doctors and very stron medication side effects.  
Truly LOVE YOU!!!!!


Maria





On Thu, Feb 19, 2015 at 11:42 AM, 'Icandoallttc' via CMLHope 
<[email protected]> wrote:


Hi Maria--I had BMA a few weeks ago.  It just confirmed my leukemia. I'll send 
a highlight of mine soon.  Are they going to put you to sleep?
Good luck -- you will be ok.  Praying for you 

Prayers & Blessings Jeanie 
<emoji_u1f420.png><emoji_u1f420.png><emoji_u1f420.png><emoji_u1f420.png><emoji_u1f420.png><emoji_u1f420.png><emoji_u1f420.png><emoji_u1f420.png><emoji_u1f420.png><emoji_u1f420.png><emoji_u1f420.png><emoji_u1f420.png>.
 18,s



On Feb 19, 2015, at 6:37 AM, Marty Gartenberg <[email protected]> wrote:



Hi Maria,


I'm sorry to hear about your kidney problems. If I can give you some advice? If 
you are not diabetic try drinking cranberry juice. It washes out your kidneys 
and keeps you hydrated.


Good luck with your BMA, I am praying that everything comes out well.


18's,


Marty



On Thu, Feb 19, 2015 at 1:43 AM,  <[email protected]> wrote:

Hello to all!!! I have been going to the posts, but not feeling well enough to 
comment on any until today.  I am so very happy with the news about your 
advancement on the list for kidney transplant Marty!!!! God bless you and I do 
hope that it happens soon!!!


I am having serious kidney problems myself.  Have an appointment with the 
nephrologist later this morning...My kidneys are small.  Had a sonogram done 
Saturfay and results do not look favourable...


Wainting for aproval of Bosulif and wondering if I might still be able to use 
it.  MY doctor fears that my CML is back.  However, my PCR/Fish results from 
last November were completely negative... I am also having a bone marrow 
aspiration done tomorrow.  We will see what develops.  I still have a couple of 
hours to try and get some sleep..


Please take care and above all be HAPPY!!!!!!! :)


On Tuesday, February 10, 2015 at 5:57:49 PM UTC-4, wa2yyx wrote:
First I would like to thank each and every one of you for your prayers. As I 
pray for all of you I know that you have been also praying for me.


This web site makes all of us as one caring family and it is always of help for 
all of us.



I was just called by my transplant coordinator to inform me that I am now in 
status 5. As soon as a B+ matching comes along and if is a good cross match I 
will be called. It could be anytime or maybe a month or longer. There is no way 
of knowing. At least now I know that it is almost there. Hopefully very soon. I 
have been looking for this for almost four years.


All of my doctors have been writing letters to the Cleveland Clinic and 
yesterday my kidney doctor also wrote one asking for me to be elevated on the 
list.


Again, I am really blessed by having all of you as my friends. I will keep you 
informed of any further news.


18's


Marty







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