Jump to content


Photo

Who are you?


  • Please log in to reply
168 replies to this topic

#1 JPD

JPD

    Advanced Member

  • Members
  • PipPipPip
  • 258 posts

Posted 15 October 2014 - 10:34 PM

If we are gonna be hanging out here for a while... and I hope we all are... I'd like to get to know one another.  So, I guess Ill start.  Maybe just the basic info and a couple of trivial things...

 

 

I live in Bloomington, Indiana.  I own a liquor store (and a useless BA in History).  Have three kids (age 18, 15, 11).... am 45 years old.  Seperated (it is what it is)  I saw the Grateful Dead 35 times in concert.  My favorite TV show of all-time is Breaking Bad.  I'm heavily involved in youth hockey in a basketball-centric area. The only food I refuse to eat is liver. 

 

Dont really care if if this thread fades away... but seeing as though I check this page everyday, Id like to get to know who I'm talking to... ;)


January 15: .53%

April 15:       .78%

July 15:      1.1% - upped dosage to 400mg after this test

Oct 15:       .85%

December 15:  .28%

March 16: .29%

July 16: .34%

October 16: .11%

January 17: .081%

April 17: .055%

July 17: .135%

Oct 17: .008%


#2 pammartin

pammartin

    Advanced Member

  • Members
  • PipPipPip
  • 631 posts
  • LocationPennsylvania

Posted 16 October 2014 - 05:34 AM

Hi,

 

I live in Western PA, have a useless BA in psychology, one son, in a few days 52 years old, married, and have been to over 20 Jimmy Buffett concerts all over the U.S.  I would have to count ticket stubs for correct #.  I love the Atlantic and Gulf but not the Pacific, professional hockey - especially when Rick Tocchet played for the Pitt Pens was my all time favorite sport, then strikes and greed removed my interest and I will not eat liver, fungi, or sushi. 

Pam



#3 Floa7

Floa7

    Advanced Member

  • Members
  • PipPipPip
  • 53 posts
  • Locationindiana

Posted 16 October 2014 - 06:01 AM

I live in Columbus, Indiana. I have been widowed 5 years. I just had my 64th birthday. My son has CML, diagnosed Nov 2011, I was diagnosed in Jan 2012. He is also diabetic and is legally blind, for the past year. I am on Gleevec and he is on Sprycel, now.  I eat everything also except liver, tripe and turnips. I also read this page everyday, but don't post much.


1 2012 CML detected Started Gleevec 400 mg

In nov 2014 my pcr started to rise by Feb I stopped Gleevec and went onto

2 2015 Tasigna 600 mg/day

I have been PCRU for 2 years and stopped Tasigna 4 7 2017

5 8 2017 results 0.008

5 30 2017 results 0.028 

6 30 2017 results 0.3, I have restarted the Tasigna because it went above 0.1 

 

My son

11 2011 CML detected Started Gleevec 400 mg

He went 2 1/2 years on gleevec and lost PCRU

Started Sprycel went PCRU for 2 years and stopped the Sprycel, went back for 3 month checkup and PCR was 8.0

He went back onto Sprycel and now is PCRU again

3 16 2017 results 0.008

6 1 2017 results 0.002


#4 tinman1939

tinman1939

    Advanced Member

  • Members
  • PipPipPip
  • 53 posts
  • LocationRockwall, TX

Posted 16 October 2014 - 09:49 AM

Hi -

I live in the Dallas area after relocating here from metro Detroit in 2007. Said relocation is related to my company's hq move here; I came along for the ride.  I have a lovely wife and two grown children. I graduated from Michigan State University with a degree in International Relations (attained after six years in the Navy); the university has pretty darn good football and basketball programs.

 

I was diagnosed with CML just after Thanksgiving Day in 2006. I thought I had a hernia and went to get it checked out at the hospital; the joke was on me after the real diagnosis.

Bands that mattered to me through the years included the Moody Blues (my late 60s prog rock fixation), Crosby Stills, Nash & Young (the early 70s), and Neil Young, and Bruce Springsteen since. Last outdoor concert I went to was this past spring to see the Boss here in Dallas (great show) on the evening prior to starting Iclusig. With all the bad press about that TKI, I figured if I was going to go see my maker, I'd like to do it after having a great time at a Springsteen concert (by the way, the entire, nearly three hour concert is available on YouTube; check it out). I visited Austin a couple of weeks ago and saw Ian Anderson, who can still rock it after those Jethro Tull days in the early 70s.

Although a bit weaker from TKIs, I still put in 10-11 hours of work/day.  On most weekends I like to hit a little golf ball around, thinking it is exercise (it's not; it's an exercise in futility).

Take care.

Wayne
aka TinMan1939

 



#5 mlk210

mlk210

    Advanced Member

  • Members
  • PipPipPip
  • 158 posts
  • LocationIllinois

Posted 16 October 2014 - 11:57 AM

Hi Everyone! I'm Michelle. I'm 38, married and have twin (boy/girl) five-year-olds (almost six). I got diagnosed by a routine blood test in July of this year. I'm on Sprycel 100mg.

 

I have a useless BA in Children/Family Studies. Left my job as an Accounting Manger last December to pursue my love for writing. I've self-published eight fiction novels and it's nice to lose myself in my characters. Although, it's been harder for my mind to get off my own issues lately.

 

Can I just say JPD, I laugh every time I see your pic. My husband and I LOVE An Idiot Abroad and Karl! So, every time I see a comment by you, it brings smile to my face!

 

I'm on here at least once a day as well, but don't have much to add since I'm so new!


7/2014 Diagnosed,8/14 Started 100mg Sprycel, 9/14 Thyroidectomy (thyroid cancer)

8/2015 Undetectable, 12/15 Plural Effusion (3 wk drug break)

1/2016 Started 70mg Sprycel, 3/16 Plural Effusion (4 wk drug break)

3/16 .014 after a wk w/o meds

4/16 Started 400mg Gleevec

4/16 Undetectable, 7/16 Undetectable, 10/16 Undetectable, 2/17 Undetectable, 5/17 Undetectable, 8/17 Undetectable

 
 

#6 Jerry.s

Jerry.s

    Advanced Member

  • Members
  • PipPipPip
  • 128 posts

Posted 16 October 2014 - 01:51 PM

Hello everyone


I am really new to this site maybe two to three weeks . I love all food including liver and onions not my favorite but if made right, I'll eat it . I was diagnosed on the the 19th and confirmed on the 23rd of September via bone m test ! I have been practicing martial arts for over 4 years and unusual bruising is the reason my blood was checked in the first place. I guess you could say jujitsu may have saved my life of course with gods help . My favorite show is also breaking bad with Sapranos a close second.

I live in Albuquerque NM with my wife and two kids a 14 year old girl and a 18 month old boy. I'll post a pic soon

#7 Bobi AZ

Bobi AZ

    New Member

  • Members
  • Pip
  • 1 posts
  • LocationArizona

Posted 16 October 2014 - 04:31 PM

Hello everyone!  I just joined this today.  I was diagnosed with CML on July 3rd of this year, and like most of you was totally shocked!  Mine was diagnosed due to routine bloodwork by my Primary Doctor.  One and a half years ago I went through treatment for Hep C and was cured - yep cured!  It was not possible until now.  Then, 1 year later here I get diagnosed with CML. :huh:  I thought I was handling it pretty well, until recently...I have been in my own head a lot.  I have an amazing support group of people - family (especially my hubby and children), friends, and employer.  I'm looking forward to more support from people that are in the same shoes that I am.

 

I am a huge NFL New England Patriots fan.  Yep, I live in Arizona but New England is my team for 15 years now!  I also enjoy camping and 4-wheeling in our 4-seater Artic Cat - with friends and family.  In Arizona, we can only go in the winter, so it's right about time for us to get started!!  I also am a NASCAR fan, Brad Keselowski is my driver and hope to see him in the final chase.

 

I'm excited to join and get to know everyone!

 

SMILES and SUNSHINE



#8 JPD

JPD

    Advanced Member

  • Members
  • PipPipPip
  • 258 posts

Posted 16 October 2014 - 09:05 PM

106 views and 6 replies... come on people dont be shy. :ph34r:


January 15: .53%

April 15:       .78%

July 15:      1.1% - upped dosage to 400mg after this test

Oct 15:       .85%

December 15:  .28%

March 16: .29%

July 16: .34%

October 16: .11%

January 17: .081%

April 17: .055%

July 17: .135%

Oct 17: .008%


#9 Damerault

Damerault

    Advanced Member

  • Members
  • PipPipPip
  • 51 posts

Posted 16 October 2014 - 09:14 PM

Hello, my name is Diane. I am a 47 year old mother of two teenagers (15 and 18) and also was diagnosed with CML the day after Thanksgiving 2014. I live with my husband (a firefighter and my hero) and kids ( oldest now off to college) in a suburb outside of Boston. I work as a software developer for a healthcare information systems company but now a days find it hard to work a full work week. I love hockey though tonight the Bruins are losing to the Montreal Canadiens. But, the Pats are winning so that is good. Go Patriots! Love that I found this site and looking forward to getting back to normal someday. Be well.

11/29/2013 Diagnosis PLT 538 K/uL HGB 6.2 G/DL, HCT 18.5% WBC 557.00 K/uL Enlarged Spleen
Sprycel 100 MG
Hydroxyurea initially 4 capsules daily
By 4/2014 PLT 27, WBC and RBC Low. Off Sprycel for 3 weeks
After 3 weeks, blood counts normal, no mutation, back on Sprycel 50 MG
5/2014 PLT too Low off Sprycel 4 weeks
6/2014 started Tasigna
Side Effects- Nauseous, Headaches, Tired
8/2014 second opinion Mass General CML Specialist
Continuous transfusions of RBC, PLTs and NEualasta to temp increase blood cells to fight off infection.

Remain on full dose Tasigna

Major p210 International Scale

05/11/2015 0.0950
09/08/2015 0.0782
01/19/2016 0.0310
04/28/2016 0.0161
07/25/2016 0.0244
11/04/2016 0.0140
02/06/2017 0.0129
05/23/2017 0.0087
Today 0.0000



Be well, Diane.


#10 leejoshuajohn

leejoshuajohn

    New Member

  • Members
  • Pip
  • 9 posts

Posted 16 October 2014 - 09:23 PM

Hi Everyone! My name is Joshua and I am 30. I was diagnosed when I was 26 while I was living on Miami Beach. I had been feeling run down and had lost quite a bit of weight. When I came home for Christmas, my mother took one look at me and had me at the hospital. The nurse practitioner I saw tried to send me home with a script for prozac because she thought I was depressed. My mom convinced her to run routine blood work and behold! CML. I now live in Pittsburgh with my awesome fiancee. We are both classical musicians. I play the tuba and work at Trader Joe's and she is a cellist in the Pittsburgh Symphony. I have a bachelors in music/anthropology and a masters in music as well. I have a cute australian shepard named Fuzz and enjoy walking, eating "everything" bagles, drinking coffee, and watching tv shows! I've been around the board quite a bit since being diagnosed and am so thankful it is here!!!



#11 Antilogical

Antilogical

    Advanced Member

  • Members
  • PipPipPip
  • 284 posts
  • LocationPittsburgh, PA

Posted 16 October 2014 - 09:47 PM

I'm a systems analyst for a Pittsburgh PA steel manufacturer. Female, age 62, married, 1 son, 1 labrador retriever. I was diagnosed with CML several years ago when I was preparing for a knee replacement.

Three years ago, I was active, rode my mountain bike for exercise, worked crazy hours, volunteered with a wildlife rehab facility, and expected a quick recovery from knee surgery. Today - older (!) and wiser (?) - I am still rehabbing my new knee (I had a revision surgery due to scar tissue buildup this year), and have cut way back on work hours due to extreme fatigue. If it wasn't for the cost of Gleevec, I'd consider retiring to some little place overlooking a lake.

I, too, have a useless degree:  A BS in Secondary Education / Social Studies.  HATED IT!


Dx: Sudden severe anemia detected 07/2011, followed by WBC spike. CML Dx 02/2012.

Rx: 03/2012-Gleevec400.  Reduced 02/2013 to Gleevec300 due to side effects (low blood counts).

Response: PCR-Und within 7 mo. on G400. Maintained MMR4-MMR4.5 on G300. PCR-Und since 02/2016.


#12 CallMeLucky

CallMeLucky

    Advanced Member

  • Members
  • PipPipPip
  • 216 posts
  • LocationCT

Posted 16 October 2014 - 10:27 PM

Hi - 42 years old, living in northeast us. I'm 4+ years with cml and doing ok. I used to think about a lot now not as much, unless I see a number go up then I panic a bit. I struggle with anxiety but most days I get by fine. I'm married with two boys 8 and 10. They give me purpose and a reason to press on even when I don't feel like it. I have a semi useless BA but I put my MBA to pretty good use. I actually like my job for the most part so that's a plus. I was dx during routine blood work, I was trying to get in good shape and exercising a lot. I learned my lesson and don't do that anymore:). My first concert I saw was Kiss and the last concert I saw was Aerosmith. My biggest regret is that I didn't invest more in friendships I had over the years.
I'm kind of a computer geek and I like to watch tv.
:)
Date  -  Lab  -  Scale  -  Drug  -  Dosage MG  - PCR
2010/Jul -  MSKCC  -  Non-IS  -  Gleevec  - 400 - 1.2%
2010/Oct -  MSKCC  -  Non-IS  -  Gleevec  - 400 - 0.25%
2010/Dec -  MSKCC  -  Non-IS  -  Gleevec  - 400 - 0.367%
2011/Mar -  MSKCC  -  Non-IS  -  Gleevec  - 400 - 0.0081%
2011/Jun -  MSKCC  -  Non-IS  -  Gleevec  - 400 - 0%
2011/Sep -  MSKCC  -  Non-IS  -  Gleevec  - 400 - 0.00084%
2011/Dec -  MSKCC  -  Non-IS  -  Gleevec  - 400 - 0%
2012/Mar -  MSKCC  -  Non-IS  -  Gleevec  - 400 - 0.004%
2012/Jun -  MSKCC  -  Non-IS  -  Gleevec  - 400 - 0%
2012/Sep -  MSKCC  -  Non-IS  -  Gleevec  - 400 - 0%
2012/Dec -  MSKCC  -  Non-IS  -  Sprycel  - 100 - 0%
2013/Jan -  Quest  -  IS  -  Sprycel  -  50-60-70  - 0%
2013/Mar -  Quest  -  IS  -  Sprycel  -  60-70  - 0%
2013/Apr -  CUMC  -  Non-IS  -  Sprycel  - 50 - 0.036%
2013/May -  CUMC  -  Non-IS  -  Sprycel  - 50 - 0.046%
2013/Jun -  Genoptix  -  IS  -  Sprycel  - 50 - 0.0239%
2013/Jul -  Genoptix  -  IS  -  Sprycel  - 70 - 0.0192%
2013/Jul -  Genoptix  -  IS  -  Sprycel  - 70 - 0.0034%
2013/Oct -  Genoptix  -  IS  -  Sprycel  - 70 - 0.0054%
2014/Jan -  Genoptix  -  IS  -  Sprycel  - 70 - 0.0093%
2014/Mar -  Genoptix  -  IS  -  Sprycel  - 100 - 0.013%
2014/Apr -  Genoptix  -  IS  -  Sprycel  - 100 - 0.0048%
2014/Jul -  Genoptix  -  IS  -  Sprycel  - 100 - 0%
2014/Nov -  Genoptix  -  IS  -  Sprycel  - 100 - 0.047%
2014/Dec -  Genoptix  -  IS  -  Sprycel  - 100 - 0%
2015/Mar -  Genoptix  -  IS  -  Sprycel  - 100 - 0%
2015/Jun -  Genoptix  -  IS  -  Sprycel  - 100 - 0%
2015/Sep -  Genoptix  -  IS  -  Sprycel  - 100 - 0%
2015/Dec -  Genoptix  -  IS  -  Sprycel  - 100 - 0%
2016/Mar -  Genoptix  -  IS  -  Sprycel  - 100 - 0.0228%
2016/Jun -  Genoptix  -  IS  -  Sprycel  - 100 - 0%
2016/Sep -  Genoptix  -  IS  -  Sprycel  - 100 - 0%
2016/Dec -  Genoptix  -  IS  -  Sprycel  - 100 - 0%
2017/Mar -  Genoptix  -  IS  -  Sprycel  - 100 - 0%
2017/Jun -  Genoptix  -  IS  -  Sprycel  - 100 - 0%
2017/Sep -  Genoptix  -  IS  -  Sprycel  - 100 - 0%
2017/Dec - Genoptix  -  IS  -  Sprycel  -  100 - 0%
 

 


#13 rcase13

rcase13

    Advanced Member

  • Members
  • PipPipPip
  • 523 posts
  • LocationCharlotte, NC

Posted 17 October 2014 - 01:53 PM

Hello, my name is Rodney and I am 44 years old. I was diagnosed 3 weeks ago just 2 weeks before my birthday. Happy Birthday!

I love my family. Its just my wife and our 12 year old son. They have been very supportive. It has been tough on them. I could not do this without them.

We live here in NC in an old house in the country surrounded by huge 100+ year old oaks, hickories and maples. My hobbies are trying to make a 42 year old home new ago. The restoration has been but on hold until all the medical bills are paid and the Tasigna starts doing its magic. The house is old and a lot of work. Hopefully I get better and can continue our dream. It would be sad if we had to sell it.

10/01/2014 100% Diagnosis (WBC 278k, Blasts 6%, Spleen extended 20cm)

01/02/2015 0.06% Tasigna 600mg
04/08/2015 0.01% Tasigna 600mg
07/01/2015 0.01% Tasigna 600mg
10/05/2015 0.02% Tasigna 600mg
01/04/2016 0.01% Tasigna 600mg
04/04/2016 PCRU Tasigna 600mg
07/18/2016 PCRU Tasigna 600mg
10/12/2016 PCRU Tasigna 600mg
01/09/2017 PCRU Tasigna 600mg
04/12/2017 PCRU Tasigna 600mg
10/16/2017 PCRU Tasigna 600mg
01/15/2018 PCRU Tasigna 600mg

 

Cancer Sucks!


#14 JPD

JPD

    Advanced Member

  • Members
  • PipPipPip
  • 258 posts

Posted 17 October 2014 - 07:37 PM

Rodney,

The Tasigna will do its magic and you'll get to work on that house (cant promise anything about the bills).  I think it was about the three week mark when I finally started feeling good again (blood counts were a little pesky to get stablized, but I felt a whole lot better after my spleen shrunk and my RBC/Hemo got higher.

 

How are your side effects on Tasigna?


January 15: .53%

April 15:       .78%

July 15:      1.1% - upped dosage to 400mg after this test

Oct 15:       .85%

December 15:  .28%

March 16: .29%

July 16: .34%

October 16: .11%

January 17: .081%

April 17: .055%

July 17: .135%

Oct 17: .008%


#15 Marnie

Marnie

    Advanced Member

  • Members
  • PipPipPip
  • 396 posts

Posted 18 October 2014 - 12:18 PM

Sorry. . pretty busy with work lately.  Finally have some time to check in.

 

Diagnosed 2009.  On Gleevec for awhile, then switched to Sprycel due to sub-optimal response. 

 

I'm a teacher (nearing retirement. . .can hardly wait!!).  In my free time I enjoy reading, gardening, playing my many musical instruments (piano, flute, piccolo, harp, hammered dulcimer, guitar, ukulele).  In the rest of my free time I enjoy motorcycle touring and trail riding (easy stuff. . .I'm a bit of a wimp when it comes to difficult trails), whitewater kayaking, snowboarding, camping, etc. 

 

Don't watch much t.v. but have gotten hooked on a few Netflix shows which I am embarrassed to admit to (Breaking Bad. . .gah!!  a teacher turned meth dealer!!,  The Walking Dead, and Orange is the New Black).  My weaknesses are sparkling wine and Cheetos.  Not together. 

 

My husband and I have had a number of adventures where we've found ourselves in ridiculous situations and we look forward to my upcoming retirement so that we can find ourselves enmeshed in more of the same.

 

Marnie



#16 Marnie

Marnie

    Advanced Member

  • Members
  • PipPipPip
  • 396 posts

Posted 18 October 2014 - 12:20 PM

Hello, my name is Rodney and I am 44 years old. I was diagnosed 3 weeks ago just 2 weeks before my birthday. Happy Birthday!

I love my family. Its just my wife and our 12 year old son. They have been very supportive. It has been tough on them. I could not do this without them.

We live here in NC in an old house in the country surrounded by huge 100+ year old oaks, hickories and maples. My hobbies are trying to make a 42 year old home new ago. The restoration has been but on hold until all the medical bills are paid and the Tasigna starts doing its magic. The house is old and a lot of work. Hopefully I get better and can continue our dream. It would be sad if we had to sell it.

Rodney. . what part of NC do you hail from?  My in-laws used to live in New Bern.  We spent a fair amount of time there.  It's a beautiful area. 

 

Marnie



#17 rcase13

rcase13

    Advanced Member

  • Members
  • PipPipPip
  • 523 posts
  • LocationCharlotte, NC

Posted 19 October 2014 - 08:23 AM

Rodney. . what part of NC do you hail from?  My in-laws used to live in New Bern.  We spent a fair amount of time there.  It's a beautiful area. 
 
Marnie


I am from Huntersville

10/01/2014 100% Diagnosis (WBC 278k, Blasts 6%, Spleen extended 20cm)

01/02/2015 0.06% Tasigna 600mg
04/08/2015 0.01% Tasigna 600mg
07/01/2015 0.01% Tasigna 600mg
10/05/2015 0.02% Tasigna 600mg
01/04/2016 0.01% Tasigna 600mg
04/04/2016 PCRU Tasigna 600mg
07/18/2016 PCRU Tasigna 600mg
10/12/2016 PCRU Tasigna 600mg
01/09/2017 PCRU Tasigna 600mg
04/12/2017 PCRU Tasigna 600mg
10/16/2017 PCRU Tasigna 600mg
01/15/2018 PCRU Tasigna 600mg

 

Cancer Sucks!


#18 hannibellemo

hannibellemo

    Advanced Member

  • Members
  • PipPipPip
  • 728 posts
  • LocationNorth Central Iowa

Posted 19 October 2014 - 08:55 AM

Hi, JPD,

 

I love it when someone starts one of these, it's been awhile. I was diagnosed in 2008 at 57. I started on Gleevec which I loved but unfortunately my liver took exception to after 9 months. On to Sprycel, which I didn't like nearly as well, reaching MMR. Developed a pleural effusion at 2.5 years on Sprycel, reduced dosage to 50mg and regained MMR, where I find myself today.

 

I live in north central Iowa, I work for the municipality in which I live and I enjoy sailing, reading, most anything in the outdoors and enjoying my new granddaughter, Isabel!!

 

Thanks to the development of these miracle drugs I was around to see my youngest son get married and to greet my grandchild who is now 10 days old. It doesn't get much better than that!

 

Pat
 


Pat

 

"You can't change the direction of the wind but you can adjust your sails."

DX 12/08; Gleevec 400mg; liver toxicity; Sprycel 100mg.; CCyR 4/10; MMR 8/10; Pleural Effusion 2/12; Sprycel 50mg. Maintaining MMR; 2/15 PCRU; 8/16 drifting in and out of undetected like a wave meeting the shore. Retired 12/23/2016! 18 months of PCRU, most recent at Mayo on 7/25/17 was negative at their new sensitivity reporting of 0.003.<p>


#19 Marnie

Marnie

    Advanced Member

  • Members
  • PipPipPip
  • 396 posts

Posted 19 October 2014 - 12:37 PM

Pat. . congratulations! 



#20 Melanie

Melanie

    Advanced Member

  • Members
  • PipPipPip
  • 219 posts
  • LocationArizona

Posted 19 October 2014 - 07:12 PM

Hello,

Dx May of 2011, after being sent to hospital for high fever and flu like symptoms. My response has been slow due to cytopenias and I've tried every TKI, except Ponatinib. I'm on 400 mg of Bosulif now and have finally reached CCyR this Septemeber.

I just turned 60, live in Tucson, AZ, still madly in love with my amazing husband, have 3 children, 11 grandchildren, and a small rescue dog. Love to hang out with family and friends, garden, read, walk/hike, quilt, cheer on AZ wildcats in basketball, and do genealogy. We do enjoy watching college football and basketball, a little NFL and NBA, and Breaking Bad was a favorite till Walt made me hate him in the end.

First concert I went to was "The Doors" and the last one was "Boston" in July. Going to see Fleetwood Mac in December.

So grateful to have had the life I've had with my wonderful husband and praying to be able to enjoy my grandchildren for many more years to come. Also so grateful for this forum that has been and continues to be such a huge support system.

Best to all,
Melanie
Dx - 05/2011; PCR: 15.04; Fish: 87% Slow responder due to pancytopenia. Current - Bosulif - Nov: 2012, Mar 2016 lowered to 300 mg. 07/16 back to 400 mg. Clinical trial drug, Promacta, Feb 2013, for low Platelets.
CyCR - Aug 2014, Positive for 1 chromosome Sep 2015. PCR: 12.77 in Oct, 2012 to 0.04 (MDA) in Mar, 2016. 4/2016 - 0.126 (Local lab (IS); 05/2016 - 0.195 (local); 6/2016 - 0.07 (MDA); 7/2016 - 0.03 (local) 9/13/2016 - 0.16 (MDA); 9/26/2016 - 0.31 (MDA); 11/2016 - 0.012 (local); 01/2017 - 0.24 (MDA); 04/2017 - 0.09 (MDA); Cytogenetics show der(1:7)(q10;p10)7 chromosome mutation. Repeat of Sep 2015. PCR - 6/2017- 0.035 (local); 10/2017- 0.02 (MDA)




1 user(s) are reading this topic

0 members, 1 guests, 0 anonymous users