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hairycellleukemiainfosharing · hairy cell leukemia info sharing - share experience as a patient/health providr/resea
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I was treated in August 2008 for HCL.   By the end of the year, my white cell count was above 4,000.  Yesterday (3/11/09), my cell count was in the 3,000...
11 Mar 14, 2009
12:29 pm

fordp2002
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Here is a good hairy cell site with lots of supportive and active members! http://www.network54.com/Forum/263810/...
1 Feb 10, 2008
5:22 pm

jcjr7
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Perhaps it was there before but I never noticed, but after HCL, I have a delay in my brain wiring. ie. I was in a parking lot getting out of my car and some...
2 Jan 4, 2008
11:34 am

Diane Lindsey
deedhl
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Hi I live in New York and have a great team of Doctors and they are experts on HCL They saved my life in July 2005 Like most people who get HCL I had no idea...
2 Dec 29, 2007
6:55 am

Diane Lindsey
deedhl
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Hello everyone, I hope the holidays are treating you well. I am writing on behalf of my mom, who has Hairy Cell and has been treated twice now with Cladribine....
10 Jan 3, 2008
11:50 pm

Diane Lindsey
deedhl
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Hi HCL Survivers Been in remissions seven years, interluken receptor tests, indicate my hairy cells are gathering strength, 4K, at last test, white blood cell...
2 Dec 20, 2007
12:42 am

Diane Lindsey
deedhl
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Hi, my name is Peg and I am 43 years old. I was diagnosed last year Dec.8, 2006. I spent 20 days in the hospital for my chemo, pancyopenia, and double...
7 Dec 20, 2007
12:48 am

Diane Lindsey
deedhl
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I'm coming up on my 3rd round of chemo it seems. After 5 years my counts are dropping slowly. I came back to this group and found only a few posts in one...
9 Dec 4, 2007
5:46 am

Diane Lindsey
deedhl
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It has been two years now Hard to believe I am living a normal life I watch what I eat rest limit my alchol intake I have only had the flu once and it only...
2 Nov 20, 2007
12:02 am

Paul Jaeger
wizard954
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We have a cancer bowl a thon on June 16 07 here on Yonsan Garrison Seoul Korea We are putting together a cancer survivior walk and continue monthly cancer...
2 Jun 12, 2007
5:29 am

deedhl
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lots of hcler's at http://www.network54.com/Forum/263810/...
1 Jun 10, 2007
4:53 am

jcjr7
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Hi Diane, Could you maybe have the flu? Hairy cell Leukemia is a very slow cancer, doesn't usually come that fast. What kind of treatment did you get for your...
8 May 8, 2007
12:40 am

Diane Lindsey
deedhl
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If the hcl slow returns every two yrs(after 2cda for me) or if rituxan results in a longer remission(4 yrs on my first course), mywbc would start dropping...
5 May 8, 2007
12:32 am

Diane Lindsey
deedhl
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When I was diagnosed I had one third of the blood in my body and my body was shutting down Within 2 hours hematomas formed on my inner thighs I spent 53...
3 May 6, 2007
2:10 am

deedhl
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I was diagnosed with hairy cell leukemia 12 30 05 I received cd2 chemo and am now 16 months cancer free For two days now I have been experienceing...
1 May 6, 2007
1:32 am

deedhl
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Dear Chris, The side effects from 2 CDA are negligible in comparison to other chemo treatments. The success rate is very high. I had chemo 3 years ago and did ...
3 Oct 7, 2006
6:44 pm

gary pennacchio
gpmesaaz
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2CDA, also called Leustatin or Cladribine, can be given several different ways, shots or IV and other than feeling weak for a few days or few weaks, that was...
1 Oct 5, 2006
2:18 pm

jcjr7
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My father is suffering from Hairy Cell Leukemia. At this point he is very weak.He has chosen not to do common treatments such as chemotherapy, because of side...
3 Oct 4, 2006
6:37 pm

imozes
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Hello, Has anyone experience both general(Valum, demarol, etc.) Anesthesia or local Anesthesia from a bone marrow biopsy? I have general Anesthesia before and...
3 May 8, 2006
8:09 pm

Joseph_LD
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Does anyone know if any exist in S. California? I'd like to join one? thanks, Joseph...
3 May 8, 2006
8:05 pm

Joseph_LD
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Hello Joseph My name is Dianne and I also live in So. Cal. My md not nothing for me in terms of any support groups other than existing groups - mostly breast...
1 Apr 17, 2006
6:02 pm

dsfar@...
ojaidi
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Thank you for letting me join your group. I am afraid I will not be online much untill I get broadband connected, which was promised November 12th. I am 40...
4 Mar 10, 2006
3:16 pm

Paul
wizard954
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Hi Peter, Thank you for the good wishes and the same from me to all of you. Happy New Year. How are things going with you? Jane in Canada [Non-text portions of...
1 Jan 14, 2006
4:27 pm

Jane Kalkman
bjk34m2000
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To all members, have a Happy & Healthy New Year From Peter...
1 Jan 14, 2006
2:38 pm

peteswebmail
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Lot of patient stories on the other site. And everyone is very nice and supportative. Here is the link: http://www.network54.com/Forum/263810/...
1 Dec 6, 2005
8:49 pm

jcjr7
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Peter, I was first diagnosed 10 years ago.. I have been in remission until recently, but the progression is very slow. The hairy cells were seen over 1 year ...
11 Dec 6, 2005
3:03 am

Jane Kalkman
bjk34m2000
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Thank you all for your replies to my message. It is great to hear from people in the same boat. Peter...
1 Nov 29, 2005
9:58 pm

peteswebmail
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I've placed this article's link at the bottom of this message. ... "According to a recent article published in The Lancet, a marker identified by gene...
1 Feb 7, 2005
6:20 pm

Bentley Retail
beresys
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hey all, i was one of the only female patients to be diagnosed with hcl in 2001. i had one week of treatments. it took me almost 1 year to get in remission....
1 Nov 15, 2004
4:07 am

alcaholicdemon
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Just a short note to wish you all well, Ray has been one year now since treatment with CDA and is going well. I still keep up with all of your messages and...
1 Aug 28, 2004
4:33 am

saabpam
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