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  #1  
Old Jan 06, 2006, 02:37 PM
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Join Date: Dec 2005
Waldenstrom's Disease

Has anyone known anyone with Waldenstrom's Disease? My girlfriend just got diagnosed with it, and I know what it is, but wondered if anyone has any experience with it. It seems like a disease she can live with for a long time, but some literature is confusing. Thanks for your help.

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  #2  
Old Jan 06, 2006, 11:02 PM
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EricEnfermero (Male)
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Post Re: Waldenstrom's Disease

If you haven't already found it, check out www.iwmf.com . It seems to have quite a bit of info, from support groups to an Internet listserv to a telephone hotline.

Don't have any personal experience with WM though.

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  #3  
Old Jan 06, 2006, 11:13 PM
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Join Date: Dec 2005
Re: Waldenstrom's Disease

Thanks Eric,
That website was really encouraging!

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  #4  
Old Jan 28, 2006, 11:18 PM
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Join Date: Jan 2006
Re: Waldenstrom's Disease

http://www.cancer.gov/cancertopics/f...Sites-Types/WM

It's not bad, but does need to be monitored closely.
And Velcade is evil, just in case they start talking about that.


Last edited by missy2b : Jan 28, 2006 at 11:26 PM.
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  #5  
Old Jan 03, 2008, 01:28 PM
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Join Date: Jan 2008
Re: Waldenstrom's Disease

I'm a chemo patient with chronic lymphocytic leukemia. My nephrologist was concerned about my creatinine (1.6) and GFR (47) before chemo. Told me to stay off the NSAIDS. Now my numbers are much better (1.0 and 72) after rituxan and fludara. The neph speculated WM yesterday and said that my chemo for CLL was already the first line treatment for WM, both being B-cell lymphoma. I envision it as looking at the same disorder from two sides of a crystal. Whichever disorder is doing it, my main physical symptom is lower back, hip and leg weakness. The oncs hope that treating CLL will improve mobility and call me a unique case.

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  #6  
Old Jan 12, 2008, 10:41 PM
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Join Date: Jun 2003
Re: Waldenstrom's Disease

I have a couple (3 I believe in the practice) of patients with this. It characterized by an abnormal group of plasma cells that produce the paraprotein, IgM. It can transform into a high grade lymphoma, worst case or it can be a smoldering disease, best case. Prognosis/staging is done using the amount of beta2 microglobulin, serum IgM concentration, and hgb. It is not a benign disease.

Our doctor said treatment is not indicated unless symptoms occur, hyperviscosity (one patient had strokes and was treated initially with plasmopheresis) B symptoms (fever sweats wgt loss) lymphadenopathy or hepatosplenomegly. Otherwise it is wait and watch we usually follow up every 4 months with B2M, SIEP, CBC, CMP and LDH. Can you tell I am training as his NP yet? LOL!

He has told me several times in patients with smoldering multiple myeloma, treating early is detrimental. I don't specifically know if this is true with Waldenstrom's but I suspect it is. The last thing I read was that there was no one treatment better than the other. The oncologist/hematologist I work with gave Rituxin and chlorambucil. The patient is doing great.

I think Velcade is a wonderful drug. We are having some success with myeloma patients using Velcade. I saw a patient Thursday whose SIEP was totally normal after treatment with Velcade, thalidomide, and prednisone

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  #7  
Old Jan 16, 2008, 07:17 PM
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Join Date: Jan 2008
Smile Re: Waldenstrom's Disease

I saw the oncologist yesterday and told him that my nephrologist thought I might have Waldenstrom's because of my high IgM. The onc looked at my SPEP and said that the IgM was never high enough to indicate WM. So, cross that one off. I commented that he would probably prefer that my other docs would not give amateur diagnoses and would leave it to the specialist (him). He was professional enough to not agree out loud. Also off the table is CLL. I'm done with chemo after a total of 8 weeks--only 9 infusions. Since I'm on a nurses' site I want to praise the nurses at the infusion center. What a positive place!

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