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Re: Re: Green Tea - Sue

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Joe, please let us know about the blood work. It will be very interested in

knowing the results. Good luck to you and have a nice weekend.!

Re: Green Tea - Sue

Hi all-

I haven't posted in a while, but I thought I would share my

experience. Diagnosed 9/03, FISH was not great (some bad and some

good), ZAP-70 >20, WBC bloods climbing, nodes enlarging, etc. I've

emailed some of you off-line and Dr. Gribben and I were assuming a

late 04 treatment. Six months of RFC.

I read the article from the Mayo clinic several weeks back and

decided to give it a shot( green tea that is). I started taking 4

pills of GT extract per day about 6 days ago. In 6 days, my nodes

are gone on my neck (right side), reduced on the left. I'm not

feeling any discomfort in the spleen region and I feel great. I have

NOT had any blood work since then, so I'm looking forward to seeing

my counts on 6/1, but I can't believe how much better I feel. I

know, sound's crazy, placebo effect, etc. But, I'm very excited

about the results so far.

> I don't have any info on t-cell and green tea. Anyone?

>

>

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I don't know the dosage but I will bathe in the stuff it will keep me from

having to repeat what I've been through. Has anyone checked to see if dosage is

mentioned anywhere? It sure would be nice to know how much the people in the

study were given.

I sent the article on to my Nurse Practitioner at Stanford and she was very

interested also. Wouldn't it be wonderful if something as simple as Green Tea

would " cure " CLL? At least slow the progression? I would drink it til I burst

if it meant no chemo treatments. And taking it in concentrated tablet form,

even better. Green Tea doesn't taste all that wonderful. It certainly isn't

Cherry Coke anyway.

As of my last bone marrow biopsy I am in Complete Response but I'm drinking it

just for a little extra insurance. Can't hurt. June 9th is the 4 year

anniversary of my BMT and I fully intend to stay in CR.

Sue Bunte

jb50192@... wrote:

Sue - super fantastic - I just went out and bought some - think we're on to

something here - what's the dosage?

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I found the following on the Mayo website. Does anyone know what (3 ug/ml) or

(3-25 ug/ml) means in English?

Sue Bunte

Yean K Lee, D Bone, Ann K Strege, Diane F Jelinek, and Neil E Kay*

Department of Medicine/Division of Hematology, Mayo Clinic, Rochester, MN, USA

Department of Immunology, Mayo Clinic, Rochester, MN, USA

* Corresponding author; email: kay.neil@....

We recently reported that chronic lymphocytic leukemia (CLL) cells synthesize

and release VEGF under normoxic and hypoxic conditions. CLL B cells also express

VEGF membrane receptors (VEGF-R1 and VEGF-R2), suggesting that they use VEGF as

a survival factor. To assess the mechanism of apoptosis resistance related to

VEGF, we determined the impact of VEGF on CLL B cells, and we studied the impact

of epigallocatechin (EGCG), a known receptor tyrosine kinase (RTK) inhibitor, on

VEGF receptor status and viability of CLL B cells. VEGF165 significantly

increased apoptotic resistance of CLL B cells and immunoblotting revealed that

VEGF-R1 and VEGF-R2 are spontaneously phosphorylated on CLL B cells. EGCG

significantly increased apoptosis/cell death in 8 of 10 CLL samples measured by

annexin V/propidium iodide (PI) staining. The increase in annexin V/PI staining

was accompanied by caspase 3 activation and PARP cleavage at low concentrations

of EGCG (3 µg/ml). Moreover, EGCG suppressed the

proteins Bcl-2, XIAP and Mcl-1 in CLL B cells. Finally, EGCG (3-25 µg/ml)

suppressed VEGF-R1 and VEGF-R2 phosphorylation, albeit incompletely. Thus, these

results suggest that VEGF signaling regulates survival signals in CLL cells and

that interruption of this autocrine pathway results in caspase activation and

subsequent leukemic cell death.

Sue Bunte <zamar1@...> wrote:I don't know the dosage but I will bathe in

the stuff it will keep me from having to repeat what I've been through. Has

anyone checked to see if dosage is mentioned anywhere? It sure would be nice to

know how much the people in the study were given.

I sent the article on to my Nurse Practitioner at Stanford and she was very

interested also. Wouldn't it be wonderful if something as simple as Green Tea

would " cure " CLL? At least slow the progression? I would drink it til I burst

if it meant no chemo treatments. And taking it in concentrated tablet form,

even better. Green Tea doesn't taste all that wonderful. It certainly isn't

Cherry Coke anyway.

As of my last bone marrow biopsy I am in Complete Response but I'm drinking it

just for a little extra insurance. Can't hurt. June 9th is the 4 year

anniversary of my BMT and I fully intend to stay in CR.

Sue Bunte

jb50192@... wrote:

Sue - super fantastic - I just went out and bought some - think we're on to

something here - what's the dosage?

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