Cord Blood Stem Cell Treatment

[Guest guest]

Thanks Sally, or your thoughts and good wishes. I am doing well, I

had some improvement after the first week and then most of that went

away. I was very upset and then I talked to a doctor who does the

treatments and was told there are cytokins in the vial of stem cells

and some people show signs of improvement foe a week or two

afterwards from that and then the improvement goes away. I was told

that the cells take many months to begin working. One week is

certainly not long enough for the cells to ingraft with my cells and

start repairing anything, neither is one month. This healing takes a

long time. I relate it to what the stem cells purpose was origionally

for: growing a baby! How long dos it take an unborn baby to grow?

Nine whole months! So it will take a long time for me to see results

also. An unborn baby is not dealing with repair of an already damaged

and diseased body. They are also continually fed, can sleep all of

the time, don't have to fix meals, no responsibilities, kept warm and

have their mother's immune system taking care of them so they can

grow unhindered. Thinking about it this way has helped me to relax

and focus on helping my body by taking care of it.

[Guest guest]

:

You are correct in your statement that it takes time. According to the

following excerpt taken from the Biomark web site;

" Once in the body, the cells migrate to the site of disease and begin

replacing damaged or missing cells. This process of noticeable

reconstitution usually peaks between 3 and 6 months following treatment.

Often significant results are noted at the one month mark. "

Noland

----- Original Message -----

From: " " <linda@...>

<low dose naltrexone >

Sent: Tuesday, December 02, 2003 1:40 PM

Subject: [low dose naltrexone] Cord Blood Stem Cell Treatment

> Thanks Sally, or your thoughts and good wishes. I am doing well, I

> had some improvement after the first week and then most of that went

> away. I was very upset and then I talked to a doctor who does the

> treatments and was told there are cytokins in the vial of stem cells

> and some people show signs of improvement foe a week or two

> afterwards from that and then the improvement goes away. I was told

> that the cells take many months to begin working. One week is

> certainly not long enough for the cells to ingraft with my cells and

> start repairing anything, neither is one month. This healing takes a

> long time. I relate it to what the stem cells purpose was origionally

> for: growing a baby! How long dos it take an unborn baby to grow?

> Nine whole months! So it will take a long time for me to see results

> also. An unborn baby is not dealing with repair of an already damaged

> and diseased body. They are also continually fed, can sleep all of

> the time, don't have to fix meals, no responsibilities, kept warm and

> have their mother's immune system taking care of them so they can

> grow unhindered. Thinking about it this way has helped me to relax

> and focus on helping my body by taking care of it.

>

>

>

>

>

>

[Guest guest]

To the best of my knowledge, FDA started an investigation for Biomark's

stem cell transplantation, and the stem cell transplantation is halted

indefinitely within the boundaries of USA. If somebody has the info on

the current situation, he/she can inform us.

Regards

Ergin

Hi Mike,

> My name is and I live in Australia. I read you post about your

> stem cell treament with Biomark. Fantasic !!! are you still continuing

> to improve. I have PPMS not as bad as you were but only had MS for

> couple years and it gets worse all the time.

> In you email to Bev you mention you are looking at another place for the

> same thing. Does that mean Biomark are not doing it now?

> In Australia they are in the process of opening a Stem Cell Centre at

> Monash University BUT is very early days here, in fact it sounds like

> they could be years off.

> I would love to hear from you on how you are doing now.

>

>

>

[Guest guest]

Thank you for the info that you have provided. It seems to me that cord

blood stem cell treatment is in early stages, and needs some addtitonal

research and time. Long term effects are not known. However, the results

are promising. Who knows, in the near future, MS can be completely

eradicated for the patients who receve this treatment, anyway, I think it

is best to wait and see additional results obtained by this treatment.

Ergin

> Biomark is back up and running. You can now go to their website

> again. They are still doing the cord blood stem cell treatments, just

> are not doing them in the United States anymore. I haven't

> talked to them but someone who has talked with them since they

> started back up told me that they have sites in Canada, Mexico and

> Europe where they will do the treatments.

>

> Hope that helps.

>

> Diane

>

>

[Guest guest]

would you give more info on cord cell(the company/clinic)??website?phone

number?

thanks

=hm=

> IM SORRY I HAVENT HAD IT DONE AS OF YET I AM ONLY GATH ERING

INFO. THE OTHER

> PLACE IM LOOKING IS CALLED " CORE CELL

>

> Mike

[Guest guest]

Hi ,

Thanks for your e mail.

Did they say how much money it costs?

Thanks,

Bev.

-------Original Message-------

From: low dose naltrexone

Date: Saturday, May 15, 2004 04:04:21

low dose naltrexone

Subject: Re: [low dose naltrexone] Cord Blood Stem Cell Treatment

Hi Bev,

Sorry to be so long replying. In his email dated 11th May Subject INFO he says Here is where you can find more info on this treatment, good luck to you. I am also looking for another place for the same thing. I will post that if it looks good. Underneath he gives you some phone numbers.

OK since then I have gone into the Biomark website and they are up and running in England and Europe and there is a stack of info on the site. Also you can email them and they will email you some detailed info. It sounds fantastic but way out of my price bracket. I've just got to hope it's not too long before it gets started in Australia. I wish he had told us how he is today as well.

-------Original Message-------

From: low dose naltrexone

Date: 05/11/04 09:43:11

low dose naltrexone

Subject: Re: [low dose naltrexone] Cord Blood Stem Cell Treatment

Hi ,

I hope you get this.....I am confused..in the e mail from Mike (to me) I don't have the part about "looking for another place to do the stem cell'... can you fill me in?. Did he say anything more about where and how you can get in touch with the right people?

I wish he would have told us how he is today.

Thanks and lets keep in touch.

Bev.

-------Original Message-------

From: low dose naltrexone

Date: Tuesday, May 11, 2004 02:18:55

LDN

Subject: [low dose naltrexone] Cord Blood Stem Cell Treatment

Hi Mike,

My name is and I live in Australia. I read you post about your stem cell treament with Biomark. Fantasic !!! are you still continuing to improve. I have PPMS not as bad as you were but only had MS for couple years and it gets worse all the time.

In you email to Bev you mention you are looking at another place for the same thing. Does that mean Biomark are not doing it now?

In Australia they are in the process of opening a Stem Cell Centre at Monash University BUT is very early days here, in fact it sounds like they could be years off.

I would love to hear from you on how you are doing now.

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