Article stating that HBOT mobilizes stem cells (from CK2) (1/1/6)

Stem Cells (December 19, 2005) question from ChelatingKids2 yahoo group:

How much are stem cells? They are $8,000 per treatment in the form of a cash check or money order, no credit cards yet. You receive a receipt. Suggestion is every three months if positive response is observed.

Kerrie...we just did the stem cells with Dr Ramirez on

Nov 30th. Dr Steenblock feels the stem cells could be

very effective for my son because he has a visible

lesion on his MRI (mold exposure, not present on

previous MRI

http://abcnews.go.com/GMA/OnCall/story?id=1291345 ) &

he has been extensively detoxed. We started the MME

(10 ton magnet) on December 2 with Dr Dean Bonlie (not

with Dr Steenblock's permission but it tested really

well together & should be synergistic except if too

much metal dumps). We also have finished 2

neuropeptide shots with Dr Steenblock. (potentially

VERY powerful...but also expensive @ $300 a shot.

I am trying to keep up to date with a journal at:

http://www.defeatautismyesterday.com/dayblog.htm

After we decided it was the right choice to do stem

cells (Dr Klinghardt suggested & tested) We were very

aprehensive about going to TJ in Mexico, but after

extensive talks with Steenblock, his wife whose

brother drives & assists you during the whole thing,

Dr Payne (Dr S's research doc) & Dr Ramiriz we felt

safe & bit the bullet. Knowing other parents would be

cautious & curious as well, I video taped the whole

thing, start to finish, including across the border

both times (1st building in TJ from border). Felt very

safe...& i'm an overprotected girl from Kansas. If

anyone is really ready to do this email me directly &

i will try to get a copy of it to you. They are

supposed to start the stem cells in Nevada Jan 1 per

Dr Steenblock, but not sure of his involvement, which

is the only reason I trusted the shot actually being

what it was supposed to be.

Again...links for all of this stuff are at:

http://www.defeatautismyesterday.com/dayblog.htm...I will

be trying to give updates on my son's progress there,

but here are some relavent websites:

http://www.amri-wa.com/index.html Dr Bonlie's machine

in WA with good information on MME

http://www.stemcelltherapies.org/index.htm Dr

Steenblock's stem cell site

http://www.strokedoctor.com/ Dr Steenblock's main site

(nothing on neuropeptides just call)

http://www.mercola.com/forms/seminars/2006/jan/klinghardt_energy_medicine.htm

http://www.vsan.org/events.shtml#DKC Dr Klinghardt's

Autism conference at ASU

Hope this helps...Good Luck! Dana

ps son's progress ...about a week ago my son noticed a

Wendy's outside the window after having had fries from

there twice. He HAS NEVER NOTICED ANYTHING OUT THE

WINDOW WORTH INDICATING IT EVER IN HIS LIFE! His

babysitter feels what we are doing appears to be

moving him in the right direction (the only other two

times she has indicated success was 'Amarillo mui

bueno" -when we were doing Dr John Martin's anti-viral

fulvic acid with the energizer in it - also at site &

Dr Vinitsky's folic acid/B12 protocol). His excema is

gone. Dr Bonlie is disappointed we are not seeing more

progress (with his cp kids he usually sees stuff

between 80 & 100 hours) so he is letting us stay until

Jan 2 & hopefully we will be at 300 hours. The only

parent of a child with Autism doing MME that I have

feedback from came from Melanie Gentile (TD-DMPS Rx @

AMT pharmacy, great friend) who called to tell me this

mom called to say that she was pleased with the MME

for her daughter but not until between 200 & 300

hours. more at dayblog.htm ...& about HBOT ...i'm

going to finish this rambling there!

http://www.defeatautismyesterday.com/martin.htm - Dr

Martin's protocol

http://www.defeatautismyesterday.com/FolicCobalamine.htm

- Dr Vinitisky's protocol

(Note on this one...Dr Amy Yasko (brilliant) & Dr

Patricia Caine (based on my experience with her &

reputation...not sure how to take her advice) have

both pointed out to me how this protocol should not

work in fact should be counter-productive based on

genetic mutations...& I am sure Dr Neubrander would

same...but bottom line it really appeared to be

effective for our son, energy tests really well & Dr

Klinghardt has found it to be a foundational peice for

8 out of 10 of kids with Autism he sees)

I vowed not to ramble here...& yet on & on I went...I

hope all of this helps! Feel free to email me directly

with any questions regarding this...I only scan this

group occasionally!

Also important: We also banked all of our children's

umbilical cord blood & have inquired with Dr

Steenblock about what we can do with it. Bottom Line:

in the good ole USofA we can't even get our blood out

of the bank unless it is delivered directly to a

government sanctioned study...basically no use at

all...& even if we could get it, it isn't the blood

itself that is valuable but the very specific types of

stem cells they grow over years from it! If you find

out something different please let me know!

Again...hope this helps...that is all i have ever

wanted to accomplish beyond healing my own son...Good

Luck! Dana

Email from Dr Payne (Dr Steenblock’s research doc)

From: "Dr. Anthony G. Payne" <dragpayne@yahoo.com>

Date: Tue Dec 20, 2005 5:02:13 AM US/Pacific

To: "Anthony Payne, Ph.D." <biotheoretician@gmail.com>

Subject: RE: New book - Human Umbilical Cord Stem Cell Therapy for Certain Eye, Brain & Circulatory Conditions

This is (so far as I can ascertain) the first book ever written on human umbilical cord stem cell therapy for non-blood borne disorders:

http://www.basichealthpub.com/detail.php?ProductID=6

If you buy and read this minor tome, please let me know what you think.

Carpe punctum!

Anthony G. Payne, Ph.D.

Biological Theoretician

Steenblock Research Institute

1064 Calle Negocio #B

San Clemente, CA. 92673

Phone: (949) 248-7034

FAX: (949) 388-3441

Article: Clinical trial to test stem cell approach for children with brain injury

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