Cystic Fibrosis

[Guest guest]

I'd be curious if anybody else besides me (and Cleary) has had

a family member with cystic fibrosis (in my case she was my first

cousin). Thank heavens that research has extended the lifespan for CF

patients -- Margie Lynn died at 11, which was about the expected

lifespan in the 1960s.

The reason I ask is that the genetic basis for cystic fibrosis requires

not merely ONE altered gene, but SEVERAL. If a patient has just one of

the genes, he/she may have other problems -- for example, one

combination gives a patient chronic respiratory problems, but not CF (CF

as in Cystic Fibrosis, not CFS as in Chronic Fatigue Syndrome).

My father, my sister and I have all had ongoing, inexplicable problems

with respiratory illnesses. In my own case, retrospectively we

conjecture that it was related to my vulnerability to all viruses

(caused by the defective 37kDa). But I have wondered if we might carry

a smaller subset of the CF combination.

Which has led me to wonder if other PWC's might carry it. I haven't

seen much discussion of this illness by PWC's -- whereas with crossover

diseases such as lupus and hypothyroidism you read a LOT on these lists

and BB's.

If you have had CF in your family -- either immediate or extended --

write me privately -- just click here:

mailto:schweit2@...

or if you are on AOL, click here:

<a href= " mailto:schweit2@... " >schweit2@...</a>.

I'll let the list know if it turns out there's anything there. (And

I'll let the list know if nobody responds, which is a finding in

itself.)

Schweitzer

mailto:schweit2@...

[Guest guest]

Well you've asked some complicated questions.

1. CAN you work on a pregnant lady is different than SHOULD I work on a pregnant lady. CAN you is yes, and I have done so (very carefully and with full knowledge of the possible outcome), SHOULD you is depending on your insurance you have covering you or the risk you are willing to take should anything go wrong, because YOU will not succeed should you be taken to court over this issue, even though it would not be your fault.

2. Can the QXCI heal genes? WE HEAL NOTHING, EVER, NEVER... PAST, PRESENT OR FUTURE. Please, do not use this term even on this chat line, it is to easy to slip when it would matter. Can we help the frequencies which may have caused the stress to these genes, probably. No biofeedback equipment is capable of adding, subtracting a gene but stress is stress and it comes in all forms.

3. Can the babies be worked on in utero? Should you choose to work on a pregnant woman at 4 weeks (approx) the machine automatically switches over to the fetus (that is the reason you answer how many weeks they are pregnant.) This helps to guarantee safety for the infant, but the legal risks are still great. As to therapy, proceed as any other issue with stress to the dna or genes. There are many areas to work for this specifically deal with Trivector DNA and/or genes on the test matrix.

Yours in Health,

Kathy

cystic fibrosis

I have a client in at the end of her first tri-mester with twins. Both she & the father have cystic fibrosis genes.

1. Can I work on a pregnant lady.

2. Can the qxci heal the genes?

3. Can the babies be worked on in utero?

Does anyone have any suggestions. The grandparents are really worried.

Thanks for all of your help.

Blessings,

Marilee Snyder

............................................

[Guest guest]

You might check out www.askdrdavid.com I think I remember seeing good info on this. Ana Garza <luisaana9@...> wrote: Does anyone have a protocol on Cystic fibrosis? I havea four year old client with this problem, she istaking pancreatic enzymes, please help me. Thank you ___________________________________________________________

[Guest guest]

Dear Ana, I am an inactive QX owner/operator. We had a QX seminar in Las

Vegas

about 3 years ago where I presented Mannatech product info. Basically, the

patented product, Ambrotose

restores the body's ability to make stem cells and the body heals itself of

every known problem. I don't

know where you are at, Dr. M. Schlachter, MD, of Las vegas, NV has a book on

Amazon.com titled; In

Search of Manna " , Your Guide to Glyconutrients and Meridians. It has over 300

references to various

illnesses and what nutrients to take for them, however CF not included, unless

the term Pulmonary Fibrosis

qualifies. We have several publications with CF testimonials and a new DVD;

Wellness Up Close, that has 8

doctors and health professionals, 5 MD's and 10 testimonials on many problems,

including Downs, Cereberal

Palsey, Cystic Fibrosis, Cancer, MS, Diabetes, etc. The DVD subtitle is, " How

Glyconutrients help your body's

ability to defend, RESTORE, repair and protect itself against disease " . I've

been in nutrition for over 26 years

and in Mannatech nearly 11 years. Our science web site has won several

international awards, www.glycoscience.

org has over 8,500 references. Our company site, www.mannatech.com/alholter is

extensive. This is an R & D

Network Marketing Company with a seamless downline from Germany to UK to

Australia, Japan, S. Korea,

Taiwan, Canada, U.S. New Zealand and Denmark. Next month, Mannatech is

introducing a new skin care line,

first in Japan, that will have no synthetic (propolyne or ethanol glycol) or

natural preservatives, the water is

from a patented Japanese filter that is bacteriostatic. My cousin's wife in

Tokyo is Japanese so I'm going to have

her ship me some sets to get a head start on the American market.

If you have any interest in the above, give me your address and phone number and

we can talk on my nickle.

My phone # is 763-537-1843. Crystal, MN a suburb of Mpls.

Sincerely,

Al Holter

cystic fibrosis

>

>

>Does anyone have a protocol of cystic fibrosis I have

>a client is a 4 years old girl she is having problems

>with her pancreas. Thankyou for your help

>

>

>

>

>

>___________________________________________________________

>

[Guest guest]

I'm sure that the vaccinations would only diminish his immune system but CF is

genetic so he would have had it anyway. It is indeed probably worsened due to

vaxes. So sad for this family.

Sheri B.

www.shaklee.net/simplevitality

" Where the best of science & nature come together. "

---------------------------------

Want to start your own business? Learn how on Small Business.

[Guest guest]

Hi,

I have a client who is a carrier of the CF (Cystic Fibrosis) gene. Although he

has no effecting symptoms. He has two siblings that have the illness CF.

He has medical evidence that he is a carrier of the CF Gene. He is after the

root causes, wants to change his way of thinking or way of being that supports

this gene to ultimately change the faulty gene.

He asked me for a serie of biofeedback sessions to support him in the process.

I am aware of beneficial protocols re autoimmune diseases but so far no

experience with CF.

Is there any therapist in this group that worked with a client with CF. If so

would you be willing to share your experiences and approach using the

SCIO/INDIGO.

Thanks!

Maarten - Australia

[Guest guest]

Hi ,

I do have two daughters with cystic fibrosis. The carriers, as I am,

are assymptomatics. I do treat them with SCIO, and all the advises

that you give in your mail are very reasonable. The diet has to be

high in DHA (suplement is needed) and low in EPA, Arachidonic Acid

and the rest of W6. Inflammation, infection and mucus is the big

problem, as well as the digestive (specially pancreas. Is important

not to increase the digestive enzimes produced in pancreas

and liver, as it can cause in them a pancreatitis, but is important

to treat these organs).

Actually there are different aproaches depending on the mutation.

For example, genisteine corrects G541D mutation, crataegus corrects

DF508 mutation, gentamicine corrects G542X mutation.

Hope it can helps,

Paloma

El 17/12/2010 15:25, Branco escribió:

 

Since this is supposedly an inherited gene malfunction. I

would work on Trivector DNA panels. Support the

corresponding organs in Short sarcodes and Biofeedback

panels eg.: Lungs, Gastro Intestinal, Endocrine.

I would definitely support it with Professor Arnold

Ehret's Mucusless Diet Healing

System. I would also instead of antibiotics

use MMS Miracle Mineral Solution.

You can do a google and find out where to get those two

items...

Of course homeopathic support, check miasms, treat lower

as well as the higher reaction miasms, below 60 very

important! use the remedies in homeopathy to make bottle

with two or three remedies, add 5 drops of brandy to the

water, it olds better the frequencies, go from 30

potency upwards to the full range changing potency weekly.

Ask patient to energise the remedy by shaking vigorously

each time before taking.

Keep us informed of results...

Love

QuantuMedical

BioEnergetic

Medicine

SCIO-INDIGO

”No problem can be solved from the

conscious that

created it. We must learn to see the world anew.”Albert Einstein

Branco Dipl. Hom. LCPH MARH FBIH ILQBT

Terminvereinbarung:

Baseler

Straße 12

12205

Berlin

Fon 030 30

10 11 63

Mobil

0176

20796804

www.quantumedical.com

[Guest guest]

I like to add here that the Mucusless Diet by Prof. Arnold Ehret is the most important factor in treating this type of disease and almost all disease. Reason being that if the cells are covered in mucus then obviously there is low functionality of all organs ofcourse affecting nutrient absorbion...could go on here for a while on this theme, but it is good to make a start with this healing diet...further info here: http://www.arnoldehret.org/healthclub/index.htmlLove

QuantuMedical

BioEnergetic Medicine

SCIO-INDIGO

”No problem can be solved from the conscious that created it. We must learn to see the world anew.”Albert Einstein

Branco Dipl. Hom. LCPH MARH FBIH ILQBT

Terminvereinbarung:

Baseler Straße 12

12205 Berlin

Fon 030 30 10 11 63

Mobil 0176 20796804

www.quantumedical.com

CC: mvanbokkel@...From: zshapeshifter@...Date: Wed, 29 Dec 2010 16:58:57 -0800Subject: Re: Cystic Fibrosis

CF is a recessive gene(s) trate that 1 in 25 White People carry, support the pancreas naturally on a low or no mucus forming diet, good exercise and good SOC improvement coaching. www.QuantumBiofeedback.info :Subject: Cystic Fibrosis

Hi,I have a client who is a carrier of the CF (Cystic Fibrosis) gene. Although he has no effecting symptoms. He has two siblings that have the illness CF.He has medical evidence that he is a carrier of the CF Gene. He is after the root causes, wants to change his way of thinking or way of being that supports this gene to ultimately change the faulty gene.He asked me for a serie of biofeedback sessions to support him in the process.I am aware of beneficial protocols re autoimmune diseases but so far no experience with CF.Is there any therapist in this group that worked with a client with CF. If so would you be willing to share your experiences and approach using the SCIO/INDIGO.Thanks!Maarten - Australia------------------------------------............................................

[Guest guest]

There are so many wonderful programs to work with the DNA and Chromosomes.  In Trivector on the hololinguistic page is one area that has lots of things to do with the DNA. There are places to write in Cystic Fibrosis and direct the energy there.  Also I learned last year to put something like Cystic Fibrosis into one of the hold trays on the test page and test it in the Chromosome chapter to see what comes up and then click the yellow lines on the right to balance the energies. You can do all kinds of variations of that technique like put the first Chromosome that comes up after your search for Cystic Fibrosis in the Chromosome chapter into the red tray on the bottom of the test page and run the 4 buttons on the bottom clicking the yellow lines that come up on the right after each button is run.  Sorry, I am not well versed in the names of all the areas that I am speaking of but I do know they all work to bring energy to areas that need balancing. It is always an education to see what issues are connected.  Things you might never have thought of.  Be creative, it can't hurt.  Kim

On Sat, Dec 11, 2010 at 7:26 PM, soul_communications <mvanbokkel@...> wrote:

 

Hi,

I have a client who is a carrier of the CF (Cystic Fibrosis) gene. Although he has no effecting symptoms. He has two siblings that have the illness CF.

He has medical evidence that he is a carrier of the CF Gene. He is after the root causes, wants to change his way of thinking or way of being that supports this gene to ultimately change the faulty gene.

He asked me for a serie of biofeedback sessions to support him in the process.

I am aware of beneficial protocols re autoimmune diseases but so far no experience with CF.

Is there any therapist in this group that worked with a client with CF. If so would you be willing to share your experiences and approach using the SCIO/INDIGO.

Thanks!

Maarten - Australia

[Guest guest]

Hi,

I think it is e.

Regards,

Manochithra

On 14 Apr 2012 09:45, " Balsam_Majid " <balsam_majid@...> wrote:

 

Plz help in this Q

Oral manifestation of cystic fibrosis include all the following except

A tend to be mouth breathers

B salivary gland enlarge

C increase in dental caries

D increase in calculus deposits

E Intrinsic teeth staining due to tetracycline

Thanks

Sent from my iPad

[Guest guest]

Salivary glad enlargement,page 340 Cawsons Sent from my iPhoneOn 14 Apr 2012, at 09:45, Balsam_Majid <balsam_majid@...> wrote:

Plz help in this Q

Oral manifestation of cystic fibrosis include all the following except

A tend to be mouth breathers

B salivary gland enlarge

C increase in dental caries

D increase in calculus deposits

E Intrinsic teeth staining due to tetracycline

Thanks

Sent from my iPad

=

[Guest guest]

Thank u..... Sent from my iPhoneOn 15 Apr 2012, at 12:57, ghazala farid <drghazalafarid@...> wrote:

HI Seethalmark IN SCULLY THE SENTENCE READS AS"THE LOW FAT AND HIGH CARBOHYDRATE DIET AND DRY MOUTH MAY PREDISPOSE TO CARIES BUT SOME STUDIES HAVE SHOWN FEWER CARIES IN CF PATIENTS"

FOR FURTHER CONFIRMATION OF THE ANSHERE IS AN EXTRACT FROM :- PEDEATRIC DENTISTRY ,OXFORD UNIVERSITY PRESS

management of cystic fibrosis

There are reports of decreased caries prevalence attributable not only to the long term

use of antibiotics and pancreatic enzyme supplements but also to increased salivary

buffering. HOPE IT CLEARS THE DOUBTGHAZALA