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Hi ,

 

First, CONGRATULATIONS!  I'm so happy for you.

 

I have had CFS for 28 years and am the group member who got the placenta stem

cell treatments.  Although the stem cells did physical repairs that I needed,

they don't kill pathogens, restore the gut, or handle oxalates so I still have

CFS and not much in the way of a real life.  Wish I had known about stool

infusions, oxalates, biofilms, etc before but the important thing is that

because of many of your contributions, I know about them now.

 

, could you please explain how taking antibiotics help the gut flora. 

I thought it was the opposite.  Since antibiotics kill bacteria and

not viruses, why did you take antibiotics, which did you take, and how did they

help the gut if you don't mind my asking.  Also, what did you do and how to

break down the bilfilm?  

 

Sure wish we had stool infusion treatment in this country.  I'm researching now

to find the most comprehensive probiotic.  Does anyone have any suggestions? 

Would also like suggestions on what to do for leaky gut.  My urine test

showed I needed the low oxalate diet so I started it almost 2 weeks ago.

 

, your improvement is so encouraging.  Thank-you.  Kay

 

 

 

Hi Louella and Marti

I have had success also, even returned to work part time 4 hrs 4 days a week,

its 7 years since I had to leave work due to cfs. Had two pay cheques already,

(spent them on clothes - I'm having a ball). No relapses, walking 40

minutes everyday at 6.30am. Significant changes, have my life back, the last

part in my recovery after the biofilm treatment, antibiotics for gut flora and

stool implant was discovering I had high oxalates in my urine from a Great

Plains Lab organic acid test. Joined the trying low oxalate group, then went on

a low oxalate diet, put in mag and cal citrate with meals to bind oxalates in

food and supplemented B5 (coenzyme A, krebs cycle). Haven't looked back, not

cured, but the body is healing and everything is humming along brilliantly. Job

now is to heal the leaky gut. Still on methylation sups and lots of other sups.

>

>

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Hi Kay,

thank you, like you there a few things in hindsight I would have done in a

different order. Firstly is getting to grips with the oxalate issue - that I

believe is perpetuation the oxidative stress/depleting glutathione, which I

don't think can be corrected until you go on a low oxalate diet and supplement

mag & cal citrate to bind oxalates with meals.

The oxalate issue is not like an intolerance to a substance, it is actually a

poison that is entering the body because of a leaky gut. The body does not have

a mechanism to deal with this toxin and so stores the crystals in the brain,

organs anywhere, a bit like what happens with mercury. Actually they are are

suspecting mercury is implicated with oxalates as well.

Join Trying Low Oxalates, very supportive and informative, run by Owens a

researcher whose daughter has oxalate issues and has been researching oxalates

for 16 years. Given you have a urine test showing oxalates I would highly

encourage you to address this issue.

Yes antibiotics are the worst thing to take, you are right, kills the good

bacteria and allows undesirables to flourish. I first started with Kenny

DeMeirlier (Canadian CFS/ME doctor) who is attempting to the correct the gut

flora imbalances by cycling antibiotics with probiotics. I have been on sooooo

many antibiotics over the years for such extended periods of time, (5 years

whilst we were trying to kill chlamidia pn. is one example) I attribute the

progression of my cfs to the use of antibiotics. But they are a necessary evil.

However, the good bacteria must be replaced otherwise the bad bacteria just

flourish once you come off antibiotics. I kept relapsing on Kenny DeMeirlier's

protocol like I did any other time I took antibiotics and that is why I had the

stool implants. I still take oral probiotics VSL#3 as these are also known to be

useful for oxalate degradation.

Dr Usman's (a DAN doctor - Defeat Autism Now) biofilm protocol (using

fibrolynitic enzymes) I also incorporated with Kenny's protocol and for me I

improved very quickly doing this. But biofilms can release enormous amounts of

toxins once you start destroying them and some people have horrendous herximers

reactions, so bad they can't tolerate them. (caution must be taken with this

protocol, here is more info http://onibasu.com/archives/am/213277.html) I

managed to cope with my herximers reactions but I was a zombie for many months

but at the same time my energy and stamina increased so I hung in there. You

really need to be very careful with the biofilm protocol, as biofilms are also

part of your good bacteria and they also get destroyed. Therefore I really think

having a stool implant is the way to go especially after the biofilm protocol.

Prof Borody of the Center for Digestive Disease is the gastro behind this

radical treatment in Syd Aust he is making an impact in US and if you can get

your hands on Jan 22 issue of NewScientist there is an article there on him and

his work.

I have been my own guinea pig, everything is coming along extremely well,

however my body still has a lot of damage to heal and I think I walk a very thin

line in the management of my cfs, one wrong move ie. eat food I shouldn't and

down I go. I therefore feel it is imperative to heal the leaky gut. This I am

still learning about and only time will tell how I go with that one.

One other thing I think has helped me is addressing my methylation blocks and

supplementing with methylation supplements recommended by Dr Amy Yasko - and

adapted for cfs/me by Van Kronynenburg who runs the CFS_Yasko group.

This illness is extremely complex and takes a lot of self education, which is

near impossible when your brain doesn't function together with self awareness

and massive amounts of supplements to get the brain and metabolism working.

I better go its getting late, I better go to bed - I'm a working girl now, hee

hee - it feels soooo good to be part of the real world again. Hang in there,

keep fighting, I know it takes soo much effort and energy to pull yourself back

up when you crash, it is just part of the yoyo manner of the illness - just keep

getting back up!!! One day you will get there, believe in yourself.

>

> Hi ,

>  

> First, CONGRATULATIONS!  I'm so happy for you.

>  

> I have had CFS for 28 years and am the group member who got the placenta stem

cell treatments.  Although the stem cells did physical repairs that I needed,

they don't kill pathogens, restore the gut, or handle oxalates so I still have

CFS and not much in the way of a real life.  Wish I had known about stool

infusions, oxalates, biofilms, etc before but the important thing is that

because of many of your contributions, I know about them now.

>  

> , could you please explain how taking antibiotics help the gut

flora.  I thought it was the opposite.  Since antibiotics kill bacteria and

not viruses, why did you take antibiotics, which did you take, and how did they

help the gut if you don't mind my asking.  Also, what did you do and how to

break down the bilfilm?  

>  

> Sure wish we had stool infusion treatment in this country.  I'm researching

now to find the most comprehensive probiotic.  Does anyone have any

suggestions?  Would also like suggestions on what to do for leaky gut.  My

urine test showed I needed the low oxalate diet so I started it almost 2 weeks

ago.

>  

> , your improvement is so encouraging.  Thank-you.  Kay

>  

>  

>

>

>

>  

>

>

>

> Hi Louella and Marti

>

> I have had success also, even returned to work part time 4 hrs 4 days a week,

its 7 years since I had to leave work due to cfs. Had two pay cheques already,

(spent them on clothes - I'm having a ball). No relapses, walking 40

minutes everyday at 6.30am. Significant changes, have my life back, the last

part in my recovery after the biofilm treatment, antibiotics for gut flora and

stool implant was discovering I had high oxalates in my urine from a Great

Plains Lab organic acid test. Joined the trying low oxalate group, then went on

a low oxalate diet, put in mag and cal citrate with meals to bind oxalates in

food and supplemented B5 (coenzyme A, krebs cycle). Haven't looked back, not

cured, but the body is healing and everything is humming along brilliantly. Job

now is to heal the leaky gut. Still on methylation sups and lots of other sups.

>

>

>

>

> >

>

> >

>

>

>

>

>

>

>

>

>

>

>

>

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