from Louise OZ

[Guest guest]

hello all ,

I was treated with Ca EAP capsule form ,(Available from Pacific Biologics on the Internet the cost use to be $120 Aus back in 1997) .it was quite good and certainly helped my walking ability.

But I went off it ,cos it increased my urgency and frequency.

THIS WILL NOT HAPPEN FOR EVERY BODY IT WAS JUST MY PATICULAR REACTION TO IT.

I recommend it as a treatment if it suits you.

I was put on it by a naturopath with a Ph.d in Biochem...very useful.

No the injections are not available in Australia ,the drug evaluation board would not have a bar of it.

Niepers hypothesis was badly discredited world wide in the 80"s by conventional researchers and that is why his treatments have never received the recognition they actually deserve,with the results they have given over time.

BUT LIKE ANY MS TREATMENT .A PROPORTION OF PEOPLE GET NO BENENFIT FROM IT.

There is no magic bullet, im only putting up with LDN because it is supposed to stop or severely slow progression in approx 98% of users .( But this was a small sample size)

An update from me is that I have now moved back to the 4.5mg and am sleeping much better.

The only catch is that I fall asleep at 8.30 at night!

But im not raving about it ,cos the increased spasticity is a real worry with me.I can also fall

backwards is if somebody breathes on me!

But keep up the good work

this is a really useful and informative digest

Louise

OZ

Ps Tom ,i agree about the diet ,but you have to do everything together ,I went low fat Gluten free

in 1995 and ended losing the use of my hands .Since then i have discovered the Dairy free is more important for me ,then gluten free ,+ keeping away from all allergic .

I did have a paper way back in 1996 ,that showed that Gluten did something to the opioid receptors in the gut that prevented them working properly.Can I find it ? No

With the vitamin D stuff its all very interesting.