RE: [SPAM] Re: Multiple Sclerosis and LDN

[Guest guest]

,

I thought about Prokarin

a bunch of years ago. The information

I had was the ingredients were histamine and something else as a stimulant, the

thought was caffeine. The nurse wouldn’t tell anyone what the ingredients

were and didn’t seem interested in any kind of a trial. At that time a prescriptions was required

because of the histamine. I know

that people with MS are low on histamine and so I wanted to find what would

make my body produce its own histamine. I felt this was a safer way to go. L-histadine is

a pre-curser to Histamine. It is an

amino acid and can be purchased at a health food store.

I started the L-Histadine for the

histamine and decided, a Mocha was a great way to get caffeine.

The results were great but, totally

unexpected. I had solar erticaria, which I’d had for two years, had horrible

light treatment for two more years, and which went away

8 months after starting the L-histadine. Of

course, the doctor said the L-histadine had nothing

to do with it. I told her that if I

had any more trouble with the sun, I would come back to her. That was 10 years ago.

Histamine is supposed to be good for some allergies

and I am just glad it all worked for me.

Solar Erticaria is miserable, especially when

my work, at the time, was and outdoor job.

I am from Oregon and Elaine DeLack is from the state of Washington. Prokarin was really in the news in the

late 90’s but I wasn’t aware it was much around. Your question is the first I have heard

of it for a good number of years.

Virginia

[sPAM]

[low dose naltrexone] Re: Multiple Sclerosis and LDN

This is again. I have another question for the

group. Has any one had any experience with PROKARIN? I

just watched that audio interview with The RN, Elaine

De Lack. It sounded pretty good, but Iv'e heard that

song before. Just wondering if it is worth a try? Any

experiences out there, let me know. Thanks

[Guest guest]

I appreciate the information YOU are sharing.

My thoughts on the Prokarin are: why would someone that suffers from MS not share with others MS patients what she claims to be beneficial for MS? Why is it soooo expensive?

If I had a "cure" or great remedy for MS symptoms, I would not think twice to just give it away and let everyone know!

I hope she reads this and hears what I think about her. I have no problem signing my name.

Ivy Myers

in FloridaSee what's free at AOL.com.