Dear Wabbite,

DON'T take 33 tablets of ascorbic acid. They will probably give you acid indigestion.

Those of us who take mega-doses of vitamin C almost
always use in the forum of sodium ascorbate crystals,
a white powder. The sodium ascorbate crystals won't
acidify your digestive tract. If you go to a clinic
for a vitamin C infusion, you'll get sodium ascorbate
in liquid form.

I buy my sodium ascorbate from Bronson Vitamins, a
company I've been dealing with happily since 1977.
Their website is: http://www.bronsonvitamins.com Their
order line is 1-800-235-3200.

You want product #50, the sodium ascorbate crystals.
They sell it by the pound and also by the kilo. I buy
it by the kilo for around $36.00 (they often have sales).

However, if the cough is that bad, you may not want
to wait a week for the crystals. Some good health food
stores sell sodium ascorbate crystals OR vitamin C tablets that are non-acidic (the same thing). If you
buy a bottle of the non-acidic tablets, you can either
take them plain, or crush them into powder.

Congratulations for getting your Amalgams out, and
for cleansing with cilantro and chlorella. The vitamin
C will help you heal from that nasty extraction. It won't interfere with the cleansing. Your immune system
NEEDS a LOT of vitamin C right now, to heal the cough,
and to heal your gums.

The pressure in your throat might be coming from your
thyroid gland. That's just a guess. I think that pressure will disappear as your body gets used to your
mercury-less mouth, and as some heavy metals are
chelated.

Do some reading on the vitamin C forum to educate yourself about mega-doses. I've posted a lot of messages in the past year that can be of help to you.

Let me know on that forum, not this one, how you're
doing with your mega-dosing.

Blessings,

Owen

Hi Roc,
First of all can I give you a hug and try and reassure you that MS is certantly not a death sentence ok? I have had it since 1989 or maybe earlier and I now lead a very normal life. I still work and my employer and co-workers don't even know that I have it. Granted my good health over the years has got to be attributed to all the very vigorous exercise that I did for 10 plus years but now I truly believe that the LDN is taking over in that department. I will try to explain it here briefly but please do not hesitate to write to me at wkendz32@hotmail.com There are many of us now that are willing to share what we know about this remarkable drug that is certainly working for us. It is Naltrexone, an FDA approved drug for more then 20 years now at a higher dose. Dr. Bihari started experimenting with a low dose of it about 15 years ago. His theory was that a low dose would cause the body to create endorphins which in turn regulate the immune system back to one that works properly. More info can be had at the site sponsored by the Advocates for Therapuetic Immunology, www.ldninfo.org. Please do not be put off by the fact that the neuros for the most part have not heard of this therapy. Do your own research online and you will come to your own decision on what is right for you. There are thousands of us using it and we are spearheading some research initiatives. Go to www.remedyfind to find what some are saying. There is even an online petition to sign that hopefully will get some studies done in Ireland. www.thepetitionsite.com/takeaction/110785607 Please take a moment to go there and sign it for the sake of those in other countries that are having difficulties getting LDN.
Ok, that being said, you are in a very good position right now Chris. Take action before any permanent damage can be done. Good luck to you and please do not hesitate to write. One day there will be support groups so that this group can meet. So important, I think. Joyce F

www.thepetitionsite.com/takeaction/110785607

http://www.ldninfo.org
http://www.remedyfind.com
http://www.thisisms.com

Hi there Chris,
I am so so sorry. Have been so busy that I have completely forgotten to come here and to read and write anything in quite a long time. Please feel free to write to me anytime and I will tell you all that I know about the LDN therapy. You can find a lot at www.ldninfo.org and if you go to www.remedyfind.com you will see what actual MS patients are saying about Naltrexone/Revia. I'd pay close attention to what other people are saying about what they use for any disorder. Goes a long way with me. Please write me at wkendz32@hotmail.com. I will tell you anything that you want to know. I've been on it for just over 2 1/2 years now and it is a blessing in my life. I like to think that I will not get any worse then I am right now and that's a good feeling....{{{hugs}}}. Joyce F