posted
My local health food store will soon be stocking this stuff called CellPower. Its website is www.cellpowerusa.com
The brochure states that it is an "oxygen producing, high energy concentrate with amino acids, enzymes and colloidal minerals," and that it provides cellular oxygenation and detoxification. Etc. etc.
It sounds too good to be true to me. What do you all think?
Thanks, P
Posts: 449 | From Vermont | Registered: Nov 2004
| IP: Logged |
posted
Thanks, sparkle. They do seem to be similar or maybe even the same.
quote:Originally posted by sparkle7: I tried Cell Food for a while & didn't notice any huge improvements. It seems similar - maybe it's a "knock off" of Cell Food?
lymie_in_md
Frequent Contributor (1K+ posts)
Member # 14197
posted
I don't think so sweet pea. Although Cell food is alkalizing due to increase oxygen in the body. This product might be alkalyzing in the intestines. Big difference!
-------------------- Bob Posts: 2150 | From Maryland | Registered: Dec 2007
| IP: Logged |
Clarissa
Frequent Contributor (1K+ posts)
Member # 4715
posted
My LLMD recommended me taking the Cell Food that Sparkle mentioned (along with their Sam e product).
Haven't done it yet as Mesosilver still has me herxing. One thing at a time.
Sorry I couldn't give any further input but I know my LLMD was taking it himself.
It's not a bad thing to use a knock off - especially if it's cheaper but in some cases it's better to use the real thing.
It's sounds like a great product. I read a small book about it. I didn't notice much of a difference in my health after using it for a few months.
It's not all that cheap - so, I decided not to continue with it. I think it's around $30 for a little dropper bottle.
They have a bunch of other products that have the "proprietary formula". I think I also tried the bath product but it didn't do anything.
The CellFood has been around for a while. I think if it really helped people with Lyme, more people would be recommending it.
I like to take things that I can actually feel a difference from. There are so many products on the market - it's really hard to tell if they really work or are just some alternative form of "snake oil"...
Everyone is different, though. What effects one person may not work on everyone.
Posts: 7772 | From Northeast, again... | Registered: Oct 2006
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/
UBBFriend: Email this page to someone!
Printer-friendly view of this topic