posted
For Lyme Disease induced Rheumatoid Arthritis/Osteoarthritis, or any form of arthritis, brought on by Lyme Disease... please know that there is incredible help for putting it into remission and stops it's progression. I just returned from Mexico May 22-25,2016..where I received DMSO IV therapy which took away all my inflammation/pain. If anyone is truly interested in knowing this info, please private msg me. This has changed my life and is just another piece of the puzzle in getting my life back. Very affordable and doable!
Posts: 120 | From nashville, TN | Registered: Nov 2008
| IP: Logged |
posted
This is curious. Project asked if anything was added to the IVs -- how about the mouth rinses or topical applications? I used to use it in a lab I worked in, and if we got it on our hands (and thus absorbed into the body) it would taste gross. I can't imagine a mouth rinse, but it's better than being incapacitated.
Posts: 112 | From USA | Registered: May 2016
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- Yeah, SLH, that transfer from skin to mouth was just shockingly fast, too, in addition to vile. It sure made an impression that what goes on our skin can be absorbed into the body so quickly (even air pollution matters in that regard, too).
As it is a solvent, it seems to me putting it directly into the mouth could result in chemical burns / irritation.
But, project, you say you are using it that way -- is it diluted? Can your mouth handle things like really hot peppers, etc.? [I cannot even handle even natural toothpastes as they burn so.]
I had a different reaction to DMSO topically (never used as an IV and I cannot imagine but would think there would be something to balance out its harshness in the veins).
It caused burning and itching of my skin and a very chemical taste & almost "film" it seemed in my mouth.
Directions were followed as per the doctor who came up with this idea in the first place as he was at the time (or had been) with one of the hospitals in my city and the doctor who suggested it had some connection.
The solution I had was authentic - so no knock-off. It's been many years (maybe even more than one decade) so formula changes may have taken place since I tried to use it.
Now, I've very sensitive to chemicals (with MCS) and as DMSO is actually a solvent, my reaction makes sense. I did give it several tries over time, again, with the proper instructions (I recall it was a kind of rather thin gel so might have had other ingredients, too).
It may be, like so many other aspects to treatment - and even foods - that it may be great for one person yet not another.
Just checking the name, surprise that I recalled. Stanley Jacobs (who passed away in 2015) is the name if others want to look up his work. there are many links on the web.
As for joint and other pain, I do find Berberine to be very helpful, perhaps the most helpful support method I've tried over all these years of not really being able to directly address the various TBDs. So some might want to also look there. -
Posts: 48021 | From Tree House | Registered: Jul 2007
| 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