posted
been checking into the immune response training. Has anyone tried this lately. I have found some testimonials that seem legit and that aren't out to sell you something...Any comments? Thanks so much.
Posts: 146 | From Midwest | Registered: Feb 2005
| IP: Logged |
joalo
Frequent Contributor (1K+ posts)
Member # 12752
posted
bump!
-------------------- Sick since January 1985. Misdiagnosed for 20 years. Tested CDC positive October 2005. Treating since April 2006. Posts: 3228 | From Somewhere west of the Mississippi | Registered: Aug 2007
| IP: Logged |
I was part of the IRT Lyme classes by phone earlier this year. For me it was not the answer I had hoped for (my condition is very complex with lots of health issues and long-standing illness), but the process did help, and I followed that with another type of class at the same place that HAS been very helpful.
Several people in the IRT Lyme class I started with had great improvement early on, and their progress continued. People with very limited abilities were reporting being able to do things they had not been able to do for a number of years...simple stuff like setting the table and making a meal, or going out of the house to grocery shop, or taking a trip. Some people left the groups to go back to work.
The thing I like about the program is that Gary is very proactive about helping the program work for people. If he things you are too sick to handle much, he will suggest ways to limit herxes, like only doing one page of codes per week. He uses muscle-testing to check what participants can handle in the way of codes, plus supplements and meds, and to figure out what their problems are.
He's a great listener when he interviews participants, and he really wants people to get well. He will refund your money if the first 3 classes don't work for you, so that's a great guarantee. For me, it's been very worthwhile.
You can always call the office if you need more information or have questions.
Good luck, and please post your experiences if you decide to try it.
Nutmeg
Posts: 386 | From WA state | Registered: May 2005
| IP: Logged |
posted
Thanks for all the replies. I may end up giving it a try. I will keep everyone posted if I do.
Posts: 146 | From Midwest | Registered: Feb 2005
| 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!
![[confused]](graemlins/confused.gif)
Printer-friendly view of this topic