Many autistic children are being helped by the Body Ecology Diet.
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96227 | From Texas | Registered: Feb 2001
| IP: Logged |
surprise
Frequent Contributor (1K+ posts)
Member # 34987
posted
I opened the link, and wanted to weep.
Tried to read it outloud to my husband, got too choked.
On the medical board here, the thread pertaining to the CDC and Lyme cover up suggests evil natures.
I find the 1 in 50 children now being diagnosed with autism, and the sheer blindness by the CDC's ever increasing vaccine schedule,
without ANY attempt whatsoever to 'green' these vaccines, OR EVEN PAUSE,
unspeakable evil.
P.S. I have been through autism with one of my children.
-------------------- Lyme positive PCR blood, and positive Bartonella henselae Igenex, 2011. low positive Fry biofilm test, 2012. Update 7/16- After extensive treatments, doing okay! Posts: 2518 | From USA | Registered: Nov 2011
| IP: Logged |
lax mom
Frequent Contributor (1K+ posts)
Member # 38743
posted
Horrific!
To think my son's former pediatrician was trying to strongarm me to get this same vaccine knowing he started banging his head the day after his 18 mo shots.
I want to just vomit! What is going on in our world???
Catgirl
Frequent Contributor (5K+ posts)
Member # 31149
posted
This makes me ill.
-------------------- --Keep an open mind about everything. Also, remember to visit ACTIVISM (we can change things together). Posts: 5418 | From earth | Registered: Mar 2011
| IP: Logged |
posted
I agree. Our daughter spiked a high fever and started regressing after her 15 month MMR vaccination. Lost all speech and much of her fine and gross motor abilities. Started raging.
It took 4 years of intensive speech therapy/OT/PT to recover her.
Then when she was 8 I tried to get our PCP to at least split the doses for the booster MMR. He refused.
We ran titers, but she was low in one of them. I trusted him when he told me the vaccine/autism link was a sham, even though I had seen it with my own eyes. Shame on me!
Now after the PCP telling me that Igenex/lyme/bartonella are all shams as well I have walked away from mainstream medicine. I will never go back.
-------------------- 13 yo DX PANS/Tourette's/Asperger's/ADHD treated for Igenex positive bartonella/IND lyme with 2 years of abx treatment. Weaned off abx April 2013 at 80% improvement. Continuing with Buhner bartonella/babesia protocols. Aug 2014 99% improvement. Posts: 265 | From Canada, Ontario | Registered: Jul 2013
| IP: Logged |
lpkayak
Honored Contributor (10K+ posts)
Member # 5230
posted
i want so much for the grand kids to come along...but i dread watching what happens...from crappy food to the vaccines...to all the other stuff
the world is so changed...and i am not sure it is for the good
-------------------- Lyme? Its complicated. Educate yourself. Posts: 13712 | From new england | Registered: Feb 2004
| IP: Logged |
LisaK
Frequent Contributor (1K+ posts)
Member # 41384
posted
I can't even op this link - I have known about this cover up for 20 years. I read back them that European findings were that kids with autism had live mumps in their intestines. The ones that got help to remove it through long therapy got better!
Our country (USA) denied that this could be a true scientific research and dismissed it all.
SHAME SHAME SHAME on all the wicked!!!!!!
-------------------- Be thankful in all things- even difficult times and sickness and trials - because there is something GOOD to be seen Posts: 3560 | From Eastern USA | Registered: Jul 2013
| IP: Logged |
LisaK
Frequent Contributor (1K+ posts)
Member # 41384
posted
** I meant to say above: I can't *open* this link.
Meaning.... can't emotionally handle it
-------------------- Be thankful in all things- even difficult times and sickness and trials - because there is something GOOD to be seen Posts: 3560 | From Eastern USA | Registered: Jul 2013
| 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/