Hello All! My name is Heather and I am a Proud Mom of 2 beautiful girls, one older and "Neuro-typical", the younger vaccine injured fighting Autism daily. I am also a Autism Parent Advocate and Medical Freedom Activist. My daughter Sabrina, known as "Pepito" ,was diagnosed in 2003 at the age of 2 1/2 with PDD- ASD. Since then I have gone through what many parents whom get this diagnosis go through.. physically and mentally. I know of the worry, anger , stress , anxiety ,hurt , frustration ,sadness , fear , and the draining effect from continuous daily battle combating autism . I also know of the happiness and sheer Joy of her accomplishments , perseverance and gains she continues to show . MY Will to fight for her and all children
is very passionate, strong and natural..
After years of believing mis-lead information about my daughters diagnosis; I finally went on my Own quest for truths. I wanted, I Needed to know what happened to my girl. I feel In order to Help her, I have to fully understand what happened to her and all I could find and learn about her diagnosis. So after watching my child deteriorate before my eyes and no questions answered as to why by her 'then' doctors.. I set out for answers and knowledge. I have done all sorts of testing and blood-work and although its seemingly ongoing, I thankfully have found reliable doctor(s) whom have helped me find many answers I was looking for and have determined that my child was indeed a vaccine injury victim. She born with a predisposition, a susceptibility like so many are and since its never checked,its not known and Bina had/has a weak immune system. We also found she has mitochondrial dysfunction as well as has the MTHFR mutated gene (again which most have) , in which means her body has issues with detoxing (the methylation/metabolical system)This was indeed Epigenetic, She was susceptible and weak at birth which no doctor looked for. Her body and systems were assaulted and overrun by the toxins given to her in the vaccinations she received. Her tipping point was at the 15 month vaccinations. That is when it all changed.
I now have the confirmation I have always felt, watched before my own eyes and can see on our home videos and pictures and have known deep down but didnt want to believe..
She was in fact a victim of vaccine injury thus which lead to her Autism development...INJURIES.
I have been reading , researching all things I can and have Finally started to put Her Pieces back TOGETHER. Our blog initially started as a fund raiser for Sabrina, for family and friends to donate, but has evolved into so much more and continues to grow I am proud to say. The Blog is mainly now to share our journey. What has worked, not worked what we found learned ..our experiences in HOPES this will help others find answers in which then they can help their kids ..
More detailed information about this journey May 2013 Post,"Test results".
I am so pleased and EXCITED to say that there IS information out there to help You put your own child's pieces together as well!! I am here to offer help and guide anyone I can to the correct people and resources for you to beable to help treat, heal and recover your child! Like with everything else..time is of essence..so the sooner you get treatment..the better the outcome! Just KNOW......
There IS HOPE! We CAN help them !!
Nothing we can do can change the past, but everything we do changes the future!
My Blog is here to help show you what I have learned.
Also to hopefully Inspire, Give Hope and Information to help Educate yourself.
Knowledge IS Power!!
I wish I knew THEN what I know NOW about autism. I think its awesome that we now have these tools and opportunities to connect with others whom UNDERSTAND what we are going through.
To share advice ,.information..just plan HELPING one another. One thing I have learned is the Support System is VERY IMPORTANT. For the success and sanity for all involved.
When people think of Autism they automatically think of BOYS.....
I am here to say that YES 1 of 45 kids are diagnosed , 1 in 4 are indeed GIRLS.
This blog is for EVERYONE to use , visit , read , support in with a
non-judgmental outlook ....
Our journey has been a difficult road . I have learned SO much about myself , my daughter and the continued fight we live daily. October 2011 is when we started biomedical treatments and measures to help start this healing process. She may never be the child she was before the injuries, BUT she is definitely a happier healthier child now and her true self is finally able to show itself once again..to shine through..BREAK through the barriers that were put up from these brain, gut, immune and metabolic injuries aka Autism. The further the treatment, the further the healing..and the more gains we continue to see! Her overall quality of life has changed for the better , our whole family's quality of life has! Bottom line.. Its NEVER too late..She getting older now and proud to say that my once healthy , alert, full of life,verbal baby that regressed into a silent ,very unhappy ,sick , isolated toddler, is now a healing and recovering into a healthier happier chatter box! If this was something she was "born with" she would never have improved! NONE of these kids would be able to improve! But she HAS! And Others HAVE and continue to do so! There IS HOPE because AUTISM IS MEDICAL!
Sabrina was diagnosed at 2 1/2 years old (even though I knew she was gone much sooner ) she immediately received early intervention and Speech. At age 3 she started in a Early Autism program in which consisted of 6 hour days Intense ABA 5 days a week. Speech was 1 time a month then. They were our Angels who pulled her back through the window..brought her back to us! Back then Nothing was done medically as I was told nothing was needed to be done. ( which we all know now as to be a huge fat lie)
Since age 5 She has been attending school "in district". Her placement is called a 8:2:1 "self-contained" class for IEP work and She also gets socialized counseling once a week with 3 other "typical" peers to help support social appropriateness. Also Speech 5 times a week and OT services to work on her handwriting and fine motor skills. She has an extended school year, AKA Summer program she attends as well. ADDED:This year (2013) she started her first year of Jr.High School. There program runs abit differently. It is still considered 8:1:2 , her class is the first to "start" this in her district. She focuses on academics like Math , English , Science and Social Studies the first part of the day/periods with her "Main" SPED teacher all to IEP levels of course. Then they have lunch , then return to the main teacher for a period of social skills and then prevocational skills. Then last few periods are for Reading, Gym and then Art or Music depends on the day (Alternating days). She receives Speech 5 times a week and OT 2 times a week.
UPDATE: As of December 12, 2014 I have pulled Sabrina out of public schools for Homeschooling.
The blogpost is now done so you can learn all about it and why we choose this route.
Sabrina has come SO far, she is a true fighter, a true WARRIOR and I am SO PROUD of her!!
She continues to amaze me!!
FAITH <3 HOPE <3 LOVE is what you NEED ,
LIVE <3 LAUGH <3 LOVE is how we live.
You will learn alot about Humanity and look at life in a different view ,
NEVER GIVE UP, Anything IS Possible !!
God never said he wouldn't give me more than I can handle,
he promised he would Always be there to Carry me Through ♥
<3 Though no one can go back and make a brand new start, anyone can start from now and make a brand new ending.**
I THANK YOU in advance for your Love, Support, Prayers , Well Wishes you may give.
Also any donations made is beyond appreciated! Its not expected nor needed to visit us, but if you do
I want you to know that it is definitely appreciated as 100% funds go directly into a account in Sabrina's name and is ONLY used for HER recovery needs. So Again Thank you!
God Bless you ALL!
~ Heather Mother Warrior Mommy of Sabrina
Autism Warrior Long Island N.Y. Facebook
Email: Autismwarriorliny@gmail.com
Twitter: @Autismwarriorny
AutismWarriorLINY: Youtube
Instagram : @Autismwarriorny
Public Advocate : The True Co$t of Vaccines: My interview
Autism Parents Answer Your Questions : Listen Here
Heather, Recovered her Autistic daughter from Vaccine injury: Listen Here
Silent Epidemic the Untold Story of Vaccines (2013) Documentary by Gary Null
Bought (2014) Documentary here
Trace Amounts (2015) Documentary here
Vaxxed (2016) Documentary here
22 Medical Studies showing Vaccines can cause Autism
83 cases of Autism Associated with Childhood Vaccines
81 Research papers Showing that Vaccines can cause Autism
124 Research papers showing the Vaccine Autism link
Medical Doctors who state Vaccines and/or can cause Autism
Dtap Vaccine packet insert , Page 11 , adverse reactions : Autism SIDS
Vaccine Adverse Reactions, Do you know what they ARE and What to look for?
RED Flags and Signs for Autism
NO shots, NO school ... NOT True! There are 3 types of Vaccine Exemptions
YOUR child, YOUR Choice! Educate before you Vaccinate!
List of Vaccine Ingredients a comprehensive guide
On November 7th, 2013, members of the vaccine injury community held a briefing for congressional staffers to present many of the problems in the Vaccine Injury Compensation Program in preparation for hearings in the House Oversight and Government Reform Committee. Professor Mary Holland, Head of Graduate Legal Studies at NYU, and Rolf Hazelhurst Father in one of the test cases In the Omnibus Autism Proceeding, and Assistant District Attorney General, State of Tennessee, present the case against the VICP and call for reform. It was during this briefing that a few things were exposed publicly.... One being that Vaccine DO cause Autism, the Government has KNOWN for decades and have purposely covered it up!
WATCH
before it all changed
2014
Thank you in advanced for any Love, Support, Prayers you may give and God Bless you ALL!
~ Heather Mother Warrior Mommy of Sabrina
I am NOT a doctor or a medical practitioner...
I am a MOM,
A MOM whos child regressed into Autism after her vaccines.
A MOM who has researched and studied all she can and continues to do in order to help her child.
A MOM who has finally found a good team of doctor /practitioners whom are helping with guidance
to further heal and recover my child.
A MOM who shares her own child's story and experience in HOPES of helping others.
This is for informational purposes only.
I WILL ALWAYS SAY AND ENCOURAGE TO PLEASE:
*Always Consult your OWN doctor, MAPS/DAN before making any decisions for treatments
when it comes to your own child. Even though our kids are effected in the same areas, because
each kid is different (Epigenetics), they are effected many different ways on many different levels. Its imperative to have proper testing done so you can then find the imbalances within your own
child. Then you and your doctor can then establish a proper individualized treatment plan.
Thank you! God Bless!
What can I do Before seeing a MAPS doctor?
TACA MAPS Doctor Scholarships
Apply for Generation Rescue Bio-medical rescue family Grant
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