Various Twilight stars (including Robert Pattinson!) have shown their support for raising money for Autism research by signing an Exclusive Twilight Limited Edition Movie Masterpiece to be auctioned off at the Icare4Autism 2010: Cocktail Gala -
Twilight star, Rob Pattinson along with the rest of the cast of hit vampire movie flick Twilight are sinking their teeth into a new role. This role, however, is more sweet and savory.
Much to surprise of many, the Twilight team has created a special item that will be auctioned off at the Icare4autism 2010: Cocktail Gala. The money raised from the item will go to funding autism research and education conducted by the International Center for Autism Research and Education (Icare4autism).
What is the item?
The official item to be donated is an EXCLUSIVE Twilight Limited Edition Movie Masterpiece Collage. This fabulous item is made up of memorabilia that is out of production, collectible snippets and things unavailable to the general public.
About the Event
The Icare4autism 2010: Cocktail Gala, will be held on Thursday April 15th, from 6pm-10pm, at the Florida Aquarium; 777 Channelside Drive in Tampa, Florida. Tickets for the event go on sale on the afternoon of Tuesday, February 16th, 2010.
Absolutely amazing. And for those of you on here who know me well, you’ll know exactly what this has touched my heart. I’m totally emo right now.
I leave Tampa on April 12th 
I wish I would have known about this beforehand!
If you are interested in purchasing tickets you can do so here!
Official Eclipse Illustrated Companion
New Book by Stephenie Meyer
Buy New Moon on DVD!
Twilight Journals
New Moon "Team Jacob" Book Edition with Poster
New MoonMovie Edition Paperback
New Moon Soundtrack
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{ 53 comments… read them below or add one }
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That is so great of them!
That is a CHEATER 1st place! LMAO!
What happened to sleeping until noon? BTW there is a contest on Twitter. Please go enter for me! (I already did!)
Sweet! This is awesome! Even more reason to love Twilight!
I'm so proud of them using their star power to such good causes. Makes me proud.
awwww… that's sooo awesome of them! these are those moments that i feel proud to be a twihard!
at least i know im supporting the “good crowd”… ^_^
The twilight cast is awesome… They are always willing to help those in need and they don't do it to show off or anything… It's because they are big hearted, down to earth people. Not like other actors who lets fame go to their heads. I love you twilight cast!!!!
This is great!! Glad to see them doing something for such a great cause. As a mother of a child with Autism Spectrum Disorder I know just how important this is.
Don't call me a cheater here! People will think it's true! You of ALL people know I'm fair and mostly honest. Well, no one can tell the truth ALL OF THE TIME! lol
I didn't fall a sleep till after 3AM again but by some miracle I woke up at 9AM on my own. I'll talk to you on twitter about the contest.
I still love you B. *grumbles* Even though you called me a flipping cheater & I haven't even had my coffee yet. LIKE WHAT EVER!
You aren't the only mother here with a child classified with ASD or PDD.
I think a new support group should be created for the Mothers of Twilight. That would be nice.
How wonderful….very refreshing.
One more reason I love all things Twilight! This touches my heart cause my son has Autism and its personal.
Makes me soo happy! Love me some Twilight stars! *dreams of hugging them all*
I am so proud of them! what a great cause:)
There's a boy next to my place who suffers autism, caused by milk poisoning (yes people, milk can be poisonous if the formula isn't right, his babysitter says so herself).
It's great that our Twilight cast do some charity work once in a while. It warms my heart.
I think I'm gonna cry…
Thats sooo awesome!
we have the BEST cast ever!
STOP IT SNOWY! YOU'RE MAKING ME CRY!
I wish I could get this for you. You're money is better spent supporting your family.
I love you Snowy!!!!
This really warms my heart. Im so proud that the franchise and Stars have put this together.
It has now become a subject that is close to my heart.
My daughter is being put through tests next months to get a proper diagnoses. Her doctor has said she definitely has Autism but she needs to go to the specialists to determine what end of the spectrum she's on. I'll be the first to admit that I know nothing about Autism or how this will affect her life. All I know is that development for my daughter has been extremely slow. She doesn't doesn't show emotions very well, and gets frustrated a lot of the time. The first time she giggled was last week, two days before her 3rd birthday. You wouldn't believe how proud I was of her. But she hasn't giggled from it, but I have hope that within time things will improve.
Im just really happy that through the Twilight fandom they are helping to raise awareness and help uneducated people like me, who have to try and adjust and come to terms with something like this.
it's amazing to see that even on this site, Austism affects A LOT of people.
good on them for doing what they can to help such an a wonderful & heartbreaking cause.
I have a daughter with several disabilities but gratefully Autism is not one of them. so my heart goes out to families who deal with this stuff.
On a serious / spiritual side, it takes an amazing family to be blessed (I say blessed because I believe they are a blessing) with a child with a disability so to all of you who have been given one of them, I tip my hat to you.
the best of luck to your family & especially your daughter. I bet she is a beautiful amazing little thing. she will be in my prayers.
p.s. I love your Avi…HOT!!
ryedf
*hugs H2B tight* I love you, too, darlin'! *wipes away tears*
Girl .. we totally need to talk!!!!
That's awesome they're doing this. Autism affects too many families. I don't see this part of my family often, but some cousins of my dad's have a grown child who has autism and one who is maybe in his teens/early 20's by now.
There are great strides in helping children with autism come out of their shells. A few of the schools I've attended have integrated programs where children of different special needs are placed into the general student body. It does wonders for both groups. Teaches the special needs kids how to function in real life & teaches the “normal” people to look past ones limitations.
My high school was like the Fame school with an intense music/arts program. A few of the students in the music department with me were autistic. Some were brilliant instrumentalists! How their minds worked made their approach to music so different and their compositions were so complex and intriguing.
They also used music to help me overcome my learning disability. Snowy & I have talked about this in length. I have ADD, (I still do) which hindered my ability to read. I started the 6th grade at a 3rd grade reading level. When I graduated that year after a teacher seeing my struggles, she knew my love for music and combined the two. She taught me to sing out the spelling of words to remember my vocabulary lessons. She also had me sing what I read as a different part of my brain was used for reading and somehow, by a miracle, it worked! I now know that for me to concentrate, I must have music in the background.
To end this long reply, (sorry) I graduated the 6th grade with an 8th grade reading level and from that point on, I was placed in AP English classes up to the point of leaving college.
Please look into music therapy for your daughter. Music is the breath of life. It is for me, at least lol.
My daughter my diagnosed with Mild PDD at the age of 20 months. when she turned 5 they classified her as autism. from what i know they can t classify it as autism because the child is still developing until the age of 5. i already went throught that stage home services, preschool, now she is in 1st grade. what i can tell you is that she will make progress because they do make progress. how much progress is something no one can answer. very fustrating. But i thought my daughter would never talk and now she does but she still has a long way to go. sign language helped my daughter to start talking and it's great because it is a means of communication so they are less fustrated. i would like to tell you more but ill just end up maybe it a long comment. the good thing is that you are not alone in this and i know exactly what you re going through.:)
*hugs wifey* I didn't know that my snow princess.
As a sister of a 10 year old autistic boy, I know exactly what you mean when you say it hits close to home. My younger brother was diagnosed when he was five; he is the reason I am studying Pathology right now.
I can't express how much I love the cast for doing this. This means so much to so many people.
Wow. I appreciate the cast so much more for doing this.
We are all connected to autism one way or another, whether it's because a family member or a friend. I myself have a 10 year old brother and an 8 year old cousin who are both autistic.
We really need all the help we can get so this means a lot and really says something about them.
Yup. His parents just attributed it to stupidity and laziness. Nice, huh? And they wonder why we're not close… *growls fiercely*
SMH. Parents are the ones that are supposed to be the most supportive. That was a terrible move on their part.
I don't live in the USA but it makes me happy to see that things are made to help people with autism in other countries. My brother has autism and I know that sometimes it's really difficult. I admire my mother for being so patient. It's great that famous people talk about that because it's not always easy to understand what is autism. Thank you twilight actors
(Sorry for my english, I come from Belgium)
This touches me personally too and I appreciate the cast for contributing to this very worthy cause. My son, who is now 22 has Aspergers Syndrome. He didn't get diagnosed until his senior year in high school. Needless to say, he had a very lonely, at times brutal, (these kids are perfect targets for bullies) childhood. It was heartbreaking to witness these things and not really be able to help him. He was just “different” from other kids. There is much more awareness now for ASD's, than even a few years ago. My hope is that other children with Austism Spectrum Disorders get diagnosed earlier so they and their families can learn how to deal with it and not have to suffer the way we did. Feeling helpless, not knowing how to help your child when you know something is wrong, is the worst feeling there is. Thank you so much to the cast. Obviously, their involvement will draw attention and help this cause.
*sigh* trust me wifey, you have no idea… *hugs beloved tightly* I love you… even if you did help me create something… oddd… LMAO
Thank you for coming on here and sharing your story! Feel free to email me at LMCullen.LMHale@gmail.com
Thank you so much for taking the time to tell us about your brother.
*hugs*
Welcome! I agree, and can relate – Mr. Snowy is 38, and it's hard to hear him talk about his school years. He still has difficulties, but I'm a mama-bear about it…
my brother's autistic and it was harder when he was younger but he's at a great school now, this is such a lovely thing to do
*snickers* Ah yes. Our beautiful little angel Carlirlie. I just put him to sleep. Lmao
*smooches wife* Love you sweetheart.
aw, such a good mommy…
My son was diagnosed with autism when he was 32 months so they can diagnose it earlier than age 5- some doctors just dont like to. .::hugs::. to every one! this really touches my heart that they are doing this!
Hi everyone. I've never commented here before but have followed this site since April '09. I have a 14 year old son with Autism and other disabilities. This is really touching…not only to know what the Twilight cast is doing, but to know that I am not alone. Autism can be a very lonely disability for the one who suffers from it and for the entire family as well. Thank you all for sharing your stories.
This is incredible and I'm so happy that the cast is doing this for such a good cause…and I feel so happy because this hits close to my family….My 2yo brother has Spina Bifida and hes always taking therapy or other treatments for his development and well this money is always use for giving this children an opportunity to have a better future.this is such a good cause..I will love to bought it…but too bad that I'm not close!=S
Thank You, Twilight Cast! As a middle-aged mommy of a 6 year old son with pervasive development disorder (PDD-NOS), I am grateful to you for stepping up to the plate. We need you to help our cause and influence the teen population so that they will understand our children and open themselves up to friendships that may not be typical, but so worth their effort. I have sent emails, letters and tweets to Stephanie Meyer and the cast in hopes that someone would hear my plea. I am not that egotistical to think I had anything to do with your participation, but it warms my heart to know that somehow you found us.
If you read these comments, thank you. This is a great first step to helping the teen population gray the line between their differences and open their hearts and minds to new possibilities.
With the greatest appreciation and hugs,
Pam (mom of one of the most beautiful children I know).
Join me for my snipits of experiences at (http:/www.motheringautism.blogspot.com). I plan on posting this news to all.
this is great isnt it ? we do care and we do help! our passion for twilight will cause gr8 things ! i mean it already has but …ya know … LOLZ
aww poor snowy. i wanna cry now too. *HUGS TIGHTLY* i dont have an autistic relative but my uncle has down syndrome so i support autistic causes too. and my dad's family thought it was hereditary and that i would catch it. idiots. people should learn more about this. my uncle is a sweetheart and loves michael jackson. he knows the thriller dance moves lol!
*shakes head laughing* yup. hereditary… LOL
they still believed it despite my family telling them its not. they just didn't want my dad to have another child with another woman is all. psht.
There is more and more research that links many learning and developmental difficulties to poor communication and synchronisation between the two brain halves. An effective way of improving the processing functions in the brain is to listen to specially altered sound or music through headphones as pioneered by Dr. Alfred Tomatis (Tomatis method) and Dr. Guy Bérard (Auditory Integration Training – AIT).
Now there is a new Sound Therapy Programme which has been specifically developed with the aim to improve sensory processing, interhemispheric integration and cognitive functioning and it is entirely free to download and use at home. It has helped many children and adults with a wide range of learning and developmental difficulties, ranging from dyslexia, dyspraxia and attention deficit/hyperactivity disorder to sensory processing disorders and autism. It is not a cure or medical intervention, but a structured training programme that can help alleviate some of the debilitating effects that these conditions can have on speech and physical ability, daily behaviour, emotional well-being and educational or work performance.
Check out the Free Sound Therapy Home Programme from Sensory Activation Solutions. There is no catch, it's absolutely free and most importantly often effective. Find it at: http://www.uk.sascentre.com/uk_free.html.
My son is 10 years old and has Asperger's. He is an high functioning Asperger's child. He is in 4th grade and is in all regular classes. He was a handful growing up. There's really no way to describe my child…when I try to describe him to other people….I just end up saying…”He's Anthony.” He's smart, and extremely loving. He has lots of friends despite the fact that it is hard for him to make them because children don't understand him. He talks and talks A TON and sometimes says of the wall things. I think that's why some children don't understand him. He has to be taught Common Sense. When he was younger, he had to be taught people's expressions, how to take turns in a conversation and how to carry a conversation and not get off track. He is still working on how not to get off track in a conversation. I think that his brain is just going and going and when he should be paying attention…he's off thinking about something totally different. We will be forever working on the common sense thing. Oh yeah he also thinks very literal, and he doesn't understand sayings. Let's say his talking is driving me crazy and I say to him….”Anthony, if you don't stop talking i'm gonna kill you” When he was younger, he would've said something like, “Mom, you want to kill me?” I would laugh and say of course not Anthony…All i'm saying that you are talking too much and it's driving me bonkers. He's learning quite well. If we say something like that we just have to explain to him what we mean. He needs to learn in case someone else says that to him. Besides the little quirks, he's as normal as a 10 year old comes. It was hard when he was young, but we ended up moving to a city where they had a great small public school and the teachers were familiar with Asperger's and he got an IEP and all the help he needed. He has done nothing but get better and better every year. I think the hardest thing with him so far is discipling him. We have to change the punishment every time…it has to be different every time or else it won't work. For example, if he does something bad…i'll take away his t.v. privileges…then the next time it's his video games…next time he can't go play outside…get my drift. It's so hard coming up with things… Having a child with Asperger's is a full time job in itself. No one understands unless they actually have one themselves or spend a tremendous amount of time with one.
They are so sweet. Both my younger brothers have autism, and they are teased constantly at school because the way thay act or look. I think its sad that they look down on them. They are the two most brightest kids I have known my entire life. If you spend time with them you would think they were the sweetest rhing. I love my little brothers no matter how they act. They are human beings just like us so they do not deserve to be looked upon like outcasts.
Honestly, when I read about this for the first time, I wasn't sure whether to feel elated, excited, or just plain joyous; but I feel a combination of all three at the moment. For so long I struggled with Asperger's Syndrome with OCD tendencies and severe Anxiety Disorder, previously mis-diagnosed as ADHD (Attention Deficit Hyperactivity Disorder), and meandered among the Twilight fan sites for years, and finally the cast pays attention to autism!
To make a long story short, when I entered the world somehow I came out botched; not only due I have a huge, horrible scar on the side of my head to show for it, but also my mother theorizes that my very difficult birth caused enough damage to my brain to develop AS, OCD, and Anxiety, along with genetics. Born with a severe type of Anxiety – and possibly also AS – my father and I both get crippling panic attacks so severe sometimes I go into seizures, although now these hardly occur much anymore due to a diligent diet, drinking water 24/7, not drinking too much caffeine (or else that might send me into seizures), etc. Once, the first time I met Kellan Lutz (a.k.a. Emmett Cullen) at AccioCon, I literally almost went into a full-blown seizure right there due to my Anxiety disorder, and it didn't fare much better when I met a few of the other cast members. Due to my OCD tendencies and Anxiety Disorder, my psychiatrist and doctor both informed me that I cannot take medication for my AS, and because of this I visit a learning strategies professional to help keep focused and graduate high school.
For twelve years at school, needless to say, due to my Asperger's Syndrome and other tendencies, in addition to a mis-diagnosis of ADHD, I faced physical, verbal, and mental abuse time and time again. Due to my inability to react quickly to a situation and my poor social skills, I faced stoning with rocks and sticks, sometimes until I bled, from my classmates, and the only “friend” I managed to hold on to, another outcast with serious self-esteem issues of her own, also resorted to frequent physical and verbal abuse to prop up her own poor self-confidence. When I tried to fight back, they brutally teased and bullied me even more; when I told the school officials, they didn't believe me and branded me a “trouble maker”, and my peers also bullied me more. Eventually, I graduated, but when most of my former abusers also enrolled at the same high school, I became extremely isolated; no friends, no contact, no nothing, just floating through school trying to get through it and get out into college, where my former abusers could not follow.
Although the violence stopped four years ago, I still live in constant fear of making friends or reaching out to people, due to betrayals by even those closest to me in the past. However, recently this turned around, and slowly, step by step, I struggle hard to improve my social skills, and not to live in constant fear or depression due to years of others telling you, “you are worth nothing”. Although the same people who once abused me walk the same halls with me, the ghosts of the past still linger, irreparable damage done.
However, despite my Asperger's Syndrome, and all of the ordeals I went through in the past, I still possess an extraordinary level of intelligence, wisdom, insight, creativity, and depth; I easily top my AP English class, and my Science class, due to the nature of those with Asperger's to “interest” themselves in certain topics. Thankfully among them lies a particular, passionate love of Twilight, and due to my writing skills managed to earn the role of Jasper Hale on EquinoxRPG.com, where I work to volunteer 24/7 as an IFM moderator for the site, researching, developing, and writing Jasper's character to conform with Stephenie Meyer's and Jackson Rathbone's visions for his character. I also write the occasional Twilight fan fiction and visit Twilight fan conventions in Florida to show my support, while trying to respect and support the actors and actresses for all of their hard work and dedication.
…whew, that was long. But boy, words cannot describe how joyous I feel right now, that finally, that Twilight will help support research for those with autism and Asperger's Syndrome to raise awareness.
LOOKING FOR THE AUTISM HERO MOVIE PRODUCER
Famous Actor John Travolta lost his son to a seizure that may have contributed to autism without realizing that his son may have had Autism at the time of his son‘s death. Many Actors today have Autism Children, and most of them do not understanding how their children contracted the Autism, because Autism does not run in their immediate family.
I am a new author. Just a grandfather who wrote an incredible true story 64.000 words all true about how my grandson got Autism. After my long and exhausted research -now I am out to save millions of children who are born normal from contracting the Autism Disorder. I am out to stop what they did to my grandson that no other child should go through but unfortunately, this is happening everyday to thousands of children. I am looking for a movie producer to make this movie on what happen to my grandbaby and the sad events that we went through to save Christopher’s life, and to save the millions of children of tomorrow who are born normal to Autism. I have no-money to self publish and many publishers and agents won’t deal with a new author – a catch 22 that it has exhausted me, so now I’m forced to look for a movie producer with this shocking true story.
I know this is not the way to do this without an agent, but I cannot afford to do everything through protocol. I just have to take my chances against this cruel and greedy society looking for Mr. Autism Hero that can make this happen. It is known that a child can be born with Autism at birth because of the genes. A disease growing in unstoppable numbers both at birth and in years later after birth. It is also a well known fact that out of 1 in 90 children that are diagnose today with Autism Disorder a great majority is diagnose with this disease years after a normal birth, making it a puzzling effect on a great many families.
The mega population of Autism children that are born normal – parents find out years later when the child hits 3 to 5 years old that their children are diagnose with Autism. Fact is, for some families their child should have never been diagnosed with Autism. My findings and research took some years to authenticate. It seems that a great many families are being fed the recipe for their child to be infected in a timely manner for the Autism to take affect. This recipe is like baking a cake after a certain amount of time in the oven, the cake is baked and cooked. Same goes here for the child – after a certain amount of time adding to the deadline of no return the child starts to have developmental delays on most of his functioning mentally at 3 to 5 years of age. In Christopher I was ordered to feed this recipe to him in a nine month period which was to short to soon that he almost died. Whether this is intentional or not we would never know, what we do know is that greed and profits exist in this country. Unbelievably – this is the truth and the proof is with my grandson and my research. For a great many families their children are fed the recipe for their child to be infected in a timely manner for Autism Disorder to take affect. In the pass 3 years alone Autism has increases unbelievably. In 2007 1 in 166 children were diagnose with Autism. In 2008, 1 in 150 children being diagnose. In 2009, 1 in 130 and today 2010 the numbers now read 1 in 90 children being diagnosed with Autism. You will find that these numbers vary with different researches, but it does not change the production of Autism as we are witnessing today. In 1970, the numbers were 1 in 10.000.
In the mid 1970’s the numbers fell to 1 in 2.500 children being diagnose with Autism. Fact is – if you knew the true story as to why a child who is born normal then later at the age of 4 years old that child is infected permanently with Autism Disorder, you would be writing letters to your congressman’s and to lawmakers and the President. You would not be to kind to our government after knowing the truth that our government has been allowing doctors to do something to harm our children of America for 30 years infecting our children to reach this diagnose of Autism today. The $64.000.00 Question Is – “Why? Why would our Government allow this to happen to our children for 30 years? I can say this – that when it comes to stocks no one cares about the outcome that makes them wealthier than yesterday, no one will stand in their way. They could care less about complaints or outcome of any child dead or alive, as I have researched first hand on the many children who have died from these experiments, that if the child does not die he will defiantly become developmental delay -”Autism.” This is a Fact!
The government refuses to do anything about the leading source that is infecting our children with Autism until this day. Thirty years ago, they refuse to contact the source to look at the complaints of parents that their children are turning Autism due to this
Problem. Now, look at today 2010 with this mega population of Autism. If our government would have done something about the source causing the Autism Affect on our children back in the 1980’s today my grandbaby would not have Autism Disorder today, and we would not be seeing this mega population of Autism children today 30 years later. Vaccines are not and never have been the problem. They saw a window of opportunity to cover-up the truth that was coming out in the 80’s, to protect their new stock venture by parents following they believed. With that in mind, the medical community and suppliers threw out other excuses to pediatricians and doctors to build up ignorance and confusion. But 30 years ago a majority of parents from all over this country stood their ground on what was coursing their children’s Autism, they did not believe it was vaccines although you had a few who were filled with ignorance.
My research is full proof because Christopher is alive to show it, and the world must know what happen to Christopher and the bloody horrible tragic events that took place throughout the course of this incredible story. The medical community says Environmental or Genetics have been causing the Autism Production Problem we see today on children who are born normal to Autism, but this is a lie. Until this day, a great majority of parents will dispute that. As far as genetically inheriting the Autism disease being born with it, I fully agree to that assessment, but after my study’s I came to realize that the amount of children who fall in this category “Genetics” are not quite as many as they claim it to be for the children born normal to Autism. These two terms – Genetic and Environmental was created for one purpose only – To satisfy the parents Questions and Concerns since the 1980’s when the truth broke out, it was their way to redirect the parents. As far as “Environmental”, this is an assumption created for doctors to add it to Autism questions and concerns from parents. It is very easy to point out that you can catch something or a disease by touching something contaminated, and this is why doctors will throw in the Environmental Solution to all parents just to shut them up. It is all about money and over powering anyone who stands in their way by using these logical excuses. They will keep infecting as many children as they can with the Autism Affect destroying our children of our future. What I am saying may sound unbelievable but is all-true, and again – I can prove it! My story is filled with true facts that if and when I publish this incredible true story to the media, I would have to move out of this county and state for the security of my family. The Autism production of our children here in America can be stopped, and it will if the people and the viewers learn the truth on what happen to my grandson. We the people in this country have lived on lies long enough in just about everything that comes from the government, I think is time for them to realize that our children in this country are more important than pharmaceutical companies and the lobbyist they hold in their purse. How much more money is enough?
How much more Autism children do they need? Aren’t 1 in 90 children being diagnose with Autism today enough? Next year we will witness 1 in 50 children. If it were not for the almost dying experience that my grandson went through, I would have never found out the truth about why we have millions of children being diagnose with Autism today after being born normal. Adding my research with what happen to my grandbaby I say there is no doubt that we have so many children on Autism because of money, profit, gain, and control. This is a very serious problem that must be faced. Again, I am speaking about the children who are born normal then later when they reach the age of 3 to 5 years of age they are diagnose to Autism without families having a genetic history to the problem, and little do many families know this disease is being created deliberately.
What I need is for a Movie Producer my story and put it on the big screen. This is the story that thousands maybe millions of people have been waiting for, for over 30 years. What I’m asking for, is for God to send me a caring and giving producer to give me and my grandbaby this dream come true – to save as many children from Autism due to this 30 year crime-spree that has been infecting and in many cases killing our children – because is all true! If you cannot help me, please help me with a donation to publish my book – 3625 Grand Prix Drive Sebring Florida 33872-2954. Your donations will be paid back with the proceeds on what my book will make, because I am sure it will sell thousands of books. The Bible says – “Ask and you will receive”, so I’m asking you to please make this worth-while donation to my address above. God will bless you for it. God Bless You.
GOD BLESS OUR CHILDREN. GOD GRANT ME THE POWER TO HELP CHANGE WHAT HAS BEEN DONE TO HURT OUR CHILDREN FOR 30 YEARS THROUGH A MOVIE PRODUCER IN MAKING THIS MOVIE COME TRUE, OR HELP ME WITH A DONATION TO PUBLISH MY BOOK. AMEN!
Ralph Colon – RC GRANDPA autismhero54@yahoo.com 863-385-2030