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Re: AS Video

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Thank you for a great job in the video and for speaking up for our kids.

No one can possibly be offended by your fight to get your kid better

through biomedical intervention and your willingness to speak up about

it on camera.

Thank you.

Bob Krakow

On May 17, 2006, at 5:59 PM, annemacfarland wrote:

> I am a mother in the video. I did talk- at length- about the vaccines

> and my son's horrible regression. I did speak about the belief I have

> that he will recover. I did not edit the video or have any final say

> in the content. I hope a longer version will be available. I want to

> thank all the people for there kind words of support. The last thing I

> want is pity but Michele I. is correct when she says that it is the in-

> fighting and judgment of others within this community that needs to be

> pitied. That is exactly what our detractors want. If I have learned

> anything through this nightmare it is to have more humility and to be

> less judgmental. We work tirelessely with bio-meds to get my son

> better- but we have a long way to go. That is the reality right now

> and if that offends someone I am not sorry.

>

>

>

>

>

>

>

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Hi Anne,

Do not think for one minute that you are not a hero for your advocacy

for your child, as are all parents who give all they can to heal their

injured children. Many, many parents simply give up and leave their

children with the State who then parks them in foster " homes " . These

poor children have both their humanity crippled and they also lose

their family.

Please accept my deep gratitude for showing the world how much love a

mom, a parent like you, has for their child so that we may all be

so inspired and reinforced by your example.

Can you tell us which mom you are in the film? Are you s mom?

Hanson's? Are you the mom with the girl? Also, which one is Michele?

With all my love,

Lenny

>

> I am a mother in the video. I did talk- at length- about the vaccines

> and my son's horrible regression. I did speak about the belief I have

> that he will recover. I did not edit the video or have any final say

> in the content. I hope a longer version will be available. I want to

> thank all the people for there kind words of support. The last thing I

> want is pity but Michele I. is correct when she says that it is the in-

> fighting and judgment of others within this community that needs to be

> pitied. That is exactly what our detractors want. If I have learned

> anything through this nightmare it is to have more humility and to be

> less judgmental. We work tirelessely with bio-meds to get my son

> better- but we have a long way to go. That is the reality right now

> and if that offends someone I am not sorry.

>

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I second this. The message is there and you felt you were right in

doing what you did. That is what is most important. We've done this

also, folks have been critical of us, but too we do need to be one

community. It's not going to assist when we don't realize that yes

this is the way of life for many of us.

Thank you for putting yourself in this place and allowing your story

to be shared, many folks will be using this video for awareness, not

for folks to give funding. That in itself is something to be proud

of. It's powerful and folks do need to see something like this to

know that there are many families in these positions.

Thank-you and prayers for you and your family and your son's progress.

Carolyn

>

> > I am a mother in the video. I did talk- at length- about the

vaccines

> > and my son's horrible regression. I did speak about the belief I

have

> > that he will recover. I did not edit the video or have any final

say

> > in the content. I hope a longer version will be available. I want

to

> > thank all the people for there kind words of support. The last

thing I

> > want is pity but Michele I. is correct when she says that it is

the in-

> > fighting and judgment of others within this community that needs

to be

> > pitied. That is exactly what our detractors want. If I have

learned

> > anything through this nightmare it is to have more humility and

to be

> > less judgmental. We work tirelessely with bio-meds to get my son

> > better- but we have a long way to go. That is the reality right

now

> > and if that offends someone I am not sorry.

> >

> >

> >

> >

> >

> >

> >

> >

> >

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I sincerley give all of you who participated in the video my deepest

gratitude. It is not easy to show everyone what goes on everyday in

our worlds.

If people get offended that is a burden that they carry not parents

like you. I agree with Lenny about foster " homes " . You love and care

for your child(ren) and have not given up. Some people do not have the

courage to put themselves out there for the world to see. You did :)

Only problem is that there are people out there that will judge what

they see based on their experience and may not agree.

Blessings from our family to yours,

Cheri

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AMEN

The majority of the community THANKS you. This film will change lives.

People will finally....understand what autism is.

Ann

>

> > I am a mother in the video. I did talk- at length- about the

vaccines

> > and my son's horrible regression. I did speak about the belief I

have

> > that he will recover. I did not edit the video or have any final

say

> > in the content. I hope a longer version will be available. I want

to

> > thank all the people for there kind words of support. The last

thing I

> > want is pity but Michele I. is correct when she says that it is

the in-

> > fighting and judgment of others within this community that needs

to be

> > pitied. That is exactly what our detractors want. If I have

learned

> > anything through this nightmare it is to have more humility and

to be

> > less judgmental. We work tirelessely with bio-meds to get my son

> > better- but we have a long way to go. That is the reality right

now

> > and if that offends someone I am not sorry.

> >

> >

> >

> >

> >

> >

> >

> >

> >

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Thanks so much for your participation and your comments here. I feel

the same way!

Never give up!

>

> I am a mother in the video. I did talk- at length- about the vaccines

> and my son's horrible regression. I did speak about the belief I have

> that he will recover. I did not edit the video or have any final say

> in the content. I hope a longer version will be available. I want to

> thank all the people for there kind words of support. The last thing I

> want is pity but Michele I. is correct when she says that it is the in-

> fighting and judgment of others within this community that needs to be

> pitied. That is exactly what our detractors want. If I have learned

> anything through this nightmare it is to have more humility and to be

> less judgmental. We work tirelessely with bio-meds to get my son

> better- but we have a long way to go. That is the reality right now

> and if that offends someone I am not sorry.

>

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I totally agree with Ann...People will finally understand what autism

is thanks to this film. Most people out there still have no idea what

autism is. Those who are affected by it certainly know and they well

understand there is a spectrum and a broad range from those mildly

affected by the condition to those who are severely affected.

But the parents and families of the 165 of 166 children without autism

have little to no clue what it is.

I am a case in point albeit from some time ago. The first time I

heard the word autism was in 1988. My friend from college, a

psychology major, was working at a summer camp for autistic kids and I

went to visit her at the camp.

I had no idea what autism was. I figured it must be something akin to

depression or bad behavioral problems or some other temporary

behavioral condition because my friend, the psychology major, was

working there trying to help make things better. Plus when I got to

the camp these kids looked totally normal - they were in the 13-15 age

group.

Looking to connect and reach out to an autistic boy while I was there,

I had an unforgetable AWAKENING to what autism is. A 14ish boy had

his sony walkman on and I was walking beside him. I asked him, " what

are you listening to? " I was expecting him to say REM or Guns & Roses

or Bon Jovi or the like, and instead his response blew me away. He

put his face 3 inches from mine and yelled at the top of his

lungs, " THE RADIO!!! " I was scared by this even though he did not

appear to be violent in anyway. It just hit me really hard that

autism is different and it is NOT akin to depression or anything like

it. A neurological condition it is indeed.

Now, when I read in the paper that social skills are impaired, I know

what that means - I have seen varying degrees of it in this young man

and in others I know with autism today.

I believe the Autism Everyday video has the potential to awaken many

people to Autism and what it really is. Once human consciousness is

there then the reality and the impact of 1-in-166 will sound more

alarms and cause more to question Why is this epidemic happening?

Thanks for a great video!

>

> AMEN

> The majority of the community THANKS you. This film will change

lives.

> People will finally....understand what autism is.

> Ann

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> Thank you for putting yourself in this place and allowing your story

> to be shared, many folks will be using this video for awareness, not

> for folks to give funding. That in itself is something to be proud

> of. It's powerful and folks do need to see something like this to

> know that there are many families in these positions.

Yes! The film is wonderful, and I thought all of the mothers were

inspiring, courageous, and tough.

People are complaining because the 13 minutes didn't accomplish

*everything -- but I think it was a brilliant first step. Let people

see what life with autism is, *then we can show them how it happened

and what to do about it. My son lost his dx thanks to biomed, so

absolutely I hope those films get made too, but I don't see that being

in the scope of this one.

Thank you to the mothers and the filmmakers. I'm sending the link all

over...

Nell

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Anne,

Thank you for participating in this video.

This video will raise much Awareness.

Pamela

" Courage is doing

what you're afraid to do. There can be no courage unless you're scared. "

Eddie Rickenbacker,

top US

fighter ace, WWI

From:

EOHarm [mailto:EOHarm ] On Behalf Of annemacfarland

Sent: Wednesday, May 17, 2006 6:00

PM

EOHarm

Subject: AS Video

I am a mother in the

video. I did talk- at length- about the vaccines

and my son's horrible regression. I did speak about the belief I have

that he will recover. I did not edit the video or have any final say

in the content. I hope a longer version will be available. I want to

thank all the people for there kind words of support. The last thing I

want is pity but Michele I. is correct when she says that it is the in-

fighting and judgment of others within this community that needs to be

pitied. That is exactly what our detractors want. If I have learned

anything through this nightmare it is to have more humility and to be

less judgmental. We work tirelessely with bio-meds to get my son

better- but we have a long way to go. That is the reality right now

and if that offends someone I am not sorry.

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>

> I am a mother in the video. I did talk- at length- about the

vaccines

> and my son's horrible regression. I did speak about the belief I

have

> that he will recover.

I am extremely proud of you moms and the fine job you did. The candy

coating of autism has gone on far too long in the national media.

Thank you all!

Charlie

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