About Us

Learn More about our non profit charity car club.

Watch Our Story

Learn more about the families we've helped by watching these videos.

Cruisers in the News

Stay up to date on all the Neighborhood Cruisers News and Show Dates.

Support Our Sponsors

We can’t do what we do alone, and that’s why we’re grateful to receive support from local businesses throughout the county.

Cruisin for Kids Annual Car Show

Learn More About Our Cruisin for Kids Car Show!

Tuesday, August 22, 2017

Cruisin for Kids 2017: Marcos Molina Mazariego

2017 Recipient: Marcos Molina Mazariego.

Marcos is 2 years old and from Stony Point. He has an undiagnosed condition that is possibly genetic but the family is unable to afford testing. 


His global developmental delay includes an inability to sit, crawl or bear weight on his lower extremities. When he is supported, he can lift his arms and reach for a toy. His body can move through a range of motions, but his joints resist the movement. 

He cannot maintain eye contact or eat independently. He needs to be held in a stable position. 


As of a couple of months ago, he is receiving some physical therapy at home. 

As you can imagine, his parents and siblings are heartbroken. 

He needs so much help and they know so much is wrong, but the testing costs are astronomical.

That’s why this year we are Cruisin’ for Marcos. 

Come out to Bowline Park in Haverstraw, NY on Sunday, October 1 to help support Marcos and his family.

(Rain date is October 8).

Monday, August 21, 2017

Cruisin for Kids 2017: Car Registration Form

Click here to download a copy of the 2017 Cruisin for Kids Car Registration Form.


Cruisin for Kids 2017



Come join the Neighborhood Cruisers for their annual Benefit Car Show/ Family Fun day! 

Cruisin for Kids 2017 will take place on Sunday, October 1 (8am - 3pm) at Bowline Park in Haverstraw, NY.

For more information, visit our event page on Facebook.

This year's show is to raise money for Marcos Molina Mazariego. He is a 2 year old from Stony Point and has an undiagnosed condition, and his family cannot afford testing.

Thursday, September 1, 2016

Local Band "THE REMEDY" to Play at Cruisin for Kids 2016

Local members of the band "THE REMEDY" will be headlining at this year's Cruisin' for Kids Charity Car show!

THE REMEDY delivers classic rock favorites that range from Santana, Dire Straits, Steely Dan and The Allman Brothers, to danceable classic Motown hits.

THE REMEDY began in mid 2005, playing clubs throughout Rockland and North Jersey, building a solid fan base. 

The original guitar duo, Steve Buckley & Adam Slayton, regrouped in 2012 with an all new lineup of stellar musicians: Billy Paschall on drums, Steven Chichetti on keys, vocals and harp, and David Wasserman on bass and vocals - all of whom have been playing a variety of styles and musical genres for decades.




For more information on the band, visit their Facebook Page.


Cruisin for Kids 2016


The proceeds from this year's Cruisin for Kids will go to support Aiyanna Faria, a 14 year old from West Haverstraw, NY.


Aiyanna was diagnosed in 2009 with Davidoff Dyke Mason Syndrome.

Davidoff Dyke Mason Syndrome refers to atrophy or hypoplasia of one cerebral hemisphere (hemi atrophy) which is usually due to the developing brain in fetal or early childhood period. 

The clinical features are variable and depend to the extent of the brain injury. More commonly they are present with recurrent seizures, facial asymmetry, learning disability and speech and language disorders. 

Due to insurance we had to change doctors. We have tried every seizure medicines with no long standing results. She is currently having 10 -15 seizures a day and recently they have been more grand mal along with dizziness, migraines and vomiting. 

She has had several tests done and has no brain function on the left side of her brain. Her right side was fully functional and now since it has been so long that the right side is starting to be damaged, resulting in memory loss. 

She has had a number of surgeries recently to try to help but it is unknown what relief it will bring. 

Aiyanna is fun loving and despite these challenges has maintained a positive attitude. She is a go getter and will almost do anything just to be a normal 14 year old. 
Although we are realistic to the fact that there is no cure, we just need to give her as much time as possible. 

We want her to do as much as she can with little effects from her treatment and disease as possible. She deserves to be able to live her life as normal as possible. Thank you for your support. 


Click here to download a copy of the 2016 Cruisin for Kids Information Flyer.

Click here to download the 2016 Cruising for Kids Charity Car Show Registration form.

Friday, July 1, 2016

Cruisin for Kids 2016: Aiyanna Faria


Aiyanna Faria is a 14 year old. West Haverstraw, NY Daughter of Sabrina Figueroa.
Aiyanna was diagnosed in 2009 with Davidoff Dyke Mason Syndrome.

 Davidoff Dyke Mason Syndrome refers to atrophy or hypoplasia of one cerebral hemisphere (hemi atrophy) which is usually due to the developing brain in fetal or early childhood period. 

The clinical features are variable and depend to the extent of the brain injury. More commonly they are present with recurrent seizures, facial asymmetry, learning disability and speech and language disorders. 

Due to insurance we had to change doctors. We have tried every seizure medicines with no long standing results. She is currently having 10 -15 seizures a day and recently they have been more grand mal along with dizziness, migraines and vomiting. 

She has had several tests done and has no brain function on the left side of her brain. Her right side was fully functional and now since it has been so long that the right side is starting to be damaged, resulting in memory loss. 

She has had a number of surgeries recently to try to help but it is unknown what relief it will bring.

Aiyanna is fun loving and despite these challenges has maintained a positive attitude. She is a go getter and will almost do anything just to be a normal 14 year old.
Although we are realistic to the fact that there is no cure, we just need to give her as much time as possible. 

We want her to do as much as she can with little effects from her treatment and disease as possible. She deserves to be able to live her life as normal as possible. Thank you for your support. 




Click here to download a copy of the 2016 Cruisin for Kids Information Flyer.

Click here to download the 2016 Cruising for Kids Charity Car Show Registration form.

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