Welcome!

Celebrating Abilities Inc. started as a support group located in southwest Florida for parents of children with different abilities. We are no longer active as a group because we've all moved on to other areas of the United States. I've decided to keep the blog active so that information can be shared with our loyal families and some new ones, too.

If you have any further questions, please contact:
hawkinsj68@gmail.com or ceenic123@aol.com


Have a blessed day!

Friday, November 5, 2010

My Holland





The following was yesterday’s post over at Hopeful Parents. I’m not quite ready yet to bid it adieu, so I’ve reprinted it here.

The Welcome to Holland essay seems to engender some strong reactions, to say the least. As I said in a comment on HP yesterday, “While the original essay rings true for me, I have to acknowledge that the beauty of this life doesn’t exist without pain. BUT, neither does the pain exist without some beauty.”

That’s MY Holland. What’s YOURS?



For my Italian friends … The following is based on the beautiful essay, Welcome to Holland, by Emily Perl Kingsley.

There are the days that I wouldn’t trade Holland for the world

The days that I stand in awe of the windmills’ quaint majesty

And marvel at the overwhelming beauty of the tulip fields

There are the days that I scoff at Italy

The days that I feel downright sorry for those who have never been to Holland

Never wondered at the beauty created by Rembrandt’s brush

What they are missing here, I tell myself

Poor souls!

How much richer they’d be for a visit someday

For a walk in these wooden shoes

**

And then there are the days that I look more closely at the Dutch landscape

The days that I see past the tulip fields to the mothers wringing their hands, waiting – always waiting

The days that I see the doctors – the specialists and therapists – everywhere it seems, filling the streets, doffing their caps as they move from one house to the next – an endless conveyor belt of service and need

There are the days that I see the siblings, struggling with dual citizenship in two dramatically different nations – neither of which they can fully claim as their own

There are the days that I can no longer smell the fragrance of the flowers for the stench of desperation and fear

The days that I send my girls off on the train, backpacks full with supplies for their daily trip to Italy

Knowing that only one of them speaks a word of Italian

Relying on a host of translators and guides to keep my youngest safe on such desperately foreign soil

There are the days that my heart simply breaks because I can’t make the whole world speak Dutch

There are the days that I watch the planes flying in – filled with mothers clutching their children, looking out the window, ready to point to the Spanish Steps and the Colosseum – knowing they’ll find out soon enough, that’s not where they are

There are the days when I wonder if my girl even notices the windmills, or the tulips – if she knows there are Rembrandts here

Or if she simply wishes that she were in Rome

**

There are the days that I see my Holland for what it really is

A breathtakingly beautiful place

A place full of love and compassion

Freedom and camaraderie

And a place where children hurt and mothers’ hearts ache with the impotence of not being able to make it better

Wednesday, October 27, 2010

Thursday, October 7, 2010

Temple Grandin

As a mom and an advocate for children with Autism, I have been vaguely familiar with Temple Grandin, her studies of animals and her diagnosis of Autism. I've read several of her books, seen interviews on tv and youtube and the HBO special about her life. I have always admired her strength and her mother's undying committment to her daughter.

Born at a time when parents were told to institutionalize their child who were "different", she battled many obstacles placed in her way not just because she was autistic, but because she was a woman, as well. Her mother and her aunt didn't allow her to have any limitations.

On October 3, 2010, at the Autism Speaks Walk Now for Autism on Long Island, I had the opportunity to meet her. I missed her speech but while regrouping after the walk, she literally walked right passed us and stood with the man next to our picnic area as he showed her some sensory friendly outdoor playground equipment. I walked over to take her picture and heard her speak to the people around her.
You could tell that she had a diagnosis of Autism. She seemed slightly uncomfortable to have so many people standing around her and she didn't want to look at anyone, but yet her mere presence was inspiring.

I went home and watched the HBO movie "Temple Grandin" again.  I paid more attention to the details I missed earlier and was moved to tears, having been able to associate the movie, the books, etc with a real person.

As the parent to a child with significant disabilities, I have found that not only does my child have limitations placed on him by society, but also by me.  I struggle with that everyday.  I want him to be all he can, yet I accept reality, there are some things that he can't do like the rest of us, but that doesn't mean he can't do at all.

"Different not less" ~ Temple Grandin


If you are the parent of a child with a disability, or more specifically, Autism........please check out the movie "Temple Grandin", now available for purchase and/or rental.  Trust me, you won't regret it.

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Wednesday, July 21, 2010

More parents report student restraints; Maine Dept. of Education downplays concerns | State

Restraints and seclusion (ie: ABUSE) of children with disabilities in the school system has become a national epidemic, one that no family can fight on their own..........please call your legislators and ask them to co-sponsor the bill.  Thank God for Chris Dodd for recognizing that  there IS a problem............

SCARBOROUGH — After a story detailing one family's experience with therapeutic restraint was published last week, many other parents came forward to share their experiences, while state agencies downplayed the problem.
Wayne Jackson said his family moved after his son was reportedly restrained improperly in 2008 at Whitefield Elementary School, which is now part of the Sheepscot Valley Regional School Unit 12.
Jackson said his then 8-year-old son, Brandon, who had been diagnosed with Attention Deficit Hyperactivity Disorder and early-onset bipolar disorder, was being disruptive in class when the principal allegedly grabbed him and restrained him in a prone position on the floor.
"Prone restraint was not even supposed to be used on Brandon. He has asthma, so they're not allowed to restrict his airway," Jackson said.
He said he had spoken to the school about the possible use of restraint to bring Brandon under control, but that he had asked to be called before any restraint was used.
"They didn't call until after the restraint. I was only three minutes away," he said.
Jackson said after the restraint, his son was transferred to Chelsea School, which is run by Spurwink.
"They were able to redirect him. They never used restraint," Jackson said.
However, the family is still concerned that there are no regulations in place to protect children in public schools. Jackson said he wants to see teachers receive proper training.
"If they're not trained, they definitely should not be restraining our children," he said.
The Forecaster received calls and e-mails from parents in Lewiston, South Portland, Cumberland, Scarborough, RSU 16 (Poland, Mechanic Falls, Minot) and Brunswick, as well as from parents as far away as Florida, all of whom had similar stories of restraints and seclusions used on their children – primarily, although not exclusively, boys between the ages of 5 and 18.
Some of the children were diagnosed with autism or emotional disorders, but others were not special education students. Some were held many times, some held in prone positions for more than an hour at a time.
"We're very concerned about this," Maine Department of Education spokesman David Connerty-Marin said Monday.
However, he said the DOE does not have plans to require schools to report this information because schools already have a lot of reporting requirements. He added that the department is not allowed to exceed federal reporting requirements.
"The authority to deal with complaints is primarily at the local level. When there's a serious violation, parents bring that forward," Connerty-Marin said.
Several southern Maine school departments do not compile or report restraint data and refused to release restraint documents after The Forecaster made a Freedom of Access Act request. The schools did agree to add up the number of restraints done in the past year, but some, including parents whose children were restrained, claim the data is drastically understated.
"If a school is not reporting it to you, they're not going to report to the state either," Connerty-Marin said.
When asked if the DOE is aware that none of the six schools in the initial FOAA request had updated their policies to reflect a DOE-requested prohibition of restraints that restrict a child's airway, Connerty-Marin said the agency would look into that.
The U.S. Senate has looked into this issue. Sen. Chris Dodd, D-Conn., earlier this year introduced a bill that would prevent harmful restrain and seclusion in schools. However, if a co-sponsor does not come forward, the legislation will likely die in committee.
Dodd's bill would require each school to report the number of seclusions and restraints each year to the public and to the Department of Education.
It would also prohibit schools from using restraints that restrict breathing, require staff to receive state-approved training, require parent notification of restraints, and require that a school notify the protection and advocacy system if a child is injured or killed as the result of a restraint.
The bill states that "seclusion and physical restraint are not therapeutic; and these practices are not effective means to calm or teach children and may have an opposite effect while simultaneously decreasing a child’s ability to learn."
The bill would also prohibit restraints unless they are included in a student's Individual Education Plan. That provision, however, is causing some debate.
Advocates for disability rights are trying to keep this prohibition in place, but lobbyists have been pushing to allow restraints in a student's IEP.
The Baizley family of Scarborough, whose son Brandon was subjected to more than 25 restraints, including prone restraints, said when they began working on Brandon's IEP, there were up to 12 school staff members present.
"Our repeated requests for no holds fell on deaf ears," Bob Baizley said.
Baizley said it was not until representatives from the Disability Rights Center attended the IEP meetings with them that the school responded to their concerns.
"We feel very strongly that the prohibition remain," Denise Marshall, executive director of the national Council of Parent Attorneys and Advocates, said of the Senate bill.
Marshall said to include restraint in a student's IEP would legitimize a dangerous practice.
"These techniques are not good for anything. They are not therapeutic," she said. "If a student needs restraint again and again, there is something wrong."
She also questioned the IEP process, explaining that parents cannot always express dissent.
"Too often parents are far outnumbered. The only way they can dissent is to go through due process," she said.
Phyllis Musumeci started Families Against Restraint and Seclusion four years ago after her autistic son was restrained 89 times in 14 months at a school in Florida.
"After that happened to my son, I said, 'you can't do that to children.' But what I found out was that, yes, they can," she said.
She said she receives letters from parents whose children were tied to chairs, locked in closets, and put in crates, all in the name of therapeutic restraint.
"There's no such thing as therapeutic restraint," she said. "If anything, it escalates behaviors."
Mary Robinson, who is also a parent of a special education student in Auburn, suggested parents form a support group.
"I've gotten a bunch of e-mails from other parents looking to get together," Robinson said. "I think a lot of parents are frustrated."
Emily Parkhurst can be reached at 781-3661 ext. 125 or eparkhurst@theforecaster.net

Tuesday, June 29, 2010

Last Day of ‘Rubber Rooms’ for Suspended Teachers - NYTimes.com

Hmmmmm........interesting! Not good enough for the teachers, WAY TOO MUCH EMBARRASSMENT and spending day after day in a windowless room would make them go MAD! Um, you think?!?!? Now how about what they are doing to kids with special needs who don't have the cognitive ability to process what your trying to "teach" them OR the ones that DO have the cognitive ability and DO go mad, start fighting back and they suspend or better yet, ARREST???




Last Day of ‘Rubber Rooms’ for Suspended Teachers - NYTimes.com

Monday, June 21, 2010

Don't Kid a Kidder

Just sharing something that may be of interest to some of you.............


Don't Kid a Kidder

One of my favorite episodes of the Rockford Files was when Jim Rockford (James Garner) told the con man, Angel Martin (Stuart Margolin), "Don't kid a kidder." I would venture to say the autism community would make the same response to Lori Unumb, senior policy advisor and counsel for Autism Speaks. Unumb, an attorney and law professor, recently scribed a disingenuous memo in defense of S.7000B/A10372A, the abominable autism bill opposed by many national and local autism groups. A recent Newsday editorial, which examined this matter, diplomatically, in detail, also opposed the bill. First of all, insurance company lobbyists contributed significant sums of monies to the Insurance Committee Chairs who tried to force feed this bill to our community. Additionally, Autism Speaks consulted with one of the largest insurance company lobbyists, Manatt, who helped write and advocate for this bill. So, please, don't kid a kidder.

However, I do not think the corporate friendly Autism Speaks, or Unumb, consulted with Rubenstein, the penultimate public relation firm that Autism Speaks paid at least $455,000.00 in 2008. It is never a good idea to chide fellow parents for being objective about the fears they have for their children's health. If anything, Ms. Unumb, who portends to be representing all of our children, should be more objective. If you are going to point out that you are an attorney and a law professor, defending our children, you have an obligation, like any attorney or professor, to give us the pros and cons of pending matters. But, Ms. Unumb only wants to tell us only what is good about S.7000B/A10372A. She only wants to tell us what she wants to tell us. And, unfortunately, she may not even give it to us straight. Please see the following comments Unumb made in an interview with CNN:

"...I've met so many other moms who were doing the best they could, and I just wanted to say to them, 'You know, an hour a week of speech therapy for your child is never going to make him better,' " the mother of three says..." "...But I didn't want to tell them what they needed is 40 hours a week of therapy, because there's nothing they can do to buy that..."

The advocates that oppose Unumb's NYS bill roll their eyes when they read the above. We look at these problems a different way. We tell the moms the truth and help them advocate for those hours. We give them the science to prove they need the hours. They do not have to buy those hours if we teach them how to fight for what is rightfully theirs. It is easy to say, "Hey, I have mine. I do not want to rock the boat or start a ruckus." Non-discriminatory health care is our children's right. We will not stand for a compromise that benefits corporations instead of our children.

As per the frustration with insurance companies in Unumb's native state of South Carolina, she got that right in the interview:

"It's not like you read your insurance policy and you can see a specific exclusion," Lorri Unumb says of the early days after Ryan's diagnosis. "We submitted bills, and we'd get denials back that said 'experimental... denied,' or 'provided by a non-licensed provider... denied.' Or sometimes the insurance companies would say 'this therapy is educational in nature, not medical... denied.'" 

Ms. Unumb wanted to stop this type of discrimination, right? She did moderately well with the wording in the South Carolina autism insurance bill. In a recent memo, she proudly states: "In 2005, while I was a law professor, I wrote legislation in South Carolina to require health insurance coverage for autism. The bill broadly required that:" A health insurance plan as defined in this section must provide coverage for the treatment of autism spectrum disorder. Coverage provided under this section is limited to treatment that is prescribed by the insured's treating medical doctor in accordance with a treatment plan.

But, it is just too gosh done bad for us Yankees up here in New York. We don't get the benefit of the above, broad language. We get a different type of wording. We get a type of wording and government regulation in our NY bill, never before seen for any illness or disability. The type of wording that would stimulate and exacerbate, for us, to the 10th power, the frustrations she quotes. We get to have therapies and treatments reviewed by a multi-agency committee that will evaluate the efficacy of those therapies and treatments under the broad guidelines of: "evidence-based, peer-reviewed and clinically proven." She did not write that into the South Carolina bill. Why is it written into ours? The bigger questions that are screaming out to all in society, especially the sick and disabled are: If you take the decision of what is necessary away from the treating doctors and place it in the hands of government regulators, where does it stop? Will there be a NYS multi-agency committee for Down Syndrome? For cancer treatments? For senior care?

Aside from being so cozy with corporations, there are other good reasons to question the sincerity of, and simply not believe Ms. Unumb and Autism Speaks. They continue to forcefully indicate that S.7000B/A10372A will cover such treatments as speech therapy and occupational therapy. And, a la Angel Martin, they say this with their best poker face. Shakespeare is quoted as saying, "What's past is prologue." Originally, Unumb, Autism Speaks (and the insurance companies) were lobbying for the American Pediatric Association guidelines to be used to determine what would and would not be covered in this bill, until such time that the multi-agency committee made those determinations. It would stand to reason, if you are an educated attorney/professor, that you would have read the guidelines you are endorsing. If Unumb were solely a passionate but uniformed advocate, she would get a pass on this. But, she is not. The intentional web of lies is coalesced. Please see analysis and some quotes from the guidelines below:

Apparently, routine screening for seizure activity is contraindicated. It appears that you should not check out a child for seizure activity via EEG until he/she has a full blown out seizure. Also, you should not do gastrointestinal work-up unless there is clear indication the child is having GI issues, which could include behavioral problems (not bad idea). Therapies such as ST, OT, SI seem to be recommended as educational treatments, not medical treatments (would be just fine with the insurance companies). APA not strong on their endorsement of these helpful therapies, even under educational.
Medical Treatments

Seizures - "...Whether subclinical seizures have adverse effects on language, cognition, and behavior is debated, and there is no evidence-based recommendation for the treatment of children with ASDs and epileptiform abnormalities on EEG, with or without regression. Universal screening of patients with ASDs by EEG in the absence of a clinical indication is not currently supported. However, because of the increased prevalence of seizures in this population, a high index of clinical suspicion should be maintained, and EEG should be considered when there are clinical spells that might represent seizures..."

Gastrointestinal - "...The existing literature does not support routine specialized gastroenterological testing for asymptomatic children with ASDs..."

Speech Therapy, Occupational Therapy, Sensory Integration Therapy and Social Skills - Therapy falls under Educational, NOT medical in AAP document. Nevertheless, AAP is not really endorsing any of these therapies:

Speech Therapy - "...However, traditional, low-intensity pull-out service delivery models often are ineffective, and speech-language pathologists are likely to be most effective when they train and work in close collaboration with teachers, support personnel, families, and the child's peers to promote functional communication in natural settings throughout the day..."

Occupational Therapy / Sensory Integration Therapy - "...However, research regarding the efficacy of occupational therapy in ASDs is lacking..." "...Unusual sensory responses are common in children with ASDs, but there is not good evidence that these symptoms differentiate ASDs from other developmental disorders, and the efficacy of SI therapy has not been demonstrated objectively..."

Can Ms. Unumb and Autism Speaks tell us that the agencies will not quote these guidelines to deny treatments for our children? Of course not! Can they tell us that the agencies will agree that insurance provide speech therapy and occupational therapy? They should not! Those questions take us back to A6888a, the autism health insurance bill our community really wants. 6888a is a decent, honorable bill. It will protect the health and civil rights of individuals affected by autism. Assembly bill A6888b, sponsored by Assemblyman Koon, lays out a very clear plan, in the bill itself, for covering reasonable therapies such as PT, Speech and OT. It provides, in writing, in the bill, for psychological care, psychiatric care, anesthesiological services (when ordered by a physician or dentist), and endocrinological care. It is a thoroughly comprehensive bill (broad in the right areas) that requires insurance to pay for treatments that are prescribed by doctors to: "...prevent the onset of an illness, condition, injury, disease or disability; reduce or ameliorate the physical, mental or developmental effects of an illness, condition, injury, disease or disability; or assist to achieve or maintain maximum functional activity in performing daily activities.." It is clearly laid out in writing. There is no wiggle room. There are no committees. It is not a compromise bill. It will end insurance discrimination. This bill was well on its way when Unumb and Autism Speaks came in to bail out the insurance companies, using broad language that would give them the ability to deny coverages.

It is unfortunate that we have to confront people and organizations who pretend they are doing the right thing for our children and really are not. They make misleading statements to our community to get a bill passed, any bill passed; even if the bill puts the needs of corporations ahead of our children. Our community is taking notice of that, more and more, every year. Many of us are silent because we are completely overwhelmed by autism and just don't have the time to get involved with these matters. We take it on a faith basis that everything is fine. That's exactly what insurance company lobbyists and some autism groups count on when they besmirch the truth. And there are some groups that have the wherewithal to understand these issues, yet remain silent. They remind me of my dog, when she sits up, salivating for a treat. The continuance of, or the prospect of a paid position with Autism Speaks, funding from Autism Speaks, corporate America, or NYS legislator-administered block grants, has them, willfully, tongue-tied. I wonder how these people, and they know who they are, can look at themselves in the mirror, or sleep at night.

Such a depressing state of affairs requires a semi-humorous ending. Another entertaining television show of yesteryear was Abbott and Costello. There was a great back and forth between Bud Abbott and Mike the Cop. Mike the Cop was agitated and was ready to arrest Abbott for something or other. Abbott asked Mike the Cop a series of questions. It was a logical progression of explaining to Mike the Cop that he was being paid by the police department to protect the citizens, which department used taxpayer dollars for his salary. Mike readily agreed that Abbott was a taxpayer and was, therefore, paying Mike the Cop's salary. Once this was established, the argument was over when Abbott yelled at Mike the Cop, "You're fired!" Right now, there are thousands of families in New York who would like to say that to Ms. Unumb, and of course, Autism Speaks.

Written by Chris Petrosino
Father of Chris, a 17 year old boy affected by autism

Thursday, May 27, 2010

Proposed Diagnostic Change Not Enough To Help Children Currently Diagnosed With Bipolar Disorder


 Proposed Diagnostic Change Not Enough To Help Children Currently Diagnosed With Bipolar DisorderMay 19, 2010  
(Garrison, NY) Shifting children from the controversial diagnosis of bipolar disorder to one that more accurately reflects their symptoms will not by itself decrease the rate of psychopharmacologic treatment and is not enough to help troubled children flourish, according to a commentary in the New England Journal of Medicine by researchers at The Hastings Center, a bioethics research institute, and a physician-researcher at Stony Brook University School of Medicine.

A new diagnostic category for troubled children called Temper Dysregulation Disorder with Dysphoria (TDD), which would to a considerable extent replace the diagnosis of bipolar disorder in children, is one of the most talked-about features of recently released draft revisions to the American Psychiatric Association's Diagnostic and Statistical Manual of Mental Disorders (DSM). The new diagnosis would focus on negative mood and temper outbursts as their own symptoms, rather than as indications of mania or other elevated mood symptoms associated with bipolar disorder.

The proposal of a new category suggests that the dramatic increase in the number of children diagnosed with bipolar disorder is not appropriate. But "will the TDD diagnosis promote the ultimate goal of psychiatric classification: helping troubled children to flourish?" ask Erik Parens, senior research scholar at The Hastings Center; Josephine Johnston, research scholar at The Hastings Center; and Gabrielle A. Carlson, Director of Child and Adolescent Psychiatry at Stony Brook University School of Medicine. The answer is no, "unless we get serious about reforming pediatric mental health care," the authors write in an essay, "Pediatric Mental Health Care Dysfunction Disorder?"

"No existing DSM diagnosis conveys the appropriate severity and complexity of these children's moods and behaviors; the 'bipolar disorder' label was meant to provide a home for children who were diagnostically homeless," according to the authors. "The dispute has been about whether bipolar disorder is the right diagnostic home."
 
To read more, please visit: http://www.physorg.com/news193493276.html

Disability Benefits Are Not Just For Grown-Ups

Disability Benefits Are Not Just For Grown-Ups  
By Elizabeth Wertime
 Social Security Public Affairs Specialist in Albany, NY

When you hear about disability benefits, you probably think about adults. But disability benefits are not just for grown-ups. In some cases, children can receive benefits too.

If your child who lives with you has a disability, and you also have limited income and resources, your child may be able to receive Supplemental Security Income (SSI) disability benefits. SSI is another program run by Social Security.  SSI is a needs-based program funded through general tax revenues.

To qualify for SSI, your child must meet the following requirements:
·       Under age 18
·       Not be working and earning more than $1,000 a month in 2010. (This earnings amount changes every year.) If he or she is working and earning that much money, we will determine that your child is not disabled.
·       Have a physical or mental condition (or a combination of conditions) those results in "marked and severe functional limitations." This means that the condition(s) must very seriously limit your child's activities.
·       Have a condition that has lasted, or is expected to last, at least 12 months, or is expected to result in death.
Once your child reaches age 18, SSI disability benefits might still be payable as an adult. Also, an adult who was disabled before reaching age 22 might be eligible for Social Security benefits as a "disabled adult child." For a disabled adult to become entitled to this "child" benefit, one of his or her parents:
·       Must be receiving Social Security retirement or disability benefits; or
·       Must be deceased and have worked long enough to be covered under Social Security. 
 

TRAINING FOR ADVOCATES


SOCIAL SERVICES PROGRAMS

SPRING 2010 SCHEDULE

 
FOUR MORNING SESSIONS 9:00AM - 12:00PM, COVERING PROGRAMS AND SERVICES AVAILABLE FROM THE SUFFOLK COUNTY DEPARTMENT OF SOCIAL SERVICES. PRE-REGISTRATION IS REQUIRED.
 
DAY ONE - TUESDAY, JUNE 15, 2010
MEDICAL ASSISTANCE
 
DAY TWO - WEDNESDAY, JUNE 16, 2010
TEMPORARY ASSISTANCE, FOOD STAMPS, DISABLED CLIENT ASSISTANCE PROGRAM,
CHILD CARE

DAY THREE - THURSDAY, JUNE 17, 2010

CHILD PROTECTIVE SERVICES/ADULT PROTECTIVE SERVICES

DAY FOUR - FRIDAY, JUNE 18, 2010

CHILD SUPPORT ENFORCEMENT BUREAU/HOUSING ASSISTANCE


For more information, please
 visit:http://suffolkcountyny.gov/departments/socialservices.aspx 
 

Saturday, May 22, 2010

11th Annual AHA Abby Irwin Family Picnic

This event is a "must attend" event..........I had the pleasure of getting to know Abby Irwin when I worked at EEDA.  She fought tirelessly to advocate for her son and many other children, all while fighting her own battle with cancer...........Please take time out of your day on 6/12 to support AHA and also to remember Abby, by attending this awesome event.


Thanks,
Jacqui



11th Annual AHA Abby Irwin Family Picnic

Date:

Saturday, June 12, 2010

Time:

11:00am - 4:00pm

Location:

West Hills Country Park, Group Picnic Area

City/Town:

Melville, NY

Please join us for our annual family picnic -- everyone, all ages, welcome.

To register, please visit: http://bit.ly/aAmQwB

Suggested Donations:
$10 p/p adults over 18
$ 8 p/p children under 18

Horseback riding provided by MY SHINE - $25 p/p ages 3 and up (up to 20 riders)

- Games
- Softball
- Free Pony Rides (12:00 noon to 1:00 pm)

- Hiking
- BBQ
- Volleyball
- Counselors for games, crafts, and more activities
- Sibling activities
- Water games
- Horseback riding (offered by MY SHINE, an equine program for individuals with special needs) for up to 20 riders, 3+ years old.
Cost: $25 per person.

Directions: Northern State Parkway to exit 40 (Rt 110) South. Make first right onto Old Country Rd. Make first right onto Sweet Hollow Rd. Go under parkway and straight ahead at the intersection. Picnic ground is on the right about a 1/4 mile past the intersection. Parking fee is $2.00 per car.

Patricia R. Schissel, LMSW
President, AHA
Asperger Syndrome and High Functioning Autism Association (AHA), Inc.
PO Box 916
Bethpage, NY 11714
P/F:888.918.9198
www.ahaNY.org
PatS@ahaNY.org

Monday, April 26, 2010

Moving!

Due to the extremely high unemployment rates in SWFL, my husband and I decided to move our family out of the area.  While I can no longer be available in person, for IEP assistance, I continue to be available via phone or email.  Please do not hesitate to contact me.