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Community Blog Review posts created by all bloggers in your community with tag adhd.
Here's an article with some really good summer camp options, including sleep away camps. Could be helpful

http://www.disabled-world.com/entertainment/camps/special-needs-camps.php


Special Needs Camps Serve as Important Complement to Home and School.

As an eight-year-old, Eric Biskin wasn't -- to put it mildly -- big into sports. "This is a kid who doesn't like to move," says Eric's father, Bruce Biskin. "He could focus on Nintendo for hours. What he doesn't do, to the extreme, is any kind of physical activity."

That's not particularly unusual for a kid like Eric, now 15, who has been diagnosed with ADHD and Asperger's syndrome. What's interesting is what happened next.

In previous summers, Eric's parents had sent him to day camps, but they weren't a good fit -- they were a little too heavy on the athletics for his personality; the pool was a little bit too cold. So one summer the Biskins decided to enroll Eric at Summit Camp in Wayne County, Penn. Summit is a summer sleepaway camp for kids aged 8-17 who have what the camp's director, Gene Bell, calls "attention issues" -- these, he says, include Attention Deficit Disorder (ADD and/or ADHD), Asperger's syndrome, awkward social skills, verbal or non-verbal learning disabilities, and mild emotional concerns.

A few weeks into the session, Biskin and his wife, Barbara Gronsky, visited Eric at camp and saw something they couldn't believe: "For the first time, he jumped into the lake and swam," Biskin recalls. "He couldn't wait to show us. It was like butter melting inside my heart. Back home we couldn't even get him in a pool."

At Summit, Biskin says, "Eric felt a sense of safety, a sense of fun. He got to try out stuff in a very encouraging environment that we could never get him to do at home."

The Biskins' story is affecting but not unique. Indeed, many families with kids who have attention issues or an Autism Spectrum Disorder (autism, Asperger's, Pervasive Developmental Disorder) have had similar experiences at special-needs camps, whose 24-hour-a-day, seven-days-a-week nature sometimes leads to breakthroughs that just aren't possible in school environments. "They do things (at camp) that typically our kids don't do during an academic year," Bell says.

The National Institutes of Health estimates that the number of school-aged children with ADD/ADHD is between 3-5 percent. A recent study by the Mayo Clinic suggests the number may be as high as 7.5 percent. According to the Centers for Disease Control, the diagnosis of ADHD increased an average of 3 percent annually between 1997 and 2006. Further, as of 2006, 4.5 million children aged 5-17 years had been diagnosed with ADHD.

Further, the CDC estimates that one out of every 110 children in the United States has an Autism Spectrum Disorder.

While homes and schools remain the primary centers for educating these children, experts say summer programs can serve as an important complement.

"ADHD is often misunderstood; subsequently many individuals diagnosed with ADHD are treated as if they are willfully refusing to engage in task completion, or are being 'just lazy,' unmotivated and even uncaring," says Michael Manos, who heads the Center for Pediatric Behavioral Health at Cleveland Clinic Children's Hospital. "This is usually not the case, for children with ADHD often are quite energetic and highly focused on restricted interests. This way of finding the defect in the child, that is, calling them 'lazy' often prevents children from truly being served."

He adds: "There are teaching and behavioral strategies that really work for children diagnosed with ADHD. Many times medicine and behavioral interventions are not applied in a systematic way; so many children do not receive optimal treatment and do not have the opportunity to truly change their circumstances."

This may be so, but there is disagreement among some educators and camp professionals over whether kids with attention issues (and other special needs) are better off in special camps or in traditional summer camps that, experts say, are increasingly able to accommodate many of them.

"The debate about mainstreaming is far and wide and very hot in the educational world right now," says Elana Naftalin-Kelman, who runs the Tikvah program at Camp Ramah in Ojai, Calif. As a special-needs camp housed within a mainstream Jewish camp, Tikvah represents a middle ground between the two approaches. And Naftalin-Kelman says even she sees "advantages and disadvantages to the type of program I run."

"The benefit of a special program is that you'll usually get staffing that better understands the needs of the child," says Gary Schulman, who runs New York's Resources for Children with Special Needs, a not-for-profit referral organization that for the last 25 years has run an annual special-needs camp fair. "The curriculum itself might be more tailored to these children's needs. Most children with disabilities, if they're in a special-needs program (in school) have what's called an Individualized Educational Program. Special-needs camps are more willing to look at that plan and are more willing to follow through on it. Consistency is extremely important -- it helps them when they get back to school. "

Still, says Naftalin-Kelman, special camps aren't right for every special-needs child. Tikvah, for example, cannot accept kids who have "severe behavior issues" such as harming themselves or others. But other children, she says, can grow immensely there. "I really believe that it's right for some kids and not right for some kids," she says. "It's based on the needs of each child."

Indeed, says child-adolescent psychiatrist Larry Silver, the decision about whether or not to send a child to a special-needs camp should be based on the specific child. "If they have ADHD and medication helps them control it, they could probably go to any camp that has the capacity to monitor medication," says Silver, a clinical professor of psychiatry at the Georgetown University Medical Center and author of The Misunderstood Child. "If they have ADHD and they're not taking medication" or they have problems with time management or social skills, then they might benefit more from special camps.

Many ADHD kids have been "excluded so much from social interactions at school that they don't really know how to be accepted," Silver says. Further, he adds, many of them have motor problems. "Typical camp is a lot of baseball, basketball, soccer," he says, "and they don't do very well with that."

Special camps, he says, might offer alternatives, such as swimming and hiking, and might also help campers begin building social skills. That's the case at Summit Camp, where Eric Biskin learned to swim. Among the camp's offerings is a travel program for kids aged 15-19. This summer, participants will travel from Vancouver to Halifax by plane and train. Later, the camp will offer a bus tour of Colonial America. Finally, there will be an ecology and nature tour of Costa Rica.

"Each camper is unique and has his or her own challenges that we work to overcome in order to meet the basic needs for acceptance, recognition and respect," says Bell, who has been involved full-time in Special Education since 1972 and with Summit Camp since 1999. "But throughout all of the various sessions and activities, certain goals are constant -- we look to establish and reinforce feelings of success, confidence, enthusiasm and self-worth in all of our campers. These are the traits that they may not attain in the normal social environments, and we can fill those voids."

Establishing those traits is done through traditional camping activities -- sports, arts and crafts, hiking, and other camp programs. Yet, each program is geared towards developing the social interaction skills of the camper and allowing them to identify their special interests. Summit Camp has 250 staff to supervise and nurture the maximum 300 campers it hosts at any given time. Bell says at an average age of 22, counselors are more mature than those at a typical camp. There is a group of staff members who act as guidance counselors. The admissions director is a clinical social worker. And while most mainstream camps have counselor-to-camper ratios ranging from 1:6 to 1:10, Summit camp and others like it boast a ratio of 1:2.

"Our camp is a therapeutic milieu," he says. "We have a caring and nurturing staff who are able to identify the challenges that our children have and are able to work with their abilities as opposed to their disabilities."

Many special-needs camps boast similar benefits for their campers, but the focus can shift from camp to camp. Some put the emphasis on improving academic performance; others, such as Camp Northwood in Remsen, NY, highlight social skills. The Talisman Programs in Zirconia, NC, promotes self-regulation and self-direction among its campers. Quest Camp in Alamo, Calif. offers a therapeutic intervention program. Whatever the focus, educators warn that quality can vary. They encourage parents to do their research before choosing a camp for their child.

"Like every other program, there's quality and there are some that are not so good," says Schulman, of Resources for Children with Special Needs. "It's up to the parent really to visit the program, maybe the summer before. Ask for a video. Call professionals like myself. Ask to speak to other parents."

Parents also can do a significant amount of research online. The Web site www.4-adhd.com lists summer camps for kids with ADHD, as does the American Camp Associations site, http://www.acacamps.org/, and www.MySummerCamps.com. Further information can be obtained from CHADD (Children and Adults with Attention-Deficit/Hyperactivity Disorder), www.chadd.org; the ADDA (Attention Deficit Disorder Association), www.add.org; the National Resource Center on AD/HD, www.help4adhd.org; and ADDitude Magazine, http://www.additudemag.com.

"Because your child has a label like ADHD or ADD doesn't mean your child must go to a special camp," Schulman says. He points out that under the Americans with Disabilities Act, special-needs children are entitled to be given reasonable accommodations in regular programs. Still, he says, special-needs camps are beneficial for "children with more severe behavioral problems who need a much higher staff-to-children ratio."

"If there's a behavioral crisis that takes place, they're less likely to just send the child home," he says.

After seven years at Summit Camp, Eric Biskin's parents think it's time for him to learn that "Summit is not the only place in the world." This summer, as last, he'll be spending half of his time in a more mainstream camp -- a situation his dad says was made possible by his years at camp.

"He's more confident in his social skills now," Biskin says. "He realizes that he can do things that he's afraid to do. Getting him over the fear so that he actually does them is still an issue -- but now when you tell him that if you give yourself the chance to learn something or do something then you can do it, he believes you. And he didn't believe that before."

Firstly a bit of a rant about peoples use of the word Retarded and also a video on youtube that pokes fun at Autistic People and yet still has not been taken down:

http://www.youtube.com/watch?v=N8kCMSOOkIQ

Discrimination and Race.  I believe we should be seen as a race and have as much protection as other minority groups.  Either at Work, School, College or even in everyday life:

http://www.youtube.com/watch?v=zsbr8cpnEdU

As and Relationships.  This was mainly a reply to a person that said he was finding it hard to find anyone to date due to having Aspergers:

http://www.youtube.com/watch?v=x3JUzIJPzSE

Aspergers Syndrome and what i was told that there is no place for it in Local Mental Health Services as it is not seen as severe as Autism or Depressive Illness:

http://www.youtube.com/watch?v=ZmiYZR-W__E

The worst of Genetics and how NTs are trying to get Women to abort Autistic Babies:

http://www.youtube.com/watch?v=nLYbgMWMBG8

Mrs Barker tape one.  She was sent by my Special School to assess if people could go to mainstream.  At the time this was very rare.  But she picked me out of a lot of other children at the School to assess my abilities:

http://www.youtube.com/watch?v=3Y_4Gga7i68


Mrs Barker was an inspiration to me and was the first person that actually saw that I was not like the others at the special school and gave me encouragement.  Here is tape 2 when I was only 8 and she was assessing me:

http://www.youtube.com/watch?v=uUwM5Cey0LM

My own opinion of Psychiatrists and how I have been treated by local mental health services:

http://www.youtube.com/watch?v=2TIOc0_CUss

Part 1 of my jobs till now the first 3 important jobs since leaving School

http://www.youtube.com/watch?v=OGJRVkfRkJc


Part 2 of the jobs I have had till now and how I was treated in the workplace:

http://www.youtube.com/watch?v=Rv7bO5EhzSA

My life till now positive view on Aspergers and coping in general:

http://www.youtube.com/watch?v=dSaZrcOkjVw

Aspergers Syndrome and Dating:

http://www.youtube.com/watch?v=bfoaqC4YCPg
http://www.youtube.com/watch?v=CQ176YYilqM
http://www.youtube.com/watch?v=BqxxZ-1sAjU
http://www.youtube.com/watch?v=AgdyM1ZFE8M
http://www.youtube.com/watch?v=E3RAhgInAnU
http://www.youtube.com/watch?v=Mo9SyXKJP6k
http://www.youtube.com/watch?v=aq-8X1Xjbfw
http://www.youtube.com/watch?v=2txxgI-2e9s
http://www.youtube.com/watch?v=C0k7Rg0gFSE

Body Language makes us easy targets for bullies:

http://www.youtube.com/watch?v=XzcWytjpW_g


Firstly my life till now that is in 3 parts and cronicles my life up till now living with Aspergers:

I'll get to my Canada trip to ANCA Consulting momentarily.  I first want to acknowledge that I've been absent but, for good reason.  I'm not much of a writer but, became one out of necessity.  I feel it's important to let people know when they have a misperception about something, especially when it concerns an entire group of people and their families.  In an effort to start changing the perception about who autistic people are and how their families brave stance to help and nurture them is important for the masses to know, I wrote a book about my own Aspie life.  I now understand that without my experience as a record producer, I wouldn't be getting as much attention with this as I have.  After several months of being interviewed or chosen to partner with other organizations to boost the level of attention given to the needs of the Autistic Community, I've learned a valuable lesson.  I actually really understood it about a week ago when I talked to my long-time buddy MC Hammer on the phone. 

 

I called Hammer to find out if he would be interested in directly working with me in a professional capacity to bring more attention to the needs of families coping with autism, autistic children & autistic adults.  He simply said, "No problem. I just want to make sure all parties understand that my time is valuable."  Hmm.  For the first time since I started writing music years ago, since starting the non-profit and writing the book, I realized that I had not properly accessed the value that I bring to the message I'm trying to get across to the general public.  EVERYONE that is doing even less than I am, has put a value on their ability to bring people together or share talking points on a talk show/news program.  What TOOK me so long?!  I finally woke up and realized that I could be funding this non-profit simply if I'd set a value to what I had to offer.  ANCA Consulting out of Canada helped me with this way of thinking as well.  Always looking out for my interests, they were concerned that I might be taken advantage of because of my good nature.  This they observed just by having me stay with them when I was visiting.

 

I'm currently working on a press kit that will be available to anyone who wants to book me on a radio show, talk show or news program to discuss my experiences and thoughts on helping families and their autistic children (as well as autistic adults).  It's become clear to me that my time is valuable, too. The very thing that makes folks interested in what I have to say, is the thing that will draw in a diverse audience willing to listen.  That thing... music.  However, the stresses and strains of giving attention to the book and the non-profit have taken me away from what makes me the person that everyone is excited about listening to.  It's time to point my attention back towards being the multi-platinum record producer that helped make MC Hammer $45million dollars plus.  It's time for me to turn those talents toward myself.  I will write and produce music for myself to share with the general public.  This is the value that I bring to getting the message out.  This is the "thing" that I had not placed a figure on.  I need to do this so that I can save my efforts of starting a non-profit solely designed to help those in need.  This will also boost the visibility of the partnerships that I've made with other organizations also geared to helping the Autistic Community.

 

I'm back!  I'm back and in a BIG way!  I'm no longer going to allow my time to be unimportant or without value.  If I am speaking to anyone, it is with the mind that I have to raise $4.5million for 30 families and if you are wasting time that I could be doing that, you are not interested in helping.  My time is valuable. My time is valuable. My time is valuable. I said that three times for effect.  If Hammers time is worth money, so is mine.  I'm 50% of what HE did.  He was the guy who performed the music.  I was the guy who wrote the music he performed to.  I'm just as valuable and I will not be wasting the time of these 30 families again.  My apologies to you all.  I know better now.

 

Peace & Love,

Michael Buckholtz

 

Blog on: Sunday, August 30, 2009 @ 16:56 EST

Its not very often that I have a  web link that is so important I feel it needs to be included in the title of a post! 

As you most likely know already, I believe that - I am committed to - an understanding of cause is extremely vital to the respond we give. In my daily work, I see families completely overwhelmed by a child with autism. The child has them spinning out of control, while he or she sinks deeper into a chaotic tangle of autism driven behaviors.

Handing parents a lens for understanding that behavior is communication, and an understanding of what a child is seeking or avoiding, the world suddenly makes sense, and a tremendous positive shift takes place.

The link between inutero lead exposure and various types of permanent brain damage has been well documented for many years. We wrote about it because the facts have gotten lost in our daily routines, conveniences and consumerism. Our parents made assumptions that lead was gone when leaded gas and paint was stopped, and my generation never got properly educated about it.

The problem is, lead carries forward its damage, and children being born today have a new susceptibility to lead's damage - ironically in a time when there is more lead than ever around us - but in less obvious places.

Enter mercury - and not just vaccines. I am talking about a myriad of surprising mercury sources - eye drops, hemorrhoid ointment, dental amalgam... the list is long and always unexpected. When mercury is paired with lead, the synergistic effect ( called potentiation) increases toxicity levels - and hence damage to humans- one hundred fold.

As authors of a book that set to explain all of this, we could not be happier about the student that was just released by the Amercian Association of Promotion of Research:

The Frequency of Polymorphisms affecting Lead and Mercury Toxicity among Children with AutismBiochemistry and Biotechnology


It has not been written for your average reader, but it is worth book marking, and having a look at. 

I personally believe that this moves us forward a giant step in ending autism, and understanding those who have autism now. Please share this article with people you know. 

Dr. Sandra Cottingham

LEAD BABIES

Breaking the cycle of learning disabilities, declining IQ, ADHD, behavior problems, and autism

Joanna Cerazy and Sandra Cottingham

www.nomoreleadbabies.com






When Shawn was 6 he was diagnosed with ADHD.  The first medicine we put him on caused SEVERE weight loss (13 pounds in 1 month).  So the doctor put him on a medicine to stimulate his appetite.  Well the 2nd medicine caused another side effect which called for a 3rd medication.  I finally said enough right there and pulled him off all his medicine.  He gained weight over the summer, and was fine.  Towards the end of last year (2nd grade) I felt it was okay to try the medicine again as long as it was a different one.  He has done fine on that since April of 2008 till about 2 months ago.  He started losing weight again.  Shawn stands 4' 4 and is only weighing in at 49 pounds.  Shawn has never been chunky or even 'normal' weight.  But he has never been sickly looking.  Till now.  When he takes his shirt off, you can plainly see EVERY SINGLE ONE of his ribs.  The doctor is saying that if he gets down to 45 pounds, then they will have to put a feeding tube in place. 
   As a parent, I am concerned.  I am also angry, and lost. I feel angry because I feel like whenever I try to help Shawn, then something like this happens.  I can't just sit back and do nothing.  And that is why I feel lost.  I no longer know what I think is 'best' for Shawn.  I find myself second-guessing every single decision I make for him or about him.  Thinking about the ADHD thing, I realize it has really shaken my belief in my own wisdom, in my own knowledge.  I am just plain confused.  I have conflicting thoughts on the medicine.  The main pro for him staying on it- he makes straight A's when he is on it.  The main con against it- his weight.  Looking at it in writing makes it look, well, so black and white. I see what I need to do now.  Now how do I go about explaining this to the school? 
Today I attended the best seminar to understanding many of my son's behaviors and why they happen as they do.The reason of the "fight,flight or freeze" behaviors/reflexes and stims.Why?- because it is what happens naturally inside HIS brain.If we don't relate to the outside surroundings with our own senses of cognitive,fine and large motor control,auditory,visual,language development,and concentration.He lacks the ability to react to any outside stimuli /response to  what his  brain doesn't know how to naturally break down. The work of years and years done by international leading brain researchers from all over the world.The seminar was titled the Missing Link.I prayed and gave my challenges to my Lord and He answered ALL of my prayers and showed me now how to go about changing my son's responses/reactions to these outside stimuli and how they weren't rhythmically in sync with the brain's reasoning to surroundings,reactions,body responses(vestibular and proprioceptive).He can't focus/concentrate for long periods of time because his body is not in sync to what he is experiencing and not understanding.These techniques can be learned and managed but have to go back to how we perceive stimuli from the infancy reflexes.When we can't center ourselves we will be limited in our abilities for anything academically based,emotionally based, physically,coordination and spatial awareness.Where a weakness exists the rest is also compromised.IT IS ALL SENSORY BASED FOR CHILDREN ON SPECTRUM.
Today I saw two boys both on spectrum speaking about themselves and how they now relate to our world.They have learned calming/coping strategies for doing school work,daily routines,have confidence and have learned control of their senses in order to do it.The fits and frustration are almost non existent because they have learned to do this for themselves with help of an excellent training by an international teacher/instructor.She gave them the connection of trust and input of knowledge to control their responses to the outside world.This program should be taught to every parent and educator dealing with children who lack these skills.This same thing has been done with individuals with cerebral palsy and learning deficits.This same program is used for everyone even Olympic athletes training.Pretty much almost ALL can benefit.
This seminar is nothing short of truly amazing!! Makes me wish i had more money to actually learn this entire course and go out and teach others of it's uses.The course i refer to is Brain Gym.It is taught internationally and is trademarked.Very very worth looking into and knowing.
*****(It does say that compensation does not support efficient use of the whole brain learning process or implement efficiency of the physical side of the learning process.Should not be used on Down's syndrome,Rheumatoid Arthritis and others with weak neck conditions!!)UNDER DOCTOR'S ADVICE AND RECOMMENDATION*****
We cope on a day to day basis; it's the way that works for us. We plan outings pretty carefully because almost anything can cause either a rage or a meltdown. When we go out, we bring timers, snacks for earned good behavior (as appropriate) and gameboys, puzzles and/or dvd players with movies for keeping everyone at a reasonable energy level.

Over the last three years specifically I've become more involved in creating a web resource for parents and family members of individuals (specifically children) with behavioral and mental health issues. I have created a website that I hope can be a resource for families to find local and online support, resources and access to accurate information on some of these disorders. That website is located at www.classifiedkids.org . I'm located in Bergen County, New Jersey, USA so most of the local support info is in that area, however I've tried to include where possible resources for national organizations so local chapters across the nation can be located where needed. I'm always looking for more resources, so anything anyone can point me to I'll be happy to check it out and add it to the appropriate page on the website.

All I can say is that we are all warriors. Advocates for our kids, for other family members, and for ourselves. We are the only ones who can fight for what is needed, because we are the ones that know best what those needs are.

We are the heros.

To the world you may be one person, but to one person you may be the world.


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