Welcome to One Small Step for Parents! Our goal is to help you find the right resources, support and information that is needed to make informed choices. Without the proper tools we, as parents and adults, don't know what will help our situation or what works and doesn't work. Here at One Small Step, we have done our best to take the guesswork and confusion out of the equation by supplying tools, resources and online support.
Showing posts with label Asperger's. Show all posts
Showing posts with label Asperger's. Show all posts

Friday, August 22, 2014

Forgive me for not posting anything sooner. I have been attending college for the last year, as a Community Support Worker - Social Service.
It is a big change for me, and I am hopeful that the time I have spent furthering my education will be of use to my community. I have to say, it feels good to see some letters after my name, because now I'm not just a "Mom" who doesn't know anything. Now I am a "professional", and that carries a lot more weight when speaking with government officials.
I admit, I know a lot more than I did a year ago, and my background and experience have stood me in good stead - providing me with inside knowledge of many features of disabilities as well as a different perspective regarding treatment.
I am looking forward to my continued participation in the forum, and I invite others to share their challenges and stories, or simply be there in support of our fellow members.
Keep your chin up...it does get better!

Sunday, February 26, 2012

Social Networking and ADHD

ADHD, or Attention Deficit/Hyperactivity Disorder and ODD, or Oppositional Defiant Disorder, are not "Media Friendly" disabilities. There are few, if any, movies made about this subject, or portraying the protagonist, or supporting cast as having these disorders. There are no fund raisers, front page stories, movie star endorsements, or media coverage to bring these disabilities to the attention of John Q. Public.

The people suffering from these disorders are not generally quiet, withdrawn misunderstood individuals, rather they appear to be brash, abrasive, undisciplined, angry children/young adults who seem to delight in causing upheaval and chaos wherever they go.

This is only half the story. These children are rarely undisciplined, and their disabilities magnify 'normal' behavior to a point where 'normal' consequences or discipline appears to be ineffective. Again, this is only half the story. The only way to truly understand what these disabilities can do to an individual and their friends and family, is to live with it.

Unfortunately, if you are 'lucky' enough to have a child with these disorders, you are ostracized from normal society and relegated to the outskirts with little to no support, help or information. You feel completely alone because no one understands what you are dealing with and others view you as a poor role model and terrible parent.

This blog is attempting to change that perception through social networking. Sites like Facebook, Twitter, and others can be adopted to spread the word that support is as close as the click of a mouse. When I was immersed in the daily negative, sometimes caustic, and always stressful behaviors of my six year old, there were no support groups and very few programs designed to work with ADHD/ODD children. There was no one available to explain why my son acted the way he did, and there were no solutions either. No one seemed to understand what they were dealing with and looked to me to provide the answers. Answers? Hell, I didn't even know the questions!

However, over the years I did my own research and learned everything I could about ADHD and its attendant disorders. In short, I helped myself. It wasn't pretty, and there was a lot of trial and error, but today I am in a position to be able to help my son, and it is working. It is slow and sometimes difficult, and almost always frustrating, but it is working.

Through Facebook, Twitter and Hub Pages, I and others, are spreading the word that support and information are available for others dealing with these issues and behaviors. Everyone can write, tweet, link, or like, the content available on this blog or forum to get the word out. Let your friends and followers know about this site and spread awareness and help for anyone living with these disorders. It doesn't cost any money - just a few minutes to click a mouse, so what do you say? You can help someone else get the support and information they need simply by clicking the like, tweet/retweet or link button on your social network profile, so please, take a moment and pass it on.

Thank you!
Enelle Lamb

Friday, February 24, 2012

Community Support Forum for Parents with Attention Deficit/Hyperactivity Disorder Children

I would just like to say "Thank you!" to all the people who are using the Community Support Forum; whether for questions and answers, information or support. We may not have all the solutions, but by adding your voices, we are helping one another, and other parents find the support they need and deserve. We shouldn't discount our experiences - they are a most valuable resource!

We all knew, when we embarked on this journey, that children didn't come with user manuals, but we were safe in the knowledge that there were many tried and true remedies, handed down from generation to generation that we felt would be enough to sustain us along the way...that and what we learned from our own parents. However, we soon discovered that these same tried and true remedies had no effect what so ever with our children, and we were left adrift in a sea of misinformation, alone and cut off from our friends and family, with no one to turn to for advice or help.

Living with any disability is difficult, but when you live with and love someone whose diagnosis does not afford them the help, programs or funding to find what they need, sometimes the only thing we can do is to band together to help ourselves.

It has taken fourteen long years for me to find programs that offer specific parenting skills and parenting groups (that would have been helpful several years ago,) for children like my son. There appear to be more programs available now than there were when my son was six and seven. This is because there are more kids being diagnosed with these disabilities than ever before, and the professionals in Child and Youth Mental Health are starting to provide the necessary services that parents need.

Unfortunately, these services are not always offered in our communities, and with today's financial and/or time constraints, it can be difficult to access them on a monthly, weekly, or sometimes daily basis...hence the Community Support Forum. This feature allows us to connect with other parents who are dealing with and surviving, (sometimes barely,) the stress associated with these disabilities. We may not have degrees in psychology, and our parenting skills might be brought into question by many parents, (who, I will add, do not deal with our type of stress,) but we have a wealth of information to pass on to other parents like ourselves.

We know what doesn't work - we have tried and tested the formulas! We know what types of medications seem to help our children, and what ones don't seem to make a difference. (I will say here, that each child is different, so what helps one might not be as effective for another, but overall, some stand out more from the crowd.) We know that sleep, (or lack there of,) food additives/processed food, allergies, potty training, discipline, consequences, and a variety of other items seem to plague our children and make it harder for us to parent them.

All of this knowledge should be, and needs to be, available to every parent who is fighting the same fight we are. Simply by sharing your stories, parents realize that they aren't alone. There are other parents out there dealing with the same issues, and that tiny bit of knowledge helps them gain the stamina necessary to get out of bed each morning - witness the over one hundred and sixty five lengthy comments on my original article - almost all of them saying thank you for posting this story.

So, for those of you who find answers, support, or a measure of solace and comfort from the Community Support Forum, I ask for your help. Tweet, Facebook, or simply pass on the link so that others can benefit from our experience and knowledge. Thank you again, and now I'll pass my soap box to the next person!


Thursday, December 8, 2011

HubPages Comments, continued

Meet Christina, the mother of an eight year old boy with ADD, a high functioning form of Asperger's and possibly ODD (Oppositional Defiant Disorder.) These are her words:


My son is 8 years old, has ADD, a high functioning form of Asperger's and I think ODD. He is very intelligent, as handsome as his Daddy (who is the love of my life) and is driving us nuts. As I write this he has been doing homework for almost 4 hours. Last night was an epic 6 1/2, the same amount of time a school day lasts. It's not that he's not capable of doing the work, he manages to do it in school. I have tried everything, and I'm at my wits end. We've done the reward system, which he only managed to turn around on us by flat out refusing to do anything unless he's guaranteed getting his game system which was the reward. We've tried punishment, not allowing any TV time before homework, made sure there are no distractions, sat beside him for hours to help him, explained that if he gets his work done there will be free time to do what he wants. NOTHING works. Yet somehow he manages to do well in school. Though his teachers always talk about his focusing issues, he is performing at grade level, in a mainstream class, is two reading levels above where is expected, gets high scores on all tests, is very good at math, and can recite lessons he's been taught. Every time I walk into the school for whatever reason all I hear is "Hi Nicky!". Teachers who do not even have him in their class know who he is. Children in older grades know who he is and last year there were a group of 6th grade girls he called his "girlfriends". They were quite charmed by him. Apparently he is quite the character in school. I wish I could be a fly on the wall for a day to see it. Well behaved and well mannered I'm always told. It makes me mad and jealous that he can't show us the same respect and courtesy. We, after all, are the ones that do everything for him.
Home is another story. He's putting us through hell. My 19 year old daughter went to live with my Mother at 14 because she couldn't deal with the constant yelling, arguing and stress. It absolutely breaks my heart, as I love her dearly. She lives close by and I do see her quite often, she comes for sleepovers at our home and she and I are quite close. But I wish I had her home. She loves her brother, but gets as frustrated with him as we do. My neighbors put up with a lot as they listen to quite a bit of yelling. One has a son with ADHD so she really understands. Yet it's embarrassing as hell. This is not me. It's not the household I come from where things were quiet, and yelling just wasn't part of the program.
I have come to believe that part of his issues he is VERY much in control of. He's a devil in the morning as we get ready for school which he refers to as a "trap", but as he walks into the school yard I can literally see the transformation. He's good all day and the moment he gets out it begins to change and by the time I am pulling into my driveway it's "hello Mr. Nasty". He knows full well what he's doing. As he gets my husband and I (I am his FAVORITE target-the weakest link I guess) angrier and angrier you can almost see the twinkle in his eye. He enjoys it, which is nuts. We are not pushovers by any means, and don't let him get away with bad behavior because "he can't control it" as I've been told. BS! He likes to push our buttons, it's obvious. Our immediate family "gets it" but when you try to explain it to anyone not living with this they look at you like you have three heads. They see him as charming, witty, intelligent and oh my God do they LOVE to talk to him. "He speaks like an adult, not like a child!" If I had a dollar for every time I've heard this I'd be loaded. The cashiers in my local market are even charmed by him. None of them live with him though.
I am very involved with school and my husband has put him in Little League and Hockey (a perfect sport to release his aggression, but there Nicky acts like a wimp ) and my husband manages and coaches both teams to be involved. He himself is very athletic and the other kids and parents love his style. Nicky could be good in both, he has potential but he loves to give his Daddy a hard time. My husband has enrolled him in these sports teams to help with Nicky's social issues, which are another problem. He has befriended another boy on his hockey team with the same issues and at first we thought "Great, he's made a friend!". Well, two peas in a pod are not always the best thing when dealing with ADD. They drive my husband nuts during practice and games because they do not stop talking. It never ceases to amaze me how much he can talk, and he was delayed with his speech. He talks from the moment he wakes up until he goes to sleep. It's how we know he's fallen asleep, for we no longer hear the talking.
The level of stress is through the roof, and we both feel it taking a toll on our health. We can't ever get a break from him, as no one will take him for a sleepover. Everything we do or don't do is based upon whether Nicky will be happy, well behaved and/or entertained. It ALL revolves around him. I believe that my kids come first, but we have a life too. And that my daughter has sat out on vacations and outings because of the nonsense is so unfair. I don't invite our friends over because at any moment something can erupt, and escalate because he just doesn't know when to stop, and I don't need the added embarrassment. Holidays are pretty much the only time, and he usually makes sure to give me an extra hard time then knowing that I am busy and stressed as it is. Birthdays, anniversaries, holidays or any special day he likes to sabotage. If he knows you are not feeling well, he gets extra pleasure out of making you miserable.
I don't get to be a "Mommy" to him. Most of the time I'm angry, arguing, frustrated, annoyed and yelling. His childhood is flying by and it's so sad that things are this way. Once in a while (and I don't know why) he is a "normal" kid for a day. He's sweet, well behaved and I can breath again. It's cruel in a way because it lets me see how things could be. How I wish with all my heart they would be. It's a window to another life possibility, and I try to explain that to him. I try to point out that when he is like that there is no fighting or yelling, and there wouldn't be if he would act like that most of the time. But I think he gets bored with that. He likes the chaos.
We don't want to medicate him. I just don't feel these drugs have been around long enough, and who knows what effects will come to light in 10-20 years. Doctors and pharmaceutical companies just love to dispense a shot or a pill for everything nowadays. His pediatrician agreed that she is no fan of these medications either, and many others I've spoken to feel the same.
What do we do? I feel lost. Reading the other posts here have made me feel slightly better as I know we are not alone. We love our son dearly, and would do anything for him. We both believe he can be very successful someday, he has so much potential. But I also see a lot of trouble if he can't get his instigating and aggressive ways under control. His condition is a blessing in some ways (the intelligence) and a maddening situation in others. All I know is as I drive away from school after dropping him off I can feel the physical change in me. My chest loosens up, I can breathe, my head stops pounding, the stress fades and I can talk without yelling. And the reverse happens at pick-up time, I feel it all increasing because I know what will transpire. And I know homework hell is looming. It's a vicious cycle, and I go to sleep every night praying (sometimes crying) that my son will begin to ease up on some of this.
As more and more children seem to have this (there are about 6 boys in his class and I don't know how his teacher manages) the medical community and the schools need to step up their game. It takes a village to raise a child right? Something somewhere is causing this upswing and I do believe there is a remedy other than sedating them. I try to keep the faith that those questions will be answered, and a "cure" of some sort will be available someday. Til then the gray hairs keep coming faster and faster and my beauty supply store keeps making more money! LOL.