I am a life learning Mama and this page is where I like to share things that resonate with me in some way along this wonderful life journey we are on ♥
Showing posts with label Dysgraphia. Show all posts
Showing posts with label Dysgraphia. Show all posts

Monday, 6 April 2015

I want to shout it from the rooftops! He found his way without school ❤️

Proud Mummy Moment! I just want to shout out about my son Samuel who has just phoned me with some wonderful news. Many of you know of him and his early struggles in school and that we ended up unschooling after a long and often hair raising journey to get there. He is now at 19 in his final year of his software engineering degree at the University of Queensland. As part of the work for one of his papers he has been going into industry to interview people and after one day he received a call from a company that said they had an internship going and they thought Samuel should apply if he was interested. He was not looking for work but the sound of it was something that really interested him. The date of application closure was the day they called him. He furiously filled the application and sent off his CV (which for someone with his executive function issues is huge to get himself into gear and organised to do this!) and was then called for an interview with 40 other applicants and he being the only homeschooler. He went for the interview and felt that it had gone well but was up against some other very talented young programmers. However, he got a call last week and was told that he was wanted for a second round of interviews. The interview happened on Tuesday and he was called last night offering him the internship!! Tears of joy from this proud Mama! He will be going in one day per week paid and taught all that they can teach him and then at the end of his degree has the offer of a full time position. My out of control (to others!) boy diagnosed with ADHD/ASD/ODD/Gifted and with learning difficulties (namely dyslexia and severe dysgraphia) who was suspended from every single school bar one (and he went to quite a few schools), who we were told needed serious psychiatric help by one school principal and who left the school system crushed, depressed and with little to no self esteem has just proved them all how wrong they were about him! I always knew that they were wrong but he didn't! He came home and was allowed to be the wonderful, smart human being that he is and always was. It was just that school didn't always see that and tried to "fix" him when he was never broken! To all those parents who worry about their children - please have faith. I know sometimes it is a huge leap of faith but Samuel was allowed to follow his passions and do things HIS way and I am so very proud of the young man he has become and his achievements today. He has proved to me that you don't need others to teach you, tell you what you need to or should be learning. Having a passion, interest or aptitude in something and being allowed to follow it really does work - well it has for my family anyway and I am sure it will for most heart emoticon

Saturday, 2 July 2011

Parenting a child with 'Special Needs'





Not sure I like the term “special needs” but I use it. What does it mean? Having a quick check on Wikipedia it depends on where you live in its definition! However, the country I like best in its interpretation is Germany where special needs children are called “besondere kinder” (“special children”). I like this term best – if I bother to check every country’s definition I may find something better, but for me now this sounds right. I know all children are “special” but for some of us parents the term has a real depth of meaning that perhaps others have not experienced? I have two beautiful children, one of which is diagnosed with ADHD/Aspergers with Dysgraphia and is Gifted! Yes he is truly VERY special. In fact he is one of the most amazing people in my life. In his 15 years of life he has struggled against a system that does not always recognise difference. He inspires me, constantly challenges me in both good and bad ways and is one of the kindest kids I know! If you let me, I would like to share some of our special journey.

He was born on a beautiful sunlit morning. I remember this little bundle of newness being handed to me swaddled in a blanket opening one wise eye and checking me out. What did this cute man’s future hold? My imaginings for our journey together were not really in tune with the reality as it turned out! He was a gorgeously cute baby (as they all are!) and made everyone smile. However, from a young age I knew that something was different about him. It was always his name I heard being called – called away from mischief mostly – not an intentional mischief – it just seemed to search him out! If he could find a way of doing something differently he would. If everyone was going left, he would be going right. If they were going up, he would be going down! He could get away with it whilst he was tiny but then once past being a toddler it became a diagnosed problem. Phone calls from day care, after school clubs, swim squad, holiday programmes – you name it – they would usually call me and tell me of some sort of problem they were having with him. It is not something that I would wish on any Mother. You want to be told good things about your child. You want your child to be liked. You want your child to be invited to birthday parties, play dates and other social gatherings. It hurts to hear the whispers, the judgmental looks. I always vowed that I would speak out for these kids when mine grew up. My son is growing up and doing well now. I did not always think this would be the case! It has taken a lot of hard work, commitment and a thick skin (of which I have very little!). The journey has at times been painful and I have cried many tears. However, I want parents to know that if your child is indeed “special” like mine there is light at the end of the tunnel if you work at it.


Don’t read all the doom and gloom books (or which there are many!) Don’t listen to every specialist without questioning their advice. I have often gone against the grain with the treatment of my son’s disabilities and trusted my mothering instinct. We do not take medication. I wanted my son to know himself as he is, not a medicated version. I wanted him to learn strategies to manage his behaviours. We have looked at diet. We do not do artificial additives. It helps! We drink plenty of water and get adequate sleep. It helps! We talk and discuss things, we share ideas and try to work as a team. Some say parents should not be their child’s friend. I am. It helps (or it has for me!).

I am so proud of my son and what he has achieved in spite of his disabilities. He is an avid Surf Lifesaver serving our local community. He is known in our neighbourhood for being a kid that will help someone in need, especially the sick and the elderly. Without doubt he is “special”. I hope that this blog gives strength to other Mothers who may sometimes feel so alone living with a child who is different. I have been abused and bullied because of my son’s differences. No Mother should have to endure that. Believe in yourself and your child and you too will see the light and when you do I hope that it shines as bright as the light I see now. Blessings to our “besondere kinder”



Home Schooling a 2e Child

Home schooling a child with ADHD/Aspergers/Twice Exceptional (wow what a label!!!!)


I have been asked many times what it is like to home school my son who was diagnosed age three with ADHD and then having started school got a few more labels added namely Aspergers with a mix of Giftedness, together with a learning disability, known as Dysgraphia and all combined together makes for a beautiful but somewhat challenging young man.

I began my home school journey around six years ago when my son having been stood down from most schools (including the one at which I taught) began attending an alternative school in Auckland, that catered for children that were somewhat outside of the ‘norm’. This was a disaster and Samuel became depressed after countless episodes of bullying. My son is a very upbeat person and I really could not stand by and watch his whole personality change before my eyes and all in the name of gaining an education. Henceforth I took a deep breath, argued my case with my husband and decided to bale out of the traditional system and try ‘school at home’.

I was nervous about my decision and really wondered whether I was up to something so ‘different’. I had never questioned school really and certainly had no experience with home schooling, nor knew of an other people home schooling. However, one of the first things I did was reach out and find my local home school community and I really began to tap into what they had to offer. It was not always successful as even within that environment Samuel stood out as different, but it did give me a reference point and somewhere to turn to when I needed help.

At home, to begin with, we really did very little (unschooled), to give ourselves a breather from the stress that had amounted for us both due to what had happened at school. It was a wonderful time where we enjoyed each other’s company, relaxed and planed our way forward. I had trained as a teacher the year before I decided to home school, which is funny because it really fired my enthusiasm for leaving the system! I saw how difficult it was to cater for children who do have extra needs, whatever they may be and it gave me the passion to make a difference for at least one child who struggled against the grain, namely my son. 

Another benefit for being a ‘qualified’ teacher it gave me some kudos when people asked why Samuel was not at school. I would tell them he was ‘home schooled’ and that I was a trained teacher and they seemed to accept this as better than if I was not! The fact is ANYONE can home school and my training had no benefits to me other than enabling me to see school both from the perspective of a teacher and as a Mum with a child that has ‘special needs’.

Once we had settled more with our decision to home school and accepted this next stage in our ‘educational’ journey Samuel and I decided that a topic based approach would be best. I initially started by running our day very like school with lessons in 45 minute blocks. This really did not work for us and neither was it necessary. Children with ADHD often lack focus and are easily distracted so I found it good to have a quite space for Samuel where he was relaxed but without constant interruption or unnecessary distractions. We compiled a little timetable to help with his organisation, which he really struggles with, but flexibility within that was the best for both of us. Samuel often hyper focuses (another characteristic of both ADHD and Aspergers) and rather seeing that as a deficit we let it work to our advantage. If Samuel was really fired up about a subject and wanted to work on it all day then that was fine. It was amazing how much he covered in a few hours without all the constant interruptions. I also found that when Samuel chose his topic it gave him ownership that also fuelled his motivation, which is not always there with these children. He is a bright child who thrived on this and rather than relying on a teacher for the answers he really wanted to just problem solve and work it out for himself.

Another benefit we found was that where at school he had been conscious of his inability to write and was embarrassed by it because of remarks by other children, at home he had none of this pressure. We did not focus on writing and indeed I helped to teach Samuel to type and would also get him to use a dictaphone to transcribe his stories which I would then type for him. When he was at school he spent many lunchtimes kept in to write up what he could not do during the lesson. The fact is Samuel will never be good at writing in the traditional sense however many ‘remedial’ lessons he receives so we decided to focus on his strengths and build up his self esteem again.

He has exceptional abilities in maths and computing and I felt unskilled in those areas so we decided to tap into distance education where he was able to do papers at his level, which was above his chronological age. He loved this time and built up a rapport with his distant education teachers that did not really materialise at mainstream school. Mainstream school teachers judged Samuel on some of the more challenging behavioural aspects of his condition rather than on the ‘whole’ person. Samuel at home talking online was not judged and neither did many of those ‘behavioural issues’ surface when he was working in a more relaxed, unpressured environment.

We have carried on in this way over the years until recently when Samuel decided that he wanted to do Software Engineering at University. We approached the local University and made enquiries as to how he could get in without the traditional qualifications. On research for us we found the best way for Samuel would be to enrol in Distant Education full time and he is now doing his OP subjects. He has been accelerated a year and is also attending University one day a week which he is loving. He is now 15 and for me looking back over the years I am amazed at how far he has come. I at times worried so much for his future because I was made to worry. Since Samuel has been home schooled we have really dropped many of the ‘labels’ that seemed to be so necessary for him during his time in mainstream. We have no need for labels at home. He is just Samuel. He no longer goes to all the ‘specialists’ he used to, who tried to ‘fix’ him. I am no longer made to feel guilty because I choose not to medicate him. I have found home schooling to be the best thing that we have ever done and for anyone who has a child with ‘special needs’ it can be so rewarding. I have really seen a blossoming in my child and I hope that my story may help, inspire or encourage others to take that initial step for a better future for our children who march to a different beat. J



Our Journey without Drugs

I was told by a ‘specialist’ when I refused to give my son Ritalin that what I was doing was an “indirect form of child abuse as I was not offering him the window of opportunity to realise his full potential”. He was 3 years old. Yes, he was getting into trouble, yes he was a handful, yes he could be challenging! However, I stuck to my guns and at the age of 15 he now attends University one day a week and goes full time next year studying Software Engineering. I kind of think he is realising his potential drug free! Drugs are not always the only answer, if the answer at all for some.

Things were hard at times and it has not always been an easy journey. I am proud of my son and what he has achieved. He knows himself as he is – not a drugged version – and is doing well in all areas of his life and he is my friend as well as my son. He is diagnosed with ADHD/Aspergers and is Gifted but also has learning difficulties, namely dysgraphia. We have worked together to find solutions to problems without the use of drugs and I really had to fight hard to convince Drs, schools and the so called ‘specialists’ of whom we have seen many, that I felt my way was best. It is only now that I really know for sure that my way was the best for us and I am so proud of what we have achieved and that I stayed strong against those who tried to convince me otherwise. I hope that speaking out gives other parents the strength to follow their heart when sometimes it feels like you are really alone in your decisions. It may not always be the easiest of paths, but for us it was the right one and I hope that speaking out will encourage others to follow a similar path to our own.

On reflecting on why so many children seem to be given medication for conditions such as my sons, I cannot help but wonder if our children just need more of our time but unfortunately in this time poor age it is often somewhat lacking. I am not saying that medication does not have a place for some, but I think they are all too often given out without having tried any other interventions. Again a ‘time poor’ solution – drugs are a quick fix but do nothing for the underlying issues! My son is living proof that there are alternatives that are far better for both body and mind! It was often a lot of hard work and believe me when he was younger, I questioned my decision not to medicate at various times along our journey. Children with these conditions can be utterly exhausting. However, it is something I believed in and I am happy with my decision. I think we always need to support each other whatever our decisions and also find what works best for each individual case. I just like to get the word out that drugs are not always the answer and wish everyone the best whatever path they choose :0)