Studies suggests that between 4-7% of students have experience difficulty in math compared to 26% of children with ADHD. Here is a free download which provides resources and information on ADHD and Dyscalculia
Published by: nzherald.conz
Written by: Katie Harris
Neurodiverse Kiwis contribute significant value to the workforce, but structural problems within the interview process mean many can be locked out of the job market. Katie Harris speaks to those on the ground about how to improve interviews for neurodiverse Kiwis.
“Tell me what you’re most proud of?”
For some, this may seem like a simple question to answer, but for many neurodiverse Kiwis its vagueness can throw off even the most well-prepped applicant.
Neurodiversity encompasses neurological differences including dyslexia, autism spectrum disorder (ASD), attention deficit hyperactivity disorder (ADHD), dyspraxia, dyscalculia, dysgraphia and Tourette’s syndrome.
The neurodiverse can bring a wealth of creativity, hyperfocus and out-of-the-box thinking that many organisations need, but often interviews can pose as a barrier to success for some.
Autism NZ chief executive Dane Dougan told the Herald the whole recruitment process isn’t set up for neurodiverse people.
Autism NZ employment facilitator Megan McNeice told the Herald a big roadblock for the neurodiverse in interviews is open-ended questions. Click here to read the rest of the story.
Published by: The Herald Sun
Written by: Karina Muzhukhina
Attention deficit hyperactivity disorder (ADHD) may be linked to substance abuse, a new study found.
The study, set to be published in the journal Alcohol and Alcoholism, found that even when accounting for age, race, income, education, childhood adversities and mental illnesses aside from ADHD, people aged 20 to 39 and diagnosed with ADHD were 69% more likely to have a substance use disorder than those without ADHD.
Around half of people with ADHD will have a substance abuse disorder, the study found, compared to only about 23.6% of adults without ADHD.
Researchers collected data from the Canadian Community Health Survey-Mental Health and analyzed findings from 270 people between the ages of 20 to 39 with ADHD and 6,602 people without the disorder.
About 36% of adults with ADHD reported abusing alcohol, followed by cannabis — with about 23% of adults with ADHD abusing the substance. Those with ADHD “were also three times more likely to experience an illicit drug disorder” — not counting marijuana — compared to those without the disorder. Click here to read the rest of the story.
Prader Willi is a syndrome which involves chromes
Download the information here;
Published by: International Foundation for CDKL5 Research
CDKL5 deficiency disorder is a rare developmental epileptic encephalopathy caused by mutations in the CDKL5 gene, and this can manifest in a broad range of clinical symptoms and severity. The hallmarks are early-onset, intractable epilepsy and neurodevelopmental delay impacting cognitive, motor, speech, and visual function. Although rare, the occurrence is believed to be ~1:40,000 -75,000 live births, making it one of the most common forms of genetic epilepsy.
The CDKL5 gene provides instructions for making proteins that are essential for normal brain and neuron development. The CDKL5 protein acts as a kinase, which is an enzyme that changes the activity of other proteins by adding oxygen and phosphate atoms (a phosphate group) at specific positions. Researchers have not yet determined which proteins are targeted by the CDKL5 protein.
CDKL5 was first identified in 2004, it stands for cyclin-dependent kinase-like 5, and its location is on the X chromosome. The X chromosome is one of the sex chromosomes; females have two X’s, and males have one X and one Y chromosome. The letters are an abbreviation of the scientific name of the gene, which describes what it does. The CDKL5 gene was previously called STK9. Many cases have been identified in boys, but because of the location of the gene, CDD mainly affects girls.
We do not fully know the cause of CDKL5 deficiency disorder at this time. Mutations have been found in children diagnosed with Infantile Spasms, West Syndrome, Lennox-Gastaut, Rett Syndrome, cerebral palsy, autism, and intractable epilepsy of unknown origin.
Through scientific research and collecting information through the CDKL5 International Database and at our Centers of Excellence, we are working hard to find all of the pieces of this puzzle. It is important to note that scientists and doctors do not know the full spectrum of CDKL5 disorders at this time. There are likely many people affected by CDKL5 who have mild symptoms and no seizures. With continued research and awareness of CDKL5, we hope to build a more comprehensive understanding of the spectrum of this disorder as we continue the search for a desperately needed cure. Click here to read the rest of the story.