Lindsey Smith

Digital Communications

Lindsey Smith, a devoted mother of two autistic children, has been a vital member of PAACT for the past six years. Known as the go-to person for all things technical, Lindsey ensures the group stays up to date with the latest technology. Her expertise and dedication are invaluable to the committee, keeping everything running smoothly and efficiently. Lindsey’s contributions help PAACT provide the best possible support to families navigating autism, making her an essential part of the team.

Beverley Clark

Vice Chair

Hi all, I'm Bev, vice chair of PAACT and like with all the volunteers & committee I have lived experience of autism & associated conditions. Mine is as a mum and granny of autistic children (and adult), ADHD and sensory processing disorder. I strongly believe that all children and young people are unique and it's about getting to know each and every one as their unique self that unlocks the key to what is right for them as individuals and their families. Trying to navigate the maze is so difficult it's always easier with someone else by your side and as a whole that's what we aim to achieve.

Melissa Lacey

Secretary

My name is Melissa Lacey and I am the PAACT Secretary. I have lived experience of ASD with a PDA profile, ADD, ARFID, Dyspraxia, generalised anxiety and SPD, with my teenage son. I have a special interest in low demand parenting and all things home education. I truly believe all children thrive and learn best when their anxiety is much lower, more manageable and they are ready to learn in what they are interested in. Learning takes many different forms and thinking outside the box is vital when helping and supporting our children and young adults, whether it be education, friendships, social skills, life skills, communication and relationships.

Gordon Forsyth

Chair

I have been involved with Autism for the last 17 years when my son received a diagnosis of Pathological Demand Avoidance at the age of 9, and a few years later when my daughter was diagnosed at age 15. I have been to every workshop, training days and conferences that were available to me to increase my knowledge in this new world. The biggest and most important thing I did was to get involved with our Local support group PAACT. 10 years later I find myself chairing the group and changing the direction the group was going in, due to the reduced services available for families. My motivation to help families understand what we need to do as parents comes from the mistakes and struggles I went through due to lack of support or direction. The biggest lesson I have taken from my journey over the last 17 years is there is no answer to get your children to not have a meltdown, to fit into society, not to worry, to accept that I had to change inorder to reduce the pressure I was putting on my children, which in turn reduced their meltdowns, reduced their pressure and they started fitting into society in their own way. My aim is to share my experiences with you from a parents point of view while providing information from professionals that I feel will be useful and helpful to you.

Zoe Ives

Activities & Membership

Hi my name is Zoe I have been part of PAACT for a number of years. Being mum to an autistic child is hard work, but is also so rewarding. PAACT is a great support offering a wide knowledge and understanding. I’m proud to be a part of this group.

Charlotte Owen

Treasurer

Charlotte Owen is a dedicated mother and passionate advocate for the neurodivergent community. As a mother of two, including a son with autism, Charlotte has spent 14 years deeply involved in understanding and supporting neurodivergent conditions. For over a decade, she has been an active force in her community, serving as the treasurer of PAACT (Parents and Autistic Children Together) support group. In this role, she ensures the group remains financially strong and capable of providing crucial support to families navigating autism. Charlotte is also the chairperson of her charity, Umbrellas, where she leads efforts to create an inclusive world that celebrates neurodivergent and disabled individuals and their families. Under her leadership, Umbrellas has become a cornerstone for families seeking resources, community, and understanding. Her work extends beyond these formal roles, as she has been a committed committee member for various organisations for the past 12 years. Charlotte is known for her empathy, dedication, and ability to inspire others to embrace neurodiversity. With her extensive experience and relentless advocacy, Charlotte Owen continues to make a meaningful impact, championing a future where all individuals are valued and supported.