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Official Report: search what was said in Parliament

The Official Report is a written record of public meetings of the Parliament and committees.  

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Dates of parliamentary sessions
  1. Session 1: 12 May 1999 to 31 March 2003
  2. Session 2: 7 May 2003 to 2 April 2007
  3. Session 3: 9 May 2007 to 22 March 2011
  4. Session 4: 11 May 2011 to 23 March 2016
  5. Session 5: 12 May 2016 to 4 May 2021
  6. Current session: 13 May 2021 to 31 January 2026
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Displaying 1829 contributions

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Equalities, Human Rights and Civil Justice Committee [Draft]

Neurodivergence

Meeting date: 20 January 2026

Maggie Chapman

Good morning, everyone. I am deputy convener of the committee and an MSP for the North East Scotland region.

While I have the microphone, I also want to declare an interest. Carolyn Scott and I worked together in my previous role at the Scottish Council on Visual Impairment prior to my being elected.

Equalities, Human Rights and Civil Justice Committee [Draft]

Neurodivergence

Meeting date: 20 January 2026

Maggie Chapman

Thanks very much, Karen. Hello again, everyone, and thank you for joining us.

The first theme that I want to explore is access to assessments and any treatment or medication that comes after. How long did you have to wait to get an assessment, and what impact did that have on you, from your experience?

I do not know who wants to pick that up first. Debbie, I saw you nodding. Do you want to go first?

Equalities, Human Rights and Civil Justice Committee [Draft]

Neurodivergence

Meeting date: 20 January 2026

Maggie Chapman

I think that Kadie wanted to come in.

11:00

Equalities, Human Rights and Civil Justice Committee [Draft]

Neurodivergence

Meeting date: 20 January 2026

Maggie Chapman

Thank you all very much for sharing your personal experiences.

Leo Starrs-Cunningham and Rachel Parker talked about support or appropriate adjustments and accommodations. I would like to open up a discussion on that. What are the kind of things that you know work? Obviously, they will not necessarily be the same for everybody in different situations, but what are the kind of things that you know work and that we should be thinking about more generally across society, so that there is the awareness and understanding that Carolyn Scott indicated are so lacking in some healthcare professionals?

Equalities, Human Rights and Civil Justice Committee [Draft]

Neurodivergence

Meeting date: 20 January 2026

Maggie Chapman

Thanks very much. Do you have anything to add, Leonie?

Equalities, Human Rights and Civil Justice Committee [Draft]

Neurodivergence

Meeting date: 20 January 2026

Maggie Chapman

Thank you, Sofia—that is a helpful point to hear.

Equalities, Human Rights and Civil Justice Committee [Draft]

Neurodivergence

Meeting date: 20 January 2026

Maggie Chapman

Thank you, Debbie. Rachel, do you want to come in on this?

Equalities, Human Rights and Civil Justice Committee [Draft]

Neurodivergence

Meeting date: 20 January 2026

Maggie Chapman

Thanks very much for that, Kabie. I do not know if you could see, but there were a lot of people around the table nodding as you were speaking. What you were saying clearly speaks to other people’s experiences as well.

Equalities, Human Rights and Civil Justice Committee [Draft]

Neurodivergence

Meeting date: 20 January 2026

Maggie Chapman

I will hand back to the convener now but I thank you all for your answers to that question.

Equalities, Human Rights and Civil Justice Committee [Draft]

Neurodivergence

Meeting date: 20 January 2026

Maggie Chapman

Good morning to you both. Thank you for being here today and for the detail in your report.

I am interested in a couple of different areas, one of which is diagnosis and its value. We have heard clear evidence that shows that having some kind of diagnosis of neurodivergence, whether that is of autism or ADHD, gives people something from which to work; it is validating and gives them something that they can explain to people. That leads me to two questions: how can we ensure that people without a diagnosis are still supported, and what can be done about the long waiting times for any kind of medical assessment? Some people are waiting years for a diagnosis. Those are two quite different questions, but I would be interested to hear your thoughts about how we can deal with the issue of validation through diagnosis.