A pair of insightful new additions to the Can I Tell You About series are:
Can I Tell You About Diabetes (Type 1)?
Julie Edge
Jessica Kingsley Publishers
Debbie has had type 1 diabetes since she was six years old and is the only member of her family with the condition. She is able to do everything others can including sports but in addition has to devote time to extra things.
However, despite leading a pretty active life, Debbie’s diabetes is always with her; she cannot forget it – the testing, monitoring of blood sugar, injecting,

Debbie uses an insulin ‘pen’ for injecting herself
eating, the results of changes such as a cold or dose of flu can bring to her body and what this means for her. Despite her general up-beat tone, Debbie can at times feel a bit fed up, she says. Occasionally this is because of lack of understanding on behalf of other people, sometimes, it is because of her general mood or because her blood sugar levels are too high or too low.
We are also told about the benefits of activity weekends when the young narrator meets up with other children with diabetes. In addition, there is biological information about the role of the pancreas and how its malfunctioning causes diabetes type 1.

The final part contains information on how to help, aimed at friends, teachers, parents. There is also a list of recommended reading, websites and organisations.
The author, a doctor has been a consultant in Paediatric Diabetes for nearly twenty years and there are numerous drawings by Julia MacConville, further illuminating the written information.
This is an extremely informative, concise explanation and a testament to all those children who like Debbie, manage the complexities of life with type 1 diabetes each and every day of their lives.
I would want to see a copy in every primary school and, at least one copy in any classroom where there is a child with this form of diabetes.
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Can I Tell You About Cerebral Palsy?
Marion Stanton
Jessica Kingsley Publishers
Herein we meet bright, thirteen year old Sophie, who uses a wheelchair, and a talking computer or VOCA for short that she operates with the aid of her personal assistant, to communicate with friends and teachers.
Sophie talks in a matter of fact voice about the reason for her own cerebral palsy and how this affects her; she stresses that her mind is not slow, rather it takes a longer time for her to say something that her friends can say in seconds.
We learn how different parts of the body can be affected by cerebral palsy

and what this means for people differently affected, sometimes behaviourally or emotionally and sometimes there are hearing or visual challenges.
It’s good to be treated less ‘like a little girl’ by her PA who assists with choice of clothes on shopping expeditions and also to be taken to sporting events by her parents.
Sophie’s physio. is a great help to her as are the occupational therapist and her speech and language therapist; and she has her own communication passport, which acts as a quick, handy way for people to get to know basic things about her.

At the end is a section with suggestions for how teachers, teaching assistants, family members, PAs, community members and other professionals can be supportive. There is also a list of recommended organisations and websites.
All this and much more is packed into this short book written by a special needs teacher and mother of a child with cerebral palsy and illustrated with line drawings by Katie Stanton. I came away from it feeling I had learned a great deal, not only about CP but also about how young people such as Sophie have an amazing power to transcend their particular experiencing of cerebral palsy, no matter what.
Highly recommended for teachers, and for students in the fields of social care, health and education as well as young readers in primary schools. In fact it is an excellent starting point for anyone wanting to know more about working with individuals living with cerebral palsy.
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