My grandson who is 6 is being bullied at school. We have been in contact with the school but they don't believe it is happening. My daughter has been to the doctor where they have taken photos and given my grandson sleeping medicine. My daughter has taken my grandson to school today, and she heard the teacher telling one of the parents whose son is one of the ones bullying my grandson; it’s not your son which has upset my family. We are at our wits end now what to do and where to go for the support for my grandson. I would be grateful for any advice you can give us.
Sorry to hear about your upsetting situation and the difficulties with the school. The website below has some very useful advice under the “Getting Support from the School” section. http://www.bullying.co.uk/advice-for-parents/what-to-do-if-your-child-is-being-bullied/
What are the steps a school can take to promote mental health among students?
The mental health of children and young people is increasingly seen as a fundamental consideration for schools. This is a step in the right direction for all students but even more so for those living with chronic medical and mental health needs. A place to start is by looking at these resource https://www.gov.uk/government/publications/supporting-mental-health-in-schools-and-colleges. Lots of useful research based information on how schools can promote the mental health of students through policy and practice. Additionally, the PSHE association produces guidance and a range of teaching plans and resources for schools. https://www.pshe-association.org.uk/curriculum-and-resources/resources/guidance-preparing-teach-about-mental-health-and
We are a secondary school expecting our first student with cystic fibrosis to start school with us. We are trying to find funding to develop an existing rarely used toilet with shower into a newly refurbished room for her and subsequent CF students. Do you have a grant system we could apply for? If not do you know of any organisations we could get in contact with which may be able to help with funding?
Most hospitals that treat patients with CF have an outreach team that can advise - and the Cystic Fibrosis Trust are also available for advice and guidance - however we are not aware of any funding for disability access - maybe try your local authority?