Education and Health Care Information

     

At CMV Action we aim to provide information and support to families. We empower parents to work effectively with professionals and advocate on behalf of families affected by CMV.

There are many charities and groups that can help you.

http://www.adviceguide.org.uk/

Self help from the Citizen’s Advice

http://www.ipsea.org.uk/news/2014/education-health-and-care-plan-checklist

Checklist for Education and Health Care Plans
 

Cerebra aims to improve the lives of children with brain related conditions. They have information and leaflets and can help with completing DLA forms, grant applications, attend meetings with you, and share local knowledge on dealing with educational issues and accessing services.

http://www.ndcs.org.uk/

The National Deaf Children’s Society (NDCS) is the leading charity for deaf children and young people. They provide impartial information and individual advocacy on every aspect of childhood deafness. They can help with welfare rights and benefit claims, making education choices, advising on health, audiology and technology.

http://www.cafamily.org.uk/know-your-rights/

Help with entitlement to benefits and services.

http://www.scope.org.uk/support

Disability information, support and services.

http://www.sossen.org.uk/

Independent helpline for SEN

http://resources.ncb.org.uk/htmlemails/3c9a546d-80e0-46d7-99fe-c9a70a942944.html

Help and advice on short breaks

 

 

If you have received help from a charity or organisation please let us know and we can add them to the list.

     

Our Stories

When I was pregnant my baby was measuring small and I had to go for weekly dopplers and fortnightly growth scans. A month before my due date, I was told there was no change in my baby's... Read more
Hi everyone, meet chocolate faced Darcie. She is my beautiful 20 month old daughter. I was diagnosed CMV positive when I was 6 months pregnant. It is thought that I caught it when I was 4... Read more

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