ASSOCIATION OF YOUNG PEOPLE WITH ME LIMITED
Support, encouragement and information for children and young people under the age of 26 years who are suffering from Myalgic Encephalopathy/Chronic Fatigue Syndrome (ME/CFS). Each member receives a bi-monthly magazine and has access to a wide range of other services, including additional support to members in times of crisis; telephone Helpline and membership contact services.
Objects
1. TO ACT AS AS ASSOCIATION FOR YOUNG PEOPLE SUFFERING FROM THE DISORDER KNOWN AS MYALGIC ENCEPHALOPATHY (ME). 11. TO WORK ON BEHALF OF THOSE YOUNG PEOPLE WHOSE LIVES ARE AFFECTED BY ME THROUGH MEDIA COVERAGE, REPRESENTATIONS TO GOVERNMENT AND OTHER AGENCIES, THROUGH TALKS, PRESENTATIONS AND THE FUNDING OF RESEARCH. 111. TO PROVIDE A SUPPORT NETWORK FOR YOUNG PEOPLE SUFFERING THROUGH ME THROUGH COUNSELLING, THERAPY AND WELFARE BENEFITS ADVICE AND TO PROMOTE CAMPAIGNS FOR THE RECOGNITION, DIAGNOSIS, TREATMENT AND ACCEPTANCE OF ME.
From the charity’s annual return (Part A, self-declared)
Self-declared on the annual return for the financial year ending 31/12/2015
- Volunteers: 65
Self-declared on the annual return for the financial year ending 31/12/2014
- Volunteers: 20
Self-declared on the annual return for the financial year ending 31/12/2013
- Volunteers: 47
Register events
- Transferred assets to another charity (10/05/2017)
Income and spending
| Financial year end | Income | Spending |
|---|---|---|
| 31/12/2017 | — | — |
| 31/12/2016 | — | — |
| 31/12/2015 | £193k | £219k |
| 31/12/2014 | £209k | £193k |
| 31/12/2013 | £212k | £228k |