It is vitally important that you and your carer receive support in understanding the condition and long-term plan of care. This is the key time for you to receive the right information from the right people.
Your Healthcare Professional will be able to answer your questions and guide you to appropriate resources regarding your condition. These resources may include local and national support groups as well as recognised websites.
- Action for Pulmonary Fibrosis
- Asthma UK
- British Lung Foundation
- British Thoracic Society
- The Childrens Heart Federation
- Cystic Fibrosis Trust
- Giving up smoking
- National Bureau for Students with Disabilities
- Newlife Charity
- Ouch UK
- Parents for Inclusion
- Pulmonary Hypertension Association
- Well Child