Action for Pulmonary Fibrosis Revenue
Non-profit Organizations • 
St Johns Street, Stuart House, United Kingdom • 21-50 Employees
Action for Pulmonary Fibrosis revenue & valuation
| Annual revenue | $3,764,420 |
| Revenue per employee | $86,000 |
| Estimated valuation?This valuation is estimated based on industry average for the Non-profit Organizations industry and current estimated revenues | $12,100,000 |
| Total funding | No funding |
Key Contacts at Action for Pulmonary Fibrosis
Bradley Price
Director Of Policy, Research And Involvement
Daniel Saxton
Chief Executive Officer
Lisa Trivett
Director Of Fundraising And Communications
Lisa Trivett
Director Of Fundraising And Communications
Company overview
| Headquarters | St Johns Street, Stuart House, East Wing, Peterborough, PE1 5DD, GB |
| Phone number | +441733839642 |
| Websites | |
| NAICS | 813 |
| SIC | 839 |
| Keywords | Research, Awareness, Education, Fundraising, Support Groups, Patient Support, Phone Support Line |
| Founded | 2013 |
| Employees | 21-50 |
| Socials |
Action for Pulmonary Fibrosis Email Formats
Action for Pulmonary Fibrosis uses 3 email formats. The most common is {first name}{last name} (e.g., johndoe@actionpulmonaryfibrosis.org), used 50% of the time.
| Format | Example | Percentage |
|---|---|---|
{first name}{last name} | johndoe@actionpulmonaryfibrosis.org | 50% |
{first name} | john@actionpulmonaryfibrosis.org | 25% |
{first name}.{last name} | john.doe@actionpulmonaryfibrosis.org | 25% |
About Action for Pulmonary Fibrosis
Action for Pulmonary Fibrosis (APF) was set up in 2013 by a group of patients, family members, carers and medical specialists to provide support for patients diagnosed with the devastating terminal lung disease Idiopathic Pulmonary Fibrosis. IPF kills 5,000 people in the UK every year – more than die from leukaemia and many other cancers – but it doesn’t have a high profile and is poorly understood. It is estimated that more than 30,000 people in the UK are affected The cause is unknown (idiopathic) and life expectancy is often worse than for lung cancer with more than half of sufferers dying within three and five years of diagnosis. The condition is characterised by a build-up of scar tissue in the lungs leading to shortness of breath and eventual respiratory failure. Our work focuses on four mains areas; firstly by supporting patients with information and access to a local support group and championing their needs. Secondly, by educating healthcare professionals about the importance of early diagnosis and helping them know how to deliver the best care and treatments for patients. Thirdly, through research; we have launched the Mike Bray IPF Research Fellowship which is a £300,000 grant that will fund major IPF research, in memory of our founder and former chairman, who sadly passed away earlier this year. Lastly, through campaigning. We proactively target parliamentarians, the NHS and policy-makers to represent patient interests. Our Vision: A world in which everyone living with pulmonary fibrosis has a better future; with your help we can make this happen.
Employees by Management Level
Total employees: 21-50
Seniority
Employees
Employees by Department
Action for Pulmonary Fibrosis has 9 employees across 8 departments.
Departments
Number of employees
Funding Data
Action for Pulmonary Fibrosis has never raised funding before.
Action for Pulmonary Fibrosis Tech Stack
Discover the technologies and tools that power Action for Pulmonary Fibrosis's digital infrastructure, from frameworks to analytics platforms.
CDN
Miscellaneous
Security
United States
Canada
Frequently asked questions
4.8
40,000 users
