FOP Australia
Non-profit Organizations • 
Australia • 1-10 Employees
Company overview
| Headquarters | Australia |
| Website | |
| SIC | 832 |
| Founded | 2015 |
| Employees | 1-10 |
| Socials |
Key Contact at FOP Australia
Lydia Scott
Member Board of Directors
About FOP Australia
FOP Australia aims to improve the lives of individuals and families affected by the extremely rare genetic condition Fibrodysplasia Ossificans Progressiva (FOP) by: Raising awareness of FOP Providing a support network for families and individuals with FOP Furthering research towards treatment and a cure FOP is one of the rarest, most disabling genetic conditions known to medicine, causing bone to form in muscles (and other soft tissue) throughout the whole body leading to ongoing and permanent restriction of movement. It is a progressive disease and there is no cure. Malformed big toes are nearly always associated with FOP at birth – recognising this sign can prevent misdiagnosis and catastrophic complications from unnecessary investigations that can trigger bone formation.
FOP Australia revenue & valuation
| Annual revenue | $342,220 |
| 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 | $1,100,000 |
| Total funding | No funding |
Employees by Management Level
Total employees: 1-10
Seniority
Employees
Funding Data
FOP Australia has never raised funding before.
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