FOP affects One in 2 million...meet one...

Ali's Army against Fibrodysplasia Ossificans Progressiva. Ali McKean suffers from FOP,  one of the rarest &
 most disabling conditions in the world. Read on throughout the site to learn more about Ali and FOP.

Email us your photos of you sporting the battle gear at [email protected] be sure to reference battle gear photos in the subject line! We will add your supportive pictures to the website!!

There are several ways to contact us.
We can be contacted via email at [email protected]
We also accept mail at:
PO BOX 503
Bellevue, Ohio 44811
You can follow Ali's Army on facebook at this link: https://www.facebook.com/pages/Alis-Army/291695637556904
You can friend her parents on facebook at this link: https://www.facebook.com/Angela.and.Gabriel.McKean
You can also follow Ali's story from day one on our blog at: http://www.thoughts.com/angingabemckean

OR of course you can submit the form below!


We look forward to hearing from you! 

Please fill out the form below and click "Submit." We will get back to you as soon as possible!
**Attention to all current and future followers** We appreciate everyone's want to help and the offers that have been made, but we need to make it VERY clear, that all merchandise being sold on behalf of Ali to raise money for her medical needs is featured on her website ONLY. If you do NOT see it on her official website at www.alis-army.org, then it is NOT official gear and the purchase of said items do NOT benefit her! I would advise everyone to make sure that any FOP purchases you make for the cause are made through OFFICIAL websites, as we have several people trying to pick up on Ali's story and use it for their own personal gain. The ONLY legal site for Ali's donations will be www.alis-army.org from this day forward. We will NOT be using any other website or page, on the web. Please be sure when making a donation that the site you entered in actually reads www.alis-army.org once the page loads. I am shutting down our giveforward.com page today and will NOT be using it in the future. Unless you are on her official website, with us in person or mailing donations to the addresses listed on her official page, or at a fundraiser that was featured on her website you are NOT giving to Ali. As you also know donations can be made directly to IFOPA as well, their official website is www.ifopa.org. If you ever have any questions regarding someone's official page please contact us, we have the means to find this information for you as we are connected with the FOP community, and can ask the individuals personally. To all of our FOP'ers please feel free to post YOUR official websites or links here. We are happy to share them & are striving to prevent any misleading to our supporters. Anyone infringing on any FOP charities and using our families medical issues for personal gain will be punished to the full extent of the law. Have some compassion people, our child is suffering, numerous others are suffering, how dare you try to use someone's disability as personal gain for yourself! On another note if you would like to actually help in a LEGAL way we would love to hear from you and guide you in the right direction. If you ever have any questions please feel free to contact us personally. We would be happy to answer ANY and all questions that we can.
Thanks!


Thank you for contacting us. We will get back to you as soon as possible
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