Ali's Army against Fibrodysplasia Ossificans Progressiva


Ali McKean suffers from FOP, one of the rarest & most disabling conditions
in the world. Please continue through the site to learn more about FOP, it's
signs, and Ali's story.

The Army :) Join Site

CONGRATULATIONS  to Angel Johnson, the winner of the tshirt for the 200 member drawing! Make sure your profile is complete to be eligible for future drawings & giveaways!! As always thank you all for being part of Ali's Army!

CONGRATULATIONS to Kim Harden, who was the winner of the tshirt for the 100  member drawing! Once we hit 200 members we will giveaway another item! We are only a few away!!

Please join the army here, membership is free! We plan on many exciting things in the future for members only! So sign up today! Thank you for visiting Ali's Army and don't forget to spread the word and help us raise awareness!

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Keirsten Gildehaus
Member
Female
16 years old

topisma99
Member
Male
24 years old
About Me


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Applejackisthebestpony
Member
Female
About Me

I wub My Little Pony:D and I want to help in the fight against FOP!!!:D LET'S ALL FIGHT AGAINST FOP!!! :D:D:D



Precious LaMont
Member
Female
About Me
Hello! My name is Precious, I'm 20 years old and I know what its like living with this condition, I was diagnosed with fop when I was a couple weeks old. I've been in a wheelchair for almost 9 years now.

Hannah
Member
Female
About Me
I first heard about FOP on Youtube in list25's 25 Weird Medical Disorders, and since then I couldn't get it out of my head. I was assigned a project at school to inform people of a disorder so I chose FOP in hopes that more people would be aware, maybe even join Ali's Army :)

Amanda
Member
Female
23 years old
About Me




Tamika_lave
Member
Female
23 years old

Kylene
Member
Female
16 years old
About Me
I'm a student of Smcc, On November 20 I was blessed by meeting Mrs. McKee and Ali! I learned about Ali and her disease! It makes me very heartbroken knowing what this little girl goes through, but I think she is strong and God gives her strength! Ali is so adorable! She seems like a very smart and loving little girl ! Forever will Ali be in my prayers! ð???ð??ªâ?¤ï¸?

FOP supporter FOREVER <3
Member
Female
15 years old
About Me

I'm 14, I'm a girl, I'm from New zealand and I recently done an assignment for Health about an certain disease and I proudly chose to do mine on Fibrodysplasia Ossificans Progressiva (FOP) to make people aware of this and I also put on my page the name of this website for people to have a look and hopefully donate for little Ali(: I got an A+ on my assignment and my teacher put it up around school and allowed me to speak at assembly about it.   I know it isn't much but I'm hoping that because I done my speech at an graduation assembly where parents were present, that they registered and donated as well.   Prayers go to everyone :D



tracy
Member
Female
42 years old

Tina Shaffer
Member
Female
45 years old

BrookesMOM
Member
Female
27 years old

Bailie
Member
Female
About Me
I've seen Ali a couple of times and it kills me to have to see her with all of this pain. I am Ali's Army???

Heather Livingston
Member
Female
47 years old

Fultzy9715
Member
Female
17 years old
About Me
Junior at MHS

Gaby
Member
Female
19 years old

Hi
Member
Female
About Me
I'm 13, and I want to help Ali

MELISSA WEHBE
Member
Female
42 years old
About Me

Advocate-abused, unfortunate, civil rights. Writer, nutrition, business, 2 kids. Mary Vassallo grandaughter(friend Joe Bonanno), Alonzo Wehbe, MARSHFIELD MASSACHUSETTS USA · https://www.facebook.com/sunladybargains

 



Skyblue
Member
Male
31 years old
About Me

Spreading the word



BritBeaver07
Member
Female
25 years old
About Me

I'm Brittany. Born in Bellevue and currently living in Okinawa, Japan. I am married to a United States Marine (hence why I live in Japan :)). We have been married since 2007. I have 2 dogs which are like my small children.

I really have a heart for children born with diseases since my little nephew was born with CMV and was given a grim outlook for his life. I am always willing to help make diseases that need help getting the word out.

These poor children shouldn't have to suffer with dieases like FOP and CMV. I hope other people open their hearts and get the word out.

It's terrible as a family member watching someone you love go through the pain or the hospitalizations or just being told by doctors horrible news. So everyone needs to band together and get the word out so scientists think to help find cures for these diseases and so we can help generate the funding to develop the cures!


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