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I am Taryn, I am 22 years old From Brookville,OH.I was Diagnosed at 5 months old & currently going through the lung transplant process.I don't let anything get me down & I live my life to the fullest. I'm a firm believer that god has a reason for everything & he gave me these lungs to help inspire others to not take things for granted.
This is my son, Jayce. Jayce is 7 years old & was diagnosed with Cystic Fibrosis at 4 months old. I also have a 12 year old daughter, Makinzie, who does not have CF. My husband & I found out that we were carriers of CF when I was 5 months pregnant with Jayce. There was no history of CF on either sides of the family. Jayce has two copies of the Delta F508 mutation. Jayce is your typical 7 year old boy. He loves playing basketball, soccer, & baseball. Jayce is the comedian of the family. There isn't a day that goes by that he doesn't make me laugh! Jayce loves playing outside with his buddies.... Riding bikes, playing in the dirt, & causing ruckus! My little dare devil! Jayce is a ladies man already! He loves flirting with his big sister's friends! Jayce seems to have a mild case of CF which I'm so thankful for. However, Jayce knows & understands how important it is to do his treatments & take care of himself. I hope that one day soon, CF will stand for CURE FOUND!

Melissa Turner
A Race for Jayce
Name's Morgan. 22. Genetic disease called Cystic Fibrosis. Google it, learn it, fight for it, cure it.
I get along with everyone unless you're some racist, homophobic, ignorant douchebag. So, if you're neither of those, add me and we should get along great! :D

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Born March 16 1981, diagnosed 9 months later. Never have known anything but CF but man have things come a long way! At age 5, I gained partner in this walk my brother was born, he too would be diagnosed  as well. So to say my family's life was never dull. So blessed throughout my whole life with a wonderfully supportive family as well as friends and a great community of people always there to help no matter the need! 
I'm proud to say that help and support has never ended. I have gained a great helpmate to whom I've been married to for 13 yrs.  We also have been blessed with two beautiful  and healthy children (yes I gave birth to them), take that CF! So many obstacles so many victories, blessed beyond  words can say! FOREVER THANKFULL for the village it takes to make our family function and their never wavering support! Friends, family, and the support of our Faith is what has carried me this far, going to keep on! I always have said "I have CF but it don't have me." 
Stephanie Stephens, Peebles OH
Hello, My name is Matt Sneary, I am a 29 year old male with Cystic Fibrosis. Im a double delta 508 gene. Diagnosed at six months after getting really sick and doctors not being able to figure out what was wrong. Through the years I have had ups and downs with cf. In the last 2-3 years I have switched gears and have been focusing my career to help support nonprofits and campaigning for cf. I am currently going to college for business/marketing. I hope to be able to work full time and support cf research after I get my degree. I currently volunteer for a nonprofit called More Than Just Me and do marketing for them.

My hobbies include mainly activities outdoors. I love hunting, fishing, camping, and hiking. Spend a lot of time on the range with my friends shooting guns and building guns. I spend a good amount of time working on my cars. I live with my wife and four Siberian Huskies at our little house in Portage, MI. I have made it a goal in life to be able to travel as much as I can and also be able to work from home. So if I want to be in Michigan during the summer in the peak of fishing season, or on the beach in Fl during the chilly northern cold months, I still want to have the capability of working as much as I can. Because ultimately, the main goal is to find a cure for Cystic Fibrosis.