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Along with the Adult CF Portrait Book, the shirts also now available to help raise money to expand the Salty Girls project in Daytona. http://thecfproject.bigcartel.com/products

The adults with CF book is being printed right now!!!! Will start shipping in about a week. PLEASE see link below if you haven't already looked at the project. Also, we'll be in daytona for the CF 5K Run and will be working on the new project, "Salty Girls". To help fund the project and...

The Just Breathe book is now in its final phase and is NOW up for pre-sale. Any help to raise some awareness for Adults with CF and this project would be greatly appreciated. http://thecfproject.bigcartel.com/product/just-breathe-the-book

First of all a special thank you to everyone that has donated, both time and money, to this project. We are getting some amazing press - thus awareness - for adults with CF. And that was really the whole goal. Its now saturday AUG2 and we have 3 days left to donate. The route for the first trip...

We are almost at the goal line... 83% funded on Kickstarter now. That's incredible and I can't thank people enough. This project has been getting some great press lately... please help pass it along and hopefully we'll make out final goal. http://www.chch.com/cystic-fibrosis-lens/ xo

Now on Kickstarter - please help spread the word: https://www.kickstarter.com/projects/2131015647/just-breathe-adults-living-with-cystic-fibrosis

Special thanks to Emily at Rock CF in Detroit. After a couple weeks of a break (I figured people were probably over-donated) the project is back in full swing and what a great way to get it started then heading to Detroit and hanging out at Rock CF with Emily Schaller. Had a great time (except...

As many of you know I am planning my book or portraits of adults with CF. Donations have stalled a bit (probably various reasons for that) but I want everyone's opinion on this issue: I'd like to focus the attention a bit more on specific factors affecting adults with CF, maybe a tighter core...

Hopefully the press will keep building, because donations have really tapered off: http://www.thephoblographer.com/2014/05/19/photographing-faces-cystic-fibrosis-interview-ian-ross-pettigrew/#.U3n63F5NzRo

I am an award-winning portrait photographer from Hamilton, ON (Canada). I am also a 45 year old male with Cystic Fibrosis. Luckily my diagnosis is considered a milder variant of the disease, but it is CF nonetheless. I was diagnosed about 7 years ago. Before that I had no idea, but looking back...