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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

It's now October and the Portrait project is almost done!!!!! Please see my website for updates: http://www.ianpettigrew.com/just-breathe-cystic-fibrosis.html

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

More good press for the book. Last couple of weeks to get involved and donate: http://prophotoblog.ca/indie-of-the-week/ian-pettigrew-portraits/

http://rockcf.storenvy.com

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...

(was hoping for some more answers that were more on topic)

Press update. Hopefully this brings in at least SOME donations. http://themighty.com/2014/05/beautiful-portraits-show-cystic-fibrosis-is-not-just-a-childhood-disease/

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...

Very special thank you to (one of my favourite comedians) Lewis Black for the mention of the portrait project on his FB page. Any and all support is very much appreciated.

**UPDATE** I have a few local people lined up in the next week to do their portrait, then I may take a week break from this. Timing for this project seems to have coincided with far TOO many other CF Charity events, and donations have been too few. As it stands right now only 20 people have...

... and STILL Canada waits for the provinces and Big Pharma to try to hammer out a deal. So sad. http://www.ctvnews.ca/health/alberta-health-minister-asks-u-s-company-why-it-charges-canadians-more-for-drug-1.1820796

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

Good luck to everyone this weekend if you are taking part in Great Strides

This news will hopefully give us some press: http://www.cysticfibrosis.ca/your-impact/hear-from-our-cf-champions/ian-pettigrew/

The first portrait for my project is done, but the need for donations is urgent. Please see the link below. James is proof that donations AND signing your organ donor card works. As a double lung recipient, he's making the most out of life. These are the stories I want to tell in my portrait...