I notified national CCFA in NY city about what happened and I got their response today so I'd just like to share this with everyone:
Dear Ms. :
Thank you for contacting the Crohn’s & Colitis Foundation of America through your recent email regarding Jennifer Jaffe’s story on Change.org. This story is very disturbing to hear .
First, I want to thank you for your commitment to CCFA and for being an active volunteer in the Western New York Chapter. We appreciate your support and sharing Jennifer’s story.
We contacted the TSA to get clarification on the scanner policy. They provided the information below, also found on their website at
http://www.tsa.gov/travelers/airtravel/specialneeds/editorial_1370.shtm#3. Patients should opt out of use of the scanners and:
Advise the Security Officer if you are wearing orthopedic shoes, support appliances, or other exterior medical devices and where the devices are located.
If you are wearing an exterior medical device and are uncomfortable with going through the metal detector or be handwanded, you may request a pat-down inspection and visual inspection of your device instead.
You should be offered a private screening if clothing is required to be lifted to complete the inspection process.
Advise the Security Officer if you have an ostomy or urine bag. You will not be required to expose these devices for inspection.
The Airlines follow the guidance provided for under US Department of Transportation: Aviation Consumer Protection and Enforcement site,
http://airconsumer.ost.dot.gov/publications/horizons.htm.
We have received numerous calls and inquires regarding the TSA and how the airlines respond and treat IBD patients. Therefore, we are adding information on this topic to our website. In addition we are currently working on developing resources for the IBD community to help them navigate both the airlines and TSA. In addition, we intend to provide resources to TSA and the airline industry information about Inflammatory Bowel Disease so they are better informed about needs and resources of individuals with IBD. We are currently developing these materials and intend to have them available before the end of the year.
I have copied our integrated media specialist on your request to have the link to Change.org posted on the CCFA website and other pages. You are encouraged to share this and other information on the CCFA Facebook page:
http://www.facebook.com/find-friends/browser/?ref=ler#!/ccfafb as well as on the CCFA community website:
http://www.ccfacommunity.org/ . The Community website is a great way to connect to the online IBD community and inform them about advocacy issues and resources.
If, after reviewing the information included in the e-mail, you have further questions, please email CCFA or call our toll-free number at 1.888.MY.GUT.PAIN (1.888.694.8872), Monday through Friday 9am-5pm EST to speak with an information specialist.
Sincerely,
Laura D. Wingate
Senior Director, Field & National Programs