Arianna Faro struggled for years with the challenges of living with Klippel-Trenaunay (KT) syndrome, but has come to accept the role it plays in her life. Here, she shares her story.
Also, you can watch a video of Arianna talking about Klippel-Trenaunay.
Have thoughts or feedback? Please share them with us.
Related posts:
- Children's doctor fixes rare facial anomoly (for the second time this year)
- Empowering patients with access, control of their health information
- One mother's story: shaken baby syndrome
- A former patient's story: Regaining independence after being paralyzed at 17
- One mother's story: Help, my babies need contact lenses












{ 1 trackback }
{ 4 comments… read them below or add one }
Thank you for bringing us the story of this gutsy young woman! more power to you, Arianna!
*Comments taken from Children’s Facebook fan page*
Joanie Figueroa
What an inspiring story
Carol Rita Sylvia
Thank you, Arianna, for sharing your story! Stay well!
Good for her! I love when people have something that is “wrong” with them or makes them different and they learn to deal with it and turn it into something positive. I try to think the same. I mean, there’s always someone worse off than you.. so why be upset about life. Living is what is most important.
Thanks for your message. I will be out of the office April 13-15 and working remotely on Friday, April 16. During this time, I will have limited e-mail access. If you need to reach me immediately, please re-send your message with high importance (and it will be forwarded to my mobile) or reach me via cell phone at 617-600-8686. Otherwise, I will return your message at my first opportunity. Thank you.