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April 21, 2016 11:07 pm
4Kate Michaelis Nielsen updates us on her daughter: Rachel Nielsen is a teenager diagnosed as Undiagnosed. She has struggled with getting proper care for the past 18 months...
April 20, 2016 4:24 pm
11Sometimes, hindsight is 20/20. And when I think back on my life, I realize that I’ve always been sick. I just didn’t see it at first. When I...
April 18, 2016 2:30 am
5Dear Undiagnosed Alliance, Please find the Undiagnosed Day flyer! Thank you all for your continued support of the Undiagnosed Alliance. I had several more organizations email me to...
April 17, 2016 11:25 pm
3Mark Kristensen and his Angel’s Hands Foundation (AHR) generously donated towards our very own Rare Teen, Hailey Sampsel, for her travel to the three-week Comprehensive Pain Rehabilitation...
April 17, 2016 9:56 pm
7Welcome to Nicholas Volker One in a Billion Foundation Mission To inspire the world to improve the quality of life for those with undiagnosed and rare disease...
April 15, 2016 10:57 pm
11Andrew Scholte: “For the past two years I have been partnered with Emma, a member of the Gaucher community for the Running For Rare Team. This year I...
April 14, 2016 4:29 pm
8I am unsure where to begin, so much has changed since the last time I’ve posted. I have started college, moved into the dorms and most importantly I...
April 8, 2016 9:05 pm
12We have tirelessly searched for answers and have sacrificed nearly everything for us and for our loved ones with a rare or undiagnosed disease to receive the information and...
April 7, 2016 6:32 pm
8Senator Hatch’s remarks from the hearing yesterday: “This amendment contains the provisions of the Open act, a bill I’m sponsoring with Senator Klobuchar to promote new therapies for...
April 5, 2016 2:13 am
6The breathtaking story of a young boy with a never-before-seen disease, and the doctors who take a bold step into the future of medicine to save him—based on...