On June 12, 2007 our third beautiful child Henry Theodore Haag was born. Soon after he turned 2 we learned that he had a Neurofibromatosis (NF). NF is the term for a set of distinct genetic disorders characterized by their tendencies to cause multiple, benign (non-cancerous) tumors to grow on nerves. Henry is currently undergoing Chemotherapy for a brain tumor we discovered in February of 2011.
Thursday, March 31, 2011
July 2010
Kristen ran the Basalt half marathon in july and raised money for the Children's Tumor Foundation in Henry's behalf.
June 2010
April 2010
NF Forum 2010. We went to Las Vegas in April to the National Forum. We had a great time a meet many people in the Colorado NF Chapter. Learned about all the different fundraising efforts through the Children's Tumor Foundation. Kristen joined the NF Endurance Team and immediately started training and fundraising for the San Diego half marathon in June.
January 2010
June 2010
The MRI in May showed us a few things. Henry had an optic glioma on his left optical nerve. This is a tumor that can cause blindness. It also revealed that his growth plate on his right fibula had stopped growing. This was the main reason for him not being able to walk and we told that we needed to do surgery to correct this bone deformity. Bone deformity's are very common with kids that have NF.
May 2009
Right before Henry's second birthday he still could not walk on his own. We made an appointment with our pediatrician and during the examination we were made aware of some small spots on his stomach and back. They are called cafe au lait spots. The doctor told us that these spots were typical with children that have Neurofibromatosis (NF). We made an appointment at St. Mary's hospital in Grand Junction for an MRI. The MRI confirmed that Henry indeed had NF.
Sunday, March 27, 2011
Henry, the world. The world, Henry...
Days Before Henry
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