LUCAS MONTGOMERY
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Lucas was born July 31,1997. He was diagnosed with Sanfilippo B, MPS III - B, in January 2006. It is a life limiting disorder, there is no cure.

LAPS FOR LUCAS

Arc Newsletter

Article 11/06

Donate to the National MPS Society

2007 MPS AWARENESS DAY photos

MAY 15TH IS INTERNATIONAL MPS AWARENESS DAY

lapsforlucas@yahoo.com

KWWL AWARENESS NEWSCAST 5/07

Information on substrate deprivation therapy possible treatment to halt progression of the disorder.

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  SUNDAY, NOVEMBER 30, 2008 05:34 PM, CST
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We had a wonderful Thanksgiving. It was a relaxing 5 days home and just a wee bit of shopping. Lucas was doing awesome , full of fun and smiles. Well, out of no where he has a cold with a cough and MORE wheezing!! I have no idea where he picked it up but we spent all night last night doing albuterol treatments. It of course is not slowing him down any but I could use a well deserved nap. He watched football with Dad today and I have my fingers and toes crossed his symptoms will not turn ugly over night. Our night will determine if we head to our favorite home away from home (not!!) the doctors office...... It dropped in temperature last night and has been snowing today ... not sure if this is related or not ... barometric changes maybe??????
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PLEASE SIGN LUCAS' GUESTBOOK, WE LOVE TO HEAR FROM YOU.

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HOSPITAL INFORMATION
Lucas is at home
in Cedar Rapids, IA
United States