In addition to painting their nails light blue for laryngomalacia, a number of our families are stepping up and raising awareness for an airway defect many can not pronounce.
In Australia:
Mel says,
"My
husband's work (NSW Ambulance) is having a state wide awareness and
fund-raiser. Morning teas/ awareness drives etc are being held from the 7-12th of July."
 |
| Event Invite |
In London:
Sally says,
"We'll
be in the Everlina London on 10th July, planned procedure 8th July.
Will make sure as one of Londons largest hubs for ENT that #LuTheLamb is
with us. Our consultant last time were were there was interested to
know all about Coping With LM."
United States:
Crystal says,
"Our son (Kane)'s first birthday is July 9, 2016 so we asked our family and friends to make a donation to Coping With LM in honor of Kane and his battle with laryngomalacia."
 | |||
| Kane at 11 months old |
Megan says,
"We will be painting our nails blue and hosting our 3rd Malacia Meet Up in Illinois."
 |
| Illinois Malacia Meet Up, 2015 |
Megan says,
"My baby girl and I are painting our nails light blue and then we as a family, are wearing all light blue! I even got a light blue sling specially for the day!"
"My baby girl and I are painting our nails light blue and then we as a family, are wearing all light blue! I even got a light blue sling specially for the day!"
WHAT WILL YOU BE DOING ON WORLD AIRWAY DEFECTS DAY?
Comment below and be sure to use #AirwayDefectsDay in all of your social media posts!
Learn more about laryngomalacia and how we help at CopingWithLM.org
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