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Broonchomalacia, Tracheomalacia & Laryngomalacia
by Hunters_mom, Apr 18, 2009 03:16PM
Check out:
LMTM _ Babies @ yahoo groups . com
It's a support group for parents that have children with either Laryngomalacia and/or Tracheomalacia and/or Bronchomalacia. If the site doesn't work goggle yahoo support groups then put in Tracheomalacia. You have to be a member to see everything. Just write a brief story about your situation, it gets viewed and they you get accepted. It's a wonderful support group with 58 member around the globe. The malacia's are rare and not much is known about them. Doctors try their best.
Colleen
mother to Dominick (12) Hunter (10 TM) Jennifer (9)
This discussion is related to my son.
LMTM _ Babies @ yahoo groups . com
It's a support group for parents that have children with either Laryngomalacia and/or Tracheomalacia and/or Bronchomalacia. If the site doesn't work goggle yahoo support groups then put in Tracheomalacia. You have to be a member to see everything. Just write a brief story about your situation, it gets viewed and they you get accepted. It's a wonderful support group with 58 member around the globe. The malacia's are rare and not much is known about them. Doctors try their best.
Colleen
mother to Dominick (12) Hunter (10 TM) Jennifer (9)
This discussion is related to my son.
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