I Have Hemifacial Microsomia
Hello! I am a mommy of a 2 year old who has Hemifacial Microsomia. I have shed so many tears and I would really love some contacts and support to share my fears, tears and joy with. I have done so much research but would love to have some real life people to relate to. We are at the stage now where he is growning like a weed but his affected side of his face is not. Breaks a mommies heart to look at pictures sometimes because I just want him to be like everyone else but reality is....hes not. :(
Having said that: my angel is so bright. He is learning new words everyday and so observant of his world. He loves to explore things he shouldn't...guess that is what boys do!!!! I really have no idea if he is on target speech wise because I have noone to compare him to. I think his development of everything else is perfect tho. Well maybe I am naive IDK :)
Having said that: my angel is so bright. He is learning new words everyday and so observant of his world. He loves to explore things he shouldn't...guess that is what boys do!!!! I really have no idea if he is on target speech wise because I have noone to compare him to. I think his development of everything else is perfect tho. Well maybe I am naive IDK :)
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