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Hello all! I am new to the group and feeling the " guilt " over my 6

month old son being diagosed with torticollis and positional

plagiocephaly. We knew right away that my son definitely favored one

side of his head but being a first time mom, I didn't really think it

was a problem. I asked the pediatrican about it at our 4 week

checkup and told us to try to use wedges and sleep positioners to

help position his head. However, it didn't seem to work. It seemed

that every time we went to the doctor, he told us to just encourage a

lot of tummy time and keep using the wedges and that my son would

eventually grow out of this problem. After several other problems

with our pediatrican, we decided to switch pediatrican groups. At

our first appointment with the new doctor, they immediately referred

us to the plastic surgery dept. at Cincinnati Children's Hospital

Medical Center. We had to wait 2 months for the first appointment!

After seeing the doctors and physical therapists at CCHMC, they told

us that my son should have been seeing a physical therapist for his

torticollis since we first saw the problem. Because of his

torticollis, it prevented him from turning his head fully and thus

caused positional plagiocephaly. On top of this, my son is in the

98% for his head circumference. The doctors said that this also can

contribute to plagiocephaly since his head weighs so darn much that

it is hard for him to hold up.

I feel like our first pediatrican " dropped the ball " --especially

since they said that we should have been doing therapy for his neck

for a couple of months now. I also feel like the doctors at CCHMC

think that my son's plagiocephaly/torticollis was my fault. They

told me that if my husband and I decide to have another child, we

need to make sure that we give the baby a lot more tummy time.

My son has been fitted for his helmet and will be getting it in the

next week or two. Althought I hate the fact that he'll have to wear

it and have people stare at him, I know that this is the best thing

for him.

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Welcome!

I am sure as you start to read all the other posts - you will see you are not alone in this!!! It is NOT your fault!

Sorry your 1st dr dropped the ball - alot of parents have had to fight for treatment - you are blessed to have the 2nd dr that was so proactive!!!

Jen and Luli - 26 months

Left tort - Right Plagio - Hanger Band Grad - CA

http://www.babiesonline.com/babies/j/jens5th/

First time to group...

Hello all! I am new to the group and feeling the "guilt" over my 6

month old son being diagosed with torticollis and positional

plagiocephaly. We knew right away that my son definitely favored one

side of his head but being a first time mom, I didn't really think it

was a problem. I asked the pediatrican about it at our 4 week

checkup and told us to try to use wedges and sleep positioners to

help position his head. However, it didn't seem to work. It seemed

that every time we went to the doctor, he told us to just encourage a

lot of tummy time and keep using the wedges and that my son would

eventually grow out of this problem. After several other problems

with our pediatrican, we decided to switch pediatrican groups. At

our first appointment with the new doctor, they immediately referred

us to the plastic surgery dept. at Cincinnati Children's Hospital

Medical Center. We had to wait 2 months for the first appointment!

After seeing the doctors and physical therapists at CCHMC, they told

us that my son should have been seeing a physical therapist for his

torticollis since we first saw the problem. Because of his

torticollis, it prevented him from turning his head fully and thus

caused positional plagiocephaly. On top of this, my son is in the

98% for his head circumference. The doctors said that this also can

contribute to plagiocephaly since his head weighs so darn much that

it is hard for him to hold up.

I feel like our first pediatrican "dropped the ball"--especially

since they said that we should have been doing therapy for his neck

for a couple of months now. I also feel like the doctors at CCHMC

think that my son's plagiocephaly/torticollis was my fault. They

told me that if my husband and I decide to have another child, we

need to make sure that we give the baby a lot more tummy time.

My son has been fitted for his helmet and will be getting it in the

next week or two. Althought I hate the fact that he'll have to wear

it and have people stare at him, I know that this is the best thing

for him.

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