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Dylan's new Starband

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My son Dylan, is 10 months old. He was first diagnosed with

positional plagiocephaly at 4 months old. He was seeing our family

doctor at the time. I have had friends with babies who've had flat

spots on their heads and all of their heads rounded out. So, when

he was six months old, our doctor referred him to a cranio-facial

surgeon to see if a helmet was needed. We felt as if our doctor was

being too aggressive and didn't want to believe that Dylan might

need a helmet. So, at 8 months, we switched Dylan to a pediatrician

to get a second opinion. She recommended a helmet. He just received

his Orthomerica Starband on Friday and has adjusted so well to it.

He barely even notices it. My husband and I are not doing as well.

We are having a hard time seeing our little baby with a helmet

covering everything but his face and ears. I had no idea it would

be so big! I don't really have any questions for the group but

would like to hear how other parents have adjusted to this.

Thanks,

Beth

Grand Rapids, MI

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Hi Beth,

Welcome to the group!!! I am also from GR, as are a few other

members.

The bands are much harder for us parents than our babies. But don't

worry, you will adjust in a very short amount of time. It gets to

be such a part of them that when the band is off for a bath that

they don't look like the same baby.

Are you planning on decorating the band, or did you get one of the

patterned STARbands? If you have a plain one, I would recommend

decorating it. It helped me get over the clinical/sanitary look

that it had and it helped others approach us when we were out and

about.

Welcome again, and if you come up with any questions, ask away!

- mom to Aidan

> My son Dylan, is 10 months old. He was first diagnosed with

> positional plagiocephaly at 4 months old. He was seeing our

family

> doctor at the time. I have had friends with babies who've had

flat

> spots on their heads and all of their heads rounded out. So, when

> he was six months old, our doctor referred him to a cranio-facial

> surgeon to see if a helmet was needed. We felt as if our doctor

was

> being too aggressive and didn't want to believe that Dylan might

> need a helmet. So, at 8 months, we switched Dylan to a

pediatrician

> to get a second opinion. She recommended a helmet. He just

received

> his Orthomerica Starband on Friday and has adjusted so well to

it.

> He barely even notices it. My husband and I are not doing as

well.

> We are having a hard time seeing our little baby with a helmet

> covering everything but his face and ears. I had no idea it would

> be so big! I don't really have any questions for the group but

> would like to hear how other parents have adjusted to this.

>

> Thanks,

>

> Beth

> Grand Rapids, MI

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Hi Beth & welcome to our group:

You must be going to MFB for Dylan's STARband?! I'm in GR as are

several other members, small world!

I too had a very very difficult time seeing my Abby in her band for

the first couple wks even. I even cried about it, meanwhile, she was

happy as a clam & couldn't have cared less. You'll soon adjust to

it, trust me, if I did, you will! After the first couple wks or so,

I no longer noticed it as it became a part of her!

I'm glad Dylan is doing so well in it. He's on his way to a rounder

head. Please keep us posted on his progress.

Debbie

Jenison, MI

>

> > My son Dylan, is 10 months old. He was first diagnosed with

> > positional plagiocephaly at 4 months old. He was seeing our

> family

> > doctor at the time. I have had friends with babies who've had

> flat

> > spots on their heads and all of their heads rounded out. So,

when

> > he was six months old, our doctor referred him to a cranio-

facial

> > surgeon to see if a helmet was needed. We felt as if our doctor

> was

> > being too aggressive and didn't want to believe that Dylan might

> > need a helmet. So, at 8 months, we switched Dylan to a

> pediatrician

> > to get a second opinion. She recommended a helmet. He just

> received

> > his Orthomerica Starband on Friday and has adjusted so well to

> it.

> > He barely even notices it. My husband and I are not doing as

> well.

> > We are having a hard time seeing our little baby with a helmet

> > covering everything but his face and ears. I had no idea it

would

> > be so big! I don't really have any questions for the group but

> > would like to hear how other parents have adjusted to this.

> >

> > Thanks,

> >

> > Beth

> > Grand Rapids, MI

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Hi Beth,

I'm new to the group also, and I am hoping to get my 4 month old son

Jaden casted next month for headgear. For me, seeing him daily w/ a

flat spot on his head, not knowing if it will round out or not (even

tho our parents seem to think it will along w/ his pede, and hearing

about how all OUR friend's kids have rounded out) is very hard on

me. I'd rather see my son temporarily in a helmet NOW than have him

w/ a flat head for the rest of his life, possibly suffering from TMJ

or other effects from the plagio because I didn't treat him. When

he comes home w/ that helmet on, I am going to be thinking to myself

that it's a temporary adjustment that will last him a lifetime. And

knowing that will help me get thru the days I look at him and feel

sorry for him (or more for myself for having a child that needs

headgear because his head's not round, as if it's MY fault, when in

fact the pede should have informed us at every wellness check that

this is something we should have been on the lookout for!). Plus,

like all the other mommies are saying, the added " safety factor " w/

having their babies in a helmet is only a plus in that should they

bump their heads, they will be protected. Remember, it's only

temporary.

~Amy, mommy of Jaden 4 mo's (soon to be diagnosed and casted)

Northeastern Minnesota (howdy neighbor!)

> My son Dylan, is 10 months old. He was first diagnosed with

> positional plagiocephaly at 4 months old. He was seeing our

family

> doctor at the time. I have had friends with babies who've had

flat

> spots on their heads and all of their heads rounded out. So, when

> he was six months old, our doctor referred him to a cranio-facial

> surgeon to see if a helmet was needed. We felt as if our doctor

was

> being too aggressive and didn't want to believe that Dylan might

> need a helmet. So, at 8 months, we switched Dylan to a

pediatrician

> to get a second opinion. She recommended a helmet. He just

received

> his Orthomerica Starband on Friday and has adjusted so well to

it.

> He barely even notices it. My husband and I are not doing as

well.

> We are having a hard time seeing our little baby with a helmet

> covering everything but his face and ears. I had no idea it would

> be so big! I don't really have any questions for the group but

> would like to hear how other parents have adjusted to this.

>

> Thanks,

>

> Beth

> Grand Rapids, MI

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