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Hello and welcome to the group! I'm not from AZ (though I wish right

now I was!!) but wanted to say hello. You've come to a GREAT board

that will give you tons of support and advice.

My son is now just about 6 months old, was diagnosed with plagio at

4 months and has had a CranioCap since December 4th. His plagio is

severe, but we are seeing some correction now with the helmet. Whew,

thank goodness.

You are doing a great thing for your son, and at a GREAT age! Be

sure to post if you have questions, want to vent AND when you find

out more!!

Best wishes!

Kim

mom to Kaela (9 yrs) and Jaxson 6 months tort/plagio/CranioCap 12/4/03

> Hello to all.. I'm new to this group and reside in Glendale, AZ. My

> son, who is 3 1/2 months, is going to see a ped. neurosurgeon on

> January 31st because our pediatrician thinks he has positional

> plagiocephaly. Just wondering if there's anyone out there who is

> going through the same thing and living in the Phoenix metro area.

If

> so, what neurosurgeon did you see, what treatment did you use, did

> you have to fight the insurance companies, etc. I don't know anyone

> else whos child has had this so I need a ray of hope! Thanks!

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Hi! I am in Phoenix, AZ (Ahwatukee) and we just gratduated from our

DOCband. My sons ped noticed his plagio at about a month and we tried

repo-ing for a couple months w/o any results so we were refered to

Cranial Technolgies and my son was banded at 4 months, and he outgrew

the first band so he got a second one at 6 months. He graduated on

12/22 at 8.5 months and looks great. His head is not perfect but it

is much better than I ever expected. I look forward to getting to

know you and if you have any questions I would be happy to talk to

you, if you want my number you can send me your email adress. Good

Luck!

Donna momma to Jaxon 22 months and Xavier 9 months DOCgrad :o).

> Hello to all.. I'm new to this group and reside in Glendale, AZ. My

> son, who is 3 1/2 months, is going to see a ped. neurosurgeon on

> January 31st because our pediatrician thinks he has positional

> plagiocephaly. Just wondering if there's anyone out there who is

> going through the same thing and living in the Phoenix metro area.

If

> so, what neurosurgeon did you see, what treatment did you use, did

> you have to fight the insurance companies, etc. I don't know anyone

> else whos child has had this so I need a ray of hope! Thanks!

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Hi, I live in Mesa, AZ. My dd is seeing a ped. neurosurgeon today

at Desert Sam. Hospital (Dr. Manwaring from Phx Childrens

Hospital). My daughter is 16 wks old today and has mild to mod (we

will see what the doc says) flattening on the back right side of her

head and I can see the result in her forehead. Unfortunately I feel

like I am a pro at this because I have a now 6 1/2 yr old son that

had the DOC band at 6 mo of age. He had mod-severe flattening. I

also saw Dr. Manwaring and went to Cranial Technologies in Phx.

They are the ones who do the DOC band and they are EXCELLENT! Good

luck on your appt and feel free to email me if you want to talk

since we are both in AZ.

S.

mom to Presley

> Hello to all.. I'm new to this group and reside in Glendale, AZ.

My

> son, who is 3 1/2 months, is going to see a ped. neurosurgeon on

> January 31st because our pediatrician thinks he has positional

> plagiocephaly. Just wondering if there's anyone out there who is

> going through the same thing and living in the Phoenix metro area.

If

> so, what neurosurgeon did you see, what treatment did you use, did

> you have to fight the insurance companies, etc. I don't know

anyone

> else whos child has had this so I need a ray of hope! Thanks!

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Hi and welcome to the group! I'm not in AZ, but did treat my

daughter's Scaphy with a DOCBand by Cranial Technologies. They make

all their bands in AZ. I'm sure whatever treatment you chose to use,

will be a good one! Good Luck and let us know how the appt goes.

Also, if you go to the photo section of the group there are before

and after pictures of babies that have completed all different kinds

of treatments and been successful!

Dustie, mom to , DOCGrad'03

Texas

> Hello to all.. I'm new to this group and reside in Glendale, AZ. My

> son, who is 3 1/2 months, is going to see a ped. neurosurgeon on

> January 31st because our pediatrician thinks he has positional

> plagiocephaly. Just wondering if there's anyone out there who is

> going through the same thing and living in the Phoenix metro area.

If

> so, what neurosurgeon did you see, what treatment did you use, did

> you have to fight the insurance companies, etc. I don't know anyone

> else whos child has had this so I need a ray of hope! Thanks!

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Hi,

I'm not in AZ, I'm sure someone who is will reply to you soon. I just

wanted to welcome you to the group!

Welcome!!

> Hello to all.. I'm new to this group and reside in Glendale, AZ. My

> son, who is 3 1/2 months, is going to see a ped. neurosurgeon on

> January 31st because our pediatrician thinks he has positional

> plagiocephaly. Just wondering if there's anyone out there who is

> going through the same thing and living in the Phoenix metro area.

If

> so, what neurosurgeon did you see, what treatment did you use, did

> you have to fight the insurance companies, etc. I don't know anyone

> else whos child has had this so I need a ray of hope! Thanks!

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Hi! Welcome to the group!! You are definitely not alone in this.

We live in sdale and go to the Phoenix Cranial Technologies

office. My son, Max, is nearing the end of his treatment in the

DOCband and I cannot say enough about Cranial Technologies and our

clinician Margie. Regarding the insurance...we have BC/BS and they

paid 50% of the cost for the band. Some insurance companies will pay

more some less. It really depends on your insurance company and the

policy you have. Your son is at a great age for correction. I'm

impressed that your pediatrician is so proactive and knowledgeable

about Plagiocephaly.

All the very best to you as you make this decision!

Kathleen and Max

sdale

> Hello to all.. I'm new to this group and reside in Glendale, AZ. My

> son, who is 3 1/2 months, is going to see a ped. neurosurgeon on

> January 31st because our pediatrician thinks he has positional

> plagiocephaly. Just wondering if there's anyone out there who is

> going through the same thing and living in the Phoenix metro area.

If

> so, what neurosurgeon did you see, what treatment did you use, did

> you have to fight the insurance companies, etc. I don't know anyone

> else whos child has had this so I need a ray of hope! Thanks!

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Thanks for the kind words, I'm hoping to get this corrected before

it's too late. I loooove my pediatrician, she's a nurse practitioner

and with all the problems we've had she's a godsend. We'll see how it

goes on the 30th!

> > Hello to all.. I'm new to this group and reside in Glendale, AZ.

My

> > son, who is 3 1/2 months, is going to see a ped. neurosurgeon on

> > January 31st because our pediatrician thinks he has positional

> > plagiocephaly. Just wondering if there's anyone out there who is

> > going through the same thing and living in the Phoenix metro

area.

> If

> > so, what neurosurgeon did you see, what treatment did you use,

did

> > you have to fight the insurance companies, etc. I don't know

anyone

> > else whos child has had this so I need a ray of hope! Thanks!

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Hey, how did they appointment go? I am wondering how " severe " my

son's is, it looks pretty bad to me. How do they determine that

anyway? And what's with the 78 degree weather? :P

> > Hello to all.. I'm new to this group and reside in Glendale, AZ.

> My

> > son, who is 3 1/2 months, is going to see a ped. neurosurgeon on

> > January 31st because our pediatrician thinks he has positional

> > plagiocephaly. Just wondering if there's anyone out there who is

> > going through the same thing and living in the Phoenix metro

area.

> If

> > so, what neurosurgeon did you see, what treatment did you use,

did

> > you have to fight the insurance companies, etc. I don't know

> anyone

> > else whos child has had this so I need a ray of hope! Thanks!

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Thanks so much for the kind words! I agree, I looove my pediatrician,

she's actually a nurse practitioner and she's fabulous. Our

appointment is on the 30th so we'll see what they say, and it

couldn't be sooner, my little guy decided to start rolling over so

keeping him on his tummy to play and help out the plagio isn't as

much of an option anymore! ;-)

> > Hello to all.. I'm new to this group and reside in Glendale, AZ.

My

> > son, who is 3 1/2 months, is going to see a ped. neurosurgeon on

> > January 31st because our pediatrician thinks he has positional

> > plagiocephaly. Just wondering if there's anyone out there who is

> > going through the same thing and living in the Phoenix metro

area.

> If

> > so, what neurosurgeon did you see, what treatment did you use,

did

> > you have to fight the insurance companies, etc. I don't know

anyone

> > else whos child has had this so I need a ray of hope! Thanks!

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