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Hello everyone,

This mail comes to the group from the UK.

Our son, Joe, is now eight months old and has been diagnosed (by

ourselves, using the Internet for research) to have the condition

Positional Plagiocephaly.

Our community Doctors have repeatedly told us over that past months

that his unusual head shape is " nothing to worry about " and that " it

will return to normal " . We are now aware that, at this late stage,

that it will probably not return to normal and may even cause other

problem, such as with his sight or jaw, in later life.

We are kicking ourselves for simply trusting the local health staff

and not taking it upon ourselves to investigate earlier. With our

new found knowledge, we are obviously very worried about what can be

done him in the UK. All of the information we have found and all the

available treatment appears to be based in the US.

Can anyone advise us of any specialists or help we can get in the UK,

or how we could go about getting help in the US.

Thank you in advance.

Steve, & Joe.

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-Dear Steve and Joe

I know of two doctors in europe, one is through a DOC clinic in

Spain. i'm told it is one half of an hour outside of Barcelona. I

have two e-mail addresses from a doctor there. They are:

info@... and littefi@..., this second e-

mail is to a Dr. Joan Pinyot i Garros, whom i have corresponded with

a few times. There is also a Dr. Blecher, who is the doctor we were

seeing, he is located in Geissen, Germany, but I know he travels to

the UK and Spain and other places throughout Europe. His e-mail

address is: Joerg.c.blecher@... and his office

phone number is: 0641-99-46274. I hope this information is of some

help. If you have any questions i can help with just let me know.

Good Luck.

Oh also try the website: www.plagiocefalio.com

Marcia

-- In Plagiocephalyegroups, steve.haley@b... wrote:

> Hello everyone,

>

> This mail comes to the group from the UK.

>

> Our son, Joe, is now eight months old and has been diagnosed (by

> ourselves, using the Internet for research) to have the condition

> Positional Plagiocephaly.

>

> Our community Doctors have repeatedly told us over that past months

> that his unusual head shape is " nothing to worry about " and

that " it

> will return to normal " . We are now aware that, at this late stage,

> that it will probably not return to normal and may even cause other

> problem, such as with his sight or jaw, in later life.

>

> We are kicking ourselves for simply trusting the local health staff

> and not taking it upon ourselves to investigate earlier. With our

> new found knowledge, we are obviously very worried about what can

be

> done him in the UK. All of the information we have found and all

the

> available treatment appears to be based in the US.

>

> Can anyone advise us of any specialists or help we can get in the

UK,

> or how we could go about getting help in the US.

>

> Thank you in advance.

>

> Steve, & Joe.

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Steve, , and Joe

I know of two doctors in europe, one is through a DOC clinic in

Spain. i'm told it is one half of an hour outside of Barcelona. I

have two e-mail addresses from a doctor there. They are:

info@... and littefi@..., this second e-

mail is to a Dr. Joan Pinyot i Garros, whom i have corresponded with

a few times. There is also a Dr. Blecher, who is the doctor we were

seeing, he is located in Geissen, Germany, but I know he travels to

the UK and Spain and other places throughout Europe. His e-mail

address is: Joerg.c.blecher@... and his office

phone number is: 0641-99-46274. Also try the website

www.plagicefalio.com. I hope this information is of some help. If

you have any questions i can help with just let me know. Good Luck.

Marcia

> Hello everyone,

>

> This mail comes to the group from the UK.

>

> Our son, Joe, is now eight months old and has been diagnosed (by

> ourselves, using the Internet for research) to have the condition

> Positional Plagiocephaly.

>

> Our community Doctors have repeatedly told us over that past months

> that his unusual head shape is " nothing to worry about " and

that " it

> will return to normal " . We are now aware that, at this late stage,

> that it will probably not return to normal and may even cause other

> problem, such as with his sight or jaw, in later life.

>

> We are kicking ourselves for simply trusting the local health staff

> and not taking it upon ourselves to investigate earlier. With our

> new found knowledge, we are obviously very worried about what can

be

> done him in the UK. All of the information we have found and all

the

> available treatment appears to be based in the US.

>

> Can anyone advise us of any specialists or help we can get in the

UK,

> or how we could go about getting help in the US.

>

> Thank you in advance.

>

> Steve, & Joe.

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