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Re: Unfair competition

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No I don't think it's being unfair at all. A lot of us have a ton

of respect and faith in CT, myself included. I want to make sure I

am not holding the company in a higher regard than it is due in

regards to their motivations for helping children who are nowhere

near a CT clinic. A mom posted on their website that she lived in

the UK and wondered if anyone heard about treatments available

there. CT isn't in the UK and I can't seem to understand why they

would be opposed to having another parent point them to someone who

is able to help. I am grateful the DOC Band was available in our

vicinty. This mom wasn't lucky in that regard.

I am curious as to why they would be oppossed to a child receiving

treatment from someone else when their product isn't available in

that country.

You're right, it is their website and if they had clinics in the UK,

I think it would be fair to not want Dr. Blecher info posted on the

site. I am just trying to understand their motivation.

This mom in the UK didn't know about this group. I believe I also

sent a link to this group in the reply.

The original post from this thread also had a finger pointed right

at them for misleading her.

who is very thankful for living near a CT clinic!

Dane's mom DOC Grad

>

> >I was wondering if CT responded to this post and I missed it.

> >I am very interested in finding out why my reply on their website

to

> >the UK mom about Dr. Blecher was deleted.

>

> Hello,

>

> Don't you think maybe we are being a bit unfair to Cranial Tech?

After all, CT

> is responsibility for the information posted on their website.

Should we expect

> them to use their website to endorse competing products? Would

that be fair

> competition? I don't think so.

>

> If you want to tell people about available alternate treatments we

can use this

> mail list or you can make certain Dr. Blecher is listed at

> http://www.plagiocephaly.org/ppcs-name.asp.

>

> Just my 2 cents. I think we are judging Cranial Tech too harshly.

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