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Re: [Stickler Syndrome ] Re: New and looking for support   Message List  
Reply | Forward Message #453 of 811 |
Hi

How good is it to have someone to chat to in the UK about SS as most people I
have found are from Aus or USA and their way of treating people id so different.
I have found a site that I printed loads from but I was going to buy the book on
SS have you read it or even heard about it I think its from the site you
mentioned.
We are in the early stages of stickler so I am not sure what to expect as
everyone is so different, I no that my son is very short sighted and needs
glasses now but I have been told he is to young for them (just 7 months). I have
read that a baby in the US was given a contact lens but I guess that the UK is
not that far advanced in Sticklers as these places seem to have far more people
with the syndrom.
Anyway thanks for taking the time to mail me back I think I could learn lots
from you as you are old hat at SS and as you said the docs seem to no very
little about it and expect us to help them.

Thanks again

Carole


----- Original Message ----
From: Amy <amwshamws@...>
To: sticklersyndrome@yahoogroups.com
Sent: Friday, October 27, 2006 6:19:08 PM
Subject: [Stickler Syndrome ] Re: New and looking for support

--- In sticklersyndrome@ yahoogroups. com, "carole" <sillypilly51@ ...>
wrote:
>
> Hi I have a 5 month old little boy who has been dignosed with stickler
> syndrome.
> I have been told that it runs in his fathers side of the family but I
> have very little to do with them so I am trying to find ouy more about
> this syndrome from the internet. If antone knows of any good sites
> please e-mail them to me as all the helpI can get would be welcome.
>
> thanks
>

Hi Carole I am Amy, the best thing I would suggest is just use some
good search engines and put Stickler syndrome in and you should have
lots of sites come up. the one I use most here in the UK is
www.stickler. org.uk

This site also has lots of fact sheets you can print out to give to
doctors or teachers when the time comes as I often find I know more
about the condition than most of my doctors and they have found the
sheets most useful.
If you have any mre question feel free to email me to chat.

Amy






[Non-text portions of this message have been removed]




Fri Oct 27, 2006 10:13 pm

sillypilly51
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Message #453 of 811 |
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Hi How good is it to have someone to chat to in the UK about SS as most people I have found are from Aus or USA and their way of treating people id so...
carole pilgrim
sillypilly51
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Oct 27, 2006
10:14 pm

I have a 4 month old with SS also. He got it from his fathers side as well. His eyes seem good at the moment but he has low frequency hearing loss. He also...
Jacqui
momofbksa2001
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Oct 27, 2006
10:34 pm

hi carole. glad you found the info, that can be most useful. Are you on about wendy hughes' book? i have not actually read it bt can highly recommend it and i...
Amy
amwshamws
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Oct 29, 2006
9:58 am

Hello Carole, I live in London , my daughter is now three and she has glasses since she was 10 months. In the UK there is a support group for SS. I will give...
miranda barone
baronemiranda
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Nov 6, 2006
9:48 pm

Dear Carole, I just read Amy told you about the support group and the book The Elusive Syndrome ,I read it and I really reccomend it. My daughter is going to...
miranda barone
baronemiranda
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Nov 6, 2006
10:01 pm

Hello. I have had the cryotherapy in Cambridge on both eyes. It worked successfully on my left eye but my right eye has since detached twice and now I have...
Amy
amwshamws
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Nov 7, 2006
11:44 pm

Hi Carole, I wore glasses when I was 6 months old. If you can get your son glasses it will be to his benefit. If the Dr says no I would check with a diff dr....
MRH3125@...
margaritavil...
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Nov 8, 2006
3:11 am
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