<img src="i/expressions/face-icon-small-mad.gif" border="0">i need to ask if there is anyone from canada and if so please reply to me. my dad has cf and is being refused treatment in the UK, his home country. he has no medication and suffers every day. he has had one positive sweat test and needs to know where he can make an appointment in canada and where would be best for him to stay? please help if you can thaks in dvance nic 20 daughter of eddie wcf.
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my dad needs serious help from canada!!!!!!
- Thread starter anonymous
- Start date
Hi Nic
Your message isn't exactly clear, why is your Dad being refused treatment in the UK? Is this where he is from and where he lives? There are many good centres in Canada but of course, the one that I would say is the best, is the one my son was looked after until his passing last year, St. Michaels Hospital in downtown Toronto, Ontario. Excellent reputation, best staff you could ask for etc.
Sandy
Your message isn't exactly clear, why is your Dad being refused treatment in the UK? Is this where he is from and where he lives? There are many good centres in Canada but of course, the one that I would say is the best, is the one my son was looked after until his passing last year, St. Michaels Hospital in downtown Toronto, Ontario. Excellent reputation, best staff you could ask for etc.
Sandy
thelizardqueen
New member
There are some great centres in Canada. I'm from Winnipeg, and the centre here is great, and you get full coverage for meds and treatments. I should also mention that we have no cases of cepacia or MRSA yet. Toronto and Montreal have some good centres as well. Here is a link to all CF centres in Canada:
<a target=_blank class=ftalternatingbarlinklarge href="http://www.cysticfibrosis.ca/page.asp?id=61
">http://www.cysticfibrosis.ca/page.asp?id=61
</a>
<a target=_blank class=ftalternatingbarlinklarge href="http://www.cysticfibrosis.ca/page.asp?id=61
">http://www.cysticfibrosis.ca/page.asp?id=61
</a>
For Liz:
I was wondering how you know that your clinic has no cases of cepacia or MRSA? Do your doctors share that information with you? This is a question I never even thought to ask.
And to the daughter of Eddie: I hope your dad receives the proper treatment soon. I am sure you are a great comfort to him with all you are trying to do to help him. I will keep you both in my prayers.<img src="i/expressions/heart.gif" border="0">
I was wondering how you know that your clinic has no cases of cepacia or MRSA? Do your doctors share that information with you? This is a question I never even thought to ask.
And to the daughter of Eddie: I hope your dad receives the proper treatment soon. I am sure you are a great comfort to him with all you are trying to do to help him. I will keep you both in my prayers.<img src="i/expressions/heart.gif" border="0">
thelizardqueen
New member
Jem,
I have asked, and they've told me. They also said that while we do not have any cases yet, its almost enevitable that someday we will.
I have asked, and they've told me. They also said that while we do not have any cases yet, its almost enevitable that someday we will.
<span class="FTHighlightFont">Halifax, Nova Scotia </span ft>is where you will find any information you will need just <span class="FTHighlightFont">call 1 888 470 5888</span ft> then <span class="FTHighlightFont">ask to speak to C.F clinic</span ft> they will answer any questions or direct you to some one who will