Comments for MitoCanada http://www.mitocanada.org Supporting Families Impacted by Mitochondrial Disease Tue, 01 Feb 2011 18:19:19 -0700 hourly 1 http://wordpress.org/?v=3.3.1 Comment on Welcome to MitoCanada! by Suzanne Gowland http://www.mitocanada.org/2011/01/16/welcome-to-mitocanada/comment-page-1/#comment-6 Suzanne Gowland Tue, 01 Feb 2011 18:19:19 +0000 http://www.mattgraham.ca/mito/?p=121#comment-6 Hi Christine, My name is Suzanne Gowland and I'm the secretary for MitoCanada. Our vice-president Stephanie Roung has been trying to email you to connect more and answer some of your questions. However the email keeps bouncing back. If you don't mind, can you email her directly at: stephanie.roung@mitocanada.org? That will help us make sure we are using the right email address to communicate with you. Thanks for reaching out to us! Suzanne Gowland Secretary, MitoCanada suzanne.gowland@mitocanada.org www.mitocanada.org Hi Christine,
My name is Suzanne Gowland and I’m the secretary for MitoCanada. Our vice-president Stephanie Roung has been trying to email you to connect more and answer some of your questions. However the email keeps bouncing back. If you don’t mind, can you email her directly at: stephanie.roung@mitocanada.org? That will help us make sure we are using the right email address to communicate with you.
Thanks for reaching out to us!
Suzanne Gowland
Secretary, MitoCanada
suzanne.gowland@mitocanada.org
http://www.mitocanada.org

]]> Comment on Welcome to MitoCanada! by Christine Harmes http://www.mitocanada.org/2011/01/16/welcome-to-mitocanada/comment-page-1/#comment-5 Christine Harmes Fri, 21 Jan 2011 10:58:29 +0000 http://www.mattgraham.ca/mito/?p=121#comment-5 Hi there Im wondering how you went about setting up Mito Canada. Ive been thinking about something similar for Ireland as while UMDF and Mito Action are terrific, I think we need something more "regional" based but with afficiliations to UMDF, Mito Action in the US, Mito Canada and Mito Australia. I know through the facebook page that there appears to be a need for something in Ireland so I would appreciate any information you could give me. Some background - my 4 1/2 year old son Jack was diagnosed at 14 months with Complexes I, III & IV missing and has chronic renal failure, hypotonic and is profoundly deaf. He is on the Q10, Carnetene and Vit C for mito & other meds/feeds for the renal failure included pd dialysis 6 nights a week at home & is ng fed. Look forward to hearing from you. Christine Hi there
Im wondering how you went about setting up Mito Canada. Ive been thinking about something similar for Ireland as while UMDF and Mito Action are terrific, I think we need something more “regional” based but with afficiliations to UMDF, Mito Action in the US, Mito Canada and Mito Australia. I know through the facebook page that there appears to be a need for something in Ireland so I would appreciate any information you could give me.

Some background – my 4 1/2 year old son Jack was diagnosed at 14 months with Complexes I, III & IV missing and has chronic renal failure, hypotonic and is profoundly deaf. He is on the Q10, Carnetene and Vit C for mito & other meds/feeds for the renal failure included pd dialysis 6 nights a week at home & is ng fed.

Look forward to hearing from you.
Christine

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