Bonjour \u00e0 tous ! Cela fait un moment que je n’ai pas \u00e9crit de billet sur mon blog. Mille excuses !<\/p>\n
J’ai re\u00e7u quelques notes de vous qui vous demandez ce qui se passe. Nous avons \u00e9t\u00e9 tr\u00e8s occup\u00e9s par la planification de notre premi\u00e8re r\u00e9union de patients \u00e0 Hamilton, en Ontario, par l’organisation de notre conf\u00e9rence \u00ab\u00a0Living Well with CML\u00a0\u00bb en juin et de notre r\u00e9union de patients \u00e0 Toronto en avril, sans oublier de travailler sur des surprises sp\u00e9ciales pour le site Web afin que nous puissions passer \u00e0 la vitesse sup\u00e9rieure ! Restez \u00e0 l’aff\u00fbt d’un nouvel ajout \u00e0 notre site qui r\u00e9pondra enfin \u00e0 la demande que vous formulez depuis des ann\u00e9es : un moyen de discuter en priv\u00e9 avec d’autres personnes qui savent ce que c’est que de vivre avec la LMC. Je suis tr\u00e8s excit\u00e9 de le voir prendre forme ! Nous sommes \u00e9galement \u00e0 la recherche d’histoires de patients pour le site. Si vous avez une histoire \u00e0 raconter et que vous souhaitez la partager, envoyez un message \u00e0 info@cmlnetwork.ca.<\/p>\n
<\/p>\n
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