Guest guest Posted November 10, 2002 Report Share Posted November 10, 2002 Thank you n, My daughter Tania, being 2 years younger than , grew up with this reality. When she was younger, she thought it was normal for every children to have some physiotherapy treatments and she was asking us when hers will begin and also how come she didn't have to take some pills... When is hospitalized, his sister worries about him and finds very difficult to be separated from her mom or/and dad. We usually bring our daughter to visit at the hospital when his condition permits it. She's too young to realize all the serious side of cf but finds her brother very courageous to go through all the daily treatments. How is your health, n? And how is your son? I hope everything goes very well for you and your family. Bye, bye, >From: Mcesana@... >Reply-To: cfparents >To: cfparents >Subject: - thank you so much for your efforts, and >Welcome Back! >Date: Sun, 10 Nov 2002 00:19:41 EST > >Long, long, long ago, I first learned French in Canada--but although I >can read it, I am a long way from conversing in it or writing in it, for >which I apologize. Your English seemed very good to me, and will >doubtless come easier with use, as would any language over time. >But, as English appears to be the " Lingua Franca, " (terrible pun!) >of this list, let me welcome you and your family back and offer my >highest hopes that transplant will not prove necessary, though I do >hope that should it become necessary, we will all be here for you >throughout the wait, and the entire process. I hope that your other >child is holding up with all this, and that you are getting some rest >now that your son is home. >With hope in abundance, >n Rojas, wcf, mom of 3 adults, the youngest wcf also > > > Quote Link to comment Share on other sites More sharing options...
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