Hi--we have a niece with cf and a son with all-but-cf (celiac disease and asthma). We know that the constant meds and cpt can wear on the body and emotions...
The internet is a great way to get an ear to listen, but try a local support group...many times other families in the same situation, sitting in the same room, with the same problems and concerns helps soooooo much! And they may have found competant sitters who can safely care for your little one giving you a short break.--and even give you and your signif other a chance to breath and enjoy each other for a little while!....The support gained by local support groups can really benefit you with drs..new pt positions etc and I found just being with others knowing where I'm coming from was really beneficial....
good luck..
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