October 25, 2008

putting the word out



I am not sure how many people have stopped by this blog looking for some info on congenital heart disease (or gastrostomy / feeding issues), instead finding a whole lotta sewing going on. I would really like to share with other mums who have a child with CHD, please leave a message or send an email. I know the isolation you can feel when it seems like you are the only one living with the constant stress of an unwell child.

2 comments:

laine said...

look at that gorgeous little poppet!

Jenn said...

Aww...sweet little baby! I found you through Refabulous...Connie is a good friend (via internet only, though...wish we could meet) anyway...my sister died of congenital heart defects and my husband's brother had to have open heart surgery at age 7 for congenital heart defects...so I have always been a little nervous of our children having a problem, but we have been blessed thus far (6 kids later)

Anyway, it's nice to see your blog and hear the truth of your words.