Blog Archive 01/2008
Home sweet home
January 05, 2008 by Bill Strong
We're home!!! After three weeks and one day, the doctors let us leave the hospital. We are thrilled to be home and ready to handle Gwendolyn's care on our own -- although she will be seeing doctors two to three times a week and will have therapy as well for some time. The even better news is that... Read More >>
Update
January 01, 2008 by Bill Strong
Hi Everyone:
Unfortunately we are still in the hospital with Gwendolyn and are still not 100% certain what type of neuromuscular disease she is suffering from. The good news is that she is continuing to show slight signs of improvement in both muscle movement and direct feeding every day. The not so... Read More >>
Page 1 of 1
Popular Posts
Tags
200k for sma
gwendolyn strong foundation
gwendolyn
featured
spinal muscular atrophy
friends
teamgsf
fundraiser
parenting a child with disabilities
sma tips
sma awareness
concerned
sponsor-a-mile
hospitalization
acts of kindness
chase community giving
news
good things for gwendolyn
birthday
holidays
development
therapy
video
sma treatment acceleration act
3rd birthday
Show More
Archive
2013
May (2)
April (4)
March (3)
February (5)
January (5)
2012
December (3)
November (8)
October (4)
September (5)
August (8)
July (7)
June (7)
May (9)
April (9)
March (7)
February (8)
January (10)
2011
December (8)
November (16)
October (16)
September (14)
August (15)
July (16)
June (13)
May (27)
April (22)
March (21)
February (20)
January (21)
2010
December (19)
November (22)
October (16)
September (23)
August (22)
July (28)
June (22)
May (24)
April (23)
March (26)
February (19)
January (24)
2009
December (19)
November (22)
October (32)
September (25)
August (25)
July (45)
June (45)
May (35)
April (26)
March (35)
February (34)
January (36)
2008
December (38)
November (21)
October (30)
September (22)
August (30)
July (27)
June (18)
May (5)
April (6)
March (3)
February (1)
January (2)
2007
December (7)
October (1)