“Expectations” – Nathan
“Expectations” – Nathan Good day friends! As I am traveling a bit with work right now, I have begun to…
“Back to Blogging” – Janet
“Back to Blogging” – Janet I love reading special needs blogs. They have lifted me up and carried me through…
“Whoa” – Janet
“Whoa” – Janet Do you ever have those days or seasons where things are just ‘alot’? I know my family…
“Getting Better” – Amy
“Getting Better” – Amy Ben’s recent Creatine Transporter Deficiency (CTD) diagnosis has hit me hard emotionally, so I thought that…
“1% Chance” – Laura
“1% Chance” – Laura GAMT is so rare, just getting diagnosed seems to be quite an ordeal. I like hearing…
“Why Getting a Diagnosis Is So Much More Than a Label” – Kelly
“Why Getting a Diagnosis Is So Much More Than a Label” – Kelly My daughter Holly (9) & son Isaac…
“On Valentine’s Day” – Nathan
“On Valentine’s Day” – Nathan Well, it’s here friends, February 14th , and according to the automatic reminder on my…
“My little guy” – Jane
“My little guy” – Jane My little guy is now 8 years old and was diagnosed with Creatine Transporter Deficiency…
“The Three P’s” – Beth
“The Three P’s” – Beth My husband likes tattoos. Really likes them. I do not have one spot of ink…
“Five Years… Then and Now” – Janet
“Five Years… Then and Now” – Janet When my son Spiro was first diagnosed with CTD, I thought it would…