Posted on August 22nd, 2011 by Tracey
we’re still chugging along here in our household, but of course i think about Jovie’s situation every. single. day.
it’s tough to relay the updates to friends without breaking down slightly, because in this stage of the diagnosis – there really is no news. (we have no diagnosis yet). the only thing i can journal here on my blog is the big wide space that is ‘our future’ that we can’t fill in, yet.
Posted on August 19th, 2011 by Tracey
it’s always so nice to spend time with Jovie. this morning was gymbaroo again – she’s settling down alot more, but she still has her moments where she wants to run around or not be held too much. i guess that’s most kids though!
all tuckered out now …. she’s fallen asleep on me and i don’t want to let go
Posted on August 17th, 2011 by Tracey
today we took a drive up to Nepean Hospital to pick up Jovie’s MRI brain scan report & films.
as they mentioned last week, the report gave us the all clear – no issues to report, which is AWESOME but also is another marker in our journey to discover what is going on with Jovie. i was so curious to see what her MRI looked like – how creepy are those eye balls!
another couple of weeks until her assessment at the Children’s Hospital – i don’t know whether they’ll diagnose her that day with anything but i sure hope they shed some light.
