(Originally posted May 6, 2009)

We went to our family doctor yesterday, and she said we have to obtain clearance from J.J.'s cardiologist and neurologist to have the surgery. She has apparently forwarded the information to their offices. Good luck with getting anything from Dr. Acula, though--I have a feeling I may have to call his nurse again to see if she can help. Why did I expect this to be easy? History has proven that NOTHING has been easy since the stroke. Every day is like a string of minor miracles.

Anyway, leaving that subject for a moment...

Our doctor ordered more blood tests to check on why J.J.'s hair is falling out in clumps. His thyroid is still the leading candidate, but now we've added diabetes and anemia to the mix. Apparently insulin resistance and certain types of anemia are common reactions to stroke. So anyway, hopefully we'll get some news on this today.

On Monday, we attended another meeting of the aphasia support group. J.J. is the youngest person in the group, the closest to his stroke (most of the others are at least a year out) and by far the highest functioning. It kind of makes me feel guilty to complain about some of the issues we have when there are so many people in this group who would love to be in our shoes. It's difficult to know that J.J. will continue to improve and to look at some of the other survivors and know that this is about as good as it gets for them. J.J. did enjoy the group a little better, and I continue to get good information, so I think we'll be going back.

Today J.J. has his last session of speech therapy (only because we've now maxed out what our insurance will pay for--he could still use more) and he's also going to check out a different support group. Then he's got the kids by himself tonight--I have to work until 9:00 or so.

Now you're completely up to date!