I feel like everyday since June 1, I have been on information overload.  We get a bunch of new information thrown at us and then they ask if we have any questions.  Brent and I just wonder “Should we?”.

I have immersed myself in research, mostly trying to figure out a way to relay the information in terms that I understand.  Now that I’ve started writing on and on about our diagnosis, some of you may have questions also.

So, I am going to offer you the chance to ask any questions that you may have.  I have set up an email of lynnette@cadesjourney.com for this purpose.  Otherwise, you can ask it in the comments and I will answer those also.

If I don’t know the answer to your question, I will try to find an answer.  A couple of the websites that I check for answers are www.mda.org and www.duchenneconnect.org.

While you’re thinking of you questions, check out this logo that a friend designed for us.  I think it is pretty awesome.

Blessings.  Lynnette