I am so not one to do this sort of thing.  (meaning: me publisizing someone elses story)  I happened upon this site through one of Kev's cousins.  I could not NOT read it, curiousity got the best of me.  It is a blog dedicated to a little boy named Charlie Cooper.  He is fighting for his life to recover from Pneumoccocal Meningitis.  My heart ached as I read this little boys story - it still aches.  His parents are dealing with his circumstances in such a postive manner.  I truly admire them.  I remember the roller coaster ride we experienced when Porter was first born and how hard it is when your baby is sick. It can be unbearable and they are dealing with everything so well.  Some of the things that they are experiencing with Charlie are the same as what we went through with Porter.  I guess that's why it has touched my heart in such a big way.  I can completey empathize.

When we were dealing with Porter I never once worried about finances.  I am so grateful that I live in a country that provides health care to ALL.  Whether rich or poor.  I remember commenting to the Neonatologist one evening (DR. Rabi) about all the procedures Porter had done and how he had so many of them.  His comment to me was "He really is your million dollar baby".  That hit me hard and brought me back to reality.  Medical procedures and medicines/drugs cost so much money.  I am so grateful that the financial issue of things was never a worry or an added stress to an already amazingly emotional and stressful time.

I think of this family in the United States and I wonder how they are doing.  The financial burden must be so heavy (insured or not).  The things that this little boy needs are so extensive and expensive.  For example: Their insurance will only cover implants for one ear, but yet he needs them in both, so his parents have to appeal to the insurance company, etc., etc.  What a nightmare that is.  I wanted to add the link to his website so that if any of you are as curious as I, take the time to read his story from the beginning and if possible donate to the fund that has been set up for his medical and ongoing needs.  And if you feel so inclinded, please pass his story along to those you hold dear.  I am realizing at this point in my life how important it is to give back in whatever way I can.  I am grateful that I can do something for this special little boy and his family.

 For his blog, click here:  http://charliecooperjackjack.blogspot.com

I wanted to post a picture of the little guy, but I don't even know if that's legal!  So here's to hoping you'll check out their blog!