You only live once,enjoy it,live it! I am 7 years old and was diagnosed with an incurable disease called Spinal Muscular Atrophy(SMA). I have a huge desire to live and grow. I have created a list of wishes that could be my last but some can be possible,and some won't be possible. My blog was created to document the time I spend with my family and friends.I only have one life and I want to live it to the maximum with love and support.
HOW TO CONTACT ME
Monserrat Hernandez (Bucketlist)
5663 Balboa Ave PO Box 168
San Diego CA, 92111-2705
Phone # 619 665-3006
www.monserrathern.blogspot.com
https://www.facebook.com/monserrathernandez08
https://twitter.com/monsebucketlist.com
monserrathernandez08@gmail.comWednesday, November 21, 2012
Monserrat Hernandez My two day hospital stay
Two days ago I had to go the hospital. There was a bit of blood residue coming out of my gastric tube. I want to talk a little about my condition and how I live with it. My mom and I want to create awareness about this condition which has no cure. There are 4 known types of Spinal Muscular Atrophy, I will concentrate on type 1,which is the one I have, also known as Hoffman's Syndrome.It is the most severe and generally affects the baby during the first months of life. When born, babies appear flacid and they don't acquire motor skills the way other babies do. For example, they cannon lift their head, sit,, or crawl. It also affects the muscles of the respiratory system and digestive system. A mechanical respirator (like the one I have) is needed so that the child can bread the easily. Also a feeding tube that goes into my digestive system is needed so that I can eat and live. In general, someone with this condition has a life expectancy of 2 to 4 years, and the main cause of death is complications to the respiratory system.Cases exist where some have lived longer with the help of respirator.
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HOLA MONSERRAT GOD BLESS.
ReplyDeleteTHANK GOD BLESS.
DeleteHOLA MONSERRAT GOD BLESS.
ReplyDeleteTHANK GOD BLESS
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