artemis moon
Hero Member
- Jun 1, 2007
- 873
- 149
- Detector(s) used
- Minelab Safari
ProPointer
- Primary Interest:
- Metal Detecting
OK, with the economy in a slump and the state of the world's affairs being what they are, it's nice to be able to see some good news once in a while.
I thought I would share this with you all.
My nephew Daniel was diagnosed with a rare disease called Spinal Muscular Atrophy last February. His prognois did not look good. Last summer, he was in the hospital on a respirator for over a month, and we almost lost him when he could not be weaned from the respirator. My brother and his wife literally made the decision that they would allow the doctors to attempt to extubate him one more time and that would be all.
Well, the good news is that Daniel turned 2 in August (many children with SMA do not reach this milestone). His doctor tells us that he has not regressed since she last saw him in late winter..in fact, he's actually gained some bone and muscle mass. He is now standing with the help of a device called a stander.
We know that Daniel will never be like other children, but his family is so grateful that he is here with us today. He's truly a special little boy and anyone who spends time with him knows this immediately.
Daniel has made me mindful of feeling joy at the little things that I used to take for granted. When the world starts to wear me down, I think about this sweet little boy and his infectous smile.
To find out more about Daniel and SMA, please check out danielshope.com
Thanks to the moderators for giving me the appropriate spot to share this with everyone who may be looking for some happy news!
I thought I would share this with you all.
My nephew Daniel was diagnosed with a rare disease called Spinal Muscular Atrophy last February. His prognois did not look good. Last summer, he was in the hospital on a respirator for over a month, and we almost lost him when he could not be weaned from the respirator. My brother and his wife literally made the decision that they would allow the doctors to attempt to extubate him one more time and that would be all.
Well, the good news is that Daniel turned 2 in August (many children with SMA do not reach this milestone). His doctor tells us that he has not regressed since she last saw him in late winter..in fact, he's actually gained some bone and muscle mass. He is now standing with the help of a device called a stander.
We know that Daniel will never be like other children, but his family is so grateful that he is here with us today. He's truly a special little boy and anyone who spends time with him knows this immediately.
Daniel has made me mindful of feeling joy at the little things that I used to take for granted. When the world starts to wear me down, I think about this sweet little boy and his infectous smile.
To find out more about Daniel and SMA, please check out danielshope.com
Thanks to the moderators for giving me the appropriate spot to share this with everyone who may be looking for some happy news!