Help relocate Mikey & Help others.
Donation protected
Our goal is to secure funds to help us relocate to where we can get the care Michael deserves. After reaching our goal ALL funds over that goal will be setup in a non profit foundation in Michaels name to help the families that have been told countless times by countless foundations as we have, there are no programs like that available, our organization will be the program to provide assistance to families with children with special needs to help them relocate to so they're children can also receive the care they so desperatley deserve , the paperwork is being compiled by my Foundation counterparts so that it will be available ASAP.
please help us help Michael and other families DONATE
Let me tell you about Michael
Kristin(mom, fiancé ) had a few visits to the emergency room , they were all dismissed as different "women issues" , finally , the hospital did the test and she was pregnant and we couldn't have been happier, only lingering concern was that she had been taking psyc meds during time and we were not having sex during trying to find out what was wrong, but all ultrasounds were good and I was supper stoked, the good news was there almost no problems during the pregnancy, on November 2nd 2012 Michael was born and everything seemed OK, until he started sceaming 18 hours a day, to the point he would either have a seizure or break out in hives, our pediatric doctor said he was colic, we explained Robert had been colicy and something's wrong , they disagreed and this was an uphill battle with them until we discontinued care with them, then enrolled in him and took the education on excersising so he wouldn't get muscle atrify, the physical therapist said off the record our son was showing physical signs of cerebal palsy we needed to get him into a nerologist, but he could me a referral for his digestive problems, who then gave us a referral to a nerologist, and he was finally was diagnosed and we knew how to proceed to make sure he is as comfortable as humanly possible, we have explored all other options in "compassionate care" for Michael , fortunately he is on ssi so he will have healthcare anywhere we take him to , but we do not have the options in florida as we would in other states (California , Michigan, Colorado , etc) which I have the research to support which I'm more than willing to provide or discuss the amount total we asking for, and how the funds will be spent and updates and pictures will be posted as well. We have contacted every CP organazation and they do absolutely NOTHING in regards to recommend current programs(email lists) which most either no longer exist or give us the same asnwer, regardless they do nothing, so I am doing this as a last ditch effort to get us there as soon as possible. once there , we will get Michael the care we deserve and start working just as hard to fais funds to help famalies with children with special need relocate so that they can have the opportunity we were blessed with.
Thank You for your time
Robert Dowling
twitter: @compassionmikey
email: [email redacted]
The pictures are Mikey then Robby
.
Any questions contact me and I am more than happy to provide all information on the outline that is currently in place...
please help us help Michael and other families DONATE
Let me tell you about Michael
Kristin(mom, fiancé ) had a few visits to the emergency room , they were all dismissed as different "women issues" , finally , the hospital did the test and she was pregnant and we couldn't have been happier, only lingering concern was that she had been taking psyc meds during time and we were not having sex during trying to find out what was wrong, but all ultrasounds were good and I was supper stoked, the good news was there almost no problems during the pregnancy, on November 2nd 2012 Michael was born and everything seemed OK, until he started sceaming 18 hours a day, to the point he would either have a seizure or break out in hives, our pediatric doctor said he was colic, we explained Robert had been colicy and something's wrong , they disagreed and this was an uphill battle with them until we discontinued care with them, then enrolled in him and took the education on excersising so he wouldn't get muscle atrify, the physical therapist said off the record our son was showing physical signs of cerebal palsy we needed to get him into a nerologist, but he could me a referral for his digestive problems, who then gave us a referral to a nerologist, and he was finally was diagnosed and we knew how to proceed to make sure he is as comfortable as humanly possible, we have explored all other options in "compassionate care" for Michael , fortunately he is on ssi so he will have healthcare anywhere we take him to , but we do not have the options in florida as we would in other states (California , Michigan, Colorado , etc) which I have the research to support which I'm more than willing to provide or discuss the amount total we asking for, and how the funds will be spent and updates and pictures will be posted as well. We have contacted every CP organazation and they do absolutely NOTHING in regards to recommend current programs(email lists) which most either no longer exist or give us the same asnwer, regardless they do nothing, so I am doing this as a last ditch effort to get us there as soon as possible. once there , we will get Michael the care we deserve and start working just as hard to fais funds to help famalies with children with special need relocate so that they can have the opportunity we were blessed with.
Thank You for your time
Robert Dowling
twitter: @compassionmikey
email: [email redacted]
The pictures are Mikey then Robby
. Any questions contact me and I am more than happy to provide all information on the outline that is currently in place...
Organizer
Roberts Michael
Organizer
Hudson, FL