We are looking for people to sponsor a plant in Joshua's garden in memory or honor of someone. The family will be decorating yard stakes with the name of the individual/saying who sponsor plants/shrubs/tree. Our plan is to paint wooden stakes with colorful outdoor paint and allow the boys to decorate around the written wording placed on each stake. The stakes will be about the size of a paint stick. It will give the boys a chance to help with the project and also will remind them over the years how many people cared enough do make this happen for them. You can sponsor a particular plant or just give a donation of any denomination to offset the cost of the plants. As particular plants/shrubs/trees are sponsored I will update and it is a first come first serve basis. If the particular plant is taken we will place funds towards one of a comprable cost. Thank you so much in advance for all of your help with this.
For this project only!!!
Donations/requests can be sent/made out to: The Joshua Garman Special Needs Trust
14 Easlick Avenue
Lumberton, NJ 08048
Please list what plant if you are particular and any names or wording you would like placed on the stake. Please keep in mind there is limited space on each stake. Thank you in advance for making a sick boys wish come true!
This weekend we are still working so if you are free please stop by!
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Support For Loving Boys Fighting a Life Threatening Disease!
About Us
- Joshua and Michael Garman
- We are wonderful little boys with Mitochondrial Disease Complex I. Two loving parents and our brothers pray for us and love us every day!
Joshua's Health/Family Update Page
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My Story
Joshua was born in 2005 and developed normally until he was 4 months old, he was the perfect baby. In December, in his fathers arms, Joshua had his first seizure. We took him to the local hospital only to be sent home being told it was a childhood seizure and not to worry. The next day he had another one and we found ourselves spending 3 days at Cooper Hospital.
Doctors had no answers by the time we left and Joshua had been placed on seizure medications. Our pediatrician at the time looked at his labs and had us get new ones ran. At his 6 month old check up he told me he thought that Joshua happened to have the same disease his son had. He sent Joshuas information to a specialist in this disorder and that June right before his 1st birthday we flew him to Atlanta, GA.
The doctors did a live muscle biopsy and ran many tests to see what was causing the seizures and the developemental delays. After 4 months of waiting, right before Halloween we got the news that Joshua has Mitochondrial Disease Complex I.
Mitochondrial Disease is a life-threatening disease with no cure or medication. Joshua's body does not produce enough energy for him to sustain life properly.
Joshua has had seizures, developmental delays, loss of speech when sick, hemiparesis, dysautonomia, and a comprimised immune system. He is a tough little cookie and tries to not allow these things to hold him back. Recently, Joshua's brother Michael, was diagnosed with Mitochondrial Disease also. He was diagnosed through a mouth swab done at St. Christopher's Hospital for Chrildren.
Michael is just as fiesty but has his own set of medical issues. For Michael, the disease affects his GI system and gives him significant sensory dysfunction. He was recently diagnosed with sleep apnea and underwent surgery to remove his tonsills and adenoids in hopes to fix the problem.
Doctors at St. Christopher's are now keeping an eye on George the newest addition to our family. Dispite all of their issues the boys are happy and overcome any obstacles that this disease places on them.
Looking at Joshua and Michael you would never know that there is something wrong with them. They lighten up the lives of those who know and love them. We could not immagine life without them.
Doctors had no answers by the time we left and Joshua had been placed on seizure medications. Our pediatrician at the time looked at his labs and had us get new ones ran. At his 6 month old check up he told me he thought that Joshua happened to have the same disease his son had. He sent Joshuas information to a specialist in this disorder and that June right before his 1st birthday we flew him to Atlanta, GA.
The doctors did a live muscle biopsy and ran many tests to see what was causing the seizures and the developemental delays. After 4 months of waiting, right before Halloween we got the news that Joshua has Mitochondrial Disease Complex I.
Mitochondrial Disease is a life-threatening disease with no cure or medication. Joshua's body does not produce enough energy for him to sustain life properly.
Joshua has had seizures, developmental delays, loss of speech when sick, hemiparesis, dysautonomia, and a comprimised immune system. He is a tough little cookie and tries to not allow these things to hold him back. Recently, Joshua's brother Michael, was diagnosed with Mitochondrial Disease also. He was diagnosed through a mouth swab done at St. Christopher's Hospital for Chrildren.
Michael is just as fiesty but has his own set of medical issues. For Michael, the disease affects his GI system and gives him significant sensory dysfunction. He was recently diagnosed with sleep apnea and underwent surgery to remove his tonsills and adenoids in hopes to fix the problem.
Doctors at St. Christopher's are now keeping an eye on George the newest addition to our family. Dispite all of their issues the boys are happy and overcome any obstacles that this disease places on them.
Looking at Joshua and Michael you would never know that there is something wrong with them. They lighten up the lives of those who know and love them. We could not immagine life without them.
The Morning After The Benefit
Benefit Night
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