988
988
25

Help for special needs kid/moving

$63,210 of $75,000 goal

Raised by 959 people in 6 months
Created May 25, 2018
Fundraising Team
https://youtu.be/_Owd9bx-RCU

Hello, thank you for taking time to read my campaign for our son, David. Like any family, when our son hurts, we hurt. When my husband wakes up our son for school in the mornings it tears my soul apart when he tells me when I get home from work that David has vomited in his sleep because he had a seizure. The thought that he could have died right there in his bed is the worst possible nightmare that We could ever have and the fear of it becoming reality set us in motion to save our son. A kind service dog has eased, but not erased the worry and dread by standing guard of him and being able to detect and alert to the oncoming seizures so that my husband can now half way sleep knowing that he will hear her cries for help when David’s voice is gone.

The Doctors tried him on many medications (some all at once) to try and stop the seizures as he was having them daily. These medications almost cost him his life just because of their chemical nature. We trusted these Doctors that their medical expertise with these medications were in David’s best interest, past my own knowledge, my husband researched them and wow the side effects, and then watched these dangerous chemicals that are prescribed in good faith have a different chemical reaction in our son that could not have been foreseen, the seizures got worse, our son has fought many times for his life with Doctors fighting to bring him back and keep him here. David has a service dog, seizures, seizure medications, and Doctors. What he doesn’t have is the ability to be a child because the seizures have stolen his childhood from him. He cannot even ride his bike to the park with friends. What would happen if he had a seizure crossing the street? He cannot go to school and enjoy when he is so tired and recovering from days of seizures to the point he was going to have to be isolated even more and taught at home. David cannot just go be a kid with his friends because “What if this is THE seizure that We have been tearing our hearts and brains apart to stop, and prayerfully begging that never comes. Neither of us can protect him in his own bed, let alone away from home. His dog helps detect and alert, but she would not be able to render the medical care that he would need. We would have to just trust that some stranger would recognize it, and call for help. Also hope that someone driving the street where he fell did not look down at the radio, or to another distraction for a split second and hit David or Malory. Can any father or mother in good faith trust their child’s life to the hands of potential strangers? If a parent did, would they have their child’s best interest? Are we really doing the right thing by imprisoning him for any reason and watching his childhood pass him by? How do We keep from hating ourselves because we are supposed to be able to fix this and protect him? What can We do? Nobody can save our son, and neither of us are willing to accept letting him go, or his innocence of catching lightening bugs and bringing me a wilted flower that he had in his pocket for an hour or the dead bug to his dad that he accidentally sat on die in our faces. His eyes search us for help, and we have none.
In February 2018, after my husband did some researching and wrestling with the idea, asking myself about the law, the thought of giving something illegal to our child that was for our entire childhood “a bad and dangerous drug,” we started treating him with Marijuana. Unfortunately it is still illegal here in Georgia. We had plans and hopes of getting him on a good track with school, and referred out of state to better and broader medical practices. We both demanded to know what is going into our child, and while we did everything we could to know, neither of us had any legal access to a Doctor’s experience with different kinds. We knew the risks that we read, the medical research that We both had to pour over for hours fighting what is right/legal/safe/moral, I informed all of his medical team because we wanted our son to be safe. I was not advised to stop treating him this way along with safer medications from the Doctor. The Doctor did not comment exactly why, but I think she wanted to see for herself. The combination granted our son 71 days seizure FREE!!!!! For 71 days our son rode his bike, woke up, went to school, played with friends, played outside, and the terror for his life that gripped our hearts and souls began to lift. The smiles on our faces reflecting our child getting to be a normal child. Safe in his bed. Doing better in school. Having a great quality of life. We were breaking the law. We saved our son. We were fixing the fragments the best way we could of him being that little boy that was taken away from him by these seizures. This is our job as parents, to protect our child even with our own lives.

As I wrote above, I kept his medical team up to date. As we felt we had found his miracle, and anyone else who saw his medical history would see this too. We also felt like his entire medical team truly cared for him and wanted the same things we did, and with honesty on my part and his safety forefront of every visit, we were winning. This transparency also meant informing a new therapist who did not share our joys or beliefs that allowing him access to marijuana was worth this new life he had begun. I was reported to DCFS, and on April 19, 2018 their representatives along with deputy sheriff’s entered our home with our cooperation and full truth of what and why, and despite the evidence, demanded that I stop “abusing” our son by giving him this “dangerous” marijuana. Allowing him to have debilitating seizures that threaten his life and any quality of that life was quite okay as long as he was not using marijuana. They did not even apply his medical team’s observations and findings to their opinions. If you are unsure what is worse, look up seizure medication side effects. Then look up medical research for marijuana usage as seizure treatment. Compare the two with success rates, side effects, birth defects that are known, long term effects that are known, what class of drug they are in by abuscability, pretend David is your child, and tell us honestly that following the law, but risking his life is better than trying something that is illegal, but with mountains of medical data as to it’s worth as a treatment to the point on becoming legal in certain states. We stood behind our decision to save our son’s life even though we had not made the move yet, and openly admitted to allowing him to use it for the treatment of his seizures. We have never lied about where he got it, or our intentions. The DCFS demanded that we cease this immediately. Against our better judgement, we did. They were not there for the times my husband had to drag our son to the truck because it takes 45 minutes for help to arrive. They were not there for the times that we carried him out of the house to break the traffic laws to get him the help he so desperately needed. They were not there to see my husband loose several jobs because we were rushing our son to get medical help. They were not there when we spent almost 3 months in an emergency room everyday because our son was being transported because he’d done had another seizure either at home or at school, or that 2 weeks out of those 3 months was spent at a hospital in Atlanta begging the doctors to take him off the medication that was killing him. There was no way we could afford to get him to a state that could help him fast enough to stop what we both knew was coming and even told the DCFS representative and officer. Even working two jobs as I do and the 4 that my husband does. There was a small hope that once they could see his seizures returning, and his Doctor’s recommendations that they would see we were not any of those other types of the parents that they see so often it hardens their hearts to only seeing laws and what the state deems acceptable parenting. Maybe they would allow me just enough time to get him to the help of a medical center in an appropriate state.

Within14 hours of the marijuana being stopped without consulting his Doctor, even with the safer seizure medications still administered, his service dog was alerting my husband as I was filling out paperwork for the DCFS office, David’s eyes filled with dread, fear, and hopelessness as all Matthew could do was watch it happen and get him to the hospital, and before my heart could even beat, he was in the grips of this horrible, evil, monster that threatens his life again. We felt sure they would see now. We felt sure they would not be able to ignore the obvious and blatant evidence in front of their faces, and the loss of childhood in our son’s face. This was not correct. While our son fought for his life, officially in DCFS custody and flatlining 15 times according to medical records, my husband was arrested, they tore me from my baby’s side and told me they were going to take custody of him as I was arrested too. They say he is not safe with us while a medical team tries to start his heart again because they have stopped his treatment by what they know of the law and their opinion.

Then by opinion of the hospital’s police staff, my son’s service dog was removed and put into the city pound without allowing me the federally mandated, and legally protected, reasonable amount of time to seek someone to take custody of her. The officer from what I understand of the service dog laws outlined by the ADA website, violated federal law that protects these working animals and their handlers. We broke a state law in hopes of saving my son. In turn, our son’s federal rights as protected under the ADA laws were violated because of ignorance of what the laws state regarding service animal identification, and the federal laws dictating how a service dog with an incapacitated handler must be treated. How do we at the least help this department repair their ignorance of the federal laws? I asked people who advocate for the understanding of laws concerning service animals if I was incorrect in what I read. They explained what the laws state for each thing specifically that happened. They cannot legally tell me who was right or wrong as we all have a right to tell our own side of every story without the assumption of guilt. On my own reporting, I did, in fact, understand the laws that I believe were violated. I now have an obligation to become an advocate myself when our son is back in our arms and living his beautiful, young life.
She is our son’s link to the conscious world when he is trapped in the grips of those seizures and cannot cry for help himself. She is his voice, his hero, and his Angel. She has a job that has improved all of our lives from him choking on his own vomit in his sleep because she will make sure someone hears her and gets to him. Instead of being treated as a valuable life and life saving dog, she was thrown into her own type of prison for 7 days. “Actually innocent, but decidedly guilty based on ignorance of the law” is what I would name that kind of charge. Seven days this life saving animal went without anyone she knew, strange foods, strange scheduling, strange dogs (who knows if they were friendly or not), exposure to a myriad of diseases, and was treated like an animal thrown away. Vaccinations are our first line defense, but they do, on occasion fail our dogs. She risks that when she leaves our house. Just as we risk being attacked by a shark if we swim in the ocean. We know the risk, and that is why we do not jump into known, high shark activity laden waters with an open wound. Pounds cannot help except to be a possible breeding ground for diseases. They must house stray dogs whether they know the histories of the dogs or not. They cannot deny going and picking up a dog reported just because they do not know if it has had vaccinations. They can quarantine if equipped for that, and if the pound has adequate space and vet staff. Our son’s service dog is priceless in alerting to get David help, and she was cast aside just like our son’s childhood and quality of life. She has this way that is unique to them to speak to his whole mind and assure him that he is going to open his eyes to her again. She is amazing, and deserves to always be treated as such. We do not want to risk losing the only link we have to him to assure him that Matt and mommy are fighting for him when he cannot see and hear us. This wonderful, furry, angel tells him so. She wants her boy back almost as much as we do.
Because of all of this, we want to move our child and family to a state with the medical resources to help him. We have found a lawyer who is the best of the best. She has reviewed and has been very optimistic in her ability to help us get our son back, and move him to a place where he can be monitored with regulated, specially grown marijuana that is designed to treat his individual needs uniquely. Our son deserves life. I am asking for help to save our son. Please donate if you are able so that we can hire this attorney and save him. If you are unable to donate, please understand that we are in deepest appreciation of prayers for our son to be okay and be a little boy riding his bike, and looking forward to going to school again, and so proud and excited when he learns new things and makes good grades.

This just hurts so badly. We feel so afraid for him, and everything in both of us cries and screams to save him. We do not know if he is being cared for like a child or a case number. We only hear things that bother us deeply, and all we can do is turn it over to the lawyer to now fight the greatest battle of our lives in having our heart returned to us safe and sound and knowing that we now know the correct path of helping him, and can do this the legal way. It has proven to be the correct way by the medical evidence of only 71 days alone. Please, help us if you are able. We only want our baby back and to see him play and grow without fear of these seizures that were stealing him away from us before he was taken away by DCFS. We want all of him back, and have proven that we will do anything to protect him. The difference is that now, we are educating ourselves on the correct way, and imagining an even better outcome for his health with the proper care.

Thank You!

https://www.gofundme.com/legal-help-for-special-needs-kid?sharetype=teams&member=227462&rcid=r01-152732054834-745a05a4a60247a6&pc=ot_co_campmgmt_m
+ Read More
Was sleeping good after off and on seizures after his great grandmother went on to the glory land early in November.
+ Read More
David has been doing good for about a week now. Thankfully. Next court date is December 13 @ 9 am. And hopefully the judge will see what kind of crap is actually going on with dcfs and how they are completely responsible for the decline in his health and that they are why he has ended up in the hospital bc of the way they decided to handle things after the last court date and dismiss all of this. And as of right now we are in the process of trying to come up with the money for a down payment/closing cost to buy a house so that all this moving can stop.
+ Read More
We have been across the country searching for a way to actually take care of my son. And still end up staying in Georgia bc of the courts and dcfs. In the last 14 days David has had 2 cluster type seizures. The one on the 20th wasn’t bad. But the ones today have been going off and on strong since 8 am.
+ Read More
Never been a scam. We woke up this morning to a new set of crazy.
+ Read More
Read a Previous Update

$63,210 of $75,000 goal

Raised by 959 people in 6 months
Created May 25, 2018
Fundraising Team
Your share could be bringing in donations. Sign in to track your impact.
   Connect
We will never post without your permission.
In the future, we'll let you know if your sharing brings in any donations.
We weren't able to connect your Facebook account. Please try again later.
MB
$1,200
mitch Baruchowitz
3 months ago
$220
Anonymous
3 months ago
LD
$25
Lynn A Dougherty
3 months ago
JG
$15
JaLeisa Grayson
3 months ago
TS
$100
Thomas B Seitz
4 months ago
$10
Richard Finkel
5 months ago
MA
$30
MaryAnn Armistead
5 months ago
JP
$100
Joan Priestley
5 months ago
BK
$25
Brett Kelly
5 months ago
SG
$20
Sari Gallegos
5 months ago
or
Use My Email Address
By continuing, you agree with the GoFundMe
terms and privacy policy
There's an issue with this Campaign Organizer's account. Our team has contacted them with the solution! Please ask them to sign in to GoFundMe and check their account. Return to Campaign

Are you ready for the next step?
Even a $5 donation can help!
Donate Now Not now
Connect on Facebook to keep track of how many donations your share brings.
We will never post on Facebook without your permission.