Movies!!!!

We took Dylan to Superman versus Batman on his birthday and I do believe he enjoyed himself. I can’t believe he was that quiet through the whole movie. His favorite parts of the movie were the fight scenes and the car chases.That’s a  boy for you.  So he had a wonderful birthday. Then we took him to his favorite place to eat which of course is the Outback. He loves the bread and the blooming onion. He was really lively when got there he ending up knocking over Dacota’s glass of water and spilling it all over him. So Dacota was mad the rest of dinner. Dylan couldn’t help it he was excited I guess.I’m posting  a couple new pictures taken at school. I love seeing him smile.

 

Daily News!!!!

Dylan will be thirteen on March 25. They will be on spring at that time. So Dylan had a party at school today. He brought home a lot of presents from his teachers and friends at school. They spoil him too much. I just want to say a big thank you to everybody for all the wonderful gifts Dylan received. The best part was no seizures today.

 

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all the wonderful gifts
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Thanks for all the superman gifts!!!
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My handsome superman
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Hi is so handsome!!!!

 

 

The Real Superman Part XXII

By Jeff King

The Real Superman Part XXII

I know that I haven’t written in forever. I have been extremely busy and there has been a lot going on. Let’s jump right in. The last post I wrote about was trying to get our County Executive Steven Schuh to get on board allowing medical Marijuana to be made available to patients in the county. He and the county council just zoned their way around it though. They’re idiots in my honest opinion. Anyway here is what has been going on with Little Superman. In previous blogs, I mentioned a good friend, Chris Hartsell who I met through a friend of one of my older son’s. This gentleman wanted to help us obtain some medical cannabis to try out on Dylan. On Thanksgiving Mr. Hartsell arrived at my home with a tub of butter, which he made using cannabis and coconut oil. I gave Dylan his first dose later that night and for the first time in what seemed forever, Dylan didn’t have a seizure for 24 hours. Afterwards, though he did have a very bad tonic -clonic seizure which really did him in. We decided to increase the dosage and the frequency of the medication and after tweaking it we came up with a dosage that has definitely decreased the frequency of the seizures, but also the length of the seizures. He has also gone several days without any seizures as well. They haven’t subsided altogether, but, we have noticed a drastic change in Dylan. Dylan has been a lot more vocal and animated since he has been taking the whole plant therapy. I am aware that this medicine does have some THC in it, but it also has high amounts of CBD and that’s what we’re going for. The THC is probably minimal; however, I do believe Dylan probably is getting a high off the medication, but, it can’t be any worse than the legal poison we have to have him ingest two times a day. He has been a whole lot happier and the teacher’s and TA’s at school said that he has been more focused and is making a lot of eye contact. They said he has been very vocal and much happier than he used to be, so to me, that’s a win, win. There seems to be a little side effects, though; some nights, Dylan will not sleep. He will stay up all night and then he will sleep the entire next day. Another side effect is he is hungrier, but I believe that’s to be expected.

Anyway, we took Dylan to see his new neurologist, Dr. Tanjala Gibson at Kennedy Krieger. He was very animated and even got up out of his chair. She was happy about how well he was doing and we did actually let her know that we wanted to try the CBD oil and when she was in agreement with Terri and me, we told her that the Dylan that she was seeing before her; didn’t look like the Dylan of two weeks ago. We already have him on CBD. We didn’t tell her that it was the full plant therapy, but we’re planning on telling her at his next appointment. He has been on this now for about a month, and we have noticed some real good changes. He is trying to talk again and if he does, it wouldn’t be nothing short than a miracle. Dr. Gibson did tell us that one of her colleague’s was doing a current study on cannabis and that it has been going on for over a year, and the results were actually positive. She said once the state gives the okay that she will get her license to dispense it to us for Dylan. We are really wondering what the actual Charlotte’s Web oil would do for Dylan. Hopefully, we will be able to find out soon.

As a parent who must sit by and helplessly watch their child suffer through these demonic seizures; to see your child’s personality being stolen away by these vampires, that drain him and leave him a shadow of his former self; there is nothing you wouldn’t do to try to cure your child, or help them in any way possible. I know that what we are doing is illegal, but I can attest first hand as to the great changes that we are witnessing on a daily basis as little by little Dylan is coming out of the darkness that once held him captive. Slowly but surely his personality is returning. Make no mistake, this hasn’t stopped the seizures completely, but it sure does offer us hope. It offers Dylan hope. Every day we get another little glimpse of our champion. The little boy that does battle with the one kryptonite that has time and again brought him down. He has never given up on the fight and neither will we. Until next time!

Daily News!!!!

By Terri King

Hello everyone, Sorry it has been awhile since I have written anything. Dylan has been back at school for three days now after being out sick for a week with an ear infection and sinus infection, he seems to be pretty good. I had his I.E.P meeting yesterday everything went well.He will be attending summer school again this year.His physical therapy increased too. His seizures were really bad Sunday night he had about ten seizures just while he was sleeping. The next morning he seemed fine. The petition is doing great 83,222 signatures now. There is a meeting about law 97-15 hopefully the law will be passed.

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https://www.change.org/p/don-t-stand-in-the-way-of-my-son-s-health

Daily News!!!!

By

Terri King

Dylan was up bright and early this morning and is in a wonderful mood.I hope his mood was the same at school today. We had our granddaughter this weekend.Dylan and her seem to be getting along better. She likes to play with his toys. She loves Dylan a lot. Kendyll likes to wear his old helmet I, guess she thinks it’s cool. I want to say a big thank you to all the people who have signed our petition. We now have 6393 signatures.Dylan is still having a rough time with the seizures. He has good days and bad days. I’m to sure how they have been at school. I gotten one phone call so far this year saying he had a pretty bad one at school that lasted about three minutes.

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His shirts say’s epilepsy sucks!!!
https://www.change.org/p/don-t-stand-in-the-way-of-my-son-s-health

https://www.gofundme.com/beast

Daily News!!

By

Terri King

My little superman is growing up so fast. I was looking at him the other day and, I noticed his first chin hair. On days Dylan doesn’t have school, he sleeps downstairs with my husband because he getting to heavy to carry upstairs.On those days he thinks it’s okay to get up at five in the morning, but if he sleeps upstairs he don’t want to get.He had two seizures while he was sleeping last night so maybe that’s why he didn’t want to get up. So I had to hurry up and get everything done this morning. Bath, dressed, breakfast and brush his teeth that’s the fun part he still fights me when I’m doing that. You would think I was torturing him. This is a picture of him waiting for the bus.

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https://www.gofundme.com/beast

https://www.change.org/p/don-t-stand-in-the-way-of-my-son-s-health

Daily News!!!!

By

Terri King

Dylan’s teacher told me he’s been giving them hard time walking to class in the morning. She asked if I could send his stroller to school with him every day “if he doesn’t start walking better and even to transported to school as well”. I told her he doesn’t need to be in the stroller that much and that he couldn’t be transported to school in it due to safety concerns because it doesn’t have a harness. But I will send it in on Wednesdays for when they go out in the community. I feel he needs to walk to and from his class. Today is picture day at school. I wonder how Dylan’s pictures will turn this year because refuses to have his picture taken. He is still having multiple seizures on a daily basis. We are going to rally tonight about getting medical marijuana passed.

This is his mood today.
This is his mood today.

https://www.change.org/p/lawrence-hogan-maryland-state-house-legalizing-cbd-oil-in-maryland