CBD Oil Stops Epileptic Seizures

GOT SCIENCE? Multiple scientific studies prove that cannabinoids stop epileptic seizures: See here

 

One of the listed so-called "side-effects" on so-called "vaccine" inserts is “grand mal convulsion.”

 

For example: “Adverse events reported during post-approval use of Tripedia vaccine include idiopathic thrombocytopenic, purpura, SIDS (sudden infant death syndrome), anaphylactic reaction (a severe, life threatening allergic reaction), cellulitis, autism, convulsion/grand mal convulsion, encephalopathy, hypotonia, neuropathy, somnolence and apnea. Events were included in this list because of the seriousness or frequency of reporting." - Sanoi Pasteur DTaP Vaccine, Dec. 2005

 

I just thought that I’d hammer that point in right from the start on this topic. How many of these epilepsy cases could have been avoided by not administering toxic poison in vaccines? How many epilepsy cases were actually caused by the vaccine program? Likely many, if not most. The CDC official vaccine schedule lists shots for birth, 2-months and 4-months. Multiple shots are listed at the 2-month visit. Just a valid observation. Now go take a look at the list of ingredients for vaccines.

 

Charlotte Figi was a normal, healthy child until she was three months old, and then she had her first seizure (after a round of vaccines? I’m not sure, but it most likely was). She was diagnosed with Dravet’s Syndrome, a very rare form of epilepsy after she started having seizures repeatedly throughout the day increasing in severity as she got older. Despite being on seven different kinds of deadly toxic drugs (so-called “medications”) she continually got worse and worse due to the negligence and incompetence of the so-called “medical system” in the USA. By the time she was 5 years old she was having upwards of 300 grand mal seizures per week with her body so damaged that even her heart stopped a few times. Eventually the choice was made to put her into a medically induced coma to give her a chance to rest and recover. Medical “doctors” had told the family that all of her treatment options had been tried and that there were no more options available for Charlotte. Her Grandfather, who had been researching about cannabis being very effective for many with epilepsy including a young boy who also had Dravet’s, suggested to the parents that they should try cannabis oil because he’d read excellent reports concerning its use. They did.

 

Charlotte Figi went from having 300 seizures per week to having ZERO while using cannabis oil; in other words she went through all of those so-called “medical treatments” and all of that toxic drug therapy and almost died several times for no reason.

 

The Stanley Brothers are medical marijuana growers and dispensers in the state of Colorado and they bred their own strain of cannabis specifically to address Charlotte’s condition. Because CBD isn’t psychoactive (cause the “high” effect) they developed a strain that is extremely low in THC (the psychoactive component) and extremely high in CBD (the component that does the most good for epilepsy which is non-psychoactive). The CBD to THC ratio of the strain that they named “Charlotte’s Web” is 30:1, in other words it’s so low in THC that they call it “Hippie’s Disappointment” as a joke.

 

“The biggest misconception about treating a child, like little Charlotte is most people think that we’re getting her high, most people think she’s getting stoned.” - Josh Stanley

 

She’s not getting high at all. And the medicine is non-toxic. The same people who worry about poor little Charlotte getting high off of cannabis don’t mind the effects of all of the chemical drugs that she’s had to take, apparently, because they don’t question that process. It’s totally unnecessary child abuse and criminal negligence by the state, but no money can be made by the system for cannabis treatments therefore they refuse to acknowledge it, recognize it or use it as a medicine, nevermind that innocent children have to suffer without it. God Bless America.

 

Dr. Sanjay Gupta, well known from his CNN broadcasts, is a neurosurgeon and professor of neurosurgery. After hearing about Charlotte Figi’s case the good doctor made a statement apologizing for not condoning medical marijuana previously, and for not researching enough into the facts before he made his evaluation:

 

“It doesn’t have a high potential for abuse, and there are very legitimate medical applications. In fact, sometimes Marijuana is the only thing that works… It is irresponsible not to provide the best care we can as a medical community, care that could involve Marijuana. We have been terribly and systematically misled for nearly 70 years in the United States, and I apologize for my own role in that.” – Dr. Sanjay Gupta, CNN Chief Medical Correspondent

 

Nova Leigh wasn’t healthy at birth, she was born with Schizencephaly, from the Greek words “split brain,” an extremely rare condition that has only been diagnosed in some 7,000 kids. She had only about 24% of her brain and her seizures started very early on in her life. Soon there were so many seizures that it was a full-time job for her parents and hospitalization became necessary. “Doctors” had her taking nine different toxic drugs including Valium, Ativan, Onfi, Sabril, Keppra, Zonegran and others, none of which were working to control seizures but you can rest assured that the drug companies were profiting quite nicely from their sales! Their final plan of action was going to be either have her take so-called “medication” that causes permanent blindness OR remove two thirds of her remaining brain. That was the final verdict of the “medical” system in the USA for Nova, no other options existed, or so they said.

 

“We relocated to Colorado in 2014 to obtain legal medical cannabis for Nova when we ran out of viable options in our home state of Texas. After trying and failing nine pharmaceutical drugs to stop the seizures by the time she was two; we were given the option for brain surgery: a lobectomy and a corpus callosotomy. The idea was that we would split her brain in half, disconnecting the two sides, and then remove any brain matter left on the right side of her head. We decided to move to Colorado and try cannabis first.” – Nova’s Mom Barbara[1]

 

Enter cannabis:

 

 

“For the first time, Novaleigh is talking. Novaleigh is growing. She is thriving! One look at Novaleigh’s Facebook Community page ‘Supernova,’ and you will see photos and videos of a child who is smiling and talking, and as her mom says, ‘seems for the first time in her life, to be taking in and understanding the world around her.’ She has even recently learned to clap, and to wave at her mother, much to her mom’s delight!”[2]

 

The family now spends far more time at home than at the hospital. It was the other way around before! She is now completely off of pharmaceutical drugs with the exception of a steroid to supposedly help control inflammation. Her hormone function has suddenly and miraculously started working all by itself! She no longer has to take hormone replacements and she used to get daily hormone shots. Not anymore! At time of writing she has successfully completed over 100 days without a single seizure and she was experiencing upwards of a hundred per day without cannabis treatment. Not bad for the “Devil’s Lettuce” huh?

 

[1] https://iloveincredibles.com/testimonials/supernova/

[2] https://www.elephantjournal.com/2016/09/the-true-story-of-a-5-year-old-colorado-cannabis-refugee/

 

“What I worry about are the thousands and thousands of children like Jayden who are suffering unnecessarily, who I know we could help. The only thing separating them from help are outdated rules that need to be changed.” - Steven DeAngelo[1]

 

Jayden David was perfectly healthy until he had his first seizure at four months old, which leads me to believe that the vaccines probably had a lot to do with this case as well. Why would a healthy child suddenly develop seizures? He was having 500 or so twitching seizures per day and grand mals for up to an hour and a half. At the age of 4 ½ he was on 22 pills per day and by the age of 5 he’d already taken about 25,000 pills total. Running out of hopes for his son and knowing that time was running out, Jayden’s dad, Jason, decided to try medical marijuana.

 

“I went and picked up something that I saw in a dispensary and came home. I gave it to Jayden. After 4 ½ years of having chronic seizures, 500 a day… the first day I gave it to him was, thank God one million times, was the first day he’s ever went seizure free in his life.”

 

Harborside Health Center, a medical marijuana clinic in Oakland, CA is where he obtained the high CBD, non-psychoactive liquid cannabis tincture for Jayden. He progressively started getting better and better as time went along, his seizures dramatically decreasing. He was eventually able to go outside and swim in the front yard pool, which wasn’t possible before because he would have seizures due to the water temperature.

 

“Jayden is not just walking, he's running. He plays at a park, climbing up and down the steps of the jungle gym. He swims at his local pool, splashing in the water with his father and other children. He loves to go to Fuddruckers to dig into his favorite food, a cheeseburger with mushrooms.”[2]

 

After one month of CBD treatments Jason started weening Jayden off of the dangerous addictive drugs that the so-called “medical system” had him taking. He’d take one drug away and for two weeks Jayden would suffer, but then he’d be OK again. Then he’d take off another drug, and another. It was a long, difficult process but he finally got Jayden down to two pills. The hardest one of them all was benzodiazepine. Jason contacted about 30 benzo-withdraw clinics and they were all yelling at him on the phone:

 

“You’ve got a 7-year-old on Benzos!?”

 

They were telling him that they had big football players on those drugs that were dying trying to get off of them. They were appalled by his young son having been prescribed such drugs, which again, goes to show the negligence and incompetence of the USA’s “medical system.” They had poor Jayden addicted to that drug from the time he was 16 months old. The clinics won’t take him in as a patient so Jason is stuck trying to work that out on his own. Jason has high hopes for Jayden on cannabis oil and is looking forward to getting to know his son for the first time when he is well enough to be himself for the first time in his life.

 

Jason and Jayden’s Journey is up on Facebook.

 

[1] Executive Director of Harborside Health Center, a medical marijuana clinic in Oakland, California

[2] https://www.cnn.com/2012/12/10/health/medical-marijuana-child/index.html