A MIRACLE!

Henna was 2 years old when she was admitted to the hospital with a traumatic brain injury. She had been thrown against a concrete wall by her biological father for crying too long. She had two depressed skull fractures, old blood on the brain from previous abuse, a lacerated liver, collapsed lung, suspected sexual abuse, and shaken baby syndrome. Henna coded while on the way to the hospital via helicopter and was brought back to life only to go into surgery to relieve pressure on her brain. She was not expected to live through the night. Henna was in a coma for one month hanging on to life. Then the miracle happened! Henna woke up and was able to move all her limbs and speak, shocking all of the medical professionals. We took Henna into our home and shortly after her arrival she started having seizures.

Henna's journey continues as we try to control her seizures. She received the Vagus Nerve Stimulator (VNS) on Feb. 4, 2011 at Children's Hospital in Washington, DC. The VNS will send an electrical impulse to Henna's brain every 3 minutes for 30 seconds to interrupt her seizures. Over two months we have increased the electrical current and we have seen no change in her seizure activity. It looks as though Henna is in the third of children who receive a VNS that sees no relief from the VNS. We are very disappointed! We have started her on a new medication in addition to her current medications. Maybe it will help.

On August 6th, 2012, Henna had a full corpus callosotomy. This surgery is for people who have generalized seizures with no focal point. The corpus callosum is a band of nerve fibers located deep in the brain that connects the two halves (hemispheres) of the brain. It helps the hemispheres share information, but it also contributes to the spread of seizure impulses from one side of the brain to the other. A corpus callosotomy is an operation that severs (cuts) the corpus callosum, interrupting the spread of seizures from hemisphere to hemisphere. Seizures generally do not completely stop after this procedure (they continue on the side of the brain in which they originate). However, the seizures usually become less severe, as they cannot spread to the opposite side of the brain.

Henna received a white Labradoodle, Leo, from 4 Paws for Ability in Oct. 2010. We sent 4 Paws 2 shirts a week to help train her dog. One shirt was when Henna had a seizure and they used it for her dog to smell the chemical change during her seizure. The other shirt was when Henna had NOT had a seizure. This helped her dog differentiate between the two scents. It's a fascinating process. We trained for 10 day in Ohio with Leo and a trainer before bringing Leo home.

Leo had been going to school with Henna but started to bark and growl at different people when they came into her classroom. We worked with Leo's barking and growling when people would knock on the door and for a while he seemed better. He is very protective at home also. He then barked and growled at some boys who came into Henna's classroom and had to be removed from school. The trainer at 4 Paws said that some dogs bond so closely with their child that they become protective. Leo took on Henna's classroom as another home and felt he had to protect her. Sadly, because of his aggressive behavior, Leo can no longer be a service dog. The trainer said Leo would behave lthat way with any child he bonded to. Just his nature. We will keep Leo as a pet. Leo LOVES being just a pet. He still alerts to Henna's seizures and lives to get his hot dog reward!

Henna now has Snoball, a beautiful Golden Retriever. Snoball was born June 3, 2011. She is so sweet and a bundle of energy! Sno is doing an excellent job alerting to Henna's seizures BEFORE she has them! She is alerting up to one hour before Henna has a seizure. Sno goes to school with Henna and proudly wears her school ID badge. Snoball will be a great seizure alert dog and will serve Henna well.

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Sunday, October 19, 2014

Finally an update.....

Homecoming 2014

I have been remiss in keeping up with Henna's blog and I apologize.  Our life has been a whirlwind of activities, new foster kids, and ups and downs.  We have had 4 new foster kids for over a year now and Henna loves them very much.  The 3 boys are returning to their father on Friday and their older sister will stay with us as she heads off to college.  This is going to be a big loss for Henna.
 
We have decided to home school Henna part time and then she attends high school the other half.  It suits her well.  She is such a social girl and enjoys all the kids and activities at school.  Since Henna's brain surgery 2 years ago she has become much more aware and her cognitive abilities are improving.  It's so exciting to see her use higher level thought processing.

We still have her service dog Snoball but Sno's job has changed a bit.  Henna does not have the drop seizures since her surgery but still has grand mal and smaller seizures.  Sno attends school with Henna and goes out into the community but stays at home other times.  She is a smart dog with a great nose.  She is still alerting to Henna's big seizures.  She's hyper and a rascal at home, chasing the cats and barking at everything!

 

Henna is still taking therapeutic horseback riding lessons and Son does not like her on that huge animal!
This summer Henna attended her first overnight camp through Brainy Camps.  She went to Camp Smiles, a Downs Syndrome Camp, and was the first non-downs person to go.
  The camp is trying to integrate other disabilities into their camps.  It  was a great fit for Henna as they were all at the same emotional level.
Henna and me picking strawberries.
Cherry blossoms in Washington DC.
Last years Xmas picture...
Henna getting lovies from sister Mica.

As we come up on Thanksgiving let us be thankful for all the many blessing God has given us.  Times are getting more challenging and we much stay focused on what really matters.
Take care and God Bless,
Jan







Sunday, September 15, 2013

Special Needs Carnival fun!

Yesterday we went to a special needs carnival a local church's youth group put on.  They did such a nice job.  There were games, crafts, face painting, a petting zoo, cotton candy, snow cones, and a moon bounce.  The weather was beautiful and there was a touch of fall in the air. God is good!


 Henna trying out her golf swing!
 Henna with 3 of the 4 new foster kids we have.
 Petting zoo.  2 day old duckling.



She found a ring!  Henna has been intrigued with wedding rings.
 Sensory table.
 Of all the pictures to get painted on her face and she chooses Batman.  That's my girl!



 Samantha and Henna
 Music table.
Balloon fun!

Friday, August 16, 2013

Seizure Disorders Enter Medical Marijuana Debate

The role of cannabinoids in the treatment of seizure disorders in children has come under the spotlight in recent months amid a string of media reports of parents obtaining the substances in states where medical marijuana is now legal and claiming "miraculous" reductions in seizures with the treatment.
Among the reports was that of a 6-year-old boy with Dravet's syndrome, a rare form of childhood epilepsy, reported by CNN. In an interview, the parents said the boy was left immobilized by the 22 antiseizure pills a day required to control his seizures, but after treatment with a liquid, nonpsychoactive form of marijuana, he was able to make it through an entire day without a seizure for the first time since he was 4 months old, and continued to see substantial reduction.
"Instead of medical marijuana, this is miracle marijuana," the father told CNN.
Another child with Dravet's syndrome in Colorado, who was having 300 grand mal seizures a week and had lost the ability to walk, talk, and eat, was similarly reported to have her seizures drastically reduced to just 3 times per month after treatment with the liquidized form of cannabis, CNN reported.
In both cases, the treatment was low in tetrahydrocannabinol, or THC, the compound associated with the psychoactive properties of marijuana, and high in cannabidiol, which is not psychoactive and is instead believed to be medicinal. Both cases were also featured in a CNN documentary on medical marijuana, "Weed," that aired Sunday, August 11.
With the increasingly abundant anecdotal but very high profile reports, neurologists can likely expect a surge in interest from parents, particularly those frustrated by intractable epilepsy in their children, who are logically asking "why not?"
"When patients, children or otherwise, are faced with bad situations and no good treatment they, or their parents, look 'out of the box' to find one," said David M. Labiner, MD, a neurologist with the University of Arizona and director of the Arizona Comprehensive Epilepsy Program, in Tucson.
"Medical marijuana is one of those things being utilized now," he told Medscape Medical News.
Dr. David M. Labiner
He added, however, that despite the anecdotal reports, the bigger picture in terms of clinical evidence of efficacy, or, importantly, long-term safety on such treatments is lackluster at best. "There is limited high-quality evidence about the efficacy and virtually no data about the safety of using marijuana or cannabinoids," he said.
Medical marijuana is currently legal in 18 states and the District of Columbia, and in some states the approval explicitly includes treatment for epilepsy.
But a 2012 Cochrane review of all published randomized controlled trials involving the treatment of marijuana or one of marijuana's constituents in people with epilepsy concluded that "no reliable conclusions can be drawn at present regarding the efficacy of cannabinoids as a treatment for epilepsy."
With a primary outcome investigated for the trials of seizure freedom for 1 year or more or 3 times the longest interseizure interval, the researchers found 4 reports with a total of 48 patients randomly assigned to placebo or to 200 to 300 mg of cannabidiol per day.
Although none of the patients in the treatment groups were reported to have sustained adverse effects, none of the trials included reliable details of randomization and all were deemed to be of "low quality."
In a commentary on the review, Jonathan W. Miller, MD, PhD, noted that in addition to the inconclusive evidence of efficacy, other evidence has suggested marijuana and low-dose THC can represent a possible seizure precipitant.
"Marijuana itself has major shortcomings as an epilepsy treatment," writes Dr. Miller, who is director of Functional and Restorative Neurosurgery and director of Epilepsy Surgery at University Hospitals, Case Medical Center/Case Western Reserve University in Cleveland, Ohio. "Its psychotropic action can only be regarded as an adverse effect."
"It is a biological product containing multiple compounds with unclear, possible, anti- or pro-convulsant effects, delivered in varying amounts from dose to dose," he adds. "Long-term safety has not been adequately investigated."
With the need for new epilepsy treatments pressing, however, he underscores the importance of evaluating the potential benefits of cannabinoids with more reliable clinical trials.
"Cannabidiol or other individual cannabinoids with minimal adverse effects could be extracted and given in precise doses in rigorously designed, blinded, randomized clinical trials to test efficacy and safety," Dr. Miller urges. "This is a reasonable route for development of new antiepileptic drugs."
Safe Dispensing a Concern
In the case of the California boy described in the CNN story, the parents said they obtained the cannabis from the Harborside Health Clinic, a medical marijuana dispensary in Oakland, California, that has billed itself as the "world's largest pot shop" and sells concentrations with names such as "Deadhead OG" and "Afghani Hash."
The clinic does claim to screen all of its products for safety and tests for potency as well as the presence of pathogenic molds, but Dr. Labiner, in agreement with Dr. Miller, asserted that if cannabinoids are shown to be effective anticonvulsants, they should be provided to the public with the same safety assurances as any other epilepsy drug.
"Rather than thinking about how to keep sick people from using these compounds, as many of our elected officials and law enforcement are doing, we need to support efforts to determine how to appropriately use these compounds in a controlled fashion and not delegate that responsibility to [places like] 'the world's largest pot shop'."
Even the American Academy of Pediatrics (AAP) favors the pursuit of a better understanding of the potential benefits of medical marijuana, but, with the same concerns of operating in an unregulated environment in mind, the academy opposes laws legalizing medical marijuana.
"The AAP strongly supports more cannabinoid research to better understand both how these substances can be used therapeutically as well as their potential side effects — which we may well be underestimating," said Sharon Levy, MD, MPH, director of the Adolescent Substance Abuse Program at Children's Hospital Boston and an assistant professor of pediatrics at Harvard Medical School in Massachusetts.
Dr. Sharon Levy
"[But] the AAP does not support 'medical marijuana' laws as they circumvent regulations put in place to protect patients, and children are a particularly vulnerable population," Dr. Levy told Medscape Medical News.
While noting that the reports on children finding seizure control from cannabinoids are "quite compelling," Dr. Levy emphasized that medical marijuana as a policy misleads the public on the level of research behind the endorsement.
"It implies, incorrectly, that marijuana is an established medication and opens the doors to people and parents 'experimenting' with it for all kinds of conditions."
And when it comes to experimenting with drugs to be used particularly on children, the practice is best left to experts in highly controlled conditions, she added.
"I fully support the parents who are trying to advocate for something they believe will be helpful for their children. But let's do it the right way — the same way we develop all other medications. We are bound to make mistakes when we try and take short cuts."