Posts tagged ‘Montana’

August 16, 2012

Wuesthoff Medical Center ER – Rockledge Florida – Dope dealers for children

We’re supposed to want to keep drugs away from our kids – right?

Isn’t that the whole point of existence – is to learn when to say NO? Use the least harsh method?

Here’s a glimpse at my ER visit in Florida this morning, July 24, 2012. We are in Rockledge Florida – Brevard County – visiting my eldest daughter. Grace has just come from very arid Montana to very humid Florida. In Montana, there is no pool in the backyard. We swim in the creek, or go to town to the big pool.

Well….Miss Gracey is part fish. She LOVES to swim. She has lived in the pool to a point I almost had to drag her out physically as she was burning her skin. She has been underwater constantly – using a mask – and also used the Hooka underwater scuba trainer – which I’m sure blew some air in those ears under water……

Perfect setup for Swimmers Ear if I ever saw it. Wish I would have thought in advance for it.

Can’t win em all……

So….

Grace had an earache this morning. 4am to be exact – a REAL howler of one – had her howlin anyways.

We wake up Sis – and Tom gets the truck – and off to Wuesthoff Medical Center – Rockledge – ER

We are met with an empty waiting room – and an hour wait. It is visibly apparent Grace is in pain – and we waited….and waited….the whole time Grace lamenting “They wouldn’t do this to me in MT. They’d have me right in there!”

All I could do was hold her – and wait. We FINALLY get into a room – and after another half hour wait in a virtually empty ER we are blessed with the presence of a Dr. G Edward Mallory, DO

Dr Mallory professes that Grace’s problem is due to serious sinus infections and allergies – and recommends we have a follow up with their partner pediatrician within 2 days – to check on her serious otitis media. I asked him if those allergies could have developed in the past 10 days or so since she arrived in Florida – as she has no history of allergies, or serious sinus infections.

Mind you – Grace and I share the same family physician, who has been my personal Dr for 27 years. He delivered Grace. He delivered ALL of my children. He knows EVERY issue any of my kids have EVER had. All my kids saw Jim until they moved out and away. He knows every little intricate detail of their health issues all through their lives, as I have any records from any other visits sent anywhere else to him for his files.

I trust him with my life. I trust him with my children’s life.

Then – this ER Physician? Dr Mallory – well – he has the BALLS to ask me if I would like 2 days worth of vicodin (8 pills – to be specific) for Grace for her pain.

I informed that dumbass that I was highly offended he would even SUGGEST vicodin for SWIMMERS EAR – and told him we wanted the pain drops – and something to dry the ear up. “I am 45 years old and have never taken a Vicodin in MY life – how DARE you attempt to prescribe it for my TWELVE YEAR OLD DAUGHTER!”

Well – that dope dealer scurried right on out of there – Gracie got her drops and is sleeping soundly – and we will be sure to use the swim ear I picked up once her infection is gone.

When the RN came in after the Doc to take care of things – I told her what transpired and that I was NOT happy about it.

She gave me a double thumbs up and told Grace she had a good Mom to look out for her. Nurse Boggs – you have my undying respect.

OH MY GOD FLORIDA!!!! What in the HELL? You tolerate this? Even my 12 year old knew it was WRONG.

HELLS BALLS – get to FIRING these guys before they damage more of our kids! He wanted to be “sensitive to her pain” with Vicodin at TWELVE for SWIMMERS EAR – what the HELL would he do for her at 21 when she is fully addicted???

I learned a very valuable lesson with this one trip to a Dr in Florida. People are sheep! “Do what the Dr says”

How many of you out there would have just taken the pain meds for your children? How many parents out there question doctors? Question their treatment?

“Do what the Dr says” – we are raised with that principle.

Well…..I contend that you need to “Do what the Dr says” after you evaluate things yourself too. ASK QUESTIONS – ask for alternatives – and QUESTION AUTHORITY – especially when it comes to your children.

If I would have taken that Vicodin prescription and given it to Grace I sincerely believe we would not have had as successful day as we had. As it was – as soon as the Aralgan drops went in her ear – her pain stopped. IMMEDIATELY

We got her home – and she slept over 4 hours – very peacefully – and Mom didn’t have to keep checking her breathing or heart rate – as she has never been on a heavy narcotic like Vicodin.

Grace woke up well rested – and not groggy or out of whack.

She has been perfect ever since.

Our children are our most precious commodities – we must protect them. It’s a pretty sad day when we have to protect them from a Doctor.

May 23, 2012

Patients Out of Time Clinical Cannabis Conference

I am excited to return to Colorado from Arizona, and the Patients Out of Time 7th National Clinical Cannabis Conference in Tucson, Arizona  April 26-28, 2012.

WHAT AN EVENT!

I had waited in anticipation so anxiously for over 18 months. The weeks before the conference were maddening. I felt like a child the eve before Christmas morning.

I was not disappointed either. Almost everybody a person could hope to meet on the medical cannabis side of things was there. Dr Russo and his daughter Sarah, Dr Weil, Mary Lynn and Al, Elvy, Dr Courtney, Melanie Drehrer, the list goes on and on…..please be sure to visit http://www.medicalcannabis.com for followup. The entire conference was filmed – and is available online. The CE portions will be available for a fee in the near future. Here is a video of Dr. Andrew Weil from the conference. (Click link silly – it’s active). Also – please be sure to find Patients Out of Time on Facebook.

Please be sure to add Patients Out of Time to your groups to support. This incredible conference was their 7th national clinical conference in 14 years. They hold them every 2 years. We will be rolling out a pledge program for the group – stay tuned – and please – support the science and research.

Every bit of our efforts rely on credible science and knowledge.  It is imperative we have a strong voice, and solid support for Patients Out of Time.

I had the honor of helping Jacki Rickert prepare for her day and assisting her throughout the day on the day she spoke. Jacki is an amazing woman, I was quite stunned to learn her story. Jacki was one of the 28 patients who was completely approved for the Federal IND Program, before it was shut down. She has been waiting 22 years for the Fedral Government to send her any cannabis.

For years, Jacki Rickert has been asking, “Is My Medicine Legal Yet?”

Jacki suffers from two painful and debilitating conditions, Ehlers-Danlos Syndrome and Advanced Reflex Sympathetic Dystrophy, and was fully approved for participation in the U.S. Government‘s Compassionate Use Investigative New Drug (I.N.D.) Program at the Federal level in May of 1990, and by the state of Wisconsin in December of 1990.

I think she will be waiting until she dies…..unfortunately. When ol George W Sr. shut down the program, Jacki and 27 other folks were completely approved, and awaiting their first shipments. Not one of these folks ever received cannabis – as only the original 13 Federal patients were grandfathered into the program.

It is only through a series of Angels and Miracles Jacki is with us today.

22 years later – Jacki is STILL asking “Is My Medicine Legal Yet?” and is lucky to be alive. What a wonderful heart and spirit Jacki has – and i hope each and every one of you out there follow up on her story – reach out – support her and her group.

Ask the question – every day – “Is My Medicine Legal Yet?” and then fight like the devil to make it legal.

If Jacki can do it all these years from Wisconsin in a wheel chair…….we should ALL be able to fight just as hard.

Blessings to each and all out there in the world. Please – stay in touch – and be brave in your fight!

Hiedi

SO pleased to attend!

I was SO PROUD to be mentioned I coulda busted. Instead – I cried. This was a highlight of my career – and I hope to see many more!

March 26, 2012

Cherish what you’ve got

Because when it’s gone, it’s very painful.

How do I know?

Here’s one example:

Warrior fighting for his life 

Even LANDLORDS are affected in Montana!

So……you may be sitting there thinking “What has Montana got to do with Colorado?”

Well folks, it has everything to do with Colorado. Politically, legislatively, AND in the medical cannabis movement.

If you have followed politics in both of these states for any period of time, you will find that CO and MT are very close in many areas. Of closest interest is the whole Agricultural realm, and many state and government practices and lawmaking.

In the midwest, these two states really have the most in common, from terrain, to weather, to agriculture, livestock, water policy. I could go on and on.

Our politicians and state governments interact – and look to each other for solutions, and feedback. In many political realms, you will see them parallel, and in many instances, MT follows CO legislation within a 5 year window.

Right now – what I wouldn’t personally give to have the problems Colorado has in Montana. From the Beinor case, to the Walsh letters, to the banking issues.

I WISH we had your problems in Montana.

You may think I’m crazy for saying that, but try losing access sometime. Walk a mile in the shoes of a Montana providor or patient….it brings it all into perspective.

Do you have any idea how many folks are affected in Montana?

We had 24 raids in ONE DAY (March 14, 2011 to be exact) in a political move to push repeal through our statehouse.

Those folks are all facing their charges now, and families are being devastated.

Our lawsuit is underway, and we go to court April 30, 2012 to see if we get damaged further. or maybe some relief.

In my opinion, with how Montana’s new law is written, no matter how one interprets it – there is NO WAY to operate and function legally. There is a loophole in there one way or another to screw Montanans, and increase crime rates.

Please see new law detailed out here: See how Montana got screwed

SO – folks

CHERISH WHAT YOU’VE GOT!

I hope this will help some of you understand my views in Colorado, and why I have taken the path I have with Colorado and Montana Connect Magazines.

What happened in Montana REALLY opened my eyes, and shaped my view on how I operate and handle things. I am  “conservative with a liberal flair” and I have been all of  my adult life.

There are quite a few of us out here – and more and more are coming into the fold every day.

That’s why I have the approach to marketing I have. The attention to public view, from an objective perspective.

The world is watching Colorado – what you folks DO matters!

And folks across the nation watch……some are literally dying to get into Colorado.

I know – we just “imported” our first patient last week, from Florida. A seriously ill Crohn’s patient.

That story will be shared soon……

I meant what I said about increasing registry numbers. We have a HUGE base to draw from in Colorado – and even more from out of state who see Colorado as THE place to be.

After my experience in Montana and Colorado – that’s what I tell folks too. At least until we get Montana straightened out.

I share my experience there. The beauty of the industry – the safety of the patients.

What we have going on in Colorado is not only beautiful, it is history.

Please folks….cherish it. Exemplify the spirit of the Pioneer……lead.

You have the lead – please – act local – think GLOBAL.

So many people around the world are watching.

WIN that Beinor case – and fight for Boulder.

Please stay tuned for a story from Boulder too – there are HUGE problems in the city – and we must rally.

CHERISH what you’ve got – for it is ever so painful to lose…….

February 26, 2012

Still….a LONG road ahead

The fight is just beginning.........

Cashy is Cancer Free…..again…..for now.

By no means is the fight over.

That became quite apparent to me traveling back to Montana with the Hyde’s. As I watched the reads on Cashy’s story go up, and up…….and the relief spread across the world (we have comments from as far as South Africa)………

I cringed.

Does everybody think we’re done? Do they all think Cashy and his family are home free?

I hope not, because brutal point in fact is – the fight is NOT over. Not even for a second.

Grab a Kleenex…..and read this.

PNET Brain tumors from Wikipedia

Definition – “Primitive neuroectodermal tumor (PNET) is a neural crest tumor.[1] It is a rare tumor, usually occurring in children and young adults under 25 years of age. After successful chemo- or(and) radio- therapy the 5 year survival rate is only 7,6-8% .[2]

“Survival – Patients diagnosed with a medulloblastoma or PNET are 50 times more likely to die than a matched member of the general population. The most recent population-based (Surveillance, Epidemiology and End-results Database) 5-year relative survival estimates are 64% in children (1-9 years) and 35% in adults (20+ years). [4]

So….yes, we can breathe easy that Cashy is cancer free – for NOW.

But this fight goes on EVERY day! Every day is the battle to find the proper, safe medicine for Cashy. Ensure he has supply, and oil rich in CBD.

There are good souls out there who attempt to donate oil. Not many, but a few brave souls. I commend their efforts, and hope to educate some folks so they understand exactly how dialed in this entire process is. Encourage folks to know what is in their garden. Test it. Buy CBD strain seeds – PLEASE. Research those seed companies, ensure they are really selling CBD rich strains.

It’s not just “fill a syringe with oil, and put it into the kid.” There are three different types of oil, used at different intervals throughout the day for different purposes. They are all tested and use absolutely NO chemical processing. Water only, and suspended in a hempseed oil. 140mg/ml to be exact.

It’s not a game here, it’s serious science.

Life saving science, dialed in with an organic diet, and parents determined to see their son live, no matter what the cost.

During the drive back to Montana, Mike and I talked for a long time. The most profound statement I heard come out of Mike’s mouth, that I wish to share is soon to follow. Let’s lead up to it a bit first……

Mike has had to search diligently for oil, and product to make oil. He has spoken to many many growers in many different states. Many caregivers in many states. Business people, scientists, doctors, and “hippies”. All walks.

You’d be surprised who is actually the most compassionate and generous. One day I hope we can tell the stories……I think you would be amazed to witness who is the bravest of all, if you don’t already know.

Point is: Cashy’s life is that important. We know we can save him with cannabis oil. We are proving it every day, with every little success, every HUGE success.

Every little smidge of help counts.

On our drive – Mike had one statement to make to anybody and everybody out there flying the medical flag.

“If you aren’t testing your products, ALL of your products, you are NOT medical. You’re just playing the game.

WE NEED to know what dosages are. People can be so generous, and want to give us oil. If that oil is processed with a chemical, and is only 30mg/ml we really can’t use it. It’s too much oil to have to ingest for treatment. We cannot and will not use chemicals on our son.

I cannot have poor product for my son. The dosages have to be right on, no matter how big their hearts are and how good their intent. Cashy’s life depends on it. I will not give my son product that has not been tested.

Period.

I cannot put his life at further risk no matter how pure intentioned the donor”

That hit home for me. Our entire conversation hit home for me.

As Mike talked about the children he had witnessed die over just the past year, my heart not only broke, but my fear for Cashy increased a hundredfold.

I witnessed Mike taking calls from those very same parents. Two called to celebrate the news while I was with Mike. Their own children had died of the very same type of tumor within the past few months, yet they were so filled with hope and excitement for Cashy and his family. Thrilled with their success. Hopeful to see one child survive of the many they personally know battling the same vicious cancer.

Ever fought cancer? Ever administered life-saving oil to a patient?

Ever made the oil to save a person’s life?

Even with a 2 oz limit – that is not near enough quantity of plant and flower material needed to make a quality oil at cancer fighting dosages. It takes roughly a pound of plant material to make one ounce of oil. If that plant material is not quality – it takes MORE. Lot’s more.

To treat Leukemia effectively in an adult, I know you need about 6 pounds of product per month – to make 3 ounces of oil – to really dose an adult, and get apoptosis into effect.

The type of tumor directly affecting Cashy’s brain is very aggressive. We all witnessed that with its recurrence in 2011.

It’s gone now. I sincerely hope it will remain gone.

Before I we go any further, I ask each and every one of you to watch this:

Define Better

What is better for our children? The general populations seems to think chemical intervention is the only way.

What does Cashy’s story tell us all?

It tells me, there is a better way, and we are well on the path to it.

Last year, Racing Horse Productions was in Montana filming a documentary. It started in the fall of 2010, and they filmed through the summer of 2011. Many of us in Montana were filmed for the movie.

I believe when it began, they had one idea of the direction they were going. As they saw what transpired, it shifted.

I am excited to see the results, and I am told it depicts what happened in our legislative session well.

It’s what we were up against – it’s what we fought.

Code of the West Trailer

See that green button they pushed there in the end of the trailer?

That was the green button for repealing medical marijuana in Montana.

That green button being pushed to kill Cashy. On St. Patrick’s Day 2011 no less.

The day after Montana politicians met Cashy at the state capitol.

We can NEVER let that happen again.

Ever.

Warriors – keep up the fight! Subscribe to this blog, stay tuned. Share the postings, and share Cashy’s story.

Spread it far and wide across the world – so we can save not only Cash – but many more children just like him.

Industry people – TEST YOUR PRODUCT! Ensure your clients are getting the right medicine. Safe, with accurate dosages! No matter where you are – find a way.

People’s lives depend on it.

Also – always keep your doors open to parents like Cashy’s parents. Find a way to help. Train your staff.

Pay it Forward.

You never know who you may help one day, and just how far their gratitude will go.

Politicians – please – know what you do. Protect the innocent at all costs, and do no harm.

Cashy is the most innocent of all……and Montana politicians attempted to murder him last year. That is my honest opinion. They did not care to look at the science and truth, or protect the patients. They treated us as criminals – called us scourge.

Montana Politicians opinions.

We had a select few defenders, but the majority were out for murder.

Funny – all with the intent to “Save the Children”

If only they would have listened when they met Cashy.

If only……

Please support the Cash Hyde Foundation

Also – please support the next issue of Montana Connect. A good portion of the proceeds will be going to the Cash Hyde Foundation.

Stay tuned for details

Winning!

February 23, 2012

Boy of Steel Cancer free – Again

Yup – you read that right.

Cash Michael Hyde is Cancer Free – again.

My hero is only 3 feet tall

On Wednesday, February 22, 2012 Cash Michael Hyde was in Salt Lake City for a follow up MRI to check the status of his brain tumor. A PNET brain tumor he has been battling for almost 2 years.

For the second time in a row, Cashy has beat his tumor, and is in remission.

The Boy of Steel is Cancer Free!

How many people do you know that beat cancer once, nonetheless twice?

At THREE years of age?

Congratulations and hugest of blessing upon his parents Mike and Kalli for being the strong parents they are, and fighting so diligently to save their son’s life with an alternative option.

Thank heavens for the cannabis oil that saves Cashy’s life.

Be vigilant in your duties Pioneers……your efforts are important to people just like Cashy and his family EVERY day! Act responsibly! Keep up the great work!

And to all the politicians out there…….please support the Hyde family, and many other families out there just like them.

We are here to save children’s lives, not take them away.

Love and blessings to all…..I’m off to celebrate on the ride back to Montana with the Hyde’s.

I love them all so very much. Better be a BIG box of Kleenex on board as we will all be so HAPPY!

LOVE YOU CASHY!

Please Read Cashy’s story HERE:

Please visit their foundation and help support Cash HERE:

February 13, 2012

When your child is dying of cancer, you’ll do anything

This is what it’s all about.

Welcome to the front lines of Cancer treatment.

I would like to introduce you to my little motivator, and real life hero.

Please meet Cash Michael Hyde.

Cashy was born June 21, 2008 to Mike and Kalli Hyde in Missoula Mt. He came into the world with an older brother, Colton.  Today, he is due to become a big brother in April.

The Hyde Family - Mike, Kalli, Colton and Cashy

Cashy is very lucky to be where he is at today. You see, at 22 months of age Cashy was diagnosed with a Stage IV PNET brain tumor on his optic nerve.

It was May 3, 2010. Cashy had been sick for a couple weeks, and his mother and father became very concerned. They had been told that Cashy simply had mononeucleosis, and that it would go away.

It didn’t go away. As a matter of fact, it had gotten worse. Cashy was sleeping 18 hours a day, vomiting morning and night, and his left eye had started drifting and drooping. It felt to his parents like he was dying in their arms.

On May 3 2010 the Hydes took their son in for a second opinion, and an MRI. The doctors at first thought they were over reacting but consented to the testing. Thank heavens Mike was so persistent. The Dr entered with the devastating news of the tumor that was 4.5 centimeters in diameter, located directly behind his eyes, and wrapped into his optic nerves. Cashy was immediately life flighted to Salt Lake City.

Not two days later, they performed surgery on this sweet boys brain. They could only get 10% of the tumor and Cashy was left blind and terrified for about 6-8 weeks after this surgery.

May 10, 2010 recovering from brain surgery

It took a few stitches to sew his lil noggin back together.

Cashy was started on chemotherapy.

During Cashy’s first round of chemotherapy, he had his first seizures from the meds. They lasted 10 hours, and damned near killed his parents to witness it.

This sweet little child was OD’d at one time on Fentanyl, in the hospital.

The drug cocktails they give these children for cancer treatment are unbelievable!

Cashy celebrated his 2nd birthday in the hospital, blind, but happy to be alive with his family.

Slowly, Cashy regained his vision.

After the third round of chemotherapy another MRI was conducted. They found Cashy’s tumor to be completely gone, with only some remnants of cancer cells left at the base of the skull where they had been eroding his skull.

Poor lil blind kid.....

June 2, 2010

On to the high dose chemotherapy with 3 stem cell transplants on August 18, 2010.

This is where things got really ugly.

This process takes three “rounds” of treatment. The first round, Cashy fared well. The second round is when there started to be problems. It started with a few up and downs, extreme nausea, vomiting, chills, peeling of skin and diaper area, leaving severe diaper rash.

This was too much for Mike. Mike had become a caregiver in Montana to help sick folks, and now his son needed him. He had witnessed the success in his clients.

How could he deny the same remedy to his precious son?

Please see the Virtual Tour here. You will completely understand when you see Cashy.

Mike had some cannabis oil made…..and Cashy has been on it ever since. They started Cashy on his oil in September of 2010.

Within hours, Cashy transformed with the cannabis oil’ on board. At this point in September, Cashy had not eaten in 40 days. He had suffered cardiac arrest, and a stroke. The pain and anti nausea meds had taken their toll on Cashy. Pharmaceutical drugs were killing him.

Within hours of administering the cannabis oil, Cashy improved. He started eating almost immediately, and was again able to sit up, laugh, and play. Mike had insisted to the doctors to stop the anti-nausea and pain meds. In October while waiting for his counts to rise from the damage the chemotherapy had done, Cash developed septic shock and was immediately admitted to the ICU where he suffered stroke, pulmonary hemmhorage, pulmonary hypertenision, and 4 episodes of cardaic arrest which required full CPR, and was placed on full life support. Doctors told the Hyde’s numerous times that they didn’t think cash would make it and gave them the option to remove the life support and let him go.

Cashy’s parents didn’t give up hope and continued on with the life support. After 7 weeks of Cashy being on life support they were able to remove him completely from it and only needed a little bit of oxygen. He was out of Hopsital on December 17th, right before Christmas where they got to spend the holiday with Mike’s loving and caring family until their return home 6 weeks later.

October 18, 2010

Happy Boy

Boy of Steel

Cashy's a FIGHTER!

They returned home to Missoula on January 31, 2011 after 10 long months away. Cashy was excelling, and healthy and happy again.

On March 17, 2011 Cashy went to the Montana state capitol to meet Irvin Rosenfeld, and share his story with the politicians.

They displayed their Reggae Racers, IV poles attached to cars for kids in Cancer units. The family makes them and donates them to cancer hospitals for the children, so they can play, and have fun without wires and IV lines impeding their joy.

January 12, 2012

As Cashy charmed the politicians, they all smiled and laughed at the precious boy. Cashy was so charming and adorable!

Then, they went into session and pushed the green vote button to repeal medical cannabis in Montana, and voted to kill Cashy. The very same day they met him.

In April of 2011, Cash Michael Hyde was deemed cancer free. The boy of steel battled on.

April 6, 2011 Cancer FREE

Cancer Fears Me!

On July 1, 2011 Montana’s “blackmarket bill” aka “repeal in disguise” went into effect. SB 423 is very prohibitive.

In my opinion, no matter how you operate under SB423, you are a criminal.

To try to comply with the law, Mike Hyde cut down his garden of 16 strains and kept one. They never knew which plant had the cannabinoids that helped Cashy. They had dialed back his dosage. Cashy was cancer free.

It was a busy summer of advocacy for the Hydes, spreading the message of Cashy’s success, how the cannabis oil had helped this precious boy. Preaching a responsible message.

In October 2011, Cash went in for his routine every 3 month check up of brain and spine scans.

In July Cashy was still cancer free.

The family was devestated by the news that Cashys tumor had returned despite his energetic and playful ways, he displayed no signs of his cancer being back.

But it was back ,and the tumor was half as big as it was the first time at 2.5cm in the same place, wrapped around his optic nerves.

December 1, 2011 we find the young Hyde Family at Loma Linda Campus in California starting a serious series of chemotherapy. They are squashed into a Ronald McDonald house in a room with two twin beds, for 4 people. Keep in mind, Kalli is pregnant too. The family is undergoing serious, life-threatening treatment for Cashy through a second Christmas in a row.

Thank heavens they have the world-wide support system to keep them elevated through this time, and in good spirits. Shortly after arriving, they were blessed to be part of a fundraiser for Cashy in Beverly Hills. Tommy Chong even made an appearance.

The Hydes and Tommy Chong

Now….let’s talk about fundraisers. This is my opinion here, so please do not feel this is the Hyde’s opinion whatsoever. They were ever so grateful for the support.

The problem I have with the fundraisers is this, the benefactor walks away with very little after thousands are raised, and all the party costs eat up all the profits. Yay, we have a big party and raise awareness. Boo, the benefactor gets very little money in the end, and they are on the front lines fighting cancer. Fighting for their child’s life. Fighting to keep their family afloat, and happy and safe during such trying times.

I really hope folks think about this in the future, as fighting cancer is SO expensive! If you have a fundraiser for ANYBODY, get those expenses covered before you open the door. Sacrifice “Primo spot” for lower cost. When those parents are sitting next to a sick child receiving radiation, party location is the LAST of their worries. They still have all the regular costs of maintaining a home at home, as well as travel costs, and there is no magic money fairy there, handing over bills.

Shall we talk about medical bills?

Nah….I’m sure you get my drift.

Back to Cashy’s story……..

We were all transfixed, yet horrified to watch Cashy go through the next series of chemotherapy. Mike and Kalli kept everybody updated daily on Facebook, and eventually started Cashy’s Blog, as folks wanted to stay tuned, and follow the Boy of Steel’s progress.

Please join Team Cashy - http://www.cashhydefoundation.com

Cashy was undergoing full spinal and cranial radiation therapy. In the blog, you will be privy to all Cashy had to endure. They actually use a mask for what they had to do with Cash, and he had to be intubated and completely knocked out for the procedure each time, as it was done with him on his belly, lashed down to the table and secured so he could not wiggle and move. The radiation beams were very focused, and dialed in.

Radiation mask

Now, do you suppose ol Mike Hyde allowed those Doctors to give Cashy any of the anti-nausea cocktails or pain meds this round? He most certainly did not. Cashy Hyde went through SERIOUS full spinal and cranial radiation therapy with absolutely NONE of the pain meds, or anti-nausea cocktails. Only his cannabis oil, and a strict regemin developed by his Father.

June 2011 Cashy gets his oil

As other children lie suffering in their beds, Cashy got out of his every day, and left with his family on days he was checked out of hospital. The entire family came down with the flu in the end of it all, and cashy dropped a lot of weight.

As far as cancer treatment?

He ROCKED it!

Even with the flu and a very low white count, Cashy excelled compared to the other children. He could eat. He could play. He enjoyed his family and a much better quality of life.

These treatments could have left this child blind, or at the least brain damaged for the rest of his life. Myself and the Hydes believe the cannabis oil, with it’s neural protectant abilities, cancer fighting cannabinoids, and anti-bacterial aspects, saved Cashy.

We sincerely believe we will be changing how cancer is treated in America with Cashy’s story.

On December 29, 2011, the family celebrated with dinner at TGIFriday’s.

Celebrating tumor shrinkage 12-29-2011

Cashy’s tumor was shrinking, and the Boy of Steel was doing very well. The tumor had shrunk by over half, and the radiologists could see Cashy’s optic nerves on the MRI scans again. There was a light at the end of the tunnel, and it was not suspected to be a freight train.

Have any of you ever been through radiation treatments? Ever had a close friend or family member go through it? It’s not pretty. Their skin is literally fried off of them in some instances by the radiation therapy.

So, how did Cashy do with burns? He had very slight burns, no more than a light sunburn actually. Why? Well, his parents, yet again, see the magic in the medicine. A local man in California had heard of their story, and brought them a hemp lotion for Cashy’s head. They applied it multiple times every day, Cash even asked for it. There was no severe peeling, and shedding of skin, as the hemp lotion handled the damage to the skin beautifully. There literally was none.

The radiologists reduced the beams, and dialed in smaller to focus tighter on the shrinking tumor.

The Hyde’s hunkered down, and made it through the holidays in a hospital, for the second year in a row.

So, where are the Hyde’s today? How is Cashy?

January 17, 2012 the Hyde Family completed Cashy’s last radiation treatment at Loma Linda, waited for Cashy to recover, and piled into their van to drive back to Montana.

I called Mike shortly after they got home, to welcome them back, and inquire about Cashy. I adore the little fighter man so much.

I was so pleased to hear Mike say “He’s a Rock Star Hiedi, eating like a horse and getting his weight back from the flu. He is doing very very well!”

I cried when we hung up the phone. It’s been a long two years, a long fight, and it ain’t over.

We still have a long way to go.

Cashy IS beating his cancer, and one day I will watch that boy play Griz football. I’ll fight to my dying day to see that.

Griz Nation Loves Cashy

I sincerely believe that.

That’s not the problem.

The problem is the laws, and the Federal Government. In Montana, we have a very prohibitive law now. The politicians didn’t even have the respect to call our new law medical. It’s “The Marijuana Act”, and it is SO prohibitive that I am of the opinion that anybody operating as patient or provider in Montana is at risk. No matter how one interprets the law, in one way or another, they are a criminal.

Period.

They even took away affirmative defense……we had 36 raids in 9 months. That’s roughly one per week. The media is not good to us either, and we never receive an iota of positive press.

That’s a daunting situation for a desperately ill young boy who relies on cannabis oil to survive his cancer.

That’s also why the entire issue of the next Montana Connect is dedicated to Cashy, and his cause. We will be focusing on the Plight of the Patient. Enlisting more Warriors in the ranks of Team Cashy.

We must protect this family, and share the news of the success. We must help other children, and give them support. We must preach a responsible message, and follow through.

Children’s lives depend on it. Children just like Cashy.

I swore two years ago I would be here in 20 years smacking politicians in the forehead with my magazines, and educating them.

I meant it folks. I hope you will join me in my smack-fest, because that’s ultimately what it is. We’re waking folks up to realities mainstream media never lets them see. We’re promoting it with a responsible message. One that respects the patient. The sickest of the patients deserve respect, and rely on it to save their lives. We’re reaching outside of our industry, outside of the choir.

What is more compelling than a child? A child who knows nothing of law, social stigma, or even medicine. He only knows he wants to live, and play with his brother, cars, and puppy dog. Love his parents, and relish their embrace and love.

Please respect the patient.

Lack of respect is what cost us our law in Montana, and threatens Cashy’s life daily.

Which team are you on?

Me?

Team Cashy…..until I die.

I hope you will join us in our fight.

Please folks, realize, every day, you are fighting cancer too. Your clients who walk in the door may never share with you why they are there, many do, but many do not.

It’s personal, and it’s very frightening.

You may have a Cashy walk in one day, or parents. Desperate, seeking help.

Please, help empower your patients today. Share Cashy’s story, and give everybody a little strength from the Boy of Steel.

Love you Cashy!!!

Please be sure to go on Facebook and Like the Cash Hyde Foundation page. Tune in for Cashy’s Cupids! A fundraiser in Missoula for the Foundation.

Subscribe and donate at http://www.cashhydefoundation.com

The Hyde’s head to Salt Lake next week for another MRI. We’ll see what that tumor is up to.

I bet it’s GONE…..or danged close.

Stay tuned and find out.