Archive for the ‘Pay It Forward’ Category


This has been one of my hardest posts to write – ever – in my entire life.

It has taken quite a few days to get it together and a constant supply of Kleenex.

Yes folks – Cashy has passed on.

Believe Timeline

It was very sudden. The Hyde family was not expecting Cash to pass away. Not like this – and not so suddenly. Not ever. There was no “plan z” for a funeral.

It was November 14, 2012. I had just stopped to see the Hyde family on November 7, on my way out of state to Florida. Whenever I am in and out of Montana – the Hyde family is always my first and last stop. When I arrived back in state – Cashy was his rambunctious self – arguing with his Mama about who got to do what with him, and lively as ever. Loving his baby sister – and hassling Colty to play with him.

Always refreshing – even if he was cantankerous! That meant he was alive!

Colty met me as I parked. Colton is Cashy’s big brother – and I adore the young man. At 8 years of age – more wisdom can be seen in his dark brown eyes than many adults can fathom. He has been through and learned so much in the past three years, fighting cancer with his family.

badass colty

Colton Hyde is a Warrior in his own right.

He always greets me with a smile, and a hug when I can catch him. 😉 I adore Colty, and he knows it. That little smartass is the one who dubbed me “Hiedi Handfull” and left me speechless when he did it! Few adults can render me speechless, nonetheless a mere child?

I love you Colton! Ya twerp!

As I got out of the vehicle and went in to the house, I never dreamt it would be the last time I saw the Hyde family as a family of 5.

Not for a minute.

Cashy was sleeping that day – charging his batteries up for “Wet Wednesday” – every Wednesday the family and friends get together and go swimming in Missoula, or wherever they are. Not just 2 or 3 – but  the whole HERD. It’s a riot!

I never pushed in on Cashy – ever. I always figured he had so much intrusion in his life from all his hospital time, he didn’t need one more person pushing in on him. I let Cashy allow me on his terms, not mine. Let the lil man sleep for lands sake so he can have some fun. Kiss him for me. Give the lil stinker a squeeze.

The Hydes were the Hydes – vibrant and busy – caring and loving. Catherine Joy BEAMED her precious smile at me and I kissed her cheeks. Joy really fits in her name, as she brings so much joy to all who meet her. Precious baby girl she is!

Cashy and Catherine

Cashy and baby sis Catherine – he loved being a BIG brother

There is always family and friends at the House of Hyde. A blurring cacaphony of them at times. Laughter and happiness are more often than not the theme of the day.

Cashy, Kalli, Colton, and Mike Hyde

Cashy, Kalli, Colton, and Mike Hyde

One Love

One Heart

Yes…..they really do live it. It is wonderful, warming, and has changed my life for the better. When I ever get down and out….I remember the Hydes and embrace fond memories of roadtrips and the Bada Bing. One Love!

Fast forward one week. I am in Fort Lauderdale with Irvin Rosenfeld. I had seen the posting earlier from Kalli about Cashy not feeling well. I had seen the post of him failing.

I immediately got in contact with the family and was told Cashy had really headed downhill, and his respiration was failing. Cashy wasn’t looking good, and this was probably going to be “it”.

I asked Mike to please kiss his sweet cheeks for me. I was distraught being so far away, and only a week gone, to have this happen now. If I could have been within 1,000 miles of the Hyde’s, I would have been on my way there immediately.

As it was  I was too far away to even dream of getting there.

Irvin was so good to me, so supportive. I had pulled up Playing for Change’s version of “One Love” on my smartphone – and we were watching it when I got the text…..”Cashy has passed”.

There are no words for that moment.

Only tears.

Instant heartbreak.

Irvin and I had just been discussing how Cashy was known worldwide, how far his story had gone, how many people he affected in so many ways. Cashy’s story touched people on a level of compassion never seen before. Grown men cried in front of me when I told Cashy’s story and shared photos and videos.

Playing for Change’s version embodied Cashy for me, as it was the work of so many on a worldwide level. Many many people had worked so very hard to bring it all together. It was such a beautiful work.

Cashy accomplished the same thing. Cashy affected the world – his story has been viewed and read far and wide. At least a hundred countries just by my blog stats. Parents have been inspired, and saved their own children, thanks to Cashy and his message of hope.

The world grieves for Cash…..one very small sweet little boy with a brain tumor. He has touched and affected so many.

Those brown eyes…..exposing a soul so very much older than the vessel containing it.

Hyde 2011 (10)

One small child, with such a huge message and story. Not anecdotal. Not supposition.

Only proof.

GONE! Cancer Free! Official report dated 5/16/2012. This WAS a Stage IV PNET brain tumor on Cashy's optic nerve. How many children must die? WHY?!?!

GONE! Cancer Free! Official report dated 5/16/2012. This WAS a Stage IV PNET brain tumor on Cashy’s optic nerve. How many children must die? WHY?!?!

And with his death, proof that lack of access to medical cannabis kills people.

Yet again.

We can never forget folks like Robin Prosser, Scott Day, and Travis Michalski. Montana has had a history of serious issues with access, actually a lack of access to medical cannabis.

When will politicians quit killing Montanans?

SB423 was implemented in July of 2011. Even before implementation, a law suit was filed to stop it, and enjoin at least the most vicious parts and hold them back with a restraining order.

In July of 2011 Cashy was declared cancer free. He was again cancer free as recent as May of this year.

Rewind and go back to July of 2011. The Hydes cut down their garden, to remain within the new boundaries of the law. They had 16 strains. They had never determined exactly which one worked for Cashy. Heck – Cash was cancer free….we were home free right?

Not hardly…..

Mike had volunteered to take Cashy out in Montana to help with Initiative Referendum 124. To help educate Montanans. To help save not only his son, but other Montanans. He would take him down mainstreet in every town in Montana if he could get there.

It was that important to him. He was fighting to save his son’s life, as well as the lives of many other Montanans.

It was imperative we stop this evil and completely unconstitutional law.

Unfortunately, pediatric application is frightening to folks. Even “industry folks” in Montana……”our camp”.

The Initiative Referendum struggled forward, and the Hydes focused their energies into fighting cancer nationally after being rejected in their own state.

I still to this day cannot tell you why Montana folks didn’t take Mike Hyde up on his offer. Cashy’s message could have killed that law right out of the gate in my opinion.

Montanans are compassionate folks, and they don’t take kindly to hurting folks.

I stated then “A child shall lead them”……and it fell on deaf ears.

Hundreds of folks turned out for Cashy’s funeral November 19 in Missoula. KPAX TV was there and followed the event and the police procession through Missoula from the church to the funeral home. There were two funerals for Cash – one in Montana and one in Salt Lake City. Cashy was buried on Mount Calvary in Salt Lake City in the family plot on November 24.

My point here is….the VERY people Initiative 148 was developed and voted in by Montana voters in 2004 with more than 62% of the vote in support are who is affected directly by SB423.

The sickest of the sick. The cancer patients. The children.

SB423 is designed to repeal and destroy an industry. To reduce patient numbers to <2,000 in Montana – the Legislature’s “magic number” they desire to see in the registry.

There are more cancer patients in 3 counties than the magic number desired by the 62nd Legislature!

With the current law as it is – access for cancer patients is near non-existent. Does the Legislative body have a magic wand where they can determine there will only ever be 2,000 cancer patients in Montana? Especially after incidents like Libby and the vermiculite issues? Cancer in Libby alone is off the charts statistically.

Ever since this law – SB423 – was enacted – it has done nothing but hurt people. It hurts patients. It hurts Montana.

SB423 killed Cashy

The Hyde’s had to fight tooth and nail for access to life saving oil when his cancer came back last year after the law changed. It wasn’t easy – it was a CONSTANT battle to get the right oil – and even to find the CBD plants needed to make the right oil for Cashy.

Lab testing? Wiped out by the last session. There are absolutely no parameters for lab testing under SB423.

Dr referral? IMPOSSIBLE – or nearly impossible for a child with cancer. Children with cancer in Montana need two dr referrals to be carded in Montana at this time. If their parents are professionals who may owe on a student loan, do not even consider it. Any Federal debt is a dis-qualifier to be a caregiver for your very own child.

The law is even designed to ensure low plant volume – and immature medicine. It takes 2 pounds of plant material to make about a months supply of oil…….cancer patients will do nothing but die under this law.

We seriously need some change.

SO – what can you do to help?

First – please donate to the Cash Hyde Foundation.

CHF logo

The Hyde’s fully intend to carry on with the Foundation and fighting pediatric cancer. Folks want safer options for their children – and will go to lengths to get them. Cashy’s memory and legacy shall carry on with Reggae Runners and Reggae Rockers and Foundation events all across the country.The day after the Hyde’s buried Cashy in Salt Lake City – they went and donated 6 Reggae Runners to the Children’s hospital there in Salt Lake where they spent the first 10 months fighting cancer with Cashy.

The Hyde’s will never quit.

As you can see from this Huffpost Live story – pediatric application is really moving to the forefront rather quickly. Reggae Runners and the legacy of Cashy will help keep that momentum going forward.

In addition – a Gift Card has been established at the Good Food Store in Missoula Montana.The Hyde’s have spent the past 2 years of holidays in the hospital fighting cancer. Please help ensure they have a super nice Christmas dinner for their family.

Please dial 406-541-3663 and press 1 for customer service to get to a representative there who will collect your donation and apply the funds to the Cash Hyde Family Gift Card. They will keep a list of donors and we will be getting Thank You’s out to all.

Legislative Session starts January 7, 2012. Please be prepared in Montana for session. Soon, we will be introducing the Cash Hyde Memorial Medical Cannabis Act of Montana and lobbying for change in Montana – so we have access for all sick Montanans. We are collecting bill sponsors now, and it is going well. They know SB423 is a bad law.

Cashy’s Law will be so much better – and I truly hope you folks out there will assist in the fight to make it become a reality in Montana.

SO many Montanans rely on it.

We can memorialize this precious boy and gain proper access to safe medicine for all Montanans.

It’s long overdue.

For more information or to assist – please send an e-mail to MTConnectMe@gmail.com

Be well folks – and do good. The world needs to be a better place – and with your help – we can make it a better place.

One Love

alluneedislove

Please feel free to share this post far and wide and leave any comments below.

Thank you

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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.

 

GONE! Cancer Free! Official report dated 5/16/2012. This WAS a Stage IV PNET brain tumor on Cashy’s optic nerve. How many children must die? WHY?!?!

 

** Note from Hiedi

I re-blogged this from Colorado Connect – as Cashy’s story truly does belong in Montana – his home state. The Hydes today – June 21, 2012 – are doing very well – and this very day is Cashy’s birthday.

What are they doing? They are in California – donating a fleet of 20 Reggae Runners to children’s hospitals in Oakland and San Francisco.

What amazing, brave warriors they are. Each and every one of them I adore – and feel as close as family. No matter what hardships are thrown at them, they always face it with love, and laughter. Smiles, and hugs.

Stay positive folks, don’t let the negative eat you alive, because it will. Please Pay it Forward every day – even if it’s something as small as opening a door for someone.

You may make a difference in someone’s life with even the smallest gesture.

Cashy Crusaders are Everywhere! Think Cashy and DO GOOD DEEDS!

Also – if you can support the Cash Hyde Foundation – please do. Here’s how:

http://mtconnect.me/2012/03/19/you-want-to-save-the-children-start-here-start-now/

Become a Cashy Crusader today. It is SO worth it!


Yup – the lil cheeseballer is FOUR today!

Yippee!

Still cancer free, and lovin life, his new baby sister, and his puppy dogs and stickers. He loves his brother Colty too – sometimes. That’s just how brothers are.

It’s still hard for me to believe it was 2.5 years ago that Sweet Cashy was diagnosed with a stage IV PNET brain tumor on his optic nerve and rushed to Salt Lake City for emergency surgery.

Cashy spent his 2nd birthday in the hospital, fighting for his life. Within 3 months of his 2nd birthday, Cashy was at a point where he had not eaten in 40 days, he had suffered cardiac arrest, and a stroke. Traditional treatments were killing him.

He almost lost too……

Refresh your memory HERE if you haven’t read Cashy’s story.

Cashy’s 3rd birthday was spent in Montana, happy and healthy. Cashy was cancer free. His dad Mike had taken him to the Montana Capitol to meet the politicians. Tell their story. Lobby for compassion.

By Cashy’s birthday in 2011 – dismal times were ahead – though none of us knew it. The politicos in Montana completely ignored Cashy’s story – as did many of the medical marijuana industry folks. Cashy’s wonderful story of bravery and compassion and the fight for his life was virtually ignored.

It still is in a majority of the state of Montana.

As the law changed in July of 2011 – so did Cashy’s fate. The new law was very restrictive – very prohibitive.

NOT Compassionate to children whatsoever. Not compassionate to Montanans. Period.

Mike cut his garden down. The 16 strains that had been working for Cashy were gone. Which one helped him? We’ll never know….

Cash was cancer free. His oil consumption was greatly reduced. We shoulda been home free right?

Cancer is a bitch – and an evil one at that. It came back – with a vengeance.

The fight was on. As you know – Cashy went through another battle in December of 2011. Another Christmas in a hospital, far from his home.

Another SUCCESS too! We celebrated a cancer free MRI in Salt Lake City in February 2012 with Cashy’s family at the Badda Bing.

Cashy is surrounded by a HUGE and very loving family – and those celebrations are so wonderful – and full of love. Cashys great grandmas and elders are so grateful to have him alive – they share his story everywhere.

Cashy’s story is such a wonderful one to share re: success. As far as support from Montana and it’s politicians – it’s a disgusting crime. We could educate so many with a small child……an innocent child. A wonderful child with such a brave and loving family.

We could all learn by their example.

All Cashy knows is – he wants to live – and play with his stickers, cars, and maybe his brother if they’re not squabbling. He doesn’t know any propaganda or fear. He doesn’t worry about social stigma.

LIFE – is what matters.

LOVE – surround him with it.

SUPPORT – share their story – and please support the Cash Hyde Foundation.

This family – no matter what – despite anything thrown at them – continues every day to help others. Pay it Forward. Fight the fight against childhood cancer and help to save others children.

Even while in hospital fighting for Cashy’s life – they help others.

Currently – there are about 20 Reggae Runners distributed nationally – sharing Cashy’s message of faith and hope.

That fleet is about to double – thanks to DooBons in California. Originally from Montana – they heard of Cashys story – and chipped in to increase the fleet.

20 more Reggae Runners are being distributed to hospitals in San Francisco and Oakland California. That increases the fleet to 40 Nationally!

40 more Reggae Runners out there helping children to fight cancer with smiles and laughter – directing folks to the Cash Hyde Foundation site – where folks can find the supporters and look for help for themselves.

A note from CJ Maestas – Cash Hyde Foundation Executive Director:

The Cash Hyde Foundation will be heading back to the Bay for the HT Medical Cannabis Cup to be held in Richmond, CA, June 23-24. Additionally we will be donating a small fleet of (20) “Reggae Runners” to San Francisco and Oakland Childerns Hospitals, thanks to the generious donations from Doobons. You don’t want to miss this marijuana expo, complete with seminars, the latest pot products, and, of course, the best cannabis, edibles, and concentrates Cali has to offer! Plus, a special Saturday night VIP party featuring Del the Funky Homosapien. Go to MedCanCup.com for details or to purchase tickets.

If you are in the California area for this event – make it a point to drop in and meet the Hydes! Kc Kush Taynor made the trip from the Ohio chapter of the Cash Hyde Foundation as well. They had their own Father’s Day birthday celebration in Ohio. See it HERE

If you are not in the area and wish to help -PLEASE DO. We have bracelets available – and you too can sponsor a Reggae Runner or Wagon in a hospital near you! We need to flood these hospitals – and save the children.

See HERE for how you can help today. E-mail MtConnectMe@gmail.com or call 720-722-0501

Also – stay tuned and Watch for the Cashy Mobile…….coming soon!

Here’s some pictures of the cute lil stinker. More to come soon!

Love you Cash Man! See you in 20 years baby!


Arguments over MT medical marijuana law underway | KPAX.com | Missoula, Montana.

I have been watching this closely today……woke up with it on my brain. Have been anticipating it for weeks, no, months – as many Montanans have been.

To quote Molloy ““Look at all of the things that people do in which they give of their time, their talents and their money to support issues & causes that they believe in. I reject the notion that people will not agree to serve as providers to provide for the compassionate use,” Montana Assistant Attorney General Jim Molloy said.”

He rejects the notion eh?

Look at our healthcare system already.  Right here in Montana – we have folks of all ages suffering to attain traditional health care. “Health”care where seniors spend money on pills and starve. Didn’t they just put out a study about hunger in Montana children?

WHERE are all those good folks Molloy references in THAT situation?

And he expects folks to possibly suffer Federal Prosecution for their acts of compassion?

That’s what they face. Montana politicians let Montanans down terribly this past session with the passage of SB423.

Well folks – I hereby reject the notion that our elected officials and Attorney General’s office have ANY CLUE what is going on with Montanans.

Steve Bullock – Jim Molloy – may you never have a family member stricken by cancer.

To all of you who live in reality…..VOTE THEM OUT – every one of them.

If ANY of you out there need help – please call me. 720-722-0501

Me and mine know what compassion is…..and we ACT.

The fight is ON.


And Cashy is WINNING!

WINNING!

Our Hyde family from Missoula Montana is currently in Salt Lake City, celebrating with an elated family at beloved Uncle Sam‘s Badda Bing.

How do I know this? I was there 3 months ago – when we got results on Cashy’s first scan since his second bout with his PNET brain tumor wrapped around his optic nerve in that precious little boy’s noggin.

I sobbed that day….3 months ago. I was SO relieved….so happy.

This time – I cried when we all saw Cashy being sedated. Poor little man has been through so much – he knew what was going on. He wasn’t too happy to be going to sleep – and held his breath in defiance. He eventually relented, and his little body went limp.

To see that happen to a three year old (soon to be FOUR!) is heart wrenching – but a fact of life for the Hyde’s. A fact of life for many families around the world, unfortunately. Every day around the world thousands of children are diagnosed with cancer. When you really go looking and examine the numbers, it is chilling.

Today – we got heartwarming news – Cashy’s 2nd MRI came back with negative results. To quote Kalli Hyde’s Facebook post “SO ive tried posting this now 3 times……The verdict is in…..Cashy is still cancer free, and there is no evidence of reoccuring tumor!!! Still waiting on thoracic spine report, but cervical and lumbar spine is all clear as well! Thank you God, and thank you everyone for the prayers and support, we would’nt be where we are today without you all cheering Cashy on! Cashy your a rockstar, your my little three foot tall hero!! :)” Kalli also updated their blog – be sure to read up HERE

Cashy is such a hero and inspiration to so many. People hear about and read the news of Cashy’s success and burst out in tears of happiness. It happens in every state, every time – all across the nation, and around the world.

Cashy is a Warrior – and he is beating the scourge……that scourge is cancer.

Support the Cash Hyde Foundation TODAY! Join the Cashy Militia!

http://mtconnect.me/2012/03/19/you-want-to-save-the-children-start-here-start-now/

Help save childrens lives!

To learn about what happened to Montana’s Medical Cannabis law – please be sure to catch this documentary made entirely through the session – detailing the saga of medical cannabis in Montana. Be sure to see Code of the West

Also – I ran across this today – and felt it was important enough to share here. The author is a seated Judge in Brooklyn New York, and a Pancreatic Cancer survivor of 3 years.

He is also a medical cannabis user.

A Judge’s Plea for Pot

By GUSTIN L. REICHBACH
Published: May 16, 2012

New York Times Opinion Pages

 THREE and a half years ago, on my 62nd birthday, doctors discovered a mass on my pancreas. It turned out to be Stage 3pancreatic cancer. I was told I would be dead in four to six months. Today I am in that rare coterie of people who have survived this long with the disease. But I did not foresee that after having dedicated myself for 40 years to a life of the law, including more than two decades as a New York State judge, my quest for ameliorative and palliative care would lead me to marijuana.
Kristian Hammerstad

My survival has demanded an enormous price, including months of chemotherapy, radiation hell and brutal surgery. For about a year, mycancer disappeared, only to return. About a month ago, I started a new and even more debilitating course of treatment. Every other week, after receiving an IV booster of chemotherapy drugs that takes three hours, I wear a pump that slowly injects more of the drugs over the next 48 hours.

Nausea and pain are constant companions. One struggles to eat enough to stave off the dramatic weight loss that is part of this disease. Eating, one of the great pleasures of life, has now become a daily battle, with each forkful a small victory. Every drug prescribed to treat one problem leads to one or two more drugs to offset its side effects. Pain medication leads to loss of appetite and constipation. Anti-nausea medication raises glucose levels, a serious problem for me with my pancreas so compromised. Sleep, which might bring respite from the miseries of the day, becomes increasingly elusive.

Inhaled marijuana is the only medicine that gives me some relief from nausea, stimulates my appetite, and makes it easier to fall asleep. The oral synthetic substitute, Marinol, prescribed by my doctors, was useless. Rather than watch the agony of my suffering, friends have chosen, at some personal risk, to provide the substance. I find a few puffs of marijuana before dinner gives me ammunition in the battle to eat. A few more puffs at bedtime permits desperately needed sleep.

This is not a law-and-order issue; it is a medical and a human rights issue. Being treated at Memorial Sloan Kettering Cancer Center, I am receiving the absolute gold standard of medical care. But doctors cannot be expected to do what the law prohibits, even when they know it is in the best interests of their patients. When palliative care is understood as a fundamental human and medical right, marijuana for medical use should be beyond controversy.

Sixteen states already permit the legitimate clinical use of marijuana, including our neighbor New Jersey, and Connecticut is on the cusp of becoming No. 17. The New York State Legislature is now debating a bill to recognize marijuana as an effective and legitimate medicinal substance and establish a lawful framework for its use. The Assembly has passed such bills before, but they went nowhere in the State Senate. This year I hope that the outcome will be different. Cancer is a nonpartisan disease, so ubiquitous that it’s impossible to imagine that there are legislators whose families have not also been touched by this scourge. It is to help all who have been affected by cancer, and those who will come after, that I now speak.

Given my position as a sitting judge still hearing cases, well-meaning friends question the wisdom of my coming out on this issue. But I recognize that fellow cancer sufferers may be unable, for a host of reasons, to give voice to our plight. It is another heartbreaking aporia in the world of cancer that the one drug that gives relief without deleterious side effects remains classified as a narcotic with no medicinal value.

Because criminalizing an effective medical technique affects the fair administration of justice, I feel obliged to speak out as both a judge and a cancer patient suffering with a fatal disease. I implore the governor and the Legislature of New York, always considered a leader among states, to join the forward and humane thinking of 16 other states and pass the medical marijuana bill this year. Medical science has not yet found a cure, but it is barbaric to deny us access to one substance that has proved to ameliorate our suffering.

Gustin L. Reichbach is a justice of the State Supreme Court in Brooklyn.


Montana Connect has been championing children since it’s inception.

Please meet the first child featured in Montana Connect.

Meet Joey, and his amazing mother Mieko Hester Perez.

The Unconditional Foundation for Autism

Joey and Mieko Jan 2012

It wasn’t always smiles when I met this family 2+ years ago. It was pretty dismal actually.

Joey was at least 50 pounds lighter than he is now, emaciated, and withdrawn into his lil autistic world. He had not been eating, and Mieko discovered Cannabis, and started her fight. Please be sure to visit the foundation website for the entire story.

Mieko was a very determined mother who had never had anything to do with Cannabis. EVER. She worked in the legal profession, her family had law enforcement ties.

Cannabis was Taboo.

When a child is on the verge of dying, parents will do ANYTHING to save their child. Mieko had found herself in this position, and Joey is alive today because of a Mother’s determination.

In turn, the immersion of Mieko into the California medical cannabis community had it’s own challenges. On top of a full time job and a kid with autism, Mieko had an infant and a teenager in the house. Challenges presented themselves daily, if not hourly on some days, and Mieko battled through.

It has been a LONG haul, and I must say, I am very privileged to have had the glimpse into Mieko’s life I have had. It has been a very rewarding experience, one to be cherished for a lifetime.

Watching Joey – MAN – what a miracle. Visit the foundation site – go see for yourself. That young man was on the brink of death……

Today? Joey has gained over 50 pounds and eats foods he never experienced before. He has come out of his autistic “world” and interacts – smiles – and plays with his siblings.

Mieko – she battles on, protecting her children, and advocating for others. Always helping, always supportive for the parents who reach out.

Some may not like her advice, but rest assured, she speaks from experience. She has seen it all, and survived.

Survived and fought so Joey can have LIFE.

Isn’t that what it’s all about?

Please keep up with her story here: Mieko’s blog – a Mother’s Tale of Advocacy

Make it a point to share her story, help her to empower more parents, and bring more autistic children LIFE

Show your support TODAY visit http://www.uf4a.org to get your bracelet!

Let’s Connect!

MTConnectMe@gmail.com

406-594-7932


Partnering to Save Lives

Montana Connect is pleased to announce an alliance with The Cash Hyde Foundation

It is with great pride we announce an alliance between Montana Connect and The Cash Hyde Foundation. With this joint venture, we will be detailing the Hyde’s two year fight against their young son Cashy’s Stage IV PNET Brain tumor he was diagnosed with at the young age of 18 months. The entire publication is dedicated to their story, the fight in Montana, the science, and the medicine. In addition, we will be ensuring the Hyde’s have the security and comfort of a home to raise their family in. Proceeds from all sales are structured to support the Hyde’s, share their message, fight for Montana, and get the Cash Hyde Foundation Special Edition into the hands of educators, physicians, nurses, and politicians across our Nation. Goal: A years worth of house payments, and security for a young family. Paying off the mortgage in completion would be a DREAM.

Meet the Hyde Family

In the past two years fighting cancer, the Hyde’s have been amazing. No matter what they went through with Cashy, they gave back to others. They helped other parents in need, and in addition, developed a donation program of their own. Fighting for their own son’s life, they still find time to help others, and donate to hospitals. With Kalli’s experience working in hospitals, and the whole family living in hospitals for a year fighting Cash’s cancer, they saw an opportunity to help others, and they developed the Reggae Runner. The Reggae Runners were designed to get children out of their beds, and having fun with their families while confined to the hospital environment. It was very constrictive, and dangerous, for parents to try to play with their children with the IV poles and cords and wires and tubes. The Hydes had a brainstorm, and adapted a Reggae Runner for Cashy so he could be more mobile, get out, have fun, fight cancer with a smile, and have some independence and safety within the confines of his Reggae Runner. Mike and Kalli found they could play with their son without the hinderance of the IV poles, and Colt and Cashy could have important “Bro Time”. Other families and children saw the Reggae Runners, and wanted one for their children too. The Hyde’s obliged, and each hospital they have stayed at during Cashy’s fight has a small fleet of Reggae Runners and Wagons. Our goal is to get more out there….be sure to tune in below to see how you can sponsor a Reggae Runner or Reggae Wagon for cancer children across our Nation today.

Paying It Forward

The past two years have most certainly been a fight, sending the Hyde’s to Salt Lake City for 10 months, back to Montana, and in the fall of 2011 they spent yet another holiday season in a hospital in California. In the mean time, Kalli has maintained her employment as an RN, and Mike, Colty, and Cashy have traveled the Nation, educating others and advocating for children everywhere. Building the foundation, and ensuring Cash receives the best care. They are expecting a new baby in the first week of May 2012. We will find out if Colty & Cashy have a brother or sister come May. Colty wants a sister, as “Little brothers are a pain!” Guess Cash keeps him on his toes! Thanks heavens he’s cancer free today, and he can be here to meet his new sibling, and keep his big brother Colt on his game.

How YOU can help

Support this campaign! The next issue of Montana Connect is dedicated in entirety to the Cash Hyde Foundation. In this issue we will share the Hyde’s complete story, explore the science, and the plight of Montana. The Cash Hyde Foundation will be immortalized, and have a tool to share Nationally to advocate for the Foundation, Fight for Cashy, and share his story in both printed and digital form. It will also allow them the freedom and resources to fight for and save more children fighting cancer. The security of always having a home to return to. The ability to help so many more than they already have.

Be part of Team Cashy

Want to Monkey around?

Monkey around for $25 – your Monkey will be printed in Montana Connect AND you get a digital version to use at your discretion. Get your Cashy Monkey TODAY!

Personalized Team Cashy Monkeys will be scattered all through the magazine and hosted online. Supporters will also receive a digital copy to use at their discretion. Be sure to get YOUR Monkey TODAY! Don’t forget Grandma and the kids too! Call TODAY! 720-326-6577

Call 720-326-6577

Be a Cashy Warrior

Here’s where the Platinum, Gold, and Silver Sponsorship’s come in. For those of you who can provide more and be a Cashy Warrior, in addition to advertising opportunities in Montana Connect, we have three different levels of sponsorship available.

All level donors will be hosted and featured on the Cash Hyde Foundation website on a state by state basis, enabling these families in need to reach folks capable of helping them in such serious times in each state.

Reggae Wagons and Reggae Runners

Reggae Runners and Wagons customized for hospital use, and ready for donation.

Cash Hyde Foundation Bracelets

There are a variety of Cashy Warrior bracelets available

The Hydes and The Cash Hyde Foundation have been VERY busy, even while fighting cancer! Platinum and Gold level sponsors will secure a place in a 2 page spread celebrating their sponsorship and thanking them in Montana Connect. Each of these levels will have it’s own 2 page spread. The Silver level sponsors will have a one page spread.

Platinum Level Sponsor:

Platinum Level Sponsors will have their very own Reggae Runner for their donation. The Reggae Runner can be shipped to the sponsor for them to donate, or sponsor may delegate the donation duty to The Cash Hyde Foundation and have it donated in their honor.

Gold Level Sponsors:

Gold Level Sponsors will have their very own Reggae Wagon for their donation. The Reggae Wagon can be shipped to the sponsor for them to donate, or sponsor may delegate the donation duty to The Cash Hyde Foundation and have it donated in their honor.

Silver Level Sponsors:

Silver Level Sponsors will get 100 Cashy bracelets and brochures to distribute and share The Cash Hyde Foundation message and educate their local communities.

All level donors will be hosted and featured on the Cash Hyde Foundation website on a state by state basis, enabling these families in need to reach folks capable of helping them in such serious times in each state.

MORE INFO

Contact info:

If you are interested in becoming a Sponsor, please send an e-mail to: MTConnectMe@gmail.com

or call 720-326-6577 or 406-594-7932

Employment Opportunities:

We are also looking for temporary staff for 2-3 months to market, and help Campaign for Cashy Nationally. Please call: 720-326-6577