All posts by Jim Jax

Jim Jax has traveled abroad and is a jack of all trades with experience in many aspects of life. He's worked in the medical field and owned his own small corporation, he's played and coached in many sports, and has a vast love of news of the world, social media and technology. A lover of fun and practical jokes who loves making others laugh. If it's in politics, sports or world news, Jim will have a point of view. He comes from a family that has been politically and socially involved with many social outreaches to help others. A techy jock who loves technology. The facts are always > than opinions.

“How Emme Lentino Pursued her Dreams On the World Stage”

“How Emme Lentino Pursued Her Dreams On the World Stage”

Emme Lentino has stamps on her passport and a big heart for people. The singer-songwriter, actress and model has made a lifetime of hitting the road and taking big leaps of faith.

You might say she has “road trip magic,” to borrow a line from “Drive All Night,” a track from her latest, available on iTunes and Amazon Music. The release of “summer this, summer that” is a triumph – a mix of upbeat and soulful tunes for your next adventure. The pursuit of her artistic dreams has taken her across the United States, and even overseas to New Zealand.

She was born to an artistic and supportive family in Salem, Oregon. She started performing at the age of six and composing songs when she was only 10 years old.

The artist is always looking for a stage to inspire others.

Setting the Stage: The Early Years

As a performer, Lentino has many influences, from classic rock to modern pop. The Beatles, Norah Jones and Ed Sheeran all shaped her taste in music. She writes and sings straight from the heart. However, more than other artistic influences, her time spent in the theatre formed her artistic style. She performed across 30 states for the Missoula Children’s Theatre. Her first big leap of faith came with a move to New York City, where she played Lucille Ball in an off-Broadway production.

“I learned early on to use my imagination, says Lentino. “My mind was opened to another world through these stories and plays and characters I portrayed. My songwriting style I believe is partly inspired by my theatre background.”

Her creative talent flourished under the bright lights of New York. She collaborated with talented individuals across music and TV, going back and forth between New York and California. In addition to playing Lucille Ball, her songs were used on ABC’s One Life to Live and All My Children.

However, it hasn’t always been an easy road.

The artist spent time living out of her car in San Diego. She is grateful for the experience, looking back on it.

“I met many kind and generous people,” says Lentino. “I also met many who were struggling much more than I who didn’t have the comfort of a car to stay in… that really humbled me.”

A Leap of Faith: New Zealand

After the move to New York, Lentino was no stranger to leaps of faith. She would make another after meeting her late husband Tony – moving to New Zealand with him. The move to New Zealand is an important marker for the artist.


The cultures of New York and New Zealand could not be more different. She went from taking the subway to being surrounded by beautiful scenery.

She adjusted by being of service and teaching music to young children. Lentino has been working with youth since she was a teenager herself, and her lyrics show a passion for making a difference in the lives of young people.

Lentino’s story is one of loss, inspiration and finding yourself again. She tragically lost her husband to cancer in 2016. Her single “Seasons of Life,” written after her husband’s passing, is an anthem for anyone going through difficult times.

She credits her faith with helping her heal after tragedy.

“My faith and my music in combination have gotten me through many tough times,” says Lentino. “It is also because I have always believed that things get better.”

The singer-songwriter is currently signed with the Robert Bruce Agency and a featured artist for the Heart of Indie Radio, which celebrates unsigned artists. The music education platform provides opportunities for aspiring musicians with the help of partners such as Stax Music Academy in Memphis, TN.

The project is a subsidiary of Hands of Grace – Rae of Light, and supports Texas Children’s Hospital, Shriner’s Hospital for Children and suicide prevention programs.

As the co-host of the Eddie and Emme Show, Lentino interviews talented musicians eager to share their message with the world. She is excited about the opportunity to help young artists promote their music.

Global Family

The artist likes to refer to her TwitterFacebook & Instagram followers as a global family. Always on the move, she spends her time traveling from London to New Zealand, and back again.

What is next for Lentino? She expects new music to be released in 2020 and is collaborating with people all over the world.

The global traveler offered words of encouragement to young artists looking to follow in her footsteps.

“My advice is to know your core values,” says Lentino. “Write them down. Make a dream board, write down your goals. Surround yourself with friends and family who can nourish your soul. Be adventurous! If the opportunity to move for a job or project comes up – be open. Ask the right questions; and listen to your heart. You just never know what tomorrow may bring –
that in itself is truly exciting!”

This article was written by Ryan Wilcox.

You can find Ryan at his website or on Twitter.

Ryan Wilcox

“Pancho Billa Mourned by Fans & Players Alike, Bringing The NFL Together Like Few Could”

 

pancho billa dm.jpgllll

Pancho Billa reminded us all.

With the passing of Buffalo Bills superfan Ezra Castro AKA Pancho Billa, the NFL fandom was reminded just how fragile life can be. Fans and players of all teams came together to mourn a man that loved his team, family, & everyone that came in contact with him.

Thirty nine years is not enough for most people, but in those years Ezra gave a lifetime worth of kindness and love. After every kind act shown to him, Ezra was shocked & often humbled at the kindness that people gave him. He never got that people thought he was a big deal and downplayed his importance. In a social media world where the need for attention and self importance is the norm, Ezra was a regular guy and a breath of fresh air.

When Greg Dresko and I did our podcast with Ezra, it was obvious he did not feel good but he rarely cancelled anything. Even on his bad days he would do interviews with a smile. After our podcast I created a prayer night for him that Greg & I promoted. Literally thousands of people got involved praying for Pancho and all of those battling cancer. We did a second one not too long ago that was also greatly supported. People really cared and it was inspiring.

https://www.spreaker.com/user/10814098/1-22-2019-two-mp3-pos-edit

A Special Family Called Buffalo:

Buffalo was the perfect team for Ezra. It is a team that is set back in the time of the old AFL. A team that has not yet been ruined by the greed of NFL owners who’s only loyalty is to the money they can make.  They have an old stadium, the second lowest ticket prices in the NFL, and a raucous loyal fan base.   While everyone else changed, Buffalo didn’t.  It is a special place.

With fancy, expensive stadiums pricing out many fans, the Bills are stuck in a wonderful time warp that allows for a foundation that continues to come to the games year after year. A loyal following that braves bitter cold and wind to support their Bills. From Jack Kemp to Joe Ferguson, to Jim Kelly to Andre Reed, the Bills rich tradition is steeped in a blue collar us against the world mentality. What an amazing place.

I don’t think any fan base or team other than Buffalo could have survived losing 4 Super Bowls while still coming back with dignity and grace.   Through all of the jokes and taunting, winning 4 conference championships is still among one of the greatest achievements in NFL history & they are very proud of it.

rip pancho
Ezra Castro with girlfriend Veronica Borjon & their kids Lourdes & Ginoboli

Ezra & the Spirit of Buffalo:

In true Buffalo Bill spirit, Pancho Billa battled until the end.   Just like Steve Tasker making an amazing play in a Super Bowl that had long been lost, Ezra never gave up.   Adversity was what Ezra faced each day after being diagnosed with stage 4 cancer. Even in his darkest days he would show a positive, caring spirit that inspired so many. We DM’d each other on Twitter and his last message to me was a smiling emoji with a halo over his head. He knew. He also though remained positive asking people to never quit praying for a miracle. Giving up was never an option.

In reality the biggest gift Pancho Billa gave to people was the way he handled his illness. Even with social media bringing out the worst in people, he showed a spirit of pride and kindness that touched so many. He remained positive at the worst of times inspiring us all to not take ourselves too seriously. In a world where many get angry at the drop of a hat, he showed a calm passion and compassion for others during his fight.

The Power of NFL Fans:

Ezra reminded NFL fans everywhere that we are not gang members or part of a football militia that should hate anything not affiliated with our teams. He showed that in reality we are all on the same team of life and that football is a fun outlet & family to belong to. Happiness, health & supporting each other during the best and worst of times is what life is about. We all saw how our hearts are more powerful than any owners money or new stadium.   It’s about the fans and the amazing relationships that we create from being fans. The simplest of things.

pancho billa suit

How I’ll Remember Ezra & You:

What I’ll remember most about Ezra, was how he brought everyone together. For a moment in time fans in New England and Oakland were on the same team. Dallas and Philly fans prayed for a miracle together and people began to realize all of the petty arguments and hate was not what being a fan was about.   It’s a willingness to help when hope is hard to find, and being there to support and love someone during great times as well as their darkest hour.

Many of you have really touched me with your sincerity and compassion and I’m very proud of everyone. Your kindness touched Ezra and helped him and his family get through such an unspeakable tragedy. As much of a gift people felt Pancho was, he felt the same about you. He brought out the best in all of us and it sure felt good.

How to Keep His Legacy Alive:

If you really want to keep his legacy alive, lets be like him. Give as much as you can to others and show kindness with a calm spirit. As Ezra once said, “don’t bring flowers to my funeral. I hate flowers. Bring backpacks full of school supplies for kids”. Think of others first, and show love and appreciation and support to one another. Most of all do it without judgement or opinion. Love completely without complete understanding. What an amazing legacy that would be. And nothing would be more pleasing to the great Pancho Billa.

Florence Carmela is “In The Spotlight” With Jon Bon Jovi’s Soul Foundation

jon bon jovi dorothea
Jon Bon Jovi & his wife Dorothea

Please visit my website:  http://www.florencecarmela.com

Please visit my podcast:  https://www.spreaker.com/show/3272667

 

Florence Carmela is “In The Spotlight”✨ with Jon Bon Jovi’s Soul Kitchen

“Together, WE can make a difference…. One SOUL At A Time.”

                               JBJ Soul Foundation

What can you say about a man who not only creates music that millions of people enjoy and spent the better part of their lives swooning over.  That Musician, Songwriter, and Philanthropist Jon Bon Jovi; along with his wife of almost 30 years Dorothea; have created an amazing Foundation that helps thousands of people through out The United States. The organization is The Jon Bon Jovi Soul Foundation and it is hands down one of the best Foundations out there!

The JBJ Soul Foundation assists and supports the efforts to shed light on the issues of hunger and homelessness in our country and to produce community awareness as well. It is a non profit organization that does all this and much, much more. The Foundation has helped provide assistance and support in several states across the country for so many people who are struggling, including our veterans. Jon says that his wife Dorothea should get the credit since she is the one that has been doing most of the work to make their Foundation a success.  

Their overall mission is to help those who are in need of food & shelter. They currently have two JBJ Soul Kitchens that provide nutritional, hot meals to people in need in his home state of New Jersey. The meals are paid for by a small donation (whatever can be provided by the customer) or by volunteering in the Community Restaurant, to pay it forward in a positive, productive way. Recently, both Soul Kitchens locations in New Jersey, in partnership with The Murphy Family Foundation has provided free meals to furloughed Federal Workers who were in need of a hot meal. 

This is truly an amazing organization! If you are looking for a cause to get behind, lend your support or donate your time and money to I suggest you look towards the JBJ Soul Foundation, their partnerships and all the incredible projects they are currently working on.

If you would like more information on the JBJ Soul Foundation and Soul Kitchens go to 

You can also follow them on Twitter @JBJSoulFound

 

“Florence Carmela’s interview w/Rosanna Arquette about the Alexis Arquette Family Foundation”

rosanna arquette
Alexis & Rosanna Arquette

1-21-19 IN THE SPOTLIGHT WITH ACTRESS ROSANNA ARQUETTE✨

I love nothing more than talking to talented and creative artists with a story to tell or a cause they feel passionate about. Recently on a quiet Sunday morning, I had the pleasure of speaking with the Actress, Rosanna Arquette.

She is not only talented, creative and beautiful, but the actress; along with the entire Arquette Family; has found a way to keep the spirit of their beloved sister Alexis alive. Rosanna, along with her siblings David, Patricia, and Richmond created The Alexis Arquette Family Foundation in memory of their sister Alexis Arquette and is committed to the care and support of the LGBTQ+ community.

Alexis, who was transgendered, passed away on September 11, 2016 and was a bright light with a beautiful heart and an artistic soul. While speaking with Rosanna I realized how much she and her entire family deeply miss Alexis and want to keep her memory alive.

Rather than remembering her on the anniversary of her death with sadness, Rosanna explained “we have a big dance party every year on September 11th to celebrate her life” in just the way Alexis would want it with a lot of laughter, music and memories.

The actress also shared with me that they are trying to raise money for the Foundation explaining “Patricia was working on that (raising funds) last week, and that’s what we’ve all been trying to do and its not been easy.”  This is something they are currently working on for the Foundation, so it will continue to provide counseling, medical intervention and services for those in need.

The Alexis Project is a true partnership between The Alexis Arquette Family Foundation and the Violence Intervention Program, also known as VIP,  at the LAC+USC Medical Center. For more information on how you can support The Alexis Arquette Family Foundation & The Alexis Project visit AlexisArquette.com

For more information on Rosanna Arquette go to RosannaArquette.com to see interviews, videos, photos and the many projects she is currently working on.

florence wp

Article by:  Florence Carmela

http://www.florencecarmela.com

Twitter:  @FlorenceCarmela

Facebook:  https://www.facebook.com/profile.php?id=100005119212687

Instagram:  _florencecarmela

“The Forum” Podcast:  https://www.spreaker.com/show/3272667

 

“Remembering Penny Marshall; The Simplest of Things”

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Penny Marshall & Cindy Williams

The simplest of things.

In the 70’s and 80’s television was the opposite of television of today in so many ways. In today’s world we love bad people, violence, sex in any form, and reality shows that aren’t real. Tastes are as shallow as a puddle in the Mohave dessert. It wasn’t always that way though.

When it was announced that iconic actress and director Penny Marshall had passed away at the age of 75 due to complications from diabetes, there was a true sadness felt around the world. A simple tom boy, who grew up to be a giant giving us entertainment that the whole family could enjoy.

penny and garry marshall
Garry & Penny Marshall

Her hit show with Cindy Williams was of course Laverne & Shirley. It took television by storm with their quirky friends and honest friendship with many bumps along the way. It was innocent, fun, and made you feel good to watch it. It usually was on right after another iconic show, Happy Days. Through the innocence of the time and the overall love and compassion the characters had for one another, it allowed people to escape into a world that had a lot of craziness, but in the end was about togetherness and a feeling of belonging. From Little House on the Prairie to the Walton’s, the shows of the time made us feel good. They made us cry, laugh, and remember our own issues with friends, family and siblings. In the end though, the characters are cared about and loved.

With Marshall’s character Laverne, we all could relate to her and most of us had a friend like her. A tomboy, a little vulgar and un-lady like, who was honest and raw.   It was impossible to not fall in love with her. With Cindy Williams playing the prissy and prude Shirley, they were a television team made in heaven.

Laverne-and-Shirley-cast-photo
The cast of Laverne & Shirley

Penny Marshall was far from done when Laverne & Shirley ended. With the support of her uber talented brother Garry, she directed and produced such movies as Jumpin’ Jack Flash, Big, A League of Their Own, Cinderella Man, Renaissance Man, and Awakenings. Big became the first 100 million dollar film that was directed by a woman. Each film in their own way an inspiration into the heart of people while bringing out the best in them.

Time is a cruel mistress and it takes away the people we love and those entertainers of our youth that brought us so much joy. And many times as adults, we can get through difficult situations watching shows of the past that made us laugh, cry, and dream. Penny Marshall gave us those feelings with her amazing talent. The feelings of love, honesty, compassion and kindness.  That’s why we already miss her.

The simplest of things.

“How One Cystic Fibrosis Patient is Thriving & Not Just Surviving; The 29 Year Journey of Livvy”

*Please Follow Livvy on Instagram, Twitter, and her popular blog:

https://www.instagram.com/seabreezecorner/?hl=en

https://twitter.com/seabreezecorner

https://seabreezecorner.com/about-me/

*Please follow the Cystic Fibrosis Foundations of the U.S. & the U.K.

https://www.cff.org/

https://www.cysticfibrosis.org.uk/

 

livvyhkhkjhk

 

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Southport in Merseyside, England

In the beautiful seaside city of Southport in Merseyside, England, a scared 13-year-old girl first became aware of a monster that was literally attacking her. After begging her parents to take her home, she stayed in the hospital for days.   At a time when Olivia; or Livvy as her friends and family call her; should have been thinking about cute boys and spending time with her friends, she now realized that she was in for the fight of her life.

livy hospital

Livvy found out she had Cystic Fibrosis. Cystic Fibrosis is a progressive, genetic disease that causes persistent lung infections and limits a person’s ability to breath. In people with CF, a defective gene causes a thick, sticky buildup of mucus in the lungs, pancreas, and other organs. Year’s ago it was a death sentence with many passing away in their teens, but now the lifespan has been increased to 50 y/o with research increasing that number every year. In the U.S., famous former NFL Quarterback Boomer Esiason started a CF foundation that has raised millions for research after his 2-year-old son Gunnar was diagnosed with the disease. Gunnar is now 26 and is an advocate for CF with a fantastic website. Below are both websites to these highly regarded advocates.

https://www.esiason.org

http://www.gunnaresiason.com/

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Growing Up With CF:

“I grew up an only child,” Livvy explains. “And that was mainly because my parents were afraid they’d have another child with CF. The kids at school never teased me but I was in the hospital every 3 months, which made it hard to make close friends. When people tried to get me to tell them what was wrong with me, I’d always tell them I had an asthma condition”.

When you have CF, it is a constant stress in dealing with the people around you as well. “I got my first boyfriend at 16 and even though he understood my disease, he kept it away from his parents fearing they would no longer allow him to see me.   When he would visit me in the hospital he would have to lie about my condition. I’m 29 now and I have an understanding boyfriend but I still feel a pressure from his family thinking I’m not good for him because I can’t have any kids”.

livvy

Not only do patients have to fight the stigmatism of having a terrible disease, but they also have to endure a daily ritual of medications and treatments. Few diseases take this much effort to keep oneself healthy. Another characteristic of CF is low body weight and depressed growth. Many with CF look much younger than they are due to this factor.

livvy hospital

The Daily Battle:

The daily routine for a CF patient is a grind that can’t be compromised. “I wake up hopefully after a good night’s sleep” Livvy says. “A good night for me is waking up twice to cough up mucus off of my chest. A bad night is when I wake up every hour, or not being able to sleep at all due to the coughing”.

Treatment starts right after she wakes up as she takes 2 medications through a nebulizer called an eflow, which delivers the medications rapidly. This takes half an hour. She then has to try and do breathing exercises to bring out more mucous which seems never ending. She then takes another type of inhaler and tries to get a bite to eat. “I also have CF related diabetes which makes eating consistently really important”. After breakfast she takes more medications, which includes prednisone, which helps her breathing, but it can worsen her diabetes and thin her bones.

e flow nebulizer
Something Livvy has discovered is that being physical fit and going to the gym for an hour a day is essential for improving her health. “I have to go every single day or my lungs suffer because of the mucous buildup. When the mucous starts to build up it’s just like I’m drowning. I do mostly cardio on a treadmill, an incline, or a rowing machine, as well as lift weights. When I return home I eat a high caloric lunch to keep my weight up and drink an Ensure supplement”.

The rest of Livvy’s day is an interval of taking medications to keep her lungs open and to eliminate the mucous, which makes breathing easier.   In between these treatments it’s also important to continue to eat enough calories to keep her weight up, and then checking her insulin to make sure it’s at a normal level.

”I hate going into the hospital for a 2 week course of IV therapy, which mentally can wear me out. Even though I am lucky enough to be able to drive home between treatments, I do have to sleep there. That leaves a lot of time by myself as we all have our own rooms on the CF ward”.

The UK Drug Controversy:

http://www.pmlive.com/pharma_news/nhs_england_to_vertex_come_clean_on_orkambi_offer_1244686

Whenever profits are placed over patients, the patients always lose. Such is the case for the latest CF drug that has not been released in the UK yet because the drug company and the governmental agencies are fighting over a price. The patients that need the medications wait and can only hope of getting a drug that could greatly help their condition while rich people in suits push papers and look at dollar signs. The drug companies obviously want to get every pound or dollar that they can out of the selling of the drug, and the governmental agency wants to pay as little as possible. “All I hope is that I don’t die before the drug is finally approved” says Livvy.   “On bad days my lungs are bordering on now needing a transplant and I get frustrated. It’s ok to have a bad day and to feel bad, but you have to rebound. I can quit or just keep working hard to keep as healthy as possibble and try to be positive. I choose the latter”.

(below is a video of a day in the life of a CF Patient)

https://www.youtube.com/watch?v=qmzvCnt5cHA

livvy final

A Positive Outlook:

Livvy, like so many CF patients, is an inspiration. Their positive outlook against a terrible foe touches and motivates many around them. She has a growing Instagram and Twitter page as well as a positive and fun blog where she shares her life and her story. “If you have CF”, encourages Livvy,”then PLEASE exercise and work out every day. Also you need to have dreams.   I want to get a house with my boyfriend and work on the side part time, or even volunteer. CF patients find it very hard to work full time but right now I’m working on being as healthy as I can be”. Presently Livvy gets the UK version of what we call disability in the U.S.   She is close to her family and looks to grow her online fingerprint while improving her health.

Livvy’s health sometimes can wear her out physically and mentally. “I’ve struggled at times and it is hard to do so much to just keep my health at a stable level.   Sometimes I worry if I will ever get to use the new medication that I know would help me. What I am going to do though is keep fighting, and keep doing what my doctors tell me to do. I want to be a warrior, and not a worrier”.

livvy dog
Livvy celebrates her dog’s 11th birthday

About 16 years ago a young 13-year-old girl first saw the monster that was attacking her. Through perseverance, hard work, and great determination, she now is a lovely adult woman looking ahead to the future. It’s definitely not easy at times but she fights for every breath and every moment. With her family and friend’s support and the help of her medical team, my money is on Livvy. She is proving to be a small package of heart and spirit who is taming her goliath with a positive energy and a smile, while inspiring others along the way. A CF Warrior indeed.