LAS VEGAS, Nev. (702 Times, NV Globe) – A progressive neurodegenerative illness that destroys nerve cells in the brain and spinal cord, often known as Lou Gehrig’s disease.
A new effort born from one man’s personal experience and desire to help others.
“I have to use a chair and I can’t walk on my own and you can hear what it has done to my voice,” said Joey Porrello who was diagnosed with ALS.
Joey Porrello may be unable to walk or speak properly, but he is all smiles, focused on the happy times and people near and dear to his heart.
“I have a beautiful wife Ali and two kids,” said Porrello. “A two-and-a-half-year-old. A rambunctious little girl and a precious perfect little boy named Walden that is 5 months old.”
Joey stated that no one goes through ALS alone, and that his wife has been his support.
“You really see and feel how much people love you when they respond to adversity, and she does it with such grace and compassion,’ said Porrello.
Over 5,000 people are diagnosed with ALS each year, with a life expectancy of two to five years.
“You never know how quick or slow this is going to go,” said Porrello.
Joey stated that he purchased concert tickets prior to the onset of his ALS symptoms.
“When it finally came around, I could no longer get to the seats I purchased,” said Porrello.
He encountered a stumbling block when attempting to convert his general admission tickets to disability tickets.
“Their promoter had said we won’t refund your tickets,” said Porrello.
When the ALS Association learned of this, they decided to take action.
“The one thing an ALS patient wants is time and we can’t give them time but we can give them memories and we are going to take the Porrello project named after joey and just turn it into a new program,” said executive director for ALS Nevada chapter.
A family dealing with an ALS diagnosis spends an average of $250,000 a year just on medical expenditures.
The ALS Foundation now says it wants to assist cover day-to-day necessities, such as house improvements or money for a date night or a concert.
“To give these terminally diagnosed people a reason to get out of the house and make a memory with their family and enjoy a night when ALS is not at the forefront,” said Porrello.
The Porrello project will begin construction in 2023. The ALS Foundation obtained a $50,000 grant to get the initiative started, but it is always in need of funds.
Credits: Fox 5 Vegas
Copyright 2022 702 Times, NV Globe. All rights reserved.
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My first symptoms of ALS occurred in 2014, but was diagnosed in 2016. I had severe symptoms ranging from shortness of breath, balance problems, couldn't walk without a walker or a power chair, i had difficultyswallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Health herbs clinic. It has made a tremendous difference for me (Visit healthherbsclinic .com ). I had improved walking balance, increased appetite, muscle strength, improved eyesight and others. ]
My first symptoms of ALS occurred during covid, but was diagnosed in 2021. I had severe symptoms ranging from difficulty speaking, balance problems, couldn't walk without a walker or a power chair, i had difficulty swallowing and fatigue. I was given medications which helped but only for a short burst of time, then I decided to try alternative measures and began on ALS Formula treatment from Health Herbs Clinic. It has made a tremendous difference for me (Visit w w w. healthherbsclinic .com ). I had improved walking balance, increased appetite, muscle strength, just amazing how effective this treatment helped me
My husband was diagnosed with ALS (amyotrophic lateral sclerosis) when he was 61 years old 2 years ago. The Rilutek (riluzole) did very little to help him. The medical team did even less. His decline was rapid and devastating. His arms weakened first, then his hands and legs. Last year, a family friend told us about Health Herbs Clinic (HHC) and their successful ALS TREATMENT, we visited their website www. healthherbsclinic .com and ordered their ALS/MND Formula, i am happy to report the treatment effectively treated and reversed his Amyotrophic Lateral Sclerosis (ALS), most of the symptoms stopped, he is able to walk and able to ride his treadmill again, he is pretty active now.
My grandma has Lou Gehrig’s disease, she is about 75 years old it was diagnosed 2 years ago. Right now it’s getting more difficult to live for her, because of stiff muscles she can’t even move. Riluzole and Edaravone medicines are given, but won"t give much relief. She can"t eat food without choking. I thought this might be the last stage and the medications she was given did not help at all, so I started to do alot of research on natural treatments, I was introduced to Health Natural Centre and their ALS Herbal Protocol. She started on the ALS/MND Treatment last year, her symptoms gradually diminished including her vocal cord spasm, Body Weakness and Difficulty with swallowing. Reach them at health natural centre . org , She is getting active again since starting this treatment, she is able to walk again ( down the street and back )she have also resumed exercising to strengthen muscles!! God Bless all ALS Caregivers. Stay Strong, take small moments throughout the day to thank yourself, to love your self, and pray to whatever faith, star, spiritual force you believe in and ask for strength. I can personally vouch for these remedy but you would probably need to decide what works best for you.
My grandma who has been Lou Gehrig’s disease for 2 years at the age of 75 had all her symptoms reversed with a Ayurveda medicine from health natural centre . org after undergoing their ALS natural treatment plan. God Bless all ALS Caregivers. Stay Strong, take small moments throughout the day to thank yourself, to love your self, and pray to whatever faith, star, spiritual force you believe in and ask for strength. I can personally vouch for these remedy but you would probably need to decide what works best for you.