Welcome Everyone,

 

I want to share with you the story of my husband Michael Porcaro, bass player for the band TOTO. Several years back starting in 2005 Mike started to suffer from weakness in his hand, first starting in the one hand then moving into both hands, making it very difficult for him to play bass. After many, many visits with several different specialist trying to discover what could be creating the problems, we where eventually given the devastating news that they believed it was Amyotrophic Lateral Sclerosis (ALS) also known as Lou Gehrig’s disease. A death sentence.

 

His condition quickly progressed to the point where he was no longer able to play and had to give up his career of thirty (30) plus years as a professional musician. Not only had he just been given the horrible diagnoses, but he had also just lost his career and lively hood. ALS slowly started to rob him of more and more things that we all take for granted, slowly paralyzing this vibrant and full of life person. We struggled to deal with all of the devastating changes he faced, and we all faced as a family together. Our children’s lives where the most important thing for us, to keep their lives as normal as possible with all the overwhelming changes we faced.

 

We refused to give up hope and continued to search for other possibilities and alternative cures. We found that there where all kinds of people, websites and companies offering a cure or hope at the cost of up to tens of thousands of dollars upfront. No one was willing to prove what they had. All just wanting your money and making outrageous promises. Of course we as many others do, tried a few and to no avail, just making them wealthier and depleting the funds of families who are desperate to try anything to help save their loved one. Anyone suffering from ALS knows how devastating financially dealing with this disease is. The insurance companies do not cover very much if anything, making it so you are having to pay for all of the care required. Most ALS patients require around the clock care (which runs up to ten thousand [$10,000.00] dollars a month), which is most often cost prohibiting to most families, making it so the spouse is required to provide the care so family doesn’t lose everything. Most spouse/caregivers are physically and emotionally exhausted and overwhelmed from the level of care they need to provide for ALS and yet they still need to keep the rest of the family functionally also. It takes a lot of support from family and friends to be able to fight this disease. We could not have survived this journey thus far with out all of the generous support from some amazing friends we have gotten. Unfortunately many families are not as lucky as we are and do not have that support.

 

So we had given up on looking for alternative cures and where just focusing on making the most of everyday that we had together as a family. Mike’s condition had continued to deteriorate and was put under hospice care. When on day last October of 2013, I received a phone call from a friend who was telling me about yet another company he swore that they could help Mike. After so many years of dealing with and being approached by charlatans there was no bigger skeptic than I. I told them that I didn’t believe that they could do anything and how much did they want upfront to try. When she told me they where willing to prove that they could help, I was shocked, no company before was willing to actually prove that they could make a difference first. So that is how our relationship with Golden Sunrise Pharmaceutical started. We contacted Golden Sunrise Pharmaceutical and Michael began treatment, under their guidance, with ImunStem supplement.

 

As you can see from featured videos, Mike started making remarkable progress with the use of ImunStem supplement. I “Thank God” that we found Golden Sunrise Pharmaceutical. He is now able to have some control over certain limbs, for example, he had not been able to move at all and now he can move some of his fingers, and has movement in his arms. He is now able to breathe independently for short periods without his respirator, he can talk for hours without exhausting himself as much as it did before treatments. But to someone with ALS one of the great improvements has been to his lungs, before we used to spend hours upon hours a day trying to keep his lungs clear of fluids, which is one of most dangerous things for someone with ALS is fluid build up in the lungs. Since starting treatment Mike’s Lungs have made a dramatic improvement, we are only needing to clear his lungs once a day, this is something that he had not been able to do in quite some time. For me, the results have been nothing short of a miracle. Being able to breathe much more clearing has greatly improved his daily quality of life.

 

We have constructed this website to bring awareness to the product, and the treatment offered by Golden Sunrise Pharmaceutical to anyone afflicted with ALS. Obviously, the results are not going to be the same for everyone, but I truly believe that this product will provide hope and a better quality of life to anyone treated with ImunStem supplement.

 

Our goal with the Porcaro Charity Fund is to create awareness of the product for treatment and to help provide funding of treatment for patients with ALS, so those who qualify for financial support will receive treatment from Golden Sunrise Pharmaceutical. We sincerely hope that given the results that Mike has personally experienced, and documented, that you will donate generously to Golden Sunrise Pharmaceutical so that they may continue my treatment and provide for treatment to other ALS patients that would qualify for charitable help and also to further their research efforts for the treatment of ALS, and other conditions.

 

We feel that every family should be able to have a small ray of hope in fighting this horrific disease.

 

The treatment is quite expensive, and a portion of the donations made will benefit Mike’s personal treatment. Should you wish to simply help Mike with the cost of the treatment, please indicate specifically, but still, we will forward the donations to the general fund of Golden Sunrise Pharmaceutical, because we want to help as many ALS patients as possible.

 

We thank you in advance for your time and donations. To make a donation now, please click on the “DONATE” button. To find out more about Golden Sunrise Pharmaceutical and/or its products, please click on www.goldensunrisepharmaceutical.com.

 

ALS, also known as Lou Gehrig's disease, is one hundred (100%) percent fatal and has few treatments to improve the quality of life. We should all commit ourselves to come and understand the impact that this devastating disease has on individuals and families nationwide.