Lisa • October 15, 2021
Lisa, we have your heart. How soon can you be here?

originally posted February 24, 2017 Huffington Post by Lisa Salberg

So there I was holding my heart in my hands while a new heartbeat was in my chest. Talk about surreal moments! The path that led to this moment encompasses 36 of my 48 years on this earth and in this one moment, I came face to face with the very thing that I had hated, feared, and loved… my heart.

The story actually begins far before my birth and continues past me to my daughter, niece, and nephew. These are stories for another day. Today I want to tell you about the first and last chapter of my heart. In the next installment, I will tell you what is in store for her future, because yes, she has an important future.

I was diagnosed with hypertrophic cardiomyopathy when I was 12 years old. I was in the 7th grade at Copeland Middle School in Rockaway NJ and it was physical day. You remember those awkward events when all the girls had to take their shirts off down to bras and have the doctor listen to their heart and the nurse check for scoliosis. When I stood before the doctor, his face dropped and he told the nurse to clear the room. He then had the nurse listen as well. I knew right then that the same disease that had killed my grandfather at 43, impacted my uncle and sister, had just shown its ugly head, and my life was forever changed. I was told I had to see a cardiologist soon or not be permitted back in school. After the consult with Dr. Paul Goldfinger, he confirmed the diagnosis (then called Idiopathic Hypertrophic Subaortic Stenosis IHSS – now called hypertrophic cardiomyopathy-HCM). My first question was “do I have to do my homework?” Why that question? Because he had just told me, in 1980, there was no real treatment, no cure, and I could die suddenly at any time. Did I mention I was 12?

<p>Lisa 1980, age 12, the year diagnosed with Idiopathic Hypertrophic Subaortic Stenosis, now known as Hypertrophic Cardiomyopathy HCM. </p>
Lisa 1980, age 12, the year diagnosed with Idiopathic Hypertrophic Subaortic Stenosis, now known as Hypertrophic Cardiomyopathy HCM.

In my next posts, I will fill in the years between and explain far more about HCM, healthcare policy, and how it has impacted my life and the lives of those I serve as CEO/Founder of the  Hypertrophic Cardiomyopathy Association. But now let’s flash forward to September 2016.

HCM is a highly variable disease, some people have minimal to no symptoms at all while others are severely impacted. I spent much of my life living on a balance beam to manage symptoms. In 2011, I found out that my heart was becoming too stiff and the ejection fraction (the amount of blood your heart process per beat) had dropped. This was the indication that transplant would be my only option but I had to get sicker before I could list. You must understand that heart transplantation is  NOT  given to improve symptoms it is  ONLY  given to save a life. So you have to be well enough to withstand the surgery and sick enough to be “terminal” without the transplant.

September 2016 was a busy month for me work-wise and an exciting one. I was invited to a meeting at the White House to discuss “Cardiovascular Health in America”. This was my second time participating in this event. While I stood there to make a statement about the importance of better understanding genetic causes of heart disease something happened I felt my heart acting strange and I had to stop speaking and ask for a moment. Little did those in the audience know, I nearly passed out. I regained myself and acted as if everything was fine – I am good at that. I returned home and the next morning attended a wedding, then home for a nap because my daughter had gotten us tickets to a concert. Ironically, it was Joan Jett and the Blackhearts and Heart (a double heart concert). Sunday I rested. Monday I flew to Grand Rapids Michigan to review a new HCM program at Spectrum Health. I spent two days there and flew home Wednesday to a meeting at Morristown Medical Centers Chanin T. Mast HCM program. This is where I also received my own care for HCM under Dr. Martin Maron. When I got to the meeting, my nurse Deatrah Debose said I didn’t look right. I told her I didn’t feel right but I’d rest for a day and if I was not better I would come in for some IV Lasix therapy to get the extra fluid off of me. Friday I admitted myself. Saturday the Lasix took off 6 pounds, but I didn’t get better, I got worse. I laid in bed with oxygen and knew this time I was really in trouble and I knew where this was leading. I shut down I could hardly speak. My mind raced to my family, my community, my work how was I going to do all I wanted to do. Wait, none of that mattered anymore. How was I going to survive, that is all that mattered.

Monday a right heart catheterization indicated that my heart was simply not working anymore. My “cardiac index” which should be 2.2-4.1 was only 1.4. My heart was simply not moving blood anymore. I was given a PICC line with a medication called milrinone which did improve my index to 1.8 and I was sent home to begin the listing process. It took 2 months to complete the tests and classes and review to be listed. On November 23 I was officially listed on  UNOS  as a status 1B for transplant. I will explain more about this process in the future.

I did, however, make a deal with my transplant center  Newark Beth Israel Medical Center.   I must KEEP my heart . I wished to use it as a teaching tool. I did not think this was so strange, but as it turns out I was the first person to make this request at this hospital. I made arrangements with a program that specializes in Plastination, a process that makes organs last forever. I arranged the logistics in advance and asked my husband to please ship my heart away after my transplant (it didn’t sound odd at the time, but after it was done I wondered if I had really considered how this impacted him … he survived so I guess it wasn’t that bad).

Groundhogs day 2017 12:23 am the phone rang. “ Lisa? This is Emily from Newark Beth, we have your heart. How soon can you be here?”

HCMA Blog

By Lisa Salberg May 7, 2025
I do not claim to be a political expert, but I do know what I am - a passionate patient advocate who has seen how systems can work for and against patients, and someone willing to put thought into action, to create a plan to make healthcare safer for a population that has long been ignored and at high risk. As we prepared to take 30 patient advocates to Capitol Hill to discuss matters of importance to the community, we monitored the activities inside Washington DC. The floor kept shifting under us week after week as we attempted to prepare a cohesive message attached to policy that had a good chance of both being bipartisan and moving forward. Please go back and look at your news headlines between the beginning of February and the end of March - it was chaotic, and it sometimes appeared schizophrenic. But we had to keep searching for areas in which we could find some base definition of what it means to be a citizen or resident within the United States. There is a slow, simmering issue that has had my attention since approximately 2007, something that reaches beyond the borders of cardiac disease but gets to the very core of our shared humanity. We will all certainly need a medication, a supplement, or a food additive to ingest into our bodies at some point in time. In the late 2000s, Dr. Harry Lever of the Cleveland Clinic brought something to my attention - an observation about generic drugs not functioning in a predictable manner. To say we've talked about this hundreds of times would be a gross understatement, it's more like thousands of times over nearly two decades. You see, Harry Lever is a really unique mix of old school cardiologist and Detective Columbo, always searching for clues to the puzzle to unravel and find the bad guy. Harry and I shared observations about patients with HCM who had previously appeared stable, with no comorbidities, no lifestyle changes, no recent domestic or workplace stressors - things seemed really normal for these people, yet their symptoms vastly changed nearly overnight in some cases. Over the years other drug quality problems had come to my attention, including deaths related to a heart transplant medication I take, called tacrolimus. Eventually Harry put me in contact with other individuals who also were sharing our observations. There was a radio show producer named Joe Graedon, a researcher in Utah, named Erin R. Fox, and a pharmacist by the name of David Light. David and I had spoken a number of times and he shared with me some of his scientific findings which were quite alarming. I learned of the process of “dissolution” and how different molecules responded differently to the dissolution process and thereby would absorb differently within your body. This impacts the mechanism of action which, in my case, was to keep my heart protected from my body attacking it as a foreign entity. I learned of the problems with generic drug manufacturers through the writings of Katherine Eban ( Bottle of Lies , Harper Collins ecco, 2019 ), and Rosemary Gibson, ( China RX , Prometheus, 2018) an advocate on behalf of patient safety on multiple planes within the ecosystem. This small band of advocates is trying to sound an alarm throughout the country. Now it is time for the productive and equitable deployment of the shared efforts to keep every one of us safe and healthy. That is what we went to Capitol Hill to talk about. There is a mechanism within the National Defense Authorization Act, a piece of legislation that is voted on each year to provide funding for our national defense. It is a type of legislation that typically moves unopposed through the process as we all seek to have a strong national defense. Within this act we are advocating the Department of Defense to support the NDAA amendment “Transparency and Quality in Pharmaceuticals Act,” to support the proposed ARPA-H project “Create and Deliver Actionable Transparency to Drug Quality.” We encouraged the VA to join with the DoD project and drug procurement reform efforts. 2025 VA Appropriations language already present in House section “Prescription Drug Quality” and Senate section “Drug Quality Scoring,” and the FDA to use DoD drug quality data to further inspect “red” rated manufacturers and reward “green,” to set a “zero toxins goal” in medicines similar to EPA’s goals for water and air, and to work collaboratively with independent testing efforts similar to Europe’s approach. Lastly, we encouraged the NIH to research drug quality to better identify issues, their public health impact, and strategies to best address them. So, as we walked around Capitol Hill inviting legislators to come join us at a briefing to learn more about these initiatives. We had meaningful discussions with various members of each office’s internal administration. We spoke to legislative assistants, healthcare advisors, defense advisors, Legislative Directors, Deputy Chief of Staffs, and Health Policy Advisors. In total we met with 24 offices. This and the briefing offered them a deep appreciation for the community we are and the problem we seek to solve - primarily the quality of generic drugs in the United States. Secondarily, we spoke of step therapy and prior authorization and the meaningless waste of time, effort, money and life quality by delays costing 1.3 billion dollars a year in waste fraud and abuse. The waste and fraud is being perpetrated upon healthcare systems, physicians and patients as we waste our time and precious resources playing a game that serves no one and costs, time, money and frankly the reputation of the health insurance systems themselves. It's time for us all to be reasonable adults; to fix the problems that we know are fixable and stop fighting about the differences in how to do it. Let's start negotiating how we all can benefit from better health systems and better access to safe high-quality low- cost generic drugs. If there is anybody who has an argument as to why anything I have said about these issues is not good for all Americans, I welcome the conversation. Let's talk it out and understand how we can see the world with such different philosophies.
By Lisa Salberg May 7, 2025
Greetings to all of our Bighearted friends, We have certainly had an eventful April and there are many updates in this letter to bring you up to speed. I hope everybody had a joyful holiday season and we're able to spend time with friends and family. April completed our second visit to Capitol Hill in very interesting times. I am happy to say that the offices we met with, including Senators Tim Scott (R-SC) and Patty Murray (D-WA), Representatives Alexandria Ocasio-Cortez (D-NY), and Pete Session (R-TX), were attentive and responsive to our requests. Our focus on the topic of generic drug quality struck a cord with all offices in this completely bipartisan effort. Having meaningful conversations about the burdens of step therapy and prior authorizations really help to invigorate the staff members we met with to be prepared with strong legislation that can be widely accepted and instituted. I encourage you to take some time and watch our Hill briefing on our YouTube channel . View photos in our Gallery . We were able to secure a champion for a federal HCM Awareness Day as well as a move for appropriations for the HEARTS Act of 2024, H.R. 6829*, which was signed into law by the President on December, 20,2024. I can safely say that our trip to Capitol Hill was successful and meaningful. I wish to extend my gratitude to our entire internal HCMA team and our volunteers and industry partners. Bringing a true patient voice to our government officials is the most effective way we can advocate for changes that are beneficial to all those with chronic disease, cardiac, and otherwise. Then we were on the road to Orlando with our dear friends at AdventHealth, conducting a patient education symposium. It was wonderful to see so many Bighearted friends, it feels like family. There were so many deeply emotional moments of the weekend, including reuniting Lorianne Peachey with her plasticized human heart and watching she and her husband marvel at the thing that brought them so much love, joy and pain. Holding your own heart in your hands is something only a few have experienced. My sincere gratitude to Lori for sharing her heart with us all. We were able to go visit Brian Wolski, who was unable to attend the session because he was awaiting a heart transplant and day passes out of the hospital are really not a thing. However, the weekend became quite eventful as just a few hours after Stacy and I visited with Brian and Cassie at AdventHealth after 369 days Brian received the call that a heart had been secured for him. As I write this letter today, he is post-op and recovering well. I also had the opportunity to hug people I have known for 20 plus years but have never previously met, and those are beautiful moments. Our educational content was fantastic. I am so impressed with how AdventHealth has grown into such a robust and high quality program. My thanks Dr. Marcos Hazday, MD FACC,and all the speakers at AdventHealth and Debbie Moore, BSN, MS, RN, Sarah Blair, Tracy Demetree, Kelly Reilly, Steven Kelley, Cheryl Hammerly and Lorianne Peachey with a special thank you for handling logistical challenges at the last moment. A special shout out to Steven Kelley and Janet Gruer for their volunteerism, and being the boots on the ground HCMA representatives for the meeting. This model worked out so well that, when we come to your town next, you'll have the opportunity to step up and give us a hand. In the middle of the chaos of this month, a staff member who is also my niece lost her father. Her father was my sister Lori's first husband. As families we know divorce and separation change dynamics. There was a time that John Titus Jr., my niece and nephew's father, was a young charismatic man who stole my sister's heart and. for a period of time made her very happy. For that I will be forever grateful to John Titus Jr. My sincere condolences to my niece and nephew, John and Stacy, and their sister Heather, as they grieve the loss of this rather complicated man. And our staff deserves two special shout outs this month – to Julie Russo our Legislative Lead, who really helped make Hill Day a success and to Stacey for navigating this month with grace and professionalism. Together we can build better systems to improve and save lives, cost effectively and with equity for all. * https://www.congress.gov/bill/118th-congress/house-bill/6829 Best wishes, Lisa
A Caucasian man and women in lab coats stand over laboratory equipment.
April 30, 2025
Medical Management means using medicines and other non-invasive therapies to relieve symptoms of hypertrophic cardiomyopathy and other thick heart diseases. Knowing what is out there and what is being studied will help you navigate your treatment with your healthcare providers.
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