You just experienced the shock of learning your child has a rare disease and now your doctor recommends genetic testing as the next step.
Brace yourself for shock #2: In most cases, genetic testing is not covered by insurance. In other cases, genetic testing is covered under limited circumstances.
Insurance companies are in the business of collecting premiums, not paying claims. The term “healthcare” is a tricky word in this context: Don’t confuse a business that makes a profit from premiums with actual care. The harsh reality is that as a business model, they generally do not care about your child’s health if coverage reduces their profit margin.
Coverage for genetic testing is routinely rejected because companies can do so without fear of backlash. In other words, anything that doesn’t affect the majority of its policyholders is up for grabs. The very name “rare” disease sends a signal to the reviewer that denial of coverage won’t create a big enough stir.
Simply stated, the system is against you.
That said, we have received countless denials from two different insurance companies over the past three years, and have successfully appealed every single one. Here are a few tips for the appeals process:
1. First and foremost, have a current copy of your insurance policy.
If you don’t have one, contact them immediately and request a copy. It is your right as it contains everything covered under your policy. Keep a current copy handy for future use, because, unfortunately, this will not be the last time you’re going to need it.
2. Know your rights.
A) If your claim is denied, you have the right to an internal appeal, meaning you can ask your insurance company for a full and fair review of its decision; B) You often have the right to demand a specialist in the applicable medical field perform the review if denial was based on medical criteria. Request it. These specialists will have more independence and a better understanding of rare disease patients and the value of genetic testing; and C) You have the right to an external review from an independent, third-party – keeping in mind that their “independence” is debatable.
3. Ask your doctor to write a letter.
Most doctors are well versed in this area and will likely mention it when they discuss genetic testing with you. If not, initiate the conversation and coordinate their assistance.
4. Request all documentation related to the claim.You have the right to copies of all documents, letters, and peer-to-peer reviews related to the matter, and all guidelines, protocols or other criteria on which the decision was made for denial.
5. Consider the assistance of an attorney.
There are plenty of attorneys who offer pro-bono (FREE!) assistance. Ask around your community and groups.
Now you are ready to appeal. I like to include a photograph of my child with the appeal letter. Whether a picture is effective or not, I want the reviewer to see the human side of the appeal.
This Friday, February 28, 2014, is “Rare Disease Day.” One in every ten people will suffer from a “rare” disease at some point during his or her life. Why, then, do we call them “rare?”
The National Institute of Health defines a “rare disease” as one that affects fewer than 200,000 people in the United States. This definition of a rare disease was included by Congress in the Orphan Drug Act of 1983. There are approximately 7,000 diseases or disorders that qualify for this designation. Alone, each disease is rare. It is only when counted together that they are not.
Because of the Congressional Orphan Drug Act of 1983, the term “orphan disease” is often used interchangeably with “rare disease.” Anyone who suffers from one or, in our case, has a family member who suffers from one, can understand the harsh poetry of that term. All too often, the sufferers are children. In many ways, they are abandoned by the scientific and medical communities. Few research projects are dedicated to these conditions. Few doctors specialize in treating them. It is difficult to find support groups. It is hard to find people who understand what it is like to watch a child’s symptoms in ignorance of what is causing them and fear of what they may portend. We face life-changing decisions alone and isolated from any sort of community of peers. We are not just facing the possible suffering or death of a beloved child, but all the things that must be changed before we even know what the future holds.
Can both parents work when our child has obstacles to face? Can we enter into daycare or mainstream schools and risk the viruses and illnesses that can so profoundly affect a child with a rare disease? Can they accommodate a child with the issues our child faces? Is our house fit for someone with a disability? Can we afford to go down to one income? Can we afford to make our house accessible? Can we afford to travel to the physicians that specialize in caring for the rare disease patient? All of this is on top of the harsh reality that we or someone we love may be facing death, and while learning that the road to answers will be long and difficult.
When we were told that Katherine likely suffered from Infantile Neuroaxonal Dystrophy or “INAD,” we searched for as much information as we could find on this condition. We had never even heard of it before the neurologist uttered the words. And it is no wonder. We read that there are only nine children in the United States that are confirmed to have that condition right now, and only around 1,000 that have ever been diagnosed with it here. These numbers do not come from scientific sources, so we cannot stand by their accuracy, but the one thing we do know is that it is extremely rare.
Compare this to cancer or heart disease. Most people have been touched by both. Even small towns have more people currently living with cancer or heart disease than have ever had INAD in the history of the United States.
It is understandable that we donate our charitable dollars to studying conditions we know all too well. We race for cures and donate to heart associations. When Congress or state legislatures set aside government research dollars, most of it goes to conditions well-known to voters. On top of this, private corporations spend their money researching new drug therapies and procedures that will make them money. There is not much money to be made from nine INAD children compared to the billions to be made off of each new cancer therapy or even a minor improvement in a heart stint.
Yes, we are orphans. We are alone, with voices too small and too few in number to be heard. This is why awareness matters. If our small choir stands united with the choirs formed by families faced with the other rare diseases, we are not small, we are not few in number, and we are not powerless. Alone we are rare. Together we are strong.
There are concrete things we can change for the better.
One of the things we learned early on in our search for a diagnosis for our daughter is that these conditions are difficult to diagnose. Most “rare diseases” have a genetic cause. Our current neurologist analogized diagnosing a genetic-based condition to editing a book. This particular book consists of detailed chapters on how to build a person. It defines how each cell is constructed, will operate, will replicate, will repair itself and will be stacked to create bones, tissue, brain cells and our whole body. Current estimates are that there are around 26,000 genes in the human body (somewhere between 23,000 and 30,000 by current estimates, excluding a lot of “non-coding DNA,” which is not well understood), translating in this analogy to 26,000 chapters to edit.The genes range from a few thousand DNA bases to over two million bases per gene, translating in this analogy to chapters of a few thousand to a couple million words each. That is a very large book to edit.
What’s in your genes?
Most of these chapters–or genes–come in duplicate. One “chapter” comes from mom and one from dad. You have to know how each duplicate chapter works when the instructions are different (in our family, mom’s instructions usually prevail, but that is not always the case in genetics), and you have to know how these chapters work in unison to know how the construction is to proceed. On top of all of this, environmental factors work into the equation. How does a virus, a toxin or a trauma factor into the blueprint when the body is being constructed? How do the chapters, themselves, define that reaction?
To top it off, we all have hundreds, if not thousands, of typos and omissions. Some typos do not mean much, if anything. Some change the entire meaning of the story. Some we simply do not know.
This editing process ends up taking a lot of time and costing a lot of money. By way of example from our circumstances, for INAD, we know that typos and omissions in the chapter or gene titled “PLA2G6” are known to lead to INAD. However, this is true only 90% of the time. In the other 10% of known cases, no typos exist in these chapters and science just has not discovered another cause. So, we began with a chance that our child has INAD that this test – this edit – would not detect.
There are duplicate PLA2G6 chapters, and the condition is recessive, meaning that you have to have typos in both mom’s PLA2G6 chapter and dad’s PLA2G6 chapter for the child to have INAD.
Each of these chapters is written in script so small that our most advanced machines cannot accurately read them. As far as chapter PLA2G6, the test accurately detects known typos and omissions in a given chapter 85% of the time. In other words, they have used the test against genes that have been confirmed to contain INAD-causing typos, and only find them 85% of the time. The known typos are missed the other 15% of the time; we simply cannot read all the words. Since typos have to exist in both mom’s and dad’s PLA2G6 chapters, however, if no errors are detected in either chapter, the condition is unlikely to be present (there is only a 2.25% likelihood that errors would be present, but missed, in both parents’ PLA2G6 genes).
So, running the INAD test can result in different outcomes: (1) both mom’s and dad’s PLA2G6 have typos of a sort known to cause INAD, in which case the child is diagnosed as having it; (2) either mom’s or dad’s PLA2G6 is detected to have such an error, but not the other one, in which case, the child may be deemed likely to have INAD based on clinical manifestations of INAD and the 15% non-detection error rate in the other “normal” gene; (3) neither parent has PLA2G6 errors that are detected, in which case, the child still may have it because of the 15% error rate in each PLA2G6 editing (a 2.25% chance), or because of the atypical INAD cases where there is some other cause; or (4) errors are detected in the PLA2G6 genes, but not of a sort known to cause INAD, in which case the results are a firm “we don’t know.” The end result is a definite diagnosis of INAD, a “maybe,” a “probably not,” or a “who knows,” but never a “no.”
The cost for these tests can run at around $2,000 each. That’s right, $2,000 to test for just one condition of 7,000. Run the math. At $2,000 per test for 7,000 tests, the cost would be $14 million to edit all of the chapters known to cause “rare diseases.” Truth be told, the math is not that simple. Some tests are cheaper, while others are more expensive. In no case would they run all 7,000, as many conditions can be eliminated based on clinical signs or other blood or urine tests. However, the reality remains that many of these rare diseases share symptoms and it is often necessary to run multiple expensive tests over the course of years to finally reach a diagnosis. At the end of this long and expensive road, the physicians only come up with a definitive diagnosis half of the time. The other half of the time, we know there is some sort of metabolic disease, some rare condition, but we just do not know what it is. Our editing skills have not advanced to the point of knowing where to look for typos or what they mean.
No one can realistically edit all 7,000 chapters associated with these diseases, so doctors look for reasons to pull a particular chapter for editing. To do so, they perform less expensive (but not cheap) tests to try to figure out which chapter to edit. An MRI and MRS result justified the INAD test for Katherine. It turned out negative (but not ruling out INAD, as discussed above). So we move on to look for reasons to pull the next chapter. She had an abnormality in her acylcarnitine profile. We’ve run it again. If it turns out abnormal a second time, we have reason to suspect it may be one of the 30 known fatty acid or organic acid disorders, narrowing it down to 30 new chapters we might have to pull and edit. 30 edits at $2,000 each is still $60,000. It beats $14 million, but is still pretty expensive, particularly when there is a 50% chance that it will result in nothing definitive. We also have a follow up MRI/MRS, a genetic ophthalmologist appointment, and a spinal tap. We also are awaiting results from a skin biopsy. All of these will provide hints at what chapter to pull next for an edit.
Thank goodness for that insurance, right? Wrong.
In most cases, genetic testing is not covered by insurance. In other cases (like our’s) genetic testing is covered under limited circumstances. Insurance companies are in the business of collecting premiums, not paying claims. Therefore, it is rarer than these diseases for an insurance company to find the limited circumstances to be met.
The reason why genetic testing is routinely excluded from insurance policies or claims are rejected is simple: rare disease patients are easy to ignore, and expensive to hear. It costs nothing for the insurance company to let Katherine die, and $60,000 to see why her acylcarnitine profile is high, much less millions to see if she can be saved.
We are literal parents to figurative orphans left to die by harsh economic realities.
Considering she was thought to be the tenth child alive with INAD, she could be rejected without fear of economic backlash. All ten of us could march away in anger and it would help, not hurt, the insurers’ bottom lines. And what is our alternative? Are we to go uninsured? Are we to buy another policy if it, too, has a “let her die” policy toward genetic testing and rare diseases?
We have chosen a different alternative: To join together and be heard. We can change things for the better. We can put economic pressure on insurance companies to cover genetic testing. We can put pressure on politicians to force them to cover it. We can force states to increase newborn screening. We can expand awareness and education of the signs and symptoms of rare diseases. We can expand the flow of money into research of the genetic roots of all disease, including cancer and heart disease, leading to advances in the fight against the rare ones. We can let the lucky 90% know our cause, as many will join our choir if they just know the song.
This is for your benefit. At a 10% overall rare disease rate in the United States, it will affect your family. It is a matter of when, not if. Help us change things for the better before you discover that you or your “Katherine Belle” is among that 10%, an orphan to the medical community and a burden left to die by your insurance company.
With this blog, we stand up to join the chorus. We are singing at the top of our lungs. We contacted our state elected officials. Kentucky Governor Steven Beshear has proclaimed February 28, 2014, as Rare Disease Day in Kentucky; Representative Sannie Overly will read a Rare Disease Day citation in the Kentucky House of Representatives. It may not matter to many of you (yet, but it will affect all of you eventually) but it matters to us. Katherine’s voice matters. Katherine’s life matters. It is worth more than $60,000. It is worth more than $14 million.
And, we will not go quietly. We will be heard.
How can you help? First, you can share this post with everyone you know to help us raise awareness. Second, change your Facebook profile picture (see different examples below) to show your support for Rare Disease Day. Third, encourage your local, state and federal officials to recognize Rare Disease Day. Fourth, wear a denim ribbon on Friday to show your support (jeans for genes) and tell people why you are doing so.
The steps of the Kentucky State Capitol, House of Representatives.
If you have read our other posts, “Faith. Hope. Love.,” “Death and Resurrection” and “Dance! Dance!, ” you will know much of our individual stories leading up to the moment when our universe was turned upside down. As Dave has explained, on Friday, August 30, 2013, we received a phone call that forever changed our lives. This was a call from a neurologist telling us our two year old daughter, Katherine Belle, likely has a rare and progressive genetic disease.
What immediately followed was complete and utter numbness, disbelief, and unbearable pain. It was so hard to believe that the world was still spinning when it felt as though it had suddenly stopped and literally knocked me off my feet.
I do not remember much of the moments, days, or even weeks following this devastating news, but I do recall repeatedly asking Dave to explain to me once again what disease the doctor said he believed Katherine had. The name was so unfamiliar.
We soon learned that INAD is very rare. Naturally, I wanted to know more about this vicious intruder who had taken our family hostage and threatened to kill my only child, but truthfully, I was afraid to look in those early days. I did not want to read what science had to say about my daughter’s fate and our future.
Infantile Neuroaxonal Dystrophy (INAD) is now a name I know all too well. And, after my mother read about the affects of this rare disease, and told me she wanted to take a “sledgehammer to her computer,” I could completely relate. It took me a while, but ever so slowly, each day I was able to read more and more about INAD until finally I knew what everybody did not want me to know. Right then I knew that we had involuntarily become a part of science. INAD is so rare, in fact, there are only two labs in the entire country that do this genetic test. Yet somehow, it had found its way to our doorstep.
By mid-October, (which felt like two years later) we had entered into the “coping” phase of our journey. The immediate numbness wore off, but today we live on an emotional roller coaster that quickly shifts gears from anger, denial, grief and depression, and is susceptible to change minute-to-minute, hour-to-hour, day-to-day. We have been to grief counseling and joined support groups. Mostly, though, we try to maintain as much routine as possible for Katherine Belle so she has a sense of structure and security. This is not an easy task when some days all I want to do is crawl into my bed and cry.
Needless to say, our lives were forever changed with this news. Sick time donations from kind and loving co-workers has afforded me the opportunity to spend as much time with Katherine as allowed while we face the difficult decision whether or not we are financially able to make the transition to a single income family with growing medical bills. (Dave has Type 1 Diabetes and is insulin pump dependent.) My husband’s co-workers have cooked us weekly meals. Friends and family have offered financial assistance. We are currently in the process of selling our home to lower our mortgage payment and move into a handicap accessible home. Our doctor is in Cleveland, which is a six-hour drive. We’ve already appealed (and won!) a denied insurance claim. I take Katherine to occupational and physical therapy appointments twice a week. And, although that genetic test for INAD came back negative, as of today, we live in that “unknown” diagnosis phase where “atypical” INAD is still on the table (Dave will explain more in his next post).
However, I do feel like we are the luckier ones. We are finding strength on this journey. We have learned the true importance of living in the moment, and we have the constant support of family, friends and even strangers who give us courage, strength, hope and love. We have so much hope. And faith. And love. Even if science never catches up with our own daughter, we hope and will actively advocate for others. And, as I am learning, there are many things that science cannot explain.
The medical aspect of our story is overwhelming and we’ve had to assimilate a ton of information quickly amidst our grief. It is true that your doctors and therapists become your family. We are all partners and advocates for Katherine Belle. We all have hope. We are all advocates for a cure.
As we take on more of an advocacy role not only for our own daughter, but for others who share this unimaginable journey of hope and survival, we want to arm you with as much information as possible to share in your own communities. It takes a village. As the Rare Disease Day slogan says, “Alone we are rare. Together we are strong.”
Rare Disease Day is February 28, 2014. Dave will soon share more information about rare diseases, our own advocacy efforts, and what we are facing in the coming months and years. In the meantime, please take a moment to read about Rare Disease Day on Facebook and share information and links with your networks.
HOPE FOR KATHERINE BELLE 