William’s Story

Site created on April 12, 2018

5.2.2018

Thanks for all the kind words and well wishes! It is difficult to know how much information each of you may want about William’s journey, so we’ve compiled it all below. Please read as much as you want to read.

William Hayden Cameron was born at 4:50 pm on Saturday, March 17, in Jackson, Wyoming. Once it became clear that William was likely going to need some medical support and to avoid any additional stress on William during labor, he was born four weeks early via c-section. William was cuddled by Robin before he and Phil were transported by Life Flight to Primary Children’s Hospital in Salt Lake City. 

It’s helpful to write this out and share it with family and friends, but we are intentionally not posting it on social media. We are still moving through the various stages of processing what William’s diagnosis means for our family and how we would like the information to be broadly known. The shortest summary, if anyone asks, is that, "William is stable and doing much better at the NICU in Salt Lake. He has an underlying condition that they are learning more about and establishing a plan of care with the support of their medical team." 

In short with a bit more detail...
William remains in the NICU but is stable and doing well in so many ways. He's gaining weight and is about 8.5 pounds, eating more each day through nursing and by bottle (rather than NG tube), and behaving like a healthy baby. He's been really mellow: mostly sleeping, eating, playing, and getting some time on his belly. He’s easily consoled and loves being cuddled and swaddled and his facial expressions are adorable. William’s blood pressure requires two medications to keep it at a healthy level. He was on several additional meds that have all been curtailed. He is no longer requiring breathing support, which is remarkable considering that the doctors initially told us to expect that we would go home on oxygen. We are thrilled by his progress and hope to be discharged soon.

In long form...
William encountered and has overcome challenges with many major organs, including his heart, lungs, liver, and kidneys. He was diagnosed with early stages of an illness called hydropsy, which results in excess fluid in the body compartment. With that complication he had systemic hypertension and pulmonary hypertension, along with poor kidney function, an enlarged liver, an enlarged heart with hypertrophy in both ventricles, and high bilirubin pigments. With the exception of high overall blood pressure, we are relieved that these issues are generally resolved. We are celebrating that he appears strong and alert and is meeting developmental benchmarks.

We had been patiently awaiting a CT scan since his birth and recently learned that his kidneys could handle processing the contrast needed for the CT scan. The scan confirmed that there is narrowing (stenosis) in his lower aorta and renal arteries, and he has been diagnosed with an exceedingly rare vascular syndrome called Midaortic Syndrome (MAS). Based on what he had already overcome, we know he is a fighter and a miracle baby. Getting the news of this issue, which carries long-term implications, was crushing to both of us, though we knew that it was a significant possibility. At some point, hopefully in several years (or longer), he will require surgery (or surgeries) to help manage the narrowing in his blood vessels. We are exceedingly fortunate that we are aware of this complication now, as more often, it goes unnoticed and is not diagnosed until the the heart has been working too hard for a long time or the kidneys are failing. William is doing so amazingly well and from the outside you would have no idea what lurks beneath. The syndrome that he has is so rare that our veteran team at Primary Children's (in Salt Lake) is only aware of one case of MAS in a child at this hospital. We're currently working with the only specialty center in the US (http://www.childrenshospital.org/centers-and-services/programs/f-_-n/midaortic-syndrome-and-renovascular-hypertension-center), which is at Boston Children's, in order to have them evaluate and weigh in on his current care and future surgery. The team in Boston is meeting on Thursday, May 3rd, to discuss William’s case. At this point, we will continue to monitor his kidney function and manage the high blood pressure with meds.  Surgical intervention will be discussed in the future when his current treatment proves no longer effective or he's grown enough that his vessels are large enough for surgery. 

The doctors do not know what caused the narrowing in William's blood vessels. There are several genetic conditions associated with MAS. He has been tested for all of them and is in the clear. This information was a tremendous relief, as we do not need to worry about Dylan as well.

The Salt Lake team's goals are to allow him to continue to eat, rest, and grow with an eye towards William's discharge in the near future. We are fortunate to know precisely what ails him, and our pediatric team in Jackson is getting up to speed. With increased growth and feeds by mouth, he is very close to being able to come home.

We are grateful for the support coming from our community in Jackson and the superb medical care we have received. We've been so well supported by friends and family. Robin's parents just watched Dylan for a week after several friends helped him over the previous few weeks. We'll keep you posted on our progress as things continue to improve. Finally, please support Ronald Mcdonald House Charities; having a place to stay, meals, activities for Dylan when he's in Salt Lake, and a local network of peers and support has been invaluable to us. They are an amazing charity that has made a huge impact on us. We look forward to introducing you to sweet William soon!

Best, 
Robin and Phil


 

Newest Update

Journal entry by Robin Cameron

We are quite overdue for an update. Thanks to all who have reached out since our last update to see how our (not so) little man is doing. William has been to Primary Children's in Salt Lake several times since we last wrote an entry, and the theme from these visits was to keep doing what we're doing. William's medication doses continue to be increased to accommodate his growth. During the most recent visit at the end of February, the Head of Pediatric Nephrology recommended that we try stretching out our visits a bit more. Rather than go every three months, we will try every 4-5 months. He continues to have regular in-home blood pressure checks every two weeks (more frequently if he is out of range).

Despite the strange circumstances we are all experiencing right now, William continues to thrive. He takes his daily medications enthusiastically, looks forward to his blood pressure checks and seeing his favorite nurse, and has now shocked several phlebotomists in the last year when he does not cry during blood draws. He is a tough one and he even wears a mask (or two...see picture below) when we go to the hospital.

William spoke about ten words going into quarantine; spending all his time with his chatty older brother has made his vocabulary explode. Their relationship has evolved in so many positive ways, as they rely so heavily on each other for friendship right now. Despite Dylan's frustration with "the sickness" (Covid-19), the boys are so full of energy and silliness. We feel lucky to have these two incredible boys lifting our spirits during the challenging times our globe is facing right now through the pandemic and continued examples of social injustice.

We are on strict lockdown per William's doctors' recommendations. The fact that Covid-related illness is causing instances of kidney failure and blood vessel inflammation is great cause for concern for our one-kidneyed little man and his bottlenecked blood vessels. His incredible nurse from our pediatrician's office comes to our house to check his blood pressure, as they are trying to minimize William's exposure.

Dylan and William are absolute troopers. Dylan has demonstrated impressive patience and maturity in understanding and articulating why our family is being so careful in the interest of his brother's unique circumstances. Since the first week in March when Dylan had the flu, they have only been to the doctor. They’ve not played on a playground or had playdates. We are very glad we live in a place with so much outdoor space to explore, as Dylan would be losing his mind if we couldn't escape our neighborhood where he sees kids playing together and going to camps daily. He is able to do chaperoned bike rides with friends, since he can ride his bike and physically distance. He's also excelling on his new roller blades. Our family has been camping a lot and we're getting very good at finding beautiful new places to explore while avoiding the local and tourist crowds. These outdoor adventures are keeping us all happy and sane, although we are eagerly awaiting the day that Dylan and William can hug their friends and play freely (and Dylan can stop pointing at all the neighborhood kids and announcing that they are not being safe with the sickness). Oh, Dylan.

We're headed to Salt Lake next week for appointments, so we will write another update once we return (in a more timely manner, I hope). We are still trying to figure out the logistics of the trip, but we will only spend time in the hospital to avoid exposure to Covid.

Patients and caregivers love hearing from you; add a comment to show your support.
Help William Stay Connected to Family and Friends

A $25 donation to CaringBridge powers a site like William's for two weeks. Will you make a gift to help ensure that this site stays online for them and for you?

Comments Hide comments

Show Your Support

See the Ways to Help page to get even more involved.

SVG_Icons_Back_To_Top
Top