Yesterday morning, we spent several hours at Children’s Hospital in D.C. after what has been a stressful and scary 48 hours or so before that.
Let me start at the beginning.
Last Wednesday, Sweet Doodle (15 months old) conked her cheekbone on the picnic table bench in our kitchen. As you can imagine, she got a pretty good shiner, but I thought that was the extent of it.
Over the following 48 hours, however, the bruise continued to spread, extending up under her eye. On Saturday morning, we noticed even more bruising on her eyebrow and forehead, and it was around then that we started noticing what seemed to be excessive bruising on her legs as well.
On Sunday, as we noticed even more bruising, I Googled “toddler bruising” and was reassured by site after site that bruising in toddlers can be normal and is usually nothing to worry about. I tried to shake the awful feeling in my stomach, but when I changed her diaper before nap, I literally gasped at the sight of her bruised up legs.
That night, I typed a word into Google that I had been avoiding saying or typing until that point. I searched “toddler bruising leukemia.” The sites I came across confirmed that excessive unexplained bruising can be a sign of leukemia – as well as several other fairly serious diseases – and we made a decision to get her into her doctor’s office as soon as we could (not an easy task for a one-car family on a holiday week!).
When I woke up Monday morning, I was starting to feel a little less panicked and was thinking that maybe we could just start with a blood test and not worry about trying to get in to see the doctor. However, when I took off her pajamas to get her dressed for the day, I noticed petichiae (tiny red dots caused by blood vessels bursting under the skin) on her lower legs as well.
We made an appointment for Monday afternoon, and by the time we arrived, the petichiae had spread to her arms as well.
There was no doubt that both the nurse and our peditrician were very, very concerned by what they saw. Our doctor later told me, “My heart dropped when I saw that.” She sent us for STAT blood work at the hospital and told us to come back after the tests were done.
When we got back to the office, it was closing time and everyone was leaving, but our pediatrician (who I still love to this day!) made sure we were comfortable – or as comfortable as you can be in an exam room – while we waited for the results. Despite the fact that the phlebotomists had poked and prodded in my Baby Girl’s arm for over 15 minutes trying to find a vein before deciding to try her other arm, she was a happy girl, dragging the diaper bag around the room and playing with anything she could find.
Finally, the doctor came back with our results. She quickly explained that her white blood cell count was only slightly elevated and her hemacrit and hemaglobin (I think!) were normal, indicating that it was not leukemia or meningitis or another serious disease. She described another condition – idiopathic thrombocytopenic purpura – and explained that it was a condition with no known cause that can be triggered by a virus (i.e., the stomach flu). The body begins producing antibodies that attack the platelets in the absence of any remaining virus, which causes the platelet count to drop to dangerous levels.
At that stage, Sweet Doodle had a count of 12,000 platelets per liter, while normal levels are 150,000 or more. Because platelets are what cause clotting and prevent bleeding, the low platelet count was causing any pressure at all to leave a bruise or petichiae.
After touching base with a hematologist at Children’s Hospital in D.C., we were sent home with instructions to be at the blood disorders clinic at Children’s at 8am Tuesday morning.
We had another round of blood tests at Children’s (and thank you, Lord, that this phlebotomist simply inserted the needle, immediately got a vein and was able to get the blood sample she needed without too much trouble and no tears from my girl!), we met with the hematologist.
She explained that the counts were now 20,000, which brought us out of the critical zone where there was a high probability of internal bleeding. She explained the three treatment options to us (which I had already researched as well while I should have been sleeping) and recommended that we take a wait-and-see approach because each of the treatments does have side effects. I was very, very happy that this was her recommendation, as the treatment options all made me very nervous. While I had been willing to do them if we were still in that critical zone, I was glad that we didn’t need to take that route.
At this stage, with a firm diagnosis of idiopathic thrombocytopenic purpura (or ITP), we will continue to take Sweet Doodle for weekly blood tests (at our local hospital) to make sure that her platelet counts return to normal within the next six months. We will need to be more cautious than usual to protect her from head injury (which could result in a brain bleed) and watch for increasing bruising or excessive bleeding that would indicate that the platelets had fallen again. In almost 90% of children with ITP, there is no reoccurence or further complication, and that’s what we’re counting on for Baby Girl as well.
While we waited at Children’s Hospital yesterday morning, I was on the edge of tears most of the time. Not because of my Baby Girl’s diagnosis, because I had read enough to know that it was going to be okay, but because of all of the other children we saw – with bald heads from chemotherapy and wearing masks because of compromised immune systems. How thankful I am that our diagnosis is what it is, but my heart breaks for the parents who are watching their children fight a much bigger disease.
A week after I wrote this, we ended up being admitted to the hospital because she spiked a fever of 104 out of the blue. However, her nose started running the next morning and it turned out to be a simple cold virus. Sweet Doodle’s levels returned to better than normal within four months, and she hasn’t experienced any other symptoms or lasting effects. She doesn’t even remember any of this happening!
What experiences will you carry with you for the rest of your life?
|Mandi Ehman is the blogger behind Life Your Way. She and her husband have four beautiful girls plus one baby boy on the way, and together, they live, work and homeschool on a little slice of heaven in wild, wonderful West Virginia. She loves coffee, chocolate, easy meals, beautiful things and minimalist spaces.|