The Hardest Month of My Life

by Mandi on January 25, 2012

idiopathic thrombocytopenic purpura

source: Mandi Ehman

December of 2008 was one of the hardest months of my life. The end of the month found me curled up on the couch on Christmas day, emotionally and physically exhausted in the wake of three weeks of the stomach flu (including an ER trip for Sean), the death of a family friend and then Sean’s grandmother, my third miscarriage and this crazy scary experience with our third daughter.

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.

idiopathic thrombocytopenic purpura

source: Mandi Ehman

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.

idiopathic thrombocytopenic purpura

source: Mandi Ehman

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.

  • Elena

    How scary! I’m so glad to hear she’s doing well:) 

    • http://lifeyourway.net Mandi @ Life…Your Way

      Thanks, Elena.

  • Jamie English

    Definitely a scary event.  Never heard of the condition before, but can certainly feel the intensity of the moment.  My son had pneumonia when he was 3 days old and spent a week in the hospital.  He was in neonatal, then upgraded to a Special Care nursery.  I remember that week so well.  Like you, I looked around and felt so much compassion for what other families were going through.  He is nearly 17 now…and we never had any other health issues.  Thanks for sharing from your heart!

    • http://lifeyourway.net Mandi @ Life…Your Way

      Oh, wow, Jamie — I’m sure that was terrifying! So glad he’s okay!

  • Thaunak

    I had this when I was about 2-3. It never reoccurred and I never had any further complications (I’m 47 now). It was very scary for my parents while the doctors where ruling out leukemia and other scary possibilities. I’m so glad all is well with your adorable baby girl! Thank you for sharing, I love the Internet and that we can research and share with one another and provide encouragement and support. Your family is just adorable!

    • http://lifeyourway.net Mandi @ Life…Your Way

      I love to hear stories from other people who had it when they were little and then never had any other issues from it — thanks for sharing!

  • http://www.athankfullheart.blogspot.com/ Miranda @ A ThankFULL Heart

    I’m so glad it all turned out okay!! My uncle and aunt went to the hospital with my 6 year old nephew last year because of a bruise on his leg. They found out he had a very rare form of cancer, but after very harsh chemo and radiation and a few close-to-death experiences, he has now been cancer free for a half a year :) !

    God is good and praise Him that your little girl will never be able to remember this.

    • http://lifeyourway.net Mandi @ Life…Your Way

      That breaks my heart, Miranda — little ones shouldn’t have to endure these things. But praise God that he’s okay now!

  • Kat Cervantes

    Omgosh I can’t even begin to imagine how difficult those days of waiting for test results must have been and to see your baby’s legs like that must have been horrifying. Thank God she is ok. I get teary eyed every time I drive past the Childrens Hospital and I say a prayer for those parents and kids in there. The hardest time in my life was 3 years ago during my last pregnancy when the doctor told us that our son had a very high chance of having down syndrome. Wow had to ponder that for 6 months and all that it would mean. He was born healthy and no downs : )

    • http://lifeyourway.net Mandi @ Life…Your Way

      Oh, Kat, I’m sure that was so hard; I’m thankful he was born healthy!

  • http://www.northerncheapskate.com/ Christina@Northern Cheapskate

    Your story made my heart ache for all the moms who have ever worried about their babies! I’m happy to hear she’s doing okay now.

    • http://lifeyourway.net Mandi @ Life…Your Way

      Thanks, Christina!

  • jennifer p

    i had this when i was 9 in 1982.i had been in a school bus accident and a week later this happened to me .my platelets were 4,000.i had to have my bone marrow tested with a giant needle in my bone and no anesthesia.they had to rule out  leukemia and see if i had enough bone marrow.i did and i got better .im 39 now and havent had any problems related to this again.im so glad your daughter is okay.and that she doesnt remember any of it.i remember it.

    • http://lifeyourway.net Mandi @ Life…Your Way

      Wow, Jennifer — I can only imagine! What a brave little girl you were to endure all of that!

  • http://www.momdropbox.com Audrey

    Wow, that must have been an incredibly scary & difficult time for your family.  We’ve only had to go to the children’s hospital once, and I too found the waiting room hard.  Glad your little girl is okay!

    • http://lifeyourway.net Mandi @ Life…Your Way

      Thanks, Audrey!

  • Lisa

    I was diagnosed with ITP in 1988 at the age of 26, also because of bruising that appeared but never seemed to go away. (By the way, I don’t recommend going out and looking at some of the informational websites about it, because they scared me to death at the time with their doom and gloom stories of “life being over as I know it”! Probably holds true for most disorders though…) I have had a couple of episodes since then and I still bruise easily, but I always bounce back. Both of my children are fine (born in 1992 and 1996 without the disease – a concern of my hematologist) and I enjoyed a teaching career of over 20 years until having to retire with other unrelated health issues. I hope that your daughter has the same experience as others posting here and never has another problem. It’s scary enough to have things like ITP yourself at times…but even worse when it’s your children that you are worried about…

    • http://lifeyourway.net Mandi @ Life…Your Way

      Thanks for sharing your story, Lisa — I’m so glad you were able to overcome it in many ways to live a full, blessed life!

  • http://www.facebook.com/profile.php?id=144902419 Erin Marie Spralo

    I do not have the experience of my child having ITP, however, my father has ITP.  Almost 13 years ago, he came home from a business trip to Europe, covered in what appeared to be a rash, but which ended up being blood vessels rising to the surface of his skin because his platelet count was so low.  They put him on steroids, which brought his platelet count back up & sent him into a sort of remission.  Since then, he has come out of remission about 4 or 5 times, his lowest platelet count being 2,000.  Luckily the steroids always brought his platelet count back up.  At one time he had his spleen removed (in some cases this has caused people with ITP to go into a permanent remission).  The last time he came out of remission, they were going to try a type of chemotherapy on him.  However, they had too aggressive of a steroid regiment and his platelet count was so high he was having blood clots in his legs, so they weren’t able to do the chemotherapy.  Shortly after going back into remission, he received the sacrament of anointing of the sick.  That was 8 years ago and for whatever reason he has stayed in remission since then.  I truly believe that the sacrament healed him.

    There are some people who go into remission the first time and stay in remission, it can just depend.  It can be really scary.  I used to always live in fear that my dad would come out of remission and not realize it and bleed internally before anything can be done.  Even now, when I believe he has been healed, I still have nightmares about him dying.  But I always find hope in that my father is a man who practices his faith and that God is merciful.

    My mother works in the medical field, and she always says it’s called idiopathic because “the idiots can’t figure out what causes it.”

    • http://lifeyourway.net Mandi @ Life…Your Way

      Wow, Erin — how exhausting that must be for your family! I know that it often hits adults harder/differently than adults, and I’m sorry you all have had to walk through this. :(

      I’m cracking up at your mom, though, LOL!

  • http://makeithappenmama.blogspot.com/ Emily @ Make It Happen Mama

    How wonderful that, in the midst of such a terrible situation, you can step back mentally and see the big picture against the backdrop of other children at the hospital. Our son has a hearing impairment and we are fighting against the school district this year, which feels he isn’t “disabled enough” for services (totally illegal, but that’s another story). I have to keep reminding myself, on the days that I feel completely overwhelmed, how relatively small our problems are when compared with other children who are seriously or multiply disabled. God never gives us more than we can handle, right?

    • http://lifeyourway.net Mandi @ Life…Your Way

      Awww, Emily — that must be so hard for your mama heart. I hope you’re able to make some progress soon, and I’m glad you have the “big picture” to help you keep it in perspective!

  • Jchapman83

    Thank you for this post.  The day I read it last week, we started noticing unusual bruising on our son’s legs and some inexplicable bruising elsewhere.  At first we weren’t too concern, as he is a bit of a rough houser at 2 years old, and figured he got them from falls or playing at his sitter’s.  He had a Dr’s appointment on Friday this past week, and it was almost word for word your scenario.  The doctor did blood work, and then told us she believed it was 99% ITP.  We have to meet with a hematologist to confirm.

    Your story touched my heart, and thank you again for the post.  

    • http://lifeyourway.net Mandi @ Life…Your Way

      Wow, what incredible timing. I am so, so happy that your diagnosis was the same as ours (it really is best case scenario, I think!), and I will be praying that your recovery is as quick and smooth as hers was as well.

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