June 2014

Chase is now almost 22 months and he has been a very busy boy.  He proudly claps and cheers at himself after almost everything he does, if that gives you an idea of how much he is used to everyone around rooting for him on a daily basis.  He is climbing on the furniture, standing on top of tables, and flushing things down the toilet like a mischievous little boy.

Chase started speech therapy 6 weeks ago and the positive changes have been coming very fast.  He had started having tremendous tantrums frequently- it seemed he knew exactly what he wanted but he had no idea how to communicate.  The tantrums have stopped for the most part and he is much happier- finally pointing at things, using multiple signs and a few words just in the past couple of weeks! He is eating better too, although very particular and issues with certain textures.  He is now at 4 therapy visits at daycare each week and we cannot speak enough praise about what this has done for him and our family.  



We are unsure but I suspect that Chase had some "normal" head drop seizures last month while he had a fever.  We immediately contacted his doctors at Mayo, who said they would work with our local hospital to get tests done so we did not have to make the long trip there. We were weary based on our past experience here with Sanford Neurology, but it was interesting (and shocking) to see them hustle over a weekend to get him in for an EEG the next Monday morning.  The local neurologist called me back an hour after the test that Monday with results, which were also sent to Mayo for verification.  I cannot help but wonder if this was because Mayo ordered the tests and how things would have gone if I tried to arrange this on my own.  Regardless, the panic was because the hypsarrythimia (abnormal brain pattern) could still come back, but it had not. It is very common for kids with IS to have other seizures especially when ill, so we were advised to watch him closely.  If Chase has "normal" seizures, we can live with that.  Unfortunately in our perspective, this is really nothing compared to what he had been dealing with.  


Chase finally learned to bite off foods such as corn on the cob

The most exciting news is that Chase had his skills reevaluated last week and most of his skills are now only 1-4 months behind for his age!  That is pretty amazing, realizing that all of his skills were measured at half of his age or less when the spasms stopped.  Language was further behind, however only 6 weeks ago he was measured almost 5 months behind where he is now so he is bridging that gap quickly.  He is truly a rock star.

This little guy has had his mom and dad on their knees begging God for mercy and although we could not be more grateful for the outcome, it has still been a hard and emotional trip. We have nightmares. I personally have a hard time being around babies a certain age (about 8 -15 months) because I can't help but mourn that normally exciting time of development we truly lost with him.  I’m scared to see my niece in a few weeks, who is coming up on that age when Chase's head drops started.  I’ve been in a public place and watched a baby appear to "drop" its head (which wobbly baby heads do all of the time) and screamed out loud, then started bawling.  Time will heal and we have so much to be happy about, but the fear and pain is still fresh.  June 29th is coming up, which is the date last year that Chase had his first recognizable seizure and the spasms started happening all day long but we didn't know what they were.

Our lives have changed from this but in a good way.  It has brought my marriage and our families closer.  We have started going to church every week and praying together.  Chase's older sister Anna is the most caring little girl who loves and protects her brother to no end, and consistently talks about Jesus and prays for the sick.  I have been contacted now several times to talk to families who have infants with seizures.  Chase will be fine, but if we can help even one other family get answers sooner when they don’t know what is wrong with their child, then this has been worth it.  
Chase enjoying the water


3 comments:

  1. Hi, I found your blog as I was researching Infantile Spasms online, my niece (8m) was diagnosed with IS yesterday, understandably it's been a lot to process for my sister in law and family. How is chase doing now? I'd love to hear an update. Kind regards. Fern
    Fernshearer@gmail.com

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  2. Please give us an update. My child was diagnosed with Infantile spams June 2015 at 6 months old. I've been following you ever since. He is now 2.5 years old and he's experiencing a speech delay which I find very common for the little ones that have this condition. He receives speech but I see no progess. How is little your little man. Your update will be gladly appreciated

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  3. I need to update this blog so badly but life has been wild! In a GREAT way! Chase is starting Kindergarten next week and is perfect! We are so proud of him. I have been contacted by so many families across the globe because of this blog and I'm not sure if I've been able to help them, but hopefully give them some hope that this diagnosis does not always have to be devastating as all the doctors and literature online says. I would love to hear updates on your family members.

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