Last Monday, the 20th, we took Jaxton in to see his Dr.  At his 6 month  visit back in August, the Dr prescribed him a special multivitamin to help him gain  some weight... he was 6 months and weighed less than 15 lbs, and has yet  to double his birth weight.  While on this vitamin, he only gained 8  oz, and he went from the 8th percentile for his age to the 3rd (roughly  this means that out of 100 children, there would only be 2 smaller than  Jaxton with regards to his weight).  This is a reason for concern,  considering that when he was born, he was in the 38th percentile and has  rapidly been dropping since about 4 months.  Dr. Allen is extremely  patient with us and came in and sat us down and calmly told us that this  has nothing to do with anything we are doing as parents, we are feeding  him and taking care of him, but something must be going on to prevent  him from absorbing all of the calories and nutrients in the breast milk  and solids that he is eating. In every other way he is right on track, if not slightly ahead.  He is crawling and pulling himself up to things.  He is walking with the support of something solid to hold on to.  He plays and laughs and lately he is mimicking when we shake our head "no" or nod "yes".  Dr Allen directed us to start adding formula to  his rice cereal three times a day (and if you know me, I am not pro formula)  and feed him smaller meals every 2-3  hours (which should prevent him from spitting anything up, to retain all  that he can).  He sent us directly over to the hospital to have blood  work done and to have an ultrasound done of his stomach to see if his  stomach was preventing food from passing through, which could be a cause  of the lack of weight gain.  The orders called his diagnosis "Failure to Thrive".  They called us the next day and said that  both of those tests looked fine and that we needed to collect a stool  sample so that it could be tested as well.  And of course, being the mom, I got the extremely fun pleasure of collecting that sample.  So we spent more time waiting... and waiting. The dr's office called  yesterday and let us know that fecal white blood cells were found in the  sample and we were being referred to a specialist in St George for more  testing.  Jaxton is going to a gastroenterologist (they specialize in  disorders of the digestive system).  I am working a grave so I spent  most of the night looking up information on these specific dr's and what  he may look at with regards to Jaxton.  However, I have had little luck  because most of the information I found talked about Jax also being  "short statured"  which clearly, he is not.  I have no  knowledge of the  medical profession, nor do I pretend to, so most of the information made  no sense to me, but we are hoping to hear from the specialist in the  next day or two to make an appointment and get this show on the road.   This is extremely stressful for me (kyle seems to handle it better than I  do)  In the information I was reading, it said that surgery is not  usually something that is needed, it may be something as simple as  changing his diet.  It talked a lot about Celiac's Disease, which  basically means he can't break down gluten... however, to be honest, I  don't know really what food he has had that has it in it.  I can't wait  to find out what is going on!  I am so lucky to have my sweet and wonderful husband who insists on being as involved as possible accompanying me to multiple dr appointments and making sure he can work his schedule out so we can do these things together.  I know in my heart that my sweet boy will be just fine, but my head can't seem to wrap around that concept.  I feel nervous, anxious and sad.  All in all, we have been blessed up until this point, and I am confident that the Lord will continue to bless our family.  I have been living by this saying (and Dr. Pepper, Peanut Butter Twix,  and fudgesicles the past couple of days)
"When life becomes more than you can stand~ kneel".

We appreciate all of the love and support we are getting.  Hopefully this is an easy fix and our little boy can continue to progress on schedule.  We will keep everyone posted as we find out more and more information.
You know I'm here whenever you need anything!
ReplyDeleteHunter had to go to a gastro specialist when he was 4 months. It was not that bad, the dr. was great. I was also not pro formula, but I had to "top" Hunter off after breastfeeding the first 2 weeks of his life due to jaundice. It was not that bad either. I was able to ween him off of the formula later on. It will get better. My prayers are with you.
ReplyDeleteHey we just went through a bunch of testing with Lydia too. They ran a bunch of tests and it was not exciting. We ended up taking her to the endocinologist but things are going way better now. We ended up switching Lydia to formula and she gained four pounds in three weeks. She's growing strong now and is a happy chubby girl. I hope that things turn around for Jax!
ReplyDeleteI'm sorry you guys have to go through all that. It is scary when you don't know what's wrong. I hope the doctors figure it out soon.
ReplyDeleteThose pictures of you guys and Jax are way cute though! He's looking so old!