Tuesday, June 2, 2009

One step at a time

I'm not sure what I want to write today. I have many different feelings and the thought of trying to get them down on paper is a bit daunting right now. I guess I was hoping somehow to have the doctor tell us that all our concerns would be okay, that our littlest guy was progressing with his gross motor development at a rate that would catch him up to where he should be. I just wanted the pediatric neurologist to say that there were no concerns that she could see. On the other end of the spectrum was the thought that she might find something, even give a diagnosis that we would be able to work with--move forward with--know how we could best help our little sweetie with. Instead, we left with all the same questions we entered her office with. She acknowledged that something was wrong--was it central nervous system or peripheral nervous system--no answers. She acknowledged that from our accounts there had been great progress in the past month--crawling on hands and knees, pulling up to standing, pushing up to sitting...but said that one month wasn't enough and we needed to see this kind of progress for at least two or three months. She suggested having a MRI as well as blood tests to check how the muscles are working, but gave the suggestions with such a lack of confidence that we don't know if she was just suggesting something to say something or if she thinks that they could actually be beneficial. We want to do all that we can for our little guy, but the thought of sedating him for a test that she acknowledged might not be useful isn't very encouraging. I will choose to be grateful that she didn't have a clear diagnosis--I guess I just have to remind myself of that periodically.

Our next step is meeting with a group of pediatric physical therapists this friday for a three hour evaluation/assessment. I'm hoping we'll have more direction after that. At times I just feel like crying. I don't like being in a position of not knowing what we can do. I need to focus on the HUGE progress that has been made this past month. I am grateful for the beautiful smiles and good fine-motor skills that our little guy has. I am grateful for his excitement at playing with his older brothers and other examples of social skills. I love his first morning smile as we go into his bedroom--he is so excited to see us. I love his happy conversations throughout the day (it will be nice to understand them someday! :). I've been saying for awhile that I felt a calm optimism about all of this, even though I recognized that might not mean all would be perfect. No one wants to hear that there is anything wrong with their child--there are enough challenges they will face in this life without these additional things, but I do believe that our Heavenly Father is truly aware of each of us and He knows those challenges as well as those blessings that will help us become the son or daughter that He sees we can be. I know He loves our children even more than what my mother's heart feels, and that amazes me, so I can be calm as we continue to try and figure things out. I'm not good at waiting, so this will give me the opportunity to get better at applying patience and I'm sure there will be many other blessings that will come from this current challenge. The thing I like about challenges is that they can be overcome--regardless of the outcome. This is a challenge that will provide growth for us all. Oh the gratitude of facing challenges together as a family with the knowledge that we have a loving Heavenly Father and a Savior that knows how to soothe, comfort and direct. I guess it is literally one step at a time.

5 comments:

Emu Monkey said...

We will keep him in our prayers.

kristenhcubed said...

Hugs, my friend. Hugs and prayers and more hugs and more prayers. And some crossed fingers and toes. And eyes.

Anonymous said...

I can completly understand the mixed range of feelings you are having...for the past 2 years we have been trying to learn how best to help our son as well...he has developmental delay, speech and coordination disorder. With that being said, it is never just a clear cut diagnosis, I so wanted to have a definite answer so that I would know exactly what to do to help him...but I have to take it one day at a time too. As a mother, I think it may be more of a trial for us than for the child himself...we want the very best for them!! You are such a wonderful mom and woman and I think your son is so blessed to have parents that so care for him and will do anything for him! :) Hugs!

Dalynn said...

Our best to you and your littlest Lowe on Friday.

Jennifer said...

Just on a whim, I thought I'd check to see if you had anything new posted. I love reading your blog.
Thank you for your latest entry. There were some things in there I needed to hear. You are such a wonderful mother. It is evident that you truly love and care for your children, and that is refreshing.
We'll keep your littlest guy in our prayers.