The “Special needs mom”

This question “What is it like being a special needs mom” was asked over at “What is Normal” at the time I could not find the words to answer that particular question to the best of my ability, but God must have really wanted me to answer it because today, I was asked the very same question again!!  So that is the inspiration for todays post.

 Were do I begin, lets start with the truth, Its not easy, If I think back to some of the many emotions I felt from the time Leah was born they start at FEAR, JOY, ANGER, DENIAL, ACCEPTANCE and finally realizing that this little life is totally dependent on you, and its up to you to gear yourself with as much information and support to carry you through each day. So I had to realize that I had to take things one day at a time.

If there is one thing I know for sure God makes no mistakes, I know Leah was given to us for a reason, before I found out I was pregnant my husband and I were living life past each other, he would be doing his thing and I would be doing mine, my girls were at a age were they were also doing their thing and our idea of quality time was taking the kids to restaurants for Sunday lunch, or visiting friend while all the kids played in the back yard, we thought our lives were complete and we had everything we needed. When we found out at my 20 week scan that there was a problem with Leah, my first thought was why was this happen to me?Is it because I never spent enough time concentration on my spiritual life, did I do something wrong? Why was I being punished?!!!!! I cried for days, I was inconsolable and I mentally tried to detach myself from the baby that was growing inside me.

The turning point for me was my Fetal Abnormality Scan, instead of a little black figure squirming around on the screen, I saw Leah in 3D, I will never forget her face and seeing the blood pumping through her veins, seeing her heart beating so hard its as if she was running a race, I then realized the magnitude of this little human being growing inside me, I felt guilty for not wanting to feel anything for her, I realized all she had in order to survive was me. As I left the hospital I remember putting my hand on my tummy and sobbing as I asked God to forgive me for those thoughts of not wanting my child, I was a new mommy after that appointment, I realized that we were all in this together, we needed to unite as a family and I accepted my child and loved my child no matter what was to come our way.

It hasn’t been easy, it’s challenging because you faced with so many obstacles, in Leah’s case we were not informed of all the health issues that surround Achondroplasia, but we will face those challenges, and we will work through them.

 I would not change a thing about my life today and neither would the rest of my family, I am constantly amazed at how this little person has brought our family together, we now see life through different eyes and sometimes my husband reminds me of how we THOUGHT we were complete, little did we know that Leah was the missing piece of our puzzle. We have lost some of our old friends, but we have gained a new family, we have met the most amazing people and we have shared in their pain, we shed tears for baby Theo and Little Avery, we felt as if they were part of us, and we prayed together when Knoah was ill and we speak of these people as if we have known them for a lifetime, we make a point of trying to visit all our little friends blogs just to keep up-to-date with the progress everyone is making, and its a good feeling to see how all these families have embraced life and deal with all sorts of issues and still remain positive and happy while doing so.

There will be fears, and there will be tears but I would not have it any other way, for me being a “special needs mom” has made me more tolerant, taught me the meaning of patients, grown my relationship with God, and made me appreciate life, love and family and I thank God for my Little Leah, and the friends we have made along the way.

So when things seem hard and you feel you not cut out for the job, remember that God choose you to be a special mommy and he never makes mistakes…. I decided to add Leah’s sleep time song…..

4 thoughts on “The “Special needs mom”

  1. Charmaine- It is reason’s like this I remember why God chose us. What you wrote I can relate too 100%.

    Thank You!!!

  2. What a beautiful post! It sure doesn’t take long to realize how special and important these children our to us and our lives 🙂 I am so thankful for both of my children and am so thankful that Kaela has already been able to teach me and so many others so many things already! And it’s great having such a wonderful support system and friends out there 🙂 I look forward to the day we can all meet! 🙂

  3. I’ve read your blog for some time, but not sure I’ve posted yet. Very sweet and sincere post. Amazing how much our lives have changed. My little girl Elizabeth has achondroplasia too. She’s 3 and the light of our lives. Amazing how our journey is so different than I thought it would be – yet just wonderful.

  4. I can completely understand where you’re coming from. It’s amazing…how God knew what he was doing when he gave us our little “special” kids, isn’t it? I’ve always known that Jamie was given to us for a reason. I believe it was to teach all of us, everyone in our family, patience, compassion, and unconditional love. And Jamie has done that for a lot of us.

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