Skip to main content

"I Hear You and I See You"

A friend texted me the other day and said, "I hear you and I see you". Those words meant more to me than most other words have. Hearing that someone hears and sees me was an overwhelming sense of peace washing over me.

I don't need people to hear and see us in a "look at us and everything we do" kind of way. I don't need people to hear and see us in a "Oh, you poor things" kind of way. I so desperately want someone to come along side us and say, "This is hard. And it sucks. And it's exhausting. It's not what you expected and it's totally okay to feel whatever you feel". I want, no, I need people to come along side us and say, "I hear you and I see you".

As I think back to that text, I cannot help but think of how God orchestrated that so perfectly. I so desperately want a human, someone psychical, to come along side me and say those things but God says them to me everyday. The fact that I felt an overwhelming sense of peace wash over me after I read those words from that dear friend, tells me that God needed me to hear those words to remember that He says them all of the time. He hears us. He sees us. He's sad with us. He knows how exhausted we are but He gives us fuel to keep on going. God places people in our lives. God knew I needed that text. God knew that I needed that reminder. And I don't think wanting to hear "I hear you and I see you" from others is a bad thing, as long as I am acknowledging that God says it everyday and I am turning to him too.

Comments

Popular posts from this blog

A Letter To My Kiddo With Disabilities

Hey Kiddo,  When your dad and I first found out you were going to be part of our family; I couldn’t stop myself from dreaming and having goals for you. I was excited to watch you play soccer and be in the band. I was excited for you to love reading just as much as me. I even thought about what your long term future would hold and if you would get married and have your own kids.  The day of your birth was one of the happiest but also the scariest day of my life. We almost lost you. But thanks to an awesome, loving, gracious God and your amazing doctor, you were able to stay here on Earth with us. You survived our nightmare. You were not given very good outcomes in the NICU but that has never stopped you from progressing and flying past the expectations they put on you.  My dreams for you changed, that day in the NICU when they told us you have HIE and likely will develop CP and a list of other diagnoses and to never expect you to lead a “normal” life. Instead of dr...

NICU

The NICU. This is one post I wish I didn't have to write. And I suppose I do not really have to, but it is such an important piece to this story, that it felt wrong to leave it out. We spent 19 days in the NICU. 19 days. Those were the longest 19 days of my life. We arrived there just hours after Bren was born. He was started on a cooling treatment. This treatment cooled Bren's body down but the true intent was to stop any secondary brain damage from happening. Cooling treatment lasts for 72 hours. Bren was scheduled to end this treatment and start warming on Saturday morning. Bren had a rough time warming up and did not actually complete the treatment until Sunday afternoon. 4.5 days. That's how long the treatment took. That's how long it took for me to be able to hold my baby boy. You see, I wasn't allowed to hold him when he was cooling because holding him would allow his body to warm up too much. That was hard. Really hard. I couldn't hold and comfort my b...

Dear Mama

I recently read a blog post where a woman wrote a letter addressed to herself before her daughter was diagnosed with CP. I learned a lot from that letter and you can read it here. One of the things that really stuck out to me was when she said "Her progress doesn’t solely rely on you; she will go at her own pace. Follow her lead and be strong for her". I cannot tell you how many times a day I see Bren's lack of progress as a failure on my part. Because here's the thing; I am with him almost 24/7. I am taking him to this therapy and that therapy, this doctor's appointment and that one. It's easy for others to tell me that it's not my fault and Bren will do what he can when he can and it's so true. He will and just because he doesn't do something we have been working all day on, does not mean that I failed. I love letters. I love getting things that are thought out and filled with so much love. Words of affirmation are my thing. I love to give th...