The day before our appointment Parker projectile vomited, everywhere. This also added to my level of anxiety regarding him getting sick again. I told the doctor, "So, Parker projectile vomited everywhere. I fear this is the start of something bad. This is exactly what happened last time."
She looks at me and nods. Says nothing. Absolutely nothing.
You know those awkward times when you are waiting for a response, but you just get a stare? That was this situation. Then, I ask, "Sooo I guess we have to just sit here and wait? You can't do anything?"
"Yes," she replied. "I understand why you are scared and nervous, but he doesn't have a fever," she adds.
So, we took Parker home and continued to try to find a new definition of what our lives would be. Not going to lie, I was looking for the vomiting and fever to commence at any moment. It never did. No matter how hard it is, you have to continue living and just find a way to be normal. At this moment I still have no clue what normal is for us. I have become quite the helicopter parent, hovering over everything Parker does. I examine his diapers, monitor his food intake, take his temp several times a day and check his entire body for strange rashes. I can safely say that I drive both Casey and Parker absolutely crazy with my hovering antics. Sometimes they need to put me in time out.
While we've been home we have known about a couple of our closest friends who were planning on giving Parker two benefits. This entry is a day after our first benefit. Some of our dearest friends and family pulled off a very successful event in honor of our sweet angel baby.
When you find out that someone is giving you not one, but two benefits, you are just at a loss for words. That is hard to admit, because frankly, I am RARELY at a loss for words. The love and support people have for our family just overwhelms me - in a very good way of course.
I mean there are t-shirts out there worn by hundreds of people for my son! How freaking awesome is that!?! Talk about Hydrocephalus awareness! You can bet a ton of people at Wal-Mart check-out lines will be Googling Hydrocephalus, now.
As Casey and I were preparing for the benefit a lot went on in our little family that people are unaware of. Most of the attendees were unaware that Parker still wakes up every hour at night and I had slammed three AdvoCare Spark drinks, having only had less than 3 hours of sleep. We try everything to keep him comfortable because his incisions are still healing and he suffers terrible headaches in warm weather. The day of the benefit, Parker spit up every single bottle, which is very much not normal for him. His temp was slightly elevated and there was one point in the afternoon where I decided I wasn't going to attend the benefit because I was so worried about him.
When he spit up yet another bottle I sat on my couch and sobbed to my mom,who was all set to babysit him for a couple hours so Casey and I could attend the benefit together. I was literally crying my eyes out because I continue to fight blinding anxiety over my son's illness and when he will get sick again. I am in constant fear of losing my baby. My mom just sat there and listened to me. She listened to all of my fears and anxieties. When I was finally done sobbing she decided to speak.
"Cait you can't always worry about him. Babies spit up. Babies cry. Babies get fevers-especially teething babies," she said.
I reply, "Yeah mom, but those babies do not have a stupid brain disease. Those parents don't live every single day on edge."
"Those moms don't huge their babies not knowing if that's the last hug they will get in a while. I NEVER know when he will be taken away from me again," I add.
Her eyes fill with tears too. It pains her to see her daughter fight so hard to have a normal family. She continues on that my basket-caseness (exact words God love her) rubs off on Parker. He can sense my anxiety and when I'm a mess, he's a mess. Basically she told me to buck up and leave. She raised two children and they were fine.
Okay. I get it. There isn't anything I can do to stop an infection or malfunction. If it's happening, it's happening. Sometimes you have to let the cards play out. It's just...hard!
I was an absolute nervous wreck for this benefit. Being the center of attention is definitely not at the top of my list and if we weren't bringing Parker I'd say some of the attention was deferred to me. We took Parker in the morning to send the golfers off. When I opened the door to greet everyone, baby in hand, I couldn't believe it. I saw so many people who haven't even seen him. I have an almost 6 month old baby that people haven't been able to see because he has spent almost half of his little life in a hospital. These people not only include close friends, but family as well.
My husband was nominated to say a few words, because Lord knows, I could not handle it. I can write and hide behind the computer screen, but to get up in front of people and speak about Parker in such an emotional state, noooo way. He definitely did it and was amazing. Actually he wrote much of the speech himself only asking me for a little input. During his "Thank You" speech at dinner I started crying, shocker. I just never pictured myself, here. Who would? I know. No one would. But to be here and living this life. It was just a lot of "heavy" going on in that moment. When he was done I excused myself and sat in the bathroom to regain composure.
"How did we get here? How is this my life? How is this MY benefit?"
When i excited the bathroom, I realized that everyone was in such amazing spirits during the golf outing and dinner. I had a really hard time not crying through it to be completely honest. I wanted to cry, mostly happy tears, but sad tears too. Sad tears for my sweet baby. This was a reminder of what he has and will continue to endure with his illness. It's such a heartwarming experience to have so many people who care about you and your family, all in one room. I did not know most of the attendees, which only added to the warmth my heart was feeling. They haven't even met Parker, but their heart and prayers go out to him. People offered me words of encouragement.
"Keep on keepin' on!"
"You, my dear, are amazing. I do not know how you do it."
"I pray for your son every single night."
I mean the list goes on and on. They've never met me, but for some reason, our story has made it's way to them and touched their hearts. So much that they purchased dinner tickets, bid on silent auction items and introduced themselves to me to show their support. I still cannot believe it.
By time the night was over I literally went from feeling like the most unlucky mom to the luckiest mom in the room. All of these people. All of these smiles! The energy and optimism they had was exactly what we needed. Even if the monetary donations weren't involved, having people there to show their support was more than enough. We weren't alone in fighting this battle.
Casey and I cannot even think of a way to thank everyone. I mean, as I've said before, I am at a loss for words. We woke up today a little groggy and speechless. Parker was of course an angel for his Nana, having not spit up AT ALL after I left him. He woke up working on his fitness in his crib, entertaining himself so much that we didn't even know he was up. We had a heart attack at 6:45AM without his wake-up call.
Someday I will share these stories with Parker. I will let him read my blogs, certainly when he's old enough to understand, and express to him how much he is loved not only by his parents, but by so many others. I will stress how lucky he was to have the opportunity to grow up in such an amazing community. A community that acknowledges the hard times and celebrates the good. A community that saw him through high school graduation and continued to lift him up, when he was down. A community that prayed for him every single night. A community that shared in the tears his mother shed and helped wipe them away. Lastly, a community that showed his parents what love and support could mean.
We are forever grateful to the planning committee and participants in the benefit. You have given us so much love and support and it is our hope that this is the beginning of something very good for our little family.
Blessings and love to you all!
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