I’ve been suffering, silently, for going on eight months…I guess. And, I’ve needed and wanted to write about it. But, I’ve been afraid. Mostly, I’ve been afraid of the emotions that come flooding back to me when I think, talk, or picture the experiences that led up to this day.
Actually, I don’t know when it started. But, I finally said something last week to Mr. B and my Momma.
This suffering stems from an accident, on July 19, that involved my 7-year-old son.
Bubs was in a golf cart accident with his grandfather. The 800-pound cart, fell on a 45-pound baby and drug him on concrete for quite a distance. Bubs was air-cared to the local Children’s Hospital. And I, well I was 39 weeks pregnant. And, I fell when I saw him. Literally.
I fell because my son, my first born, and my best friend was trapped. Under a machine. He was covered in blood from “road rash” and he was broken. everywhere. He suffered with a dislocated hip, broken femur, butterfly fractured femur, crush-fracture of his foot, dislocated toes, puncture wounds and road rash all over his body and a removed quadriceps muscle. When I stood from falling, there he was, screaming for help and frantically searching for his mommy. And my heart couldn’t take it. It was broken.
In that instant, I was changed. Forever. I can’t forget the pain of driving to the scene. The soul crushing fear that flooded through my body the way I imagine Hurricane Katrina taking over New Orleans – engulfing your body with no hope or relief in sight. The fear and pain took me to a place that had not existed prior to this accident. And now I can’t seem to find my way out of it.
I still remember the scene like it was a dream. There were people rushing all around me, ambulances screaming to the scene, a helicopter circling overhead, paramedics asking questions…about him…and about me, paramedics taking blood pressure, police officers begging me to go to the hospital. I was swarmed but still felt invisible. All I wanted to do was go back in time. Just 20 minutes earlier. To make this moment disappear. All I could think about was this “never happening” and how it “couldn’t be happening” to us.
I am ashamed to admit…but, I didn’t care about the baby inside of me in that moment. Because the boy who had my heart first was seriously hurt. More serious than I even knew or wanted to know in that moment. More serious than anyone was willing to “tell the pregnant mom.” It was hard for me to consider the unborn child. I “knew” right where she was and I “knew” she was okay. All I knew was I heard words like “internal bleeding”, “head trauma,” “internal damage” and “spinal cord injuries” being thrown around…regarding my baby. MY baby. It was as if I was having an out-of-body experience.
I still remember the paramedic who took me to the hospital. His attempts at consoling me, while my son flew overhead, were heroic. He was kind and gentle and was a true professional. There are no words that can describe these moments. No words created by man that can put your thoughts and fears on paper to describe the instant you think you may lose your child. It’s a pain like I’ve never known. A pain that was sharp and reckless and it had no concern for me or the perfect family I had built.
And now, it has been replaced with fear.
As I sat in the hospital waiting room, waiting for his six hour surgery to be complete, and cried. I cried for my unborn baby, who would be born into a world interrupted. I cried for me. Because I was afraid and exhausted and broken-hearted. But mostly, I cried for my baby boy. Because I didn’t know what the future held anymore. 10 hours prior, I knew. And now my world was crashing in around me. I couldn’t breath.
See, Bubs and I started on this journey alone. Mr. B was our answered prayer that came four years later. For four years it was just us…and nothing will ever match those four years for our small family. Nothing will ever match the bond we built. He is my best friend. My confidant. My companion.
I am suffering silently with Post Traumatic Stress Disorder. I am struggling every.single.day with constant fear and irrational thoughts. I become overwhelmed with illusions, memories and possibilities…which all hold me back from living. These fears consume everything I do. Everything I let my family do. And, they consume every thought I have. I catch myself living in a world of “what-ifs” rather than just living and loving life. (Loving the life that God so graciously spared last summer.)
And, even with Bubs upstairs sleeping in his bed. Even if we made it through 12 weeks in a wheel chair and two weeks in a walker and one week of God-fearin’, earth rattling pain and torture…I still can’t shake the memory.
I still live in fear of losing someone. And not just Bubs now… Mr. B, Bubette, my mom, dad, step-dad, cousins, aunts…it is growing. And, for that reason, I have decided to talk to someone who knows more about this than I do. A professional….which makes me feel like a nut job.
Because prior to July 19, I lived in a beautiful world where horrible things happen “to other people.” and now…well, I can’t help but think that those horrible things “could happen to me.”
Last year, Stand Up to Cancer asked me if i remembered what i was doing on september 11th, 2001. I did. I still do. This is what i wrote:
su2c asked on twitter if we remembered what we were doing eight years ago on September 11th, 2001. we were living in manhattan. i was on my way to work. the streets were filled with frantic police officers. it was horribly loud, as manhattan so reliably is, but you could feel an eerie silence beginning to settle over the city.
there was a mass exodus on foot. people fled the city via every bridge possible. the subways and trains weren’t in service. grand central was locked down because of the bomb threat. our building was locked down, too. a cell phone signal near impossible to come by.
nuggetdaddy was working in new jersey then and i was finally able to get a hold of him. we decided i would take the first train out of the city and he would pick me up wherever we could both get to. i made it on the first train out of grand central. it was sweltering. the train filled with an acrid stench. most passengers were covered in a heavy white dust; most in more than their fair share of blood.
it didn’t matter where the train was going, people just got on in hopes of making it out of the city. the train stopped at every single station en route. it took forever.
nuggetdaddy picked me up at the fleetwood stop and we decided to try to drive back into the city. we had pets and friends to check on. family and friends desperate to hear our voices. we were finally able to make it back in over some tiny bridge in the bronx.
by now the city was silent. there were no planes in the air, no people on the streets. when we woke up the next morning the wind had changed direction. the stench was unbearable. we stayed in the apartment all weekend, happy to be alive and at home with the pets and dr. roommate.
so, stand up to cancer, there’s your answer.
and speaking of stand up to cancer, did you watch the telecast last night? did you donate? did you help find a cure? did you save lives? did you stand up to cancer?
Maybe a favorite piece of jewelry? Time? A friend?
My mother-in-law lost her battle with cancer just a few weeks short of my second wedding anniversary. She was an amazing woman. And I’m not just saying that. Everybody adored her. When you think of the ideal mom, that was her. She had a ton of friends that sang her praises. She volunteered with the American Cancer Society to drive elderly people that couldn’t drive to medical appointments and to run errands. She would do anything for anybody. Thoughtful, warm, beautiful smile.
Clearly, she was not a likely candidate for cancer!
Clearly God wouldn’t tear an angel from our hearts!
But we were wrong. Less than a year before her death, she was diagnosed with cancer.
Religion doesn’t play a huge role in my life. It is important to me, and I pray and thank God every night for our blessings. My mom’s best friend, a practicing Christian and strong believer, once told me, “God doesn’t care where you worship him as long as you worship him.”
So I prayed. I prayed that she would get better. I prayed that chemotherapy and radiation would work. I prayed the homeopathic treatments that she tried would work. I prayed for a miracle. I tried to bargain with God. If he let her live, I would never do X, Y, or Z again. If he let her live, I’d be a better person.
A few months before she passed, it was clear she wasn’t getting better. And that’s when I started to get mad. Why would God take someone so loved by so many? Someone that had not even met her son’s children yet? But I continued to pray.
Up until the night we got the call that she had passed away. We had been over to see her earlier that day, and knew that she was getting worse. We knew what was coming. We got to say that we loved her, and spoke to her privately. When we got the call that she was gone, I was shocked that she had actually died. I expected my miracle.
And I was pissed. Pissed off at God. All those prayers? They meant nothing. Why would he take someone that was so loved by so many people? There are thousands of murderers, rapists, and child molesters that deserve death – why not take one of them?
WHY, WHY, WHY?
The prayers stopped. I ignored him when I heard him trying to “talk” to me. Religion? Obviously a joke. Why believe in HIM if he can’t even help when you asked for it. There was no lesson to be learned. No epiphany to wait for. There was just sorrow and grief.
IT WAS NOT FAIR.
Does time really heal all wounds? I think it does. Because ever so slowly, over that first year after her death, I started to listen to him again. And I started to pray…occasionally. And when I invited him back into my life because I missed him, he gladly accepted me with open arms.
I still haven’t figured out the “why,” and I still don’t know what I was supposed to learn from her death.
In kindergarten, my daughter was singled out by her “crazy old lady/about to retire” teacher who said Maddie was “very inattentive and probably needed to be evaluated for ADD.”
I was all, “this women has a whole SEVEN kids to look after with a damn assistant! She obviously is lacking and totally sucks at life to not be able to handle SEVEN kids and she’s the one who needs to be evaluated. “
Unable to even fathom such a thing for my perfect little princess, I took her out of the expensive private school and started first grade in the public school. The local school a few blocks away is really new and great and shiny!
First grade began, and she seemed to be doing well until our first Parent/Teacher conference. Once again, ADD was brought up by her very young, energetic teacher.
Again, I couldn’t wrap my brain around this possibility. My daughter was so caring and sweet and there was no way in living hell there was something wrong with her!
But I relented, and took her to see the pediatrician armed with a heavy dose of internet literature regarding the scary ADD possibility. What I didn’t expect was to identify with most of the symptoms listed on the checklist.
So, with a heavy heart, I accepted that yes, my little angel was indeed struggling in school. She was beginning to show signs of a low self-esteem as a result of her poor behavior. She was showing the insensitiveness that comes with a child with ADD. She was unable to see how others may feel. She was pretty self-centered.
I waved my White Flag and tried to stop feeling sorry for myself or guilty for something I could have done to prevent this from happening. I gave up the idea that my daughter would be a stellar student and be the top of her class. I mourned (seriously GRIEVED) the possibilities I had built up all through her early years of how magnificent she would surely be. I shed real tears and experienced a heartbreak that I didn’t think was possible.
I felt extremely defeated until I buckled down and became her advocate. I fought long and hard to get her school to become involved in her special education program that would work for her. I went full speed ahead with every behavior modification the school could provide that might make a sliver of a difference.
Over the years, she was given an Individualized Education Plan (IEP) with in-school modifications for test-taking and a more thorough explanation for her assignments. Her seat was moved in order to minimize distractions and although she continued to struggle, she was really improving.
Along with the modifications, we began trying medication. I was overjoyed when we finally found one that really helped her without the harsh side effects. This process was heartbreaking, but we found the one that works for her and for this I am grateful.
So now, here we are in the fifth grade. Report card comes home and finally there are mostly B’s on it. There are two C’s, but compared to last year when she was mostly C’s and D’s this was such an amazing moment for me and her to see everything we were doing was paying off!
I was so excited that I wanted to dance around the room; this was not something that I am used to. This was something that has taken so long. I didn’t even it was possible to see a report card such as the one she got today.
After saying all of this, maybe you can understand why, after sharing with you my pure bliss, I would be upset when you complain to me, a whopping two minutes later, about the one B your daughter received on her report card when every other grade was an A. How I got frustrated, left the room and didn’t want to show you my daughter’s report card.
I do not make this a competition, as you so rudely accused me of. I would never have those sort of expectations for my daughter after every hurdle we have been through to get her to this point. That would just be unrealistic.
I know that your daughter is two years younger than mine and is enrolled in all advanced math and reading classes. I know that she is a very bright little girl and I would never ever try to diminish that! But I had a happy moment and you just don’t understand how complaining about that one B would make me feel. Here I was rejoicing all the B’s that were on Maddie’s report card and you were looking down on that very same grade; the one flaw on your daughter’s perfect grades.
So, just when I think we know everything about each other I suppose you don’t really know the entire story of the ADD path. And I don’t even know how to make you understand.
When you told me I was turning it in to a competition, it felt like a slap in my face. It showed me that your perception of me is way off. So now what? How do I make this better? After three and half years together, I love you. But I need you to be on my team with this. Not accuse me of a competition.
I wanted you to jump up and down with me and celebrate this victory.
Prankster, my heart goes out to you. I wish that I could wrap you up in a big hug so that you knew that you were loved. Because you are so loved. You are worth everything. I know that telling you that you need to stop won’t help and will further reinforce all that you do to yourself, so I won’t, but I am reading what you don’t say here, and it breaks my heart. You are worth saving. You can fight your dragon and you can win. Someday you will win.
We will be here waiting to celebrate when you do.
Much, much love,
Aunt Becky
I’m a sucker for it. And I could speculate about all the things that have caused it. My childhood wasn’t great. I’ve dealt with depression and all the shit it brings. I’m impulsive… but I have this feeling, deep down inside, that it’s just the way I’m wired.
The first time it happened I was 14, angry and frustrated and it just made sense. The scissors were right there… and just like that, an addiction was born. I was a cutter. I self-injured.
Of course, 14 year-olds aren’t the most logical thinkers, so I got ‘caught’. We did the whole therapy deal with a crappy counselor and I was expected to stop immediately, so I did.
But I wasn’t stupid. Since the age of 15, I’ve been dealing with an eating disorder. I’ve seen 2 shrinks since the first, and neither know about my eating disorder.
As with all addictions, I’ll never be cured. I never truly stopped, but my parents like to think I did, so I let them. I just got better at hiding it.
While I don’t cut nearly as often as I use to, I picked up a nice little friend, named trichotillomania (self-pulling of hair). It’s so great [sarcasm].
This would be one reason I think it’s instilled in me, I don’t want to give it up. It’s mine, all mine, and I don’t have to share it with anyone, which feels great.
So, maybe the day will come and I’ll be ready to give up the ghost. And if it does, I’ll come back, and I’ll let all of you know.
If you read my profile, you already know that I’m married 23 years with 2 teenagers; a daughter, almost 20 and son just turned 16. Four years ago I was diagnosed with breast cancer, went through a double masectomy, chemo, radiation and reconstruction. I was in remission up until 3 months ago when it was discovered that the breast cancer has returned, in the lining of my stomach, treatable, not curable (1% chance).
This is not to be mistaken for stomach cancer – confusing right?
Needless to say I went through the depression, anger and shock all over again. Only this time it was harder. The optimistic goal of beating it wasn’t as easy to grasp because it had already returned once.
My meds have been changed, my doctor’s visits are more frequent and the side effects more intense. Hotter flashes, sleepless nights and mood swings. I am not always the easy-going, jovial Queen that used to rule this Kingdom. No, I often become that dragon you referred to in the Bands write-up. But I allow myself to breath some fire, release some anger, then I straighten my tiara and return to my throne surrounded by my adoring and supportive family, my riches, my strength, my motivation.
I could fall in the moat tomorrow and get gobbled up by… well whatever lives in moats. I’m not going to let this Cancer defeat me and takeover my Kingdom…
I know I will have bad days but I also know that I will get through them with a little help from my army (my friends and family) …
Today was one of those bad days and then, suddenly, you appeared!