by Band Back Together | Sep 30, 2016 | Anger, Anxiety, Compassion, Denial, Depression, Emotional Regulation, Faith, Family, Fear, Feelings, Grief, Guilt, Help For Grief And Grieving, How To Cope With Post-Traumatic Stress Disorder, Post-Traumatic Stress Disorder, Self Loathing, Shame |
This is her story:
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.”
…because they did.
And I can’t seem to find my old self again.
by Band Back Together | Mar 14, 2016 | Adult Child Loss, Anger, Depression, Help For Grief And Grieving, Loving An Addict, Prescription Drug Abuse |
There are days when I sit and think about my son’s addiction. I think about everything I did do, didn’t do or should have done. I start to disassemble his entire journey in my mind trying to find the missing piece. That piece that somehow I overlooked during our struggle for recovery. You see, my son had the worst outcome. The one every parent dreads but would never allow the thought to even cross their lips. My son overdosed and died of the very pills he was given to manage his post op pain.
His addiction snuck up on us like a thief in the night. Carefully and quietly taking us by surprise. Like the elephant in the room, we all knew there was a problem but no one had the guts to say the words. I called it our dirty little secret. Keeping it safe and sound between me and my addict son. Protecting both of us from the ugliness of the stigma attached to this most misunderstood disease. We had brief periods when we were given a glimpse of normal, tricking us into believing the demons had lost their grip and moved on. Then reality would hit as my son returned to his world of darkness and chaos dragging me along for the ride of my life.
His addiction consumed me as I struggled to find places where he would stay safe and I would get a much needed break from the endless worry constantly dancing in my mind. Finding the right fit of rehab was like finding a rose in six feet of snow. I fought to get him in and he fought to get out. Never feeling like the help and support he needed was available wherever he was staying at the time. I’ve learned that helping the addict is like matching fingerprints. Almost impossible. Hindsight is such a great gift if only it arrived before things were said and done, people were trusted and money was wasted on places that made promises that could never be kept.
There are days I feel like I failed him. After all as mothers our job is to keep our children safe. I have a double whammy. I’m not just a mom but also a nurse, a fixer. The very idea that I could not fix my son horrifies me. I allowed myself the sick illusion that I was in control of his addiction and I had the power to fix him. Even when that little voice of reason resonated through my brain, and was echoed by close friends and family, “you didn’t cause it and you can’t cure it” I still continued to beat myself up dissecting every fight, every rehab, tough love, no love or tons of love that we lived during his battle. Being the lone survivor of my sons addiction is a life sentence. I’m still shocked that he is gone. It feels like the beginning of my end. I have become my own personal punching bag. I have a million reasons why his death is my fault. I should have… begins my sentence when close friends try to set me straight.
There is nothing that can change my mind. I should have been able to save him. I had years of practice. So now my painful reality is every parents nightmare. Now, I must figure out a way to go on without him. I have become a sounding board for other mothers living the nightmare of addiction. In the midst of my struggle for survival and my fighting back at the broken system, I have made many contacts. By channeling my anger to make a difference I have stumbled upon people who have started the walk of grief before I joined this club. Together we find strength and hope that the bigger we grow and the louder we become the harder we will be to ignore. Parents whose prior struggle was to save their children. Working together to fix the breaks in the system we have come to know too well. A system that fought us when we were begging for help, a system that turned its back on a generation of addicts pleading for their lives. My son’s struggle has ended. Mine has begun. Everyday is a struggle. Trying to ease the pain that grips my heart and fighting to find joy in a world that has turned upside down. My new normal is just that, so new that even I have trouble adjusting. I pray for acceptance. I pray for peace. Until then I survive one day at a time.
by Band Back Together | Oct 22, 2015 | Asperger's Syndrome, Autism, Grief, Help For Grief And Grieving, How To Help A Parent With a Special Needs Child, Parenting, Special Needs Parenting, Speech Disorders |
I am the mother of identical twin sons. They turned two in November.
At 12 months, they seemed to be moving right along in their development. They were walking, starting to say words; everything seemed fine. I was a little worried they were late in talking, but they were talking, so that was something. By 15 months, they still had very few words but they were both doing some signs and also had a full repertoire of “action” songs in their arsenal. By 18 months, there were no words. None. No signs. No action songs.
Everything was easily explained away as a boy-thing, or a twin-thing, or an identical-twin thing.
We tried not to worry.
Friday, they had their first visit with Early Intervention. I wanted to get their speech back on track as soon as possible. Language delays were our number one concern. Of course, in the back of our mind, we’d thought about autism, but we weren’t going there unless we had to. It’s too difficult.
After thirty minutes of watching the boys “play,” and watching their interactions with me, the Early Childhood Development teacher and the Speech Pathologist, there was an early diagnosis of sorts. They weren’t as concerned with the language as they were all of the other things: they didn’t really play with their toys, they didn’t really interact with, well, anyone in the room.
Early Intervention wanted to proceed with autism evaluations.
The next thirty minutes involved me, sitting on a chair nursing my four-month old. Trying to not to break into an ugly cry, trying to keep it together and sound somewhat intelligent until I could get all of these people who just brought my whole world crashing down, out my door.
My sons are perfect.
And I don’t know how to fix them.
by Band Back Together | Oct 8, 2015 | Anniversary Reactions, Baby Loss, Child Loss, Coping With Baby Loss, Coping With Losing A Child, Family, Feelings, Grief, Help For Grief And Grieving, Loss, Loved and Lost, Stress, Trauma |
First, people are afraid of what to say, and often say nothing. This is a mistake. Many people are afraid to bring up the deceased child, fearing it will open wounds and raw feelings. But in my opinion the hardest thing is when people don’t talk about Maddie. It feels like she was never here, and this is what is heartbreaking. It is nice when people say, “I thought of Maddie today,” of “I saw a kid in a dress like the one Maddie wore at whatever today.” Or “I miss Maddie.” These things help, not hurt. Make us feel she is not forgotten. Sending a keepsake with the child’s photo or name, things that help her be tangibly remembered are nice. We have received AMAZING things and we cherish everything.
Six years ago, one of my friends lost her father. I was living across the country from her, and I was terrified. I felt guilty that I had my dad and she didn’t. So I didn’t say anything, and I ruined our friendship for a while. I am very lucky she gave me another chance. She has been there for me since Maddie passed away. I have horrible regret about the whole thing – all I had to do was call her and say, “I’m so sorry.”
Religion is a potentially explosive way to comfort. Unless you absolutely know 100% percent the person will be comforted by mentions of faith, don’t go there. Religion is a very complicated thing in the wake of a child’s death, and they may be angry at God or confused as to how to incorporate the death of a child into the religion that they have known to have their best interests in mind. Even someone you know to be intensely religious may be having a crisis of faith in the wake of a child’s death, and could be angered/saddened by mention of religion. Especially stay away from, “God wanted her more than you,” or “God needed her more,” etc.
I don’t care if it is the all powerful creator of the universe, you don’t tell any Mama that anyone wants her baby more than she does.
So many people hate seeing their loved one in such pain and want to fix it. Consequentially, they start talking about how you have to move on, that you will see them again, the child is with God, it will get better in time, etc. All things they think will “fix it.” Don’t try to do this. Follow the lead of the parents. Discuss what they want…if they go to those places you can discuss those things, but don’t try to steer it there. Sometimes I want to talk about Maddie and the unfairness of it all, and other times I want to hear funny stories or talk about reality TV.
Don’t be afraid to show emotion. Many people feel they have to be strong for their friends, that they can’t cry or show emotion. I don’t think that is true. You can be strong AND be emotional. If tears come, don’t fight them. This shows your friends that you, too, are crushed and sad and lost.
Address the horror. People often worry about addressing how awful the situation is, but the parents want to hear that people get the hell they are in. The parents feel alone when they don’t think people understand how awful this is. Saying things like, “This is the worst thing. I am so sorry and sad that it had to happen to you and your child,” helps.
Food is very helpful. The last thing you want to do when mourning is worry about eating. There are always people around after a death, and the last thing you want to think about is feeding them. Mike and I never would have eaten if food hadn’t been sent to us. A gift of food also tells the parents they are loved.
Say or express something you never have before. If you have never told the person that you love them, come right out and tell them that you love them. If you’ve never held their hand, hold their hand. Give hugs. These expressions mean a lot.
Finally, my biggest advice is to not be afraid to take initiative. We often say, “let me know what I can do,” in a situation like this. Well, I can tell you that Mike and I had no idea what we needed. We were so lucky that we had friends and family rally together and just take care of things. A few came to town to help out. One friend organized food, another cleaned my house, two bought the clothes Mike and I wore to the funeral, one put together Maddie’s slide show, a few organized the reception after her service. I could go on and on. I didn’t have to worry about anything because I knew my friends and family would handle it.
Be there for your friends. Call, email, text. Tell them they don’t have to respond. Let them know you are thinking of them, and their child, all the time. Don’t drop away after the funeral – that’s when they’ll need you the most. Be the kind of friend that you would want to have.
by Band Back Together | Sep 15, 2015 | Blended Families, Cancer and Neoplasia, Caregiver, Chronic Illness, Coping With Cancer, Grief, Help For Grief And Grieving, How To Help A Friend With Chronic Illness, Loss, Parent Loss |
Part I Here
My memories of the time between when Mom was admitted and when she left for Houston are jumbled. I know with Mom gone, running the house largely fell to me. I would get me (age 8), my sister (age 3-4) and my Dad up in the mornings and make breakfast. I remember having burns on my thighs from wearing my night shirt while cooking bacon in the morning and the grease would pop and splatter me. I remember learning how to do laundry and having to have a step stool so I could climb on top of the washing machine so that I could reach the soap. I remember sitting on the sofa attempting to hand-sew a hole in my underwear closed.
Through out the summer we spent a lot of time with various family members and random people from our church who volunteered to look after my sister and I for a day. That was probably the hardest. Every house had different rules. One house I sat until I was near starved b/c I’d been taught it wasn’t polite to ask people for food. When the woman found out she was like “oh honey you just have to speak up or better yet go serve yourself!” Then the next house I got in trouble for trying to do just that. Some houses they’d tell me I could eat anything I wanted and others I was told that beggars can’t be choosers and I should eat ONLY what they offered me and eat every last bit.
Then there was the boredom. Some people had kids who would share their toys. Others did not – either the kids were grown or the kids wouldn’t share. Or they’d want to watch a movie I wasn’t interested in or what not. The sweetest woman, I have no idea what her name was or I’d write her a big fat thank you note all these years later, discovered I liked to draw and she bought me a BIG thick fat loony tunes coloring book and a box of 64 crayons. I swear that book saved my life with all those days of house hopping.
I also discovered reading. But mostly I discovered how to fake reading…. Nobody would tell me exactly what was up with my Mom. They made this big show of how Momma would do 6 weeks of chemo therapy (counted it off on the calendar with us and everything) and then she’d be all better and could come home. That was a lie. I don’t know if it was intentional or just misinformed but either way when the info changed they didn’t tell me directly.
And so I’d pretend to read a book and listen while Daddy talked on the phone. I even remember him saying “Oh nah, its okay, she’s reading a book. She’s not listening” and he would talk about chemotherapy and radiation and bone marrow transplants. I didn’t understand what those words were exactly but I caught the gist of it. Daddy seemed to underestimate my vocabulary and comprehension back then. Where as my Mom always just talked to me like I was an adult and I’d just have to stop her occasionally to have her define things.
It was funny, at one point they put me in class with one other little boy and some type of teacher there at the hospital where she tried to give us the “My Mommy has Cancer” after school special or some such thing. I was so excited to finally have a person to ask all my questions to. I immediately started asking about chemo etc and she about freaked. I think she would have put her hands over the ears of the other kid if she could.
As it was class was HASTILY broken up – me with one teacher where I asked all my questions and the little boy went with some other person to get the kiddie version.
Our days went something like this: we’d get dropped of with whoever was watching us that day, Dad would go to work, then he’d come and pick us up, we’d go visit Mom in the hospital. My sister and I would wear masks b/c the docs explained that we had cooties and would make Momma sick (oddly enough she never once got sick from my sister and I but she caught a dozen things from Dad). And then later in the evening we’d head back home and I’d lay across the foot of my Dad’s bed pretending to read Black Beauty while he talked on the phone.
In retrospect, Momma mostly looked good at the time. I remember she lost some weight and when the chemo got started a friend of hers who was a beautician came the hospital and gave her a hair cut. My Mom had had the 80′s big curly shoulder length hair and her friend cut it off to a ultra short pixie cut. They explained that this was better since the chemo would probably make her hair fall out and it wouldn’t make such a mess this way. I remember being shocked but liking it.
I missed being able to give my Momma kisses but at least we could scramble up into her bed and cuddle with her and get hugs. We’d bring her pictures we’d drawn to decorate her hospital room. And we always loved to see when other people would bring her balloons. She couldn’t have flowers so if somebody forgot and sent her them they’d hold them out at the nurses station and we’d take them home with us at the end of the night. I liked that part because I loved fresh flowers but I sure wished I could share them with Mommy.
Then they began to talk in earnest of transplants. Momma needed a donor and a hospital. At the time there were only 3 hospitals in the country that did the transplant – one in Tucson, one in Seattle and one in Houston. At the time we lived in Phoenix and so Daddy asked the doctor, “Well, Tucson is closest… whats the difference between the them?” The doctor replied that, “Well, right now, Tucson has about a 13% success rate, Seattle is running 20% and Houston is doing 50%”. My Dad stared at him for a minute and went “Ya know Houston sounds GREAT to me.”
I remember the search for a donor. They started by testing all of my Mom’s brothers. Adam and Sam went first and neither was a match. They’d wanted to avoid putting Uncle Mike through the stress because he had a heart condition, but he agreed to be tested. By this point, I’d caught on that if Mommy didn’t have a bone marrow transplant that it was going to be bad. I wanted them to test me. I didn’t care if it hurt. I was willing to do anything to save my Mommy.
Momma was dead set against my even being tested. She said it hurt too much and she didn’t want me to go through that. I was set and ready to be stubborn and fight long and hard for this if I had to but thankfully it turned out my Uncle Mike was a match.
So now we had a donor and a hospital there was just one more major roadblock: money. The insurance company was refusing to pay for treatment. There was some sort of government assistance available but they didn’t want to pay either and MD Anderson wouldn’t let us come unless they got a down payment that was either 30k or 3k I don’t remember. I was 8 at the time but I remember it was wayyyy more money than we had. My parents had always been on the verge of broke though they worked hard to provide for us but the medical bills quickly piled up and wiped out whatever was left of their finances.
And so, I don’t know who all organized it but they had a big benefit dinner to try to raise money for my Mom. A local grocery store donated steaks, family friends provided entertainment, and Kodak (my Dad was a professional photographer at the time) donated door prizes. I know the tickets were like 100 bucks each. We raised a ton of money with that dinner (I can’t remember exactly how much) but it was still far short (less than half if I recall) of what we needed.
Unbeknownst to me at the time, my father’s childhood best friend, an attorney, sent a letter to the hospital and the government and explained that if they continued to delay my mother’s treatment while they quibbled over the money and she died that we would sue them for everything that the mother of two small children was worth.
The day after the benefit dinner, we got word from the hospital that they’d let us come after all. We only needed to pay less than half the previous amount in advance. I don’t remember the numbers but I remember it was almost the exact amount we’d raised at the dinner the night before. It was a miracle.
A small army of sisters from church came to the house and packed up everything. My sister and I went to live with my grandparents while Mom and Dad went to Houston.
The day they left we went to the hospital early. Mom was in street clothes for the first time in months. They wheeled her in a wheel chair out of the hospital and to a waiting limo. I was so excited, I’d never been in a limo before. Daddy explained that taxis had too many cooties and they wanted all of us to be able to ride together so they’d gotten a limo. I remember my Mom and Dad piling into a little leer jet complete with a small medical team to monitor Mom through out the trip.
I hugged my Mother goodbye for what I was scared might be the last time. I had know idea if I would ever see her again. And then I stood next to my Grandma with her arms wrapped around me and I sobbed my little heart out as I watched the plane back up and take off.
Part III Here
by Band Back Together | Sep 13, 2015 | Anxiety, Bacterial Infectious Diseases, Caregiver, Chronic Illness, Fear, Grief, Help For Grief And Grieving, How To Cope With A Suicide, How To Help A Friend With Chronic Illness, Infectious Diseases, Invisible Illness, Lyme Disease, Stress, Suicide, Trauma |
Click here for Part I
Everyday I feel like I am going to die.
It’s pretty difficult to sleep at night when you are afraid that you won’t wake up in the morning, leaving your 18 month old motherless. And in the *capable* hands of your husband who, when it’s his night to make dinner, relies on boxed Mac and Cheese. Without me he’d probably revert back to Kraft, leaving organic Annie’s behind.
Neurologic disorders are their own beast, I think. The symptoms are literally all in your head, and yet you feel them everywhere. My feet tingle. Sometimes I can’t stand the feeling of pants on my legs because my nerves are hyper sensitive. My hands go completely numb some nights. Just a minute ago I was pretty sure that my tongue had stopped working and that maybe I was having a crazy allergic reaction. When I touch the skin of another person, sometimes it feels like it’s burning.
I’ve been to the ER too many times this last year. At first it was chest pain, which was treated with Ativan. Turns out I have chest wall inflammation. Advil was much more helpful than the anxiety drugs, but I’m a woman so must be crazy. Then I went to a doctor for what felt like the flu in the height of the swine flu outbreak. She listened to my heart, which had become tachycardic. She thought I was having a thyroid storm. Nope. Just Lyme disease. (It would have been helpful to know it was Lyme then.)
Lyme is also extra special because it causes psychiatric changes. Remember IRENE from the Real World? Don’t you wish you were my husband? I swing between uncontrollable anger to lying on the floor thinking about death. Suicide is actually the leading cause of death for people with Lyme. When I was first diagnosed and reading about the disease, I couldn’t figure out why there were links to suicide prevention lines. I get it now.
And then there’s the memory deficits. I’ve always had a really sharp memory. My mom hates me for it. Pray that your children don’t remember every phrase you ever uttered to them! I’m also a word freak and can kick some serious Scrabble ass. But now, I have trouble remembering the word for “countertop” (yep, happened the other day). I don’t know how to spell things. And I often just stop in the middle of a conversation unsure of what we were talking about or what I was saying or what I want to say next.
My stomach hurts. My knees ache. I lose my sense of taste sometimes. I can’t sleep, and yet I’m profoundly exhausted. I get night sweats. Bright lights bother me. And low lights bother me even more. I feel jittery and can’t sit still. But I’m too tired and sore to move. And I constantly feel like I’ve just gotten off a Tilt-A-Whirl, that’s how dizzy I am.
This is my life. I don’t tell you this for sympathy. I tell you it because it’s real. And frankly it scares the shit out of me.