This is Becky's story's about her babies with wings. I want to thank her for sharing it with us. This is a painful journey and I am very happy she has written this for us. All of are story's are different but the outcome is the same, When we share our story's we can each learn what has helped us heal with our loss. Thank you Becky.God bless you and your family. |
Becky's Journey
Here’s my story…….
October, 1991, brought blessed news that my husband and I would be welcoming twins into our family, we were beyond excited. These were to be my husbands’ first children, two little girls. The pregnancy went well and then at 7 months I found I had gestational diabetes. This wasn’t a surprise since I had the same condition with two other pregnancies but has been successful in controlling it with diet and exercise. It was the same with this pregnancy as well. I immediately started the diabetic diet, got plenty of walking and with three other children to care for; mine from a previous marriage, there was always lots to keep me busy. The kids were so excited about having the babies and it was great to see them talk about what they would do to help. It was a wonderful time for all of us. We worked on the nursery, and so many friends surrounded us with love and support. At 35 weeks, I went into labor and we went to the hospital. The doctor I had chosen had been highly recommended, but he did not want to let me go through with labor, nor would he send me to a higher tertiary care hospital, his arrogance stood in the way. To make a long story short, his decision cost me so very much. He knew I was diabetic, and yet he took me off food, water, and wasn’t monitoring my sugar levels as he should and I went into akido acidosis and eventually a diabetic coma. The babies perished. This was the hardest thing we had been through either individually, or together, our children and family members were devastated. The coma took a toll on me as well and after 3 weeks in ICU, seizures, and a stroke, I found myself facing the difficult task of going home with empty arms. Together my husband and I vowed this would not put us under, and we clung to each other. Our girls came and left this world on Father’s Day, 1992.
I can honestly say our faith in God was what kept us going and we each grieved in our own way. There were times when I wanted to give up, but my husband kept me going and knowing my children needed me helped too. But, it was very, very hard. We had many good friends that were there from the time we went into the hospital, until long after we came home. It seemed that God knew when to have someone drop by, and many, many meals were brought from our church and these same friends. I don’t think I could have made it without them. Anyone going through this needs a network of friends and people to help them through it.
My husband grieved differently from me, often keeping a lot to himself, or throwing himself into his work. We did the best we could to talk and stay connected. It just takes time.
That is something important to remember, husband, wife, and existing children will all grieve differently and each will take different lengths of time to come through the process. Siblings need to receive counseling in order to ensure they are processing the grief and not feeling it was their fault, which tends to happen and my oldest daughter felt that way for quite a while,
even though we constantly tried to reassure her that it was in no way her fault.
It is a difficult rollercoaster ride, getting through the grief process, I read many books regarding the loss of a child, dealing with the grief, how to go forward after such an event –
The one thing I learned is that it takes time.
One thing I found that helped me, was that when I saw an obituary in the newspaper for a baby that had passed, I wrote to that family, sending them my condolences and my prayers that they would know they were not alone. I did this much time over the next year and it did help me to reach out to others. I would include my phone number and many mothers called me and we would chat, they said they appreciated the notes. It does help to know that you are not alone in your grief.
My husband and I attended a meeting once of a local chapter of parents that had lost children. I was totally shocked when I walked in the room and saw so many parents that had been through what we were experiencing, many of them more than once. It hit me square in the face – We were not alone! Others were going through this too and it was not a personal affront to us as a couple, or as parents, these things happen. It didn’t diminish the hurt, the pain we felt over losing our girls, or the loss of the dreams that we had for them, but it did help to know we were not alone. We only went to one meeting, that we enough for us to have that realization in our minds. Joining a support group is always a big help, and we had our church groups that helped through, though they weren’t specifically grief groups. What ever works for you is what you should be; there is no definite script to get through the process.
One thing that I feel is important for anyone going through this to know, you have to keep the lines of communication open between you and your spouse, or significant other that is going through this loss with you…you have to keep talking. Tell each other when you are hurting and be there for each other. I found that amazingly enough when I was down, my husband was up, and visa versa. Counseling is always a good thing and very important, we did, and probably should have done more. But talking with a professional and making sure you are taking care of yourself and each other is vital.
I found that people don’t really know what to say when they talk to you about what you have been through, and sometimes the things they say can be hurtful. It is difficult, but I had to let a lot of what was said roll off my back because it wasn’t what I needed to hear right then. They meant well, but just couldn’t relate to what we were going through. That is why it is important to find a group or people that have been through this to talk with you and comfort you. Sometimes people would say it was ‘for the best’, or any number of other comments and it was difficult to not react defensively because how could it have been for the best? It took a long time for me to realize they were really trying to help but just didn’t know what to say.
We tried to use our experience to help others. There were several occasions when someone we knew was expecting, had gestational diabetes, or other complications and were hesitant to ask their Doctor questions, for fear of seeming stupid…..ASK! Don’t hesitate to ask, if your Doctor is too busy to answer, then find another Doctor. You do not have to accept this kind of behavior and you have the right to have the best medical care possible. Doctors are human too and sometimes they can be distracted, so wake them up to what it is you need. Because we talked with several couples, their children were actually saved and that too gave us a feeling of something good coming from all our pain.
It’s been 17 years since I held those precious girls in my arms and cried for the lives they would never have, the laughter I would never hear, the smiles that I would miss. Again my faith tells me I will see them again some day, and that brings me peace. But though it gets easier, their imprint is always on my heart. I know it would be the same for everyone that suffers this kind of loss.
We tried to do things in their honor that would leave a footprint on this earth, donations were made, trees were planted in their names, and much more. You have to find what brings you
peace and comfort, for each of us it will be different. Be willing to reach out to others, and also be willing to allow others to reach out and comfort you when you need it. It is a hole
that will forever be in your heart, it gets easier in time to face the anniversary, to face the memories, but it will never go away. My girls, Alexandria and Victoria, left their tiny footprints on my heart and I miss them every day.
You can go on, there is life beyond the loss, and I pray that if you are going through this heartbreaking experience you will seek out a group or people that know what you are feeling, and allow them to help you. As I said, you are not alone. Please let me know if I can be of help. There are many great publications out there to help you through the difficult days.
God Bless.
Becky M.
Our precious angel came to us 6 weeks early on June 13, 2007. I got a call at work from the hospital, his mother was there and he wasn't doing well so we were having a baby today! What a plethera of emotions! Fear-it's too soon! Joy-we get to see him! Hope-please God, let him be ok! I got to the hospital just before they took his mom in for an emergency C-section and frantically changed into scrubs then waited and waited for what seemed like an eternity before they let me into the OR. His mommy was scared-me too! We had sent my husband to find daddy and they weren't there yet. We both waited to see whether or not we would hear a cry when they took him ok and then...a tiny little cry but a cry none the less! We were thrilled and so were the doctors because he was breathing on his own for the moment anyway. He weighed in at 3 pounds 3 oz- so tiny! They whisked him away and I went out and there were my husband and son coming down the hall as though they were ready to break down the doors! The first 24 hours were very scary, he ended up on a ventilator and was having multiple problems with blood sugar, clotting and so many more things but he was a little fighter and rallied over the next week. He got to come home at 3 weeks old weighing not quite 4 pounds yet. What a little miracle he was!
At 4 months old, Mason came to live with me and my husband. At 6 months old he was diagnosed with cerebral palsey and epilepsy. I was devastated! I loved him even more and was worried for him but was reassured that this would not affect his life expectancy. It did however start a flurry of appointments! He had MRI's, ECG's, many assessments for his motor skills and cognitive skills along with trips to Helena for specialists. The consenses was that, yes, he was very delayed in motor skills but a smart little boy and we we pelased to watch his progress over the next 2 years.
Never has there been such a happy boy! He would break out in a smile every time he would see his daddy, mommy, Papa or me and of course his favorites were his twin uncles who helped take care of him so much of the time. It was a family venture: whoOur precious angel came to us 6 weeks early on June 13, 2007. I got a call at work from the hospital, his mother was there and he wasn't doing well so we were having a baby today! What a plethera of emotions! Fear-it's too soon! Joy-we get to see him! Hope-please God, let him be ok! I got to the hospital just before they took his mom in for an emergency C-section and frantically changed into scrubs then waited and waited for what seemed like an eternity before they let me into the OR. His mommy was scared-me too! We had sent my husband to find daddy and they weren't there yet. We both waited to see whether or not we would hear a cry when they took him ok and then...a tiny little cry but a cry none the less! We were thrilled and so were the doctors because he was breathing on his own for the moment anyway. He weighed in at 3 pounds 3 oz- so tiny! They whisked him away and I went out and there were my husband and son coming down the hall as though they were ready to break down the doors! The first 24 hours were very scary, he ended up on a ventilator and was having multiple problems with blood sugar, clotting and so many more things but he was a little fighter and rallied over the next week. He got to come home at 3 weeks old weighing not quite 4 pounds yet. What a little miracle he was!
At 4 months old, Mason came to live with me and my husband. At 6 months old he was diagnosed with cerebral palsey and epilepsy. I was devastated! I loved him even more and was worried for him but was reassured that this would not affect his life expectancy. It did however start a flurry of appointments! He had MRI's, ECG's, many assessments for his motor skills and cognitive skills along with trips to Helena for specialists. The consenses was that, yes, he was very delayed in motor skills but a smart little boy and we we pelased to watch his progress over the next 2 years.
Never has there been such a happy boy! He would break out in a smile every time he would see his daddy, mommy, Papa or would take him to physical therapy on this day and who had to work, occupational therapy, speech therapy, doctor's appointments, blood draws, dietitian appointments and on and on. We all pulled together to make sure he got everything he needed, aunts, uncles, friends-he touched everyone's lives and left footprints on their hearts.
There were camping trips where we made his bed in the bathtub of the fifth wheel, rides on the 4-wheeler, staying up all night rocking when he had ear infections and colds, a short stay in the hospital where he slept woderfully and I didn't sleep at all!
In July of 2009, our entire family took a trip to the Oregon coast for a week. Little did we know that it would be our last trip with our little angel. We had a wonderful time, walks on the beach, crabbing, playing games. He was so happy! He was starting to walk with a walker, he would "army crawl" to me across a mat, he could say on and hi! He was doing so well!
When we got back he starting having trouble keeping his medication down. We were trying a lot of different things to keep them down but it wasn't working. Thursday night he stayed with his daddy and Friday morning I got a hysterical call from him.
Mason was gone! I was trying to find clothes to put on and tell him how to do CPR at the same time all the while praying to myself and pleading that this can't really be happening! As I drove to the hospital I kept thinking, "this isn't real. It can't be real." But it was real. Mason had had a seizure in his sleep and died during the night. My husband was outside waiting for me at the hospital and I knew because he was crying. I felt like someone had sucker-punched me! But my next thought was, "I have to keep it together for my son, he needs me now." I went into the room where he was holding our precious little boy and he was crying, "Mom, my son is dead!" My heart was broken for both of them.
As we rode home together from the hospital it seemed so surreal. Already the questions were coming. Do we want a cremation? Where do we want him buried? What day will it be? This is the bill, it needs to be paid at the time of service.
How can you comprehend all of it at once? Decisions and plans and still be able to grieve for your baby?
I felt like my world had stopped and yet everyone else's was still spinning and expecting me to keep up with them! We made it through the service and the burial, getting a marker and then trying to move on. But I couldn't. I wanted to find a way that I could keep his memory alive, a way to help other parents who were going through the same devastation, but how? Through a conversation with another mother who had gone through a loss (a wonderful woman by the way) it finally hit me like a ton of bricks! And that is how this foundation came to be.
My hope is that I can help ease the horrific pain that comes with the loss of a child by easing the finacial burden that comes with it. Sometimes, helping others through a pain like your own is the only way to help yourself.
Run with the angels baby boy! I know you are up there doing summersaults and laughing, just waiting for the rest of us and saving us the best seat at the table.
Have a wonderful day!
Shana
Kelly's baby with wings....
Oh Mother, my mother by Theresa Cochrane
Oh Mother, my mother I touch your tears invisible fingers soothing your skin I know you think of me so often in the day, in the night in your dreams going into an empty nursery knowing I'll never be there but I am...in your heart in your soul, I shall always be for you gave so unselfishly of yourself. Inside of you, you created such a world for me a world of laughter, of love of sadness, of sorrow every emotion people come to know you shared with me.
And even though I may never feel your arms around me I felt your heart beating, like a lullaby, singing me to sleep and your spirit giving me a safe haven already protecting me nuturing me preparing me for things to come. But sometimes the journey of life pulls souls apart and yes, I had to go on to another place. I wish this was a decision I could make and I know you do too. Know this wherever you are: I will always remember that yours was the first love the first joy, the first soul
I will ever know you gave me the courage to go on in my journey I hope I can do the same for you Your heart beat will always call me to you. Love, Your Child
Kelly thank you for sharing Cooper with us. What a blessing from God he is to you and your family. I know he is proud of you, and is watching over you and your loved ones. God Bless
March 23 at 3:52pm On the 9th April 2009 I received the greatest news of my life, I was 2 weeks pregnant. Everyone who I told was so excited for me and people followed my pregnancy on facebook. I loved the whole experience of my pregnancy from the first scan to my bump getting bigger even loved been kicked morning noon and night.
On the 6th December I turned 38 weeks and it was then everything went tragically wrong. It was about 9:30pm when I felt a heavy drop in my womb, and the pains started. I like everyone else thought I was going into labour so had a hot bath and some paracetamol like the midwife would have told me to do. By morning the pains had not subsided, so after numerous failed attempts to contact my midwives I went to hospital.
Sitting in the Day Unit on the Maternity ward, the midwife put the heart monitor to my bump to listen to my babies heart beat, but there was silence. So I was taken to a side room where I received a scan to look for the heart beat. The worst was then confirmed, my baby had died! Devastation hit, the waves of emotions that hit everyone close to me was unbelievable. We had spent months preparing for a healthy baby, instead on the 10th December I give birth to a beautiful sleeping angel, Louis Robert Joseph Knight.
As a focus for my grief, I have decided that I would like to help mothers of babies that are stillborn and raise funds to make the experience as painless as possible. 17 babies are stillborn everyday in the UK and very little is available to help these mothers rebuild their shattered lives. We are looking to raise money for North East maternity and Neo Natal Units
We are hosting numerous events leading up to what would have been Louis’ 1st birthday on the 10th of December 2010. We are hoping to hold a number of Tom bola events in local shopping centre’s such as the Galleries in Washington. Hamper raffles and Name the Teddy competitions in local shops and businesses, host Charity Nights that will have a variety of events from live bands to auctions. We are also looking at trying to complete a sponsored event every month , including a 178 mile walk from the Maternity Unit at Sunderland Royal Hospital to the SANDS Memorial Garden in Alrewas, Staffordshire.
We are trying to raise as much money as possible so we can buy basic items to put into hospitals, initially in the North East of England, such as digital cameras, Moses baskets and stands, specially designed fold away beds that will enable fathers to spend the night comfortably in the hospital with mother and child. We would also like to provide keepsake boxes, which would contain items such as a clay impression kit for hand and feet imprints, teddy bears and an Angel, which signifies a born sleeping baby. I also have a number of people who are knitting a range of patterns of hats, booties, mittens and jackets for premature babies may they be sleeping or not
our website is www.4louis.webs.com
and the facebook link is
http://www.facebook.com/amylealand?ref=ts#!/pages/4Louis/253081067047?v=wall&ref=ts
Thanks Kirsty.
