Showing posts with label kids in wheelchairs. Show all posts
Showing posts with label kids in wheelchairs. Show all posts

Wednesday, September 18, 2013

My Dream of Hope's Seed

“You have turned for me my mourning into dancing; You have loosed my sackcloth and girded me with gladness.”  Psalm 30:11


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When Mighty Z was born, I mourned not just that fact that my child had a horrible disease and that I was told she wouldn’t make it to her first birthday, but I also mourned the friends and family I lost. Frankly, nobody knew what to say to me and at times people still don’t, and so many times they just stay away from me in hopes that they can avoid any awkward situation with me. I remember sitting up in the NICU (Neonatal Intensive Care Unit) and feeling completely and devastatingly alone.

The Devastating Silence

Of course I had my mother, father and one of my aunts who came up to show support, but even they didn’t know what to say. What do you say to a new mother who has been told there is no hope and all she can do is trach her beautiful baby, place her on life support machines, and pray, always pray, that she would survive?  I remember that traching Z was the hardest choice I had ever made in my 25 years of life and I was devastated, and nobody knew how to comfort me.  I think that if they had told me that all would be well, I might have gone over the edge because nobody could understand how hard it was.
As the years flew by and I had adapted to having a child with a trach and on a ventilator, we stilled graced the PICU (Pediatric Intensive Care Unit). I began to look through the slits in the curtains that separated me from other mothers with children who were also fighting huge battles, and slowly a little seed started forming in my heart. I thought to myself Wouldn’t it be wonderful if I knew these other women who are also going through exactly what I am?

My Dream

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I went home and I began to dream, to dream of an organization that would bind parents of special needs children together, to help mentor one another, help pray, and understand what this new world was about.  I had a burning desire that other new mothers who also had to trach their babies, place them on life support machines, or place tubes in their babies’ bellies, or have to have their babies fitted for power chairs would have the support of other mothers who had to go through the same thing so that they no longer felt alone.

Turning My Dream To A Reality

I tried for years to create such a group but every time I couldn’t get off the ground. I prayed and prayed that God would show me how to start it yet it felt like He wasn’t listening. Last December I was asked to start a local chapter of a national group that supports special needs moms.  I was told I could make it whatever I wanted; however, my ideas far surpassed the ideas of the group.  I wanted more; I wanted to empower other mothers with these special little miracles to go back up to the NICUs and PICUs and let the new mothers see that they were not alone.  I wanted to create a bond of friendship so tight that when one of our own babies was in the hospital, we would visit each other in order to fill each other’s cup full of hope.

Not So Easy

The national group didn’t want that. Their vision was strictly online and although that is so important, I wanted, no, needed, the face to face friendships. Then God sent me a friend– someone who also had felt the desire to make sure that others didn’t feel alone like we had.  Emily Minich and I began to talk and share with each other our dream for such an organization.  You see, what God was waiting on was for me to meet Emily.  I needed my other half, so to speak.  Everything I am not good at Emily is amazing at, and vice versa. Once we launched our group there was no holding us back.  God began to bring people in to the group; He aligned people with the power to get us into the NICUs and PICUs who were thankful for our presence there.

Friendship And A Vision

Emily and I named our group Hope’s Seed, because what we wanted to do was plant seeds of hope into the mothers of special needs children, so that these women can know that there is always hope and that they are no longer alone, that we will help pick up the torch in the darkest night and show them that the way is full of light.
You see, God did turn my mourning into dancing.  He gave me friends that finally understood this new normal world that I was made to live in.  He took off my sack cloth and girded me with gladness and giggles.  
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Hope’s Seed Grows


My friends at Hope’s Seed always know exactly what to say no matter what the doctors tell me. They are not frightened by machines and alarms. Trachs, ventilators, G tubes, power chairs, any trisomy syndrome, autism spectrum, and mental health issues are common among us and they bind us closer together as a family. We have all learned to see the beauty in the special needs world and now are more partial to it than the regular world.
Hope’s Seed mission is simple that no mother is left all alone with no hope in any part of this journey. We want to be that person who helps carry this weight, and we want to be the one who gives you the tools you need to walk this road. We are the people who want to plant seeds of hope in you and let you know that you are no longer alone.



edited by Emily Joy Minich
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Sunday, March 24, 2013

Abram's Story of Transverse myelitis

I first met Jen because my cousin's baby developed Transverse myelitis. I was they only person in my family who knew how to navigate this new world of Special Needs so I began teaching my cousin what to do. I spent hours looking up and researching Transverse myelitis, I also began to look for mom's of children with TM (Transverse myelitis). I ran across Abram's picture and contacted Jen I asked her a ton of questions and have been the middle man (or should I say woman) between Jen and my cousin every since. Jen is a wealth of knowledge about TM and how to advocate for your child. Here is a story of a normal little life turned upside down, and yet made whole and happy

 

 When the topic of children came up between my husband and I, it was never a discussion on having them, that was certain. It was how many we were going to have. See I wanted 4 and he wanted to have 2. So we came to an agreement that 2 was enough and if the Lord blessed us with more then so be it.


I always joke that Abram is my second and third child. I got all his firsts twice. I got to watch him gain control over his tiny body, roll over, sit up, etc. All the firsts that parents look forward to, I got to see twice with my son.



I had a very normal pregnancy and birth with A. Nothing abnormal at all. He wasn't ever sickly, grew just like he was suppose to. He crawled at 4 months and by 7 months he was walking. I breastfed him and since I work full time he slept with us. Around 8 months old we (mostly I) decided that it was time for him to sleep in his crib and sleep through the night too. We used the same routine with A that we used with our Gen. My husband started getting up with A because he didn't equate Daddy with food. Things were going great and Mommy was sleeping though the night!






7 am December 3, 2009 our lives changed forever. You know the feeling you get when your baby sleeps though the night for the first time. You wake up, it's light out and your like OMGosh! Then you have this debate with yourself about why you slept though the night. Then you wake your hubby to go check the baby. The words you never want to hear were spoke that morning “Oh God, Jennie you gotta get your car. He's not moving.”






I rushed to the ER and by rushed I mean I turned a 45 minute drive into about 20. Then we waited... Our town is small and our hospital is small. The closest children's hospital is 110 miles away and we couldn't get an ambulance to come get us. We decided to drive him ourselves. The hospital was kind enough to keep my car seat, we folded the seats down in my SUV and laid him strapped to a board in the back of the car, hung his IV bag from the coat hook and we were off. It was the longest drive of my life!  




At 9 pm on the 3rd after 4 hours of MRI and X-rays Abram was diagnosed with Acute Idiopathic Transverse Myelitis with lesions from C2 to T4. We spent 18 days in the children's hospital, 7 in PICU waiting, watching and wondering why he was still breathing. Then 11 days in Oncology. He gained 12 lbs from the steroids and possibly because all we did was nurse... We did 7 treatments of Plasmapheresis and still nothing.




He is completely paralyzed from the neck down. Couldn't make sounds couldn't move, nothing. Next came the hardest decision I will probably ever have to make in my live. They wanted to give my baby chemo. They handed me 2 pages of side effects and told me to let them know in the morning. I've never cried so hard in my life. I didn't tell a soul. The next morning the Dr's came in and took my baby away to hook him up to machines could change his life in so many ways and some of them real bad. We left the hospital 18 days later with a 5% chance of him ever walking or talking again. It was like having a 28 lb newborn all over again.



Abram turns 4 this week and though life has been a roller coaster for us he is amazing. In the 3 years since being diagnosed with TM he has regained all movement in his body although he can't feel anything on his right side and little on his left. The last MRI showed permanent spinal cord damage at C4 and T2 with continued swelling between the two points. He has days where he has to be on O2 because his muscles aren't strong enough to breath well if he is tired or sick.




 He has a wheelchair for distances or when it's to dangerous for him to walk. We live life to the fullest every minute we can. We camp, I carry him in a hiking pack so he doesn't miss out on hiking, rides ATV's and LOVES trucks! Sure life has changed for us, I mean who ever thought I would have a Urologist, Neurologist and PM&R Specialist on my speed dial! 
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