I’m a Kid too… A Foster Child’s Point of View

I am more than a foster child.  I’m a kid too.

I could be a newborn, a toddler, or a teen or maybe somewhere in between.

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I may arrive at noon or in the middle of the night.

My clothes might be to small or not fit me just right. 

I’m full of emotions. I could be shy, angry, frightened, or scared. I could be crying, withdrawn, and may even avoid eye contact.

I may be hungry I may be cold. 

School could be hard for me.  New place, new faces, new friends, and new rules.

Don’t judge me because I am in foster care…

                                                          I’M A KID TOO!!!

I laugh 

I sing 

I play 

I dance

I like sports.

I like music.

I like hanging out with friends.

I like watching cartoons.

I like to eat ice cream 

I like to play video games

I like going to the movies 

I need to feel safe

I need food in my tummy

I need to feel wanted

I need a warm place to sleep

I need to feel excepted

I need to know I am not alone

Above all, I need to be loved.  After all I am a kid too.

There are over 700,000 children in foster care across the United States, over 100,000 of them are waiting to be adopted.  These children are dealing with things that most adults could not handle and yet they are expected to “deal with it”  They don’t want to be seen as ‘”the foster child”, they want to be seen as a kid.  Don’t assume that because he or she is in foster care they are a bad kid.  Most children in foster care are in the system because of what their parents or caregivers done NOT because of their own actions. All they want is to feel safe and know that someone is looking out for them.  They want a normal life just like every other child does.  Let them have that life.  Let them be little.  Let them live a life without labels.  Let them be a KID ❤

 

 

 

Grieving a Foster Child

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I looked over at the empty crib and tears ran down my face. I need to take it down but my heart is just not ready. Being a foster mom hurts sometimes.

We loaded up the van this morning and headed off to church, daddy T and I both had this empty feeling we were forgetting something. But we were not, you are no longer here. Being foster parents brings sadness sometimes.

As I washed up last weeks laundry I ran across your favorite outfit and I lost it. Tears ran down my face and all daddy T could do was hold me and tell me everything would be alright. But he too had tears in his eyes. Being a foster parents is painful sometimes.

The kids have looked for you since you left, Wild Man does not understand why you are not here and keeps saying Momma go get Baby P bring her home please. I force a smile and tell him you are so happy at your new home and that I’m sure you are doing just fine. But my mind races and wonders if you are ok and if you are safe. Being a foster mom makes one worry sometimes.

I found myself wide awake at 2 am, that was our one on one time. I wonder if you were awake and thinking to yourself where is she? Why is she not singing to me? Why is she not holding me? Again I find the tears rolling down my face. I grab your favorite blanket, I’ve not washed it yet so it still smells like you, and I cry myself to sleep. Foster care is not easy sometimes.

In all our years of fostering we have had to say goodbye to many little loved. You my little love have been to hardest to let go. God blesses us not once but twice to be part of your story. We know that reunification or placement with a family member is always the priority, but when you came back to us we could not help but dream. I allowed myself to see you as part of our forever family. I allowed my mind to dream of first days of school and dances and family outings. I allowed myself to go where no foster parent mind should ever go. I saw our future and you were in it. This journey can be cruel sometimes.

So I didn’t see it coming. As I sat there in the courtroom listening to the judge I heard words I did not want to hear. I was not prepared for the change of events. I went in thinking you would be here forever and left with an hour to pack all your things for you to leave. Being a foster parent is heart wrenching sometimes.

But that’s how this goes. The system is not perfect and I pray those that do not know you those that have never held you those that do not love you like I do I hope they have made the decision God would have made. I pray He looks after you and keeps you safe. I pray He gives you comfort and that you feel Him near you. I pray you will always know how much we love you.

If we would not have stepped out in faith and followed Gods plan for us we would have never met you. We would have never seen your smiling face. We would have never held you or seen you crawl. We would have never falling in love with you. Being a foster parent is beautiful sometimes.

We will grieve for you and we will miss you. We will find things through the house over the next few weeks (maybe months) that will remind us of you. It will be painful but also such a blessing. For these things will remind us of YOU. A smile will cross my face and I will get to dream of you again. And that will make me happy. Foster parenting can be a blessing sometimes.

If we open our home again to the next little one who needs us, we are not replacing you. You could never be replaced. We are just answering Gods call to help one more. But that decision has not been made; for now we will just take time to heal from losing you.

Fostering is not for the weak but in our weak moments God gives us comfort and strength to carry us through. Thank you Jesus for allowing us to be part of her life over the last six months. Thank you for allowing us to see her smile and hear her laugh. But mostly thank you God for being You. Thank you for allowing us to be your hands and feet. To You oh Lord be the glory.

Robot Mom 2.0

In order to fully understand this post please go back and read my blog Part Mom/Part Robot sort of.

My last surgery, I was told the new batteries they were placing in my SCS’s (spinal cord stimulators) would last me between five and six years. That was last June. This past Friday I found myself back in the surgery room undergoing the knife one more time to replace the batteries. Where did my five years go?

Dealing with back pain/neck pain has become part of my normal. I do not complain about, it’s just part of who I am. Maybe it’s because I don’t complain that people do not see me as someone who suffers with a chronic pain. Just to clear things up not all illnesses or health issues can be seen. Just because someone is not in a wheelchair, or using an oxygen tank, or someone is not using crutches does not mean they are fine. Many chronic illnesses or pain issues can not be seen with the naked eye.

It is much easier to say I’m fine when someone asks how I’m feeling than to actually go into what all hurts. It’s been my experience that when most people ask “How are you doing?” they are just making small talk they don’t actually want to know how your doing. The truth is most days I am fine. The SCS’s have really made it possible for me to keep a somewhat normal life. But there are days I hurt, days I can’t move, days I wish the accident never happened. On those days I wish people could really see what’s it’s like for someone to live in constant pain. Days like today.

A few months ago my generator started saying it was time to replace my batteries. I thought there had to be a mistake so I called the doctor and scheduled an appointment. When I went in I was met by the doctor and the programming team. They laid me down and ran the scans to see what was going on.

They adjusted the programs and reset the batteries and sent me on my way. That lasted three weeks before my unit started flashing replace batteries soon. I called the office back and scheduled yet another appointment. At this appointment it was confirmed that my SCS’s were in fact dying. Both batteries were going bad, just my luck. After father investigation it was determined that my spine is covered in scar tissue (countless surgeries will do that) making it hard for the electrical current to get from the leds to my spine. This was making the batteries work over time to get push the current through in order to keep the SCS’s working. That in turn drained the batteries, which is why my five to six year battery life only made it a year and four months.

So Friday I had yet another surgery. New larger batteries were placed in my units (one on the left side of my lower stomach area and one on my right side lower back area). They worked on my one on my back first then flipped me over and replaced the one in my stomach. In a few days I should be back to my normal but today I feel like I’ve been hit by a truck.

This will fix the problem short term but there is still scar tissue around my spine so another, more complicated, surgery will be needed down the road. Sooner than later. It seems to be never ending.

But even with all the downsides I am thankful. I do hate surgery but because of it I am still able to walk. The scars will fade and the pain will subside. I am thankful because with each passing year the medical community gets closer to finding a way to permanently fixing those in chronic pain. I am thankful because with my SCS’s I am no longer on pain medication. I am thankful that I am still able to be the mother and wife God planned for me to be. I am thankful because I still believe in miracles and one day I will be healed. And oh what a day that will be.

From our beautiful chaos to yours don’t be so quick to judge others. Just because you can see their illness or see what causes their pain does not mean it does not exist. The strongest people I know cry behind closed doors in pain so they don’t worry those they love.

The X Factor: School Life for Our Autistic Son 


I attended my first IEP meeting for this school year for wild man a few weeks ago.  As a mom I want the best for my kids. I want them to have a great education and be able to succeed. As a mom of an autistic child I want these things and so much more.

 The meeting went well. His new teacher, OT, speech director, principal and his teacher from last year all love him.  Which makes me feel like we made the right decision on the School.  We went over his daily schedule and how we could make it better for him.  This year he will have his major subjects in a regular classroom while his afternoons will be spent in the classroom equipment for special needs (this is the classroom which make us choose the school in the first place). Change is hard for him but I want what’s best for him.  

The meeting was filled with comments like “he is doing so great” “he is working so hard” and “he has come a long way”. All of which made me smile because he is doing great and working hard. And he has come a long way, a very long way.  It’s in these moments that I get lost and almost forgot he is autistic.  Everyone bragging on him and telling funny stories about things he has done.  I love seeing other people’s faces when they talk about him.  They just light up he has that effect on people once they take time to get to know him. 

But then there comes the reality.  Take this work page for example.  He scored a 3 out of 10.  I know placing him in the regular classroom is supposed to help him build social skills and help him become more independent.  But he is so lost when it comes to the actual school work.  I don’t want him to be overlooked or just passed through because of his disabilities. I want him to have a chance to learn and to grow just like any mother would.  I know many of you are thinking “it’s just one paper or he is just in 1st grade” but that’s my point. This is just the beginning. What happens now and how he is treated will affect the way things go from here on out. He does not bring many graded papers home but when he does most notes are “he tried hard” At what point will he become completely lost and what nothing to do with School? Will he always be this happy go lucky boy or will the struggles become to much for him the bear?  I worry because it’s my job to make sure he receives the best possible education he can receive. I worry that the other kids will start calling him names or talking about him because he does not get the answers right.  I worry constantly about how his peers receive him.  

But then my son does the most wonderful thing.  As I look at all the X’s on his papers and the comments my son, my beautiful intelligent son points at the papers and says “look momma I got this one right” and smiles great big.  Even in a world full of negativity and large red and green X’s my son only sees the good, he only sees the beauty. As his mom I worry about him in this crazy world we live in.  People are so cruel to each other and I am scared that the things that make him unique in Gods eyes will get him teased or even hurt in this world.  But God has given my son a unique way of looking at things. He only sees the good in people and in things.  He does not notice those that stare at him or say hurtful things about him. I am truly thankful for that.  As his mom I need to try and see the world the way he sees it.  I need to find the good.

So yes we celebrate the three right answers, because a year or two ago none of this would have even been possible. We celebrate that he can now write his name and that his teacher said he is now sitting at his desk up to three minutes at a time. (This is huge for him) We celebrate that he has even sat at the dinner table with us a few times this month and we were able to have dinner as a family(and this is huge for him). We celebrate the red and green X’s because they show us progress. He is moving forward in all areas of his life.  We celebrate because God has made this prefect little guy ours and we are the ones that get to watch him grow and succeed at life.   

We celebrate because we are blessed.  

Thank you wild man for opening my eyes to more than just the negative.  Thank you for helping me see there is beauty in everything, even in X’s. 

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