In my life there are many issues (depression, stress, ADHD, ADD, Autism, Physical disabilities, etc.), but I hope that I can bring hope to others that have to deal with their own issues. From one person that is suffering with mental illness, I hope to break free of my dark cloud to offer help to others.

Friday, September 24, 2010

My own parenting quotes

A family member asked me to come up with some inspirational quotes that for those leaders that help special children. I took great honor in this request. I have made a list of ten inspirational quotes that I thought of for those that help these special children. Feel free to use these if you wish in anything they may help you with.


Helping others find their value by lifting spirits

Revealing the riches of others gives them light

Eliminating can’t, won’t and giving up one child at a time

Eliminating can’t, won’t and giving up one heart at a time

Understanding those that need it the most

It is never to late too show a child what they can be

Special children require special leaders

Look into the heart of a child not what you can see with your eyes

Those children that are the most lost are the most at home

Children with special needs have special hearts

All quotes by Hope L. Brock

Friday, September 10, 2010

Doctors, meds, guilt, and poor Adam

If any of my readers follow me on facebook, then you already know that my little boy has to see a neurologist. For the first time in his little life, a doctor has suggested a diagnosis of muscular dystrophy. While it does not come to a total surprise for anyone the knows him, it is still very scary. I had not known that much about it when it was mentioned in the doctors office. So I headed for the information super highway (internet) for more research. What I found could scared the living daylights out of any mother. I found myself glued to the computer screen fearing the worse. Since the MDS diagnosis is actually made up of 100 different types it is hard to know actually what the medical community is thinking. However, the one I looked at the most is commonly in boys, commonly around the age of 5 or 6 (Adam is 7), involves waddle walking, and other things that sound like my little boy. The most horrible thing about this type is that they stop walking by the age of 12 and died by 20. Just typing these words scares the crap out of me. As a mom you want to protect your children, but whatever is going on with Adam I can't stop.

I also found out the MDS is hereditary. This is where the guilt and shame come in. I feel as if it is my fault; either directly or indirectly. It was either my genes, or my choose of a father for him that caused this awful scenario.  My dad always told me never to have sex with someone that I would not want as the father of my child because it can happen the first time. I never listened to that. Here I am in the middle of what could be a very scary situation all because I could wait to have sex with the 'right' person. I wish that I would have gotten to know my ex-husbands medical background before I decided to marry him. I now wonder if others should not medical screen potential spouses. If Adam has this condition, then I will not be able to have another biological child. I feel bad enough about Adam, and if I were to have another child after knowing this then I would be making a conscious decision to give another child this horrible condition.

As you can see my mental state is like Hell right now. So I have once more tried to start my meds again. I started yesterday, and prayed that I could have started on a higher dose right away. The idea of being medicated through this ordeal does not seem like such a bad thing. I started yet another steroid for my feet and knees. That one keeps me pretty loopy. I am actually grateful for this feeling. It makes it hard to cry. I don't want Adam to see me cry. I don't want him to know what might come. I don't even know if I want to know what might come.

The only good thing about this, if there is any, is the fact that Adam will no longer slip through the cracks for help. He will get all of the help he needs through many different services, and I can't do it there are other out there willing to help. When he was considered high function disabled everyone thought his condition was not severe enough to give him the best. Now he will get the best. Please pray that God will take care of Adam. I don't know if I can. I just pray that he will watch over him and get him safe.
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