An open letter to parents of special needs children:
Dear Mom & Dad,
You are amazing! You may not realize it yet but you
are. Life probably hasn’t worked out the
way you expected it to but you can pick up the pieces and make something
wonderful out of them. Summon every bit of courage you have and keep moving
forward remembering that courage is not the absence of fear but action in the
face of it.
Look for help and support in your community, it is probably
there, not always easy to find but if you search for it, it will be found.
NEVER EVER be afraid to ask for help.
Sure, the answer you get may sometimes be no, but do not let that deter
you. Keep asking, keep looking, keeping
dreaming of the best life your child could possibly have and let that be a driving
force. Your child needs you to be their
champion. You may not be the expert on
their diagnosis but you ARE the expert on your child, you know them better than
anyone else does. So do not be
intimidated by service providers, their’ experience, their’ fancy degrees. These people are usually fabulous resources
and can be great advocates for you and your family, but if something isn’t
working, say so. If you need direction,
answers, support, do not hesitate to ask for it. Use what is helpful and ignore
what is not.
The way you see your child’s special needs and react to
them, will set the example for how others respond to your child. The teachers
your child comes in contact with probably are not experts on your child’s
diagnosis either, and that’s okay.
Educate them about what your child’s special needs are, how they affect
your child. Let your child’s teacher know your child’s strengths and
weaknesses. If you have strategies that help with their weaknesses, share
those. You may have had to set aside the
expectations you had for your child when you discovered their special needs,
but that doesn’t mean you can’t have hope. Inform the people who work with your
child what your hopes and dreams and goals are for them. Inspire them to believe in your child as you
do.
Your job raising a child with special needs is probably one
of the most difficult things you will ever do.
But it can also be one of the most gratifying. Remember to take time for yourself, yes I
know this can be difficult to arrange but do whatever you can to make it
happen. It is not a luxury that you can’t afford; it is a necessity that you
can’t afford to do without. You
effectiveness in your child’s life is largely dependent on your emotional well
being which requires rest and breaks and time away occasionally. Do your best to build a support group around
you that can help you with the needs of your entire family. Make time for your spouse and if you have typical children as well, do everything
you can to spend one on one time with them, and teach them to love and care for
their sibling. If you are so wrapped up
in the needs of your special needs child that your spouse and other children feel their
needs are ignored or overlooked, they could feel resentful toward that child. Help them to want to be a champion for their sibling as well.
Know that God sees you and loves you beyond all measure. God didn't give you a special needs child as some form of punishment. In fact, the opposite is true, God has entrusted you with a very precious child and He is there for you to lean on. Trust Him, let Him be your peace and your guide and your strength. Allow Him to show you great & mighty things in the journey of special needs parenting and remember that His idea of great & mighty things are often quite different than ours.
I know, it is all so overwhelming and seems difficult to
balance and manage everything. But you can do this. Believe in yourself, rise to the challenge,
don’t give up, don’t feel guilty for needing help, ask for it! Do not be
intimidated by people who do not know your child as well as you do, make your voice heard. Hope
for the best, dream big dreams for your child.
You CAN become the champion your child needs you to be!
Sincerely,
A parent who has been there.
3 comments:
A most encouraging post. Applies to the parent of any of God's children.
As I read this I am in the process of moving my 25 year old Adpergers daughter home. She started out in special ed preschool and now has a college degree. My heart still aches wondering what is next for her.l continually remind myself she is in His hands & I just need to do my best. Thank you for your encouraging words when I'm needing them most.
Linda, I understand, my kiddo with Asperger's will graduate from High School next year. Praying that he will find a good place in life for himself. I'm glad my letter was encouraging.
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