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Now Reading: 2 Reasons Why My Wife Is The Coolest Autism Mom
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(originally written & published on November 15, 2013)
My wife is the best, most different autism mom that I know…and I love her for it.
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If you’re gonna shop Amazon anyway, can I ask that you enter Amazon by using the search box above or by going to http://www.amazon.com/?tag=a050ef-20?  This way I can make a little money to help pay for my son’s after school & weekend therapies.  This blogging thing has been awesome & life changing for me… but I must admit that it’s taking up a lot more time than I ever thought… so if I can make a few bucks it’ll make it easier for me to justify….Love you all! Thanks!!
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Written by
Frank CampagnaIâm a 48 year old neurotypical dad with a 14 year old son with severe, non-verbal autism & epilepsy. I created this blog to rant about autism & epilepsy while celebrating my son who I affectionately call âthe kingâ :-).
Love it so real
I can totally relate to this. When we first got our son's diagnosis, I was all about the autism and the "What will we do?" "What therapies do we need?" Spiraling around and around and worried about the future. My husband really struggled with the diagnosis, and would get angry any time I tried to talk about it. I would get really depressed about life and the future because autism was my focus. I really try to focus on the now, and my husband and I take turns getting out of the house to do "frivolous things". We are much happier people when autism isn't the center of the world, but something that we deal with when it throws the walls up in front of us, and we keep on going.
I am filing for divorce, as my soon to be ex husband, does not understand Autism. ..such a 'know it all' that it makes me want to choke him. Ty for making me feel like my gym time is ok…such guilt I feel at times for wanting a 15 min alone time…I love my son and if you ( not you per say) are not supporting and loving and ACCEPTING him then there is no me.
I have so much respect for you and your wife!!! I get one weekend a month respite… I definitely use it. My son is 13 with verbal autism..I would say he is in the middle as far as how serious it is..he also has MR which makes him more like a 8 yr old. My mom gets upset when I talk about autism all the time. I understand where she is coming from.. she wants me to have activities outside of the "illness". I wish she would understand it is hard not to think about itall the time. I am a single mom so it seems like I just try to find ways to make things better for my son. Anyway the whole point ofthis post is to say parents need breaks when they have special needs kids!! Sorry forthe long post. đ
My husband is the best for this. Always encouraging me to go with friends, indulge in a hobby. Over time, I have realized how right he is. He's in the shower right now getting ready to spend the day with his buddies.
So glad that I have found you guys to connect with.
Oh WOW!! As an "Autism mummy" I REALLY needed to hear this tonight… thank you for reminding me to be ME not just the crazy mum who has a mixed up kid….
AD… You know how amazing you are. However, I give all the hard work and patience to the super autism mommy. She the best best,,,, I wish I could be her friend. As autism mom I always make plans to breath or have me time but end up reading or thinking about autism…..ugh
AD…if this Autism mom could do it…I WOULD! NOW, how to help the single parents out there….UGH!
Must be nice! I would love to send mine away for a week but his father wouldn't hear of it. He's not the one with him all day obviously.
Speak to the social worker at your child's school and find the nearest respite program in your area. My kids had one since they were as young as 4 – and now at 18 and 22, still are entitled to respite services including overnight and week long stays. You need this. As a single mom, you cannot do it alone. You need time to breathe.
as a single autism mom I can only dream of getting the chance to meet a dedicated man like you… unfortunitly I don't get to leave the house by myself as I have no one to watch her for me or anyone to help. This blog really hit home for me as I will be in survival mode until she grows up and moves out… I am holding up the hope that she will be able to function as an adult by herself. In which time I will finally have the chance to go out on a date if I do ever meet someone…
I read your post all the time. Our son has Aspergers. You are a great husband and father. Your wife is very lucky and I love how involved you are with everything to do with your son. Thanks for the stories.
You are an amazing dad and husband!! The world could sure use more of you đ
You hit the nail on the head Ol'AD-Survival. The cards that ourselves and are children have been delt are very hard.We live with this pain forever pushed to the back of our minds in order to survive.If we let it sit up higher in our brain-it would just hurt so much-leaving it very difficult for us to function.So I keep pushing it down deep-put on my smily face and super mom cape and try to enjoy life
Exactly!