What Would I Want a Mother of a Typical Needs Child to Know

Recently a question was posed on the web which asked, as a mother of a special needs child, what would you want a mother of a typical needs child to understand? As a mother to both a special needs child and a typical needs child, I found the question very difficult to answer.

Recently there was a discussion question put out on the web which asked what I would want a mother of a typical needs child to know about mothering a special needs child. As a mother to both a typical needs child and a special needs child, this question is really difficult to answer. Our son has both learning disabilities and ADD.

I have to say that I have written and re-written my answer probably a dozen of times. Finally, I think my answer comes down to what I feel is obvious. What mothers of typical needs children, family and friends need to understand is that we, families of special needs children, need understanding and consideration of our situation. Not unlike those with physically visible handicaps, those with invisible to the eye special needs require consideration, accommodations, respect and understanding. Invisible special needs can make daily situations no less daunting than for those with physical handicaps.

What is especially tricky with learning disabilities and ADHD, especially when a child is young, is that understanding the special needs and challenges takes time and work to understand and address. It has taken us a great deal of time, awareness and education to understand our son’s needs and to respect them. By respecting his needs, I mean that the way he is taught, communicated with, motivated and disciplined is done in a way specific to him and his needs. If you have a close friend or family member with a special needs child, educate yourself on the special needs of the child so that you too can RESPECT the needs that the child has.

My mother and sister have both read books to educate themselves. It has meant such a great deal to us that they took the time to understand our situation. You can read some articles online. It does not have to take a great deal of time. A little effort can go a long way.

We are extremely proud of both our son and our daughter. We love them both and recognize that each of them have their special strengths and their weaknesses.

With a special needs child, however, their weaknesses can make every day living very difficult. The difficulties can affect academics, social situations and the mundane tasks of every day life. Even with the effort we have put in to understand our son’s strengths and weaknesses, we don’t always understand how his issues will come into play in different situations. As a result, we are always on the alert with our son and we always have our “armor” on, as a favorite blogger of mine, canmombecalm, says.

We have our armor on when it comes to school and home work. His needs have to be individually understood and addressed. Even though he is in a small classroom setting, we work with the teachers closely to understand what is most effective for him in learning. Homework is never easy and takes a great deal of vigilance, creativity and patience. It has to be a part of our daily routine all year long. We need to be as or more observant about his successes and his challenges as his teachers.

We have our armor on when it comes to social settings. Group situations can be stressful for our child. Changing from one activity to the next activity can be stressful for our child. Answering on demand questions from adults can be stressful for our child. Social situations for our son can be tougher than for the typical child but they are extremely important to him. Maybe it is because he is in a small group classroom or because his homework takes longer and has to be part of a six day a week routine. Whatever the reason, when he has an opportunity to have a play date, it is extremely important to him and if something happens which causes the play date to be canceled, it is very upsetting to him.

We have our armor on for every day living. He needs time to transition from one activity to the next such as from play time to dinner time and from dinner time to homework time. Each transition requires forethought and warning. Instructions need to be broken down into one or two discrete tasks that can be communicated easily and completed quickly. He needs reminders for most daily activities.

As a result, I may seem high-strung or over-protective to a typical needs mother but I assure you that I am neither. I am simply a mother that is being respectful of the needs of her child. Because our son’s challenges are not visible to the eye, we have to be the buffer zone for our child making sure that he gets the consideration and understanding that he needs.

Is our day-to-day life more challenging with a special needs child? Absolutely. Do we worry? Absolutely. However it has made us realize that, in life, you have to celebrate each small success. We celebrate little notes written to us, we celebrate books completed, we celebrate small instructions followed and we celebrate fun, successful play dates. Life is good and we would not want it any other way!!

7 Responses to “What Would I Want a Mother of a Typical Needs Child to Know”

  1. Mommyaulait Says:

    I love this. I am called a Helicopter parent. Over protective. Over indulgent..so many ridiculous names by other parents. In the end I’m just trying to help my kid adjust to a world that is different for us. It’s so infuriating. In the end. I have to be true to my son. Listen to him and not others who don’t understand. I don’t have time to explain to every single one of them who decides to judge me and my kids. I have to much living to do with my wonderful kids. Thank you for this post.

  2. ginabad Says:

    Here, here! As the mom of 2 vastly unique LD childrens, I appreciate this post and am linking it on my blog and sending to some very special moms. Thank you!

  3. Jean Says:

    My 3 year old is Autistic. I had a lightbulb moment one day at Target. My son threw a massive 30 minute tantrum on the floor and he was so upset I just didn’t care about anyone else. In that moment all I cared about was me and him.

    And another evening at a nighttime care center my son was really out of control. Screaming and crying at the top of his lungs. And the lady behind the counter gave us the most horrid looks you could imagine. Needless to say I grabbed the business card from the counter and sent a nice little letter to the manager.

  4. Barbara Says:

    “understanding the special needs and challenges takes time and work to understand”

    I would boil it down to “just be polite”. Being polite means NOT giving some non-verbal and disapproving look, nor asking prying questions. Being polite respects that each parent manages their child to the best of their ability.

    Unfortunately, a hyper-awareness of potential child abuse (thank you media-types) has given the public an empowerment-feeling for intervening with parents and children.

    I suspect you will be dealing with other person’s responses for the duration of your child’s childhood. Social changes for understanding ‘invisible’ disabilies is not near complete. However, I think you can hope to educate within smaller communities – the businesses you frequent, your child’s school, and your family.

    Nice post. I will look for an opportunity to link to it.

  5. Holly Schwendiman Says:

    Karen, so nice to *meet* you. I appreciated your comment on my post about fear. :) I have shared several thoughts on my blog about ADHD as well. It appears we have something in common as mothers. :) It is an amazing learning curve isn’t it?

    Hugs,
    Holly

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