Becoming a Parenting Team

September 25, 2012 by · Leave a Comment 

Any parent knows that one of the biggest challenges of being a parent in a two parent family is working with the other parent.  You can be in agreement about décor, finances and many other things, but it is likely that parenthood will bring out differences that you were only dimly aware of before.  Add to that a challenging or quirky child, and the differences can quickly become polarized so that you feel that one parent is too strict and the other is too lenient.  In all likelihood both parents hold part of the solution.

Any two people have definitely had different experiences growing up.  All of us had parents who did things we pledged we would never repeat.  At the same time there might be aspects of your parents’ practices that you feel were wise, and you would like to repeat.   Whether in trying to do as well as our parents did, or in trying not to repeat their mistakes, each of us can become rigid in our own approach.

Add to the mix a quirky child who might not be much like the way you were as a child, and the situation is primed for conflict.  There is no doubt that the situation challenges parents to negotiate and treat each other with respect under pressure.

Children learn very quickly where the differences are and how to exploit them.  I tell parents that any child worth her salt will sort this out and aim for the space in between the parents.  The child feels a great deal of control in this situation, too much control, and this contributes to a feeling of careening near the edge when it goes unaddressed.  Especially if parents disagree in front of the child, the child then feels empowered to ignore limits set by one parent.  The child then feels entitled to provoke that parent.  This is often when parents seek outside help.

The situation requires a kind of respectful listening and negotiation that will in the long run be good modeling for the child.

What to do?

  1. Agree to address the differences in a respectful way out of your child’s earshot.
  2. Listen to your partner.  Perhaps there is something useful in what she or he has to say.
  3. If you cannot come to agreement, seek outside help.
  4. Agree to try an approach and come back to it later to see how it is working.
  5. When either parent is in an unsure situation with a child (for instance, “Can we rent an R rated movie?” when you and your partner haven’t developed a clear policy on this), feel free to say, “I need to talk to Dad (Mom) about this.  We’ll get back to you.”  It is OK to let the child know you don’t know.

Children feel safer when they know their parents are working together, and this alone helps them maintain better behavior.  They are no longer “careening out of control” wondering who will put the brakes on and when.

Good luck with this challenging but rewarding endeavor in raising quirky kids.

 

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Photo Credit: Scott Ableman on Flickr

Strength in Community

September 11, 2012 by · 4 Comments 

Last week I wrote about the complicated feelings that parents have when their child is diagnosed with a learning disability.  While these feelings are all a normal part of coping with a special needs child in your family, they can interfere with your well being and your ability to advocate for your child unless you find ways to support and take care of yourself.

There is nothing like community to heal the shame, sadness, fear and anger that parents feel in this situation.  If it is painful for you to talk to parents of “typical” kids, find other parents whose children have special needs and cultivate relationships with them.  Below I’ll list some useful organizations.  At these meetings there is no shame in having a child with special needs because everyone is in the same boat.  Before you know it, you’ll be meeting with others for coffee or calling each other on the phone to share the latest outrageous story (sad or funny, or both).

When you become part of a community of this sort you experience many benefits.  You’ll find others who are more experienced and can share tips that have been useful to them.  You will find out about services in the community or school system.  Your fear about the future might decrease because you might learn about kids like yours who have had successful outcomes.  In time you will be the one to offer useful information to a newcomer, and this also feels good.  There is no doubt that community is healing.  Where can you find it?

  1. Under IDEA, the federal law that mandates special education, all school systems have PAC’s or Parent Advisory Councils.  These meetings can inform you about your rights and the services in your school system.
  2. In my area the Asperger Association of New England offers a wealth of educational and support services for parents and children.  Their website, www.AANE.org, even offers a listserv useful to people outside the immediate area.
  3. Another organization that offers very useful information is the Federation for Children with Special Needs (www.fcsn.org).  Within this organization parents can find useful information, support, and opportunities to volunteer and give back.  FCSN even has webinars on their page.

These are ways you can find and develop community that might help you diminish your shame, sadness, fear and anger.

Next, let’s think about how you see your child and where her strengths might offer community for her and you.  When you first get a diagnosis, you might only see her shortcomings.  But it is likely that there is much more to her than that.  Try to recover a more full understanding of who she is.    Does she have an encyclopedic knowledge of some topic?  I knew one boy who had nonverbal learning disability whose knowledge of geography took him to the state level competition in the National Geographic Geography Bee.  This gave him a little social capital in middle school.

Does she do well at individual sports rather than team sports?  Many children who cannot manage the social and physical complexity of team sports can excel at track or swimming where the main competition is against oneself.  I knew another boy who excelled on a swim team.  He enjoyed the camaraderie and the exercise helped manage his weight and his anxiety.

Can she play a musical instrument?  How about a sense or humor? What about art?  Theatre can be a helpful way for some kids with Asperger Syndrome to try out different ways of being. Finding these areas of competence and nurturing them will be good for your child and you.  It gives you both something to feel proud of when school is tough.  Activities that draw on your child’s strengths can also give her a social network in which she can feel strong.

I would be interested to hear how others have coped with having an “atypical” child.

 

Click here to sign up for my newsletter, Parents’ Corner, and receive my free report, “Living With and Loving Your Disorganized, Impulsive, Forgetful, Yet Delightful, Funny Child”.

 

Photo Credit: Melissa Wall on Flickr

Five Difficult Feelings Parents Have About Their Child’s Learning Disability

September 7, 2012 by · 8 Comments 

Often children get diagnosed with learning disabilities after some amount of time of difficulty at home, in nursery school, or in public school.  Parents or teachers have recommended an evaluation. The report comes back with a description of how your child learns and participates in the classroom as well as in social and family situations. A good report points out strengths and weaknesses and gives useful recommendations about how to be helpful to your child in and out of school.

Sounds good, right?  With a good evaluation, report, helpful educators and therapists children begin to do better and even thrive.  I want to focus on what parents experience when they confront their child’s difficulties, such as ADHD, a specific learning disability like dyslexia, Asperger Syndrome, nonverbal learning disability, or something else entirely.

Instead of feeling relief that they are at the beginning of remediation, many parents feel some uncomfortable feelings.  In my work as a Parent Coach I find it important and rewarding to give parents a place to acknowledge and come to terms with these feelings.

Shame:  Let’s face it—parents often feel that their children’s accomplishments reflect on them.  It hurts to find out that your child has an invisible difficulty that is interfering with her education and likely her friendships as well.  Even if you requested testing because you suspected a difficulty, most parents still hope to find out that there’s no problem and just a simple adjustment in school or life will help.  Maybe just an after school tutor.  Now that you know that there is a problem that can be managed but not necessarily be fixed, you might feel ashamed, as though there is something wrong with you that your child has a learning disability.

Anger:  I think that people tend to be more aware of this one.  Many people feel angry at school personnel for not understanding their children and causing unnecessary pain.  And one can be angry at your child (even if it isn’t rational) for having a problem that makes daily life more complicated.

Sadness:  This is a big one, especially when parents first get the news that there is a problem.  It is sad to accept that your child has a problem that will not go away.  This difficulty will probably affect your child’s life in some degree forever.  It changes the future for you and your child, and you need to rewrite the family narrative.

Fear:  What will the future look like?  I have often had parents sit with me and ask, “Will she be able to go to college?” “ Will she ever leave home and have a job?”  Often when children are struggling enough that people get an evaluation, the child may look very impaired.  After all, there are probably no services in place.  As a result, parents worry that things will never change or get better.  They have no experience with this new world of parenting a child with a learning disability.  With the people I see, I tell them that they just need to keep working to get their child the services she needs and not to give up on a bright future.  It will be a different future, but it does not need to be bleak.

These are uncomfortable feelings that are a normal part of coming to terms with your child’s learning disability.  It is helpful to accept the feelings as you move along to advocate for your child.  In next week’s blog I will talk about ways parents can take care of themselves to manage these feelings and become effective advocates for their children.

 

Click here to sign up for my newsletter, Parents’ Corner, and receive my free report, “Living With and Loving Your Disorganized, Impulsive, Forgetful, Yet Delightful, Funny Child”.

 

Photo Credit:  Keltron (So far behind,  I’m in front of me!)