How  Do  I Support Without Enabling  Our Physically Challenged,  Adult Son?


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Caring for an adult child with a physical disability is extremely challenging 

Half the time I have no idea what my role is. I am Mom, caretaker, nurse, counselor, all at the same time. 

All very unique roles and all very important but to do all of them at the same time is hard and very challenging.


Guilt... Help!

Mom guilt...frustration, anxiety, worry, feelings of... I'm doing it all wrong. The question I ask myself, what if? What If I would have checked on him sooner in his apartment? What if I had found him sooner after his seizure? Surely we could have avoided all this and he wouldn't need to deal with these stroke like issues.


The day life changed...

 Our adult son had some sort of episode (we still don't know what happened) and lost mobility to walk and use his upper limbs due to stroke like symptoms. 

He's single and came home to live with my hubby and I for a period of time to nurse him back to health. It's going on 3.5 years.

 Just prior to this my husband retired so... this was not in the plans of how we we had planned to do life after retirement. 

But then again, life is not made up of "drinking sweet lemonade" every day... sometimes we're handed a bitter lemon.

 It's life, things happen. What we do with the lemon is really the most important. 


I’m the kind of person that wants to fix everything and make everyone happy. I often feel angry and frustrated because I can't. I can't fix it all.

I spend hours researching hoping to find the next right thing. Because I feel sorry for him,  I do things for him that he could maybe do himself just so I don't need to see him struggle or... the fact that I could do it faster for him.

I struggle with feelings of helplessness, feeling like I don't do enough but then guilt because I do to much. It's a vicious cycle in my mind.


Am I An Enabler? 

When does doing to much for your adult child hinge on the side of an enabler? I certainly am guilty of that and struggle with it constantly. 


To enable is to inadvertently reinforce an undesired behavior.
I think we all do this to some degree because it’s only natural to want to shield our children from pain, fear, failure, difficulty and embarrassment. I try not to be that helicopter parent but that's not easy! I'm a server and nurturer, sometimes to a fault. My time and energy is spent on him. I spend hours researching for a new med, searching for solutions or more answers to make his life better. It consumes me at times and literally drains and sucks the energy out of me. 

 If I could simply refrain from asking too many questions or let him figure things out on his own such as...
 -Did you take your medication?
-What did you eat?
-Are you drinking enough water?
-Perhaps covering up for things he did o...r forgot to do or did poorly 
-Protecting him from an uncomfortable situation
-Speaking up on his behalf instead of letting him learn to express his own thoughts and feelings
-Helping him with a task so I don't have to watch him struggle to do it on his own.

 It's a frustrating, emotional rollercoaster...

I will say though that I often find internal strength that I never thought I had. God desires that we be utterly dependent upon Him and when we trust in him he will never leave us alone. He is always there and he will always provide a way even where there seems to be no way. God is ever so faithful and I often hear him say, "Don't panic, I've got this. Simply trust me. 


So... I come up for air and I become intentional about looking at the progress that was made. I savor the good moments and realize how blessed we are. I thank him for the progress our son has made and continues to make. 

I'm thankful he can walk again even though he struggles with his balance. 

I'm thankful he can use his upper limbs again even though he only has use of one hand. It's peepy steps but it's progress in the right direction and for that I am thankful. I savor the good days and moments and... I don't take them for granted.

 I look for and find  joy in even the smallest milestones reached that were predicted never to occur. Yet, I will occasionally feel like I failed my son when we have our moments of lashing out on each other because one of us or both of us are not in our lane. Thats the emotional rollercoaster ride I speak of.


Here's what I'm still learning, 
-Where to draw the line 
-Staying in my lane 
-When to stay silent and when to speak
-When to back off
-How to give him structure and support yet give him the freedom to be.
- Allowing him to fall and make mistakes yet be there to pick him back up? 

I don't pretend to have the answers. I'm still learning and grappling each day to do it right. Not perfect ... but right. 

One thing I take serious is to support my immune system everyday. I do that by drinking at least 2-4 oz. of NingXia Red Juice, I make sure I have my super B for energy and keep my mood in check along with omega for the brain, and a few others. 

And then of course I always have my oils close by and apply them daily or through out the day depending on my stress level or... I even have an oil called clarity to help my brain think more clearly.
 It still amazes me even after 7 years of using oils, how beneficial a drop or two is. 

Do you relate? If so lets chat, lets connect. I'd love that!
Connect with me and... to read more of our story go to...https://getoiling.com/VernaSmoker
To order any of the supplements or oils mentioned above, you can order here.
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