Skip to main content

About Me

My photo
Humbly Courageous
Hi, I’m Amy. I live life with a condition called Bethlem Myopathy which is a rare form of Muscular Dystrophy. I like to help others by showing how I live well with a debilitating condition. I was born with this disease, so it’s the only way I know life. I continue to work on embracing myself and using that to help others.

Followers

Self-Blame

Hello and welcome to another week at Humbly Courageous. I’m glad you are here!

Living my life with a progressive muscle disease, I’m no stranger to the self-blame game. Whether it be brought on from outside sources or my own thoughts, self-blame towards my lack of physical abilities is always waiting in the wings to attack. It’s an automatic go to if I’m not careful. It’s not helpful to me in any way. If I’m not my own cheerleader in a situation like this, how can I expect anyone else to be?

I’ve spent the last several years trying to correct damaging thought patterns. Most of my life, I was extremely negative towards myself and my disability. Retraining your brain is definitely possible, and it is something I’m capable of doing. 

I’ve seen a lot of progress in myself. However, it takes consistency and diligence, and a whole lot of patience. You have to go into it accepting you will take two steps forward and one step back over and over. 

Recently, I thought about how not that long ago most of the time I could choose to leave my cane behind in the car for a quick trip into the store. Now, I panic when I think about not using it. What was once more of a security blanket, now feels like something I can’t live without. I found myself thinking, did I not do enough? Should I have tried to exercise more? Am I letting fear take over and cloud my reality?


Part of overcoming self-blame is to work on your defense. Your battle against those thoughts. It's not just knowing your truth, it's believing it. In reality, I know I’m doing the best I can. I’ve got nothing left to give. I’m going down swinging that’s for sure.

What happens though when the self-blame is born from the things others say? That’s hard to hear from others that they think you could be doing more. If you’d just do it this way or that way maybe you could cure your genetic disease? I’ve heard a lot of those type of comments/unsolicited suggestions in my lifetime. It’s deeply hurtful and damaging to lay that kind of pressure on someone. It’s just ignorance. 

I’m not a confrontational type of person, so I usually just stay quiet. I get frustrated with myself that I don’t stand up for myself more and defend my truth. Another thing on the long list to work on. One thing at a time. On the other side of that, I also think the ability to hold your tongue doesn't always make you a weak person. Sometimes, that is the right thing to do.

It takes humble courage to fight self-blame head on. Are you too struggling with self-blame towards something out of your control? I encourage you to work towards changing those thought patterns. It’s good to hold ourselves accountable when it’s appropriate. However, when it turns into constant self-deprecation for something that isn’t in your power to change, that’s a problem. It’s so freeing to gain confidence and feel good about how you are facing the difficult circumstances in your life. 💚

For more on my story follow me on Instagram @ashinneman

Check out my weekly column “Disability in the City” in The Hamilton County Reporter. https://readthereporter.com/the-same-but-different/


Comments

Popular posts from this blog

Dear Muscular Dystrophy

A letter to Muscular Dystrophy on the eve of my 49th birthday. This has been a lifelong journey…. Dear Muscular Dystrophy, At times you dazzle me, showing me the heights of human love and kindness, and at other times you take me to the deepest, darkest parts of my soul. I have silently pleaded, please just let this end. I don’t want to do this anymore. I’d like to say that was a one-time thought, but you’ve made it impossible to tell that as a truth.  I want to love you because you are a part of me, but you make it so hard at times. You feel like a best friend when I achieve feats that seem impossible due to my physical weakness, but also you feel like my worst enemy living inside of my body when you fail me, and I’m once again lying on the floor. You robbed me of big chunks of childhood joy, while I sat in silent envy of my friends, as I watched them effortlessly turn cartwheels, run and jump.  You are stuck to me like glue during the countless hours in waiting rooms, operati...

Recovery Week 1, SVF Stem Cell Treatment #2

Welcome back! Well, I survived week one post double SVF stem cell procedure, and also got word that the half of my cells I am banking arrived safely at the cell bank. That was a relief! One thing is for sure, there was a definite difference in the single procedure recovery vs. the double procedure recovery. There has been a lot more pain this time. I am still very sore from the procedure. The bruising is getting better, but definitely still there. Also, the area is still swollen and very tender to touch. Each day I have just taken it day by day. I have had some good days, combined with some really painful days. The pain is from the actual procedure, but also I have had some achiness all over that has been pretty persistent and miserable this time, as well as feeling very fatigued. However, I know I am only about a week post procedure, and all of this is to be expected. Allowing your body to heal is important to the process! The first couple of days, I just had a hard time finding a com...

Dear Disabled Motherhood

Dear Disabled Motherhood, As a child, I never dreamed being a mother could be my reality. As I got older, I boldly proclaimed I did not want kids every chance I got.  I was suiting up in an armor of protection, thinking if I told myself that long enough, I would believe it.  My childhood years spent playing with my dolls pretending to be a mother, but not really believing that would ever by my reality. Now I know, that was a lie I told myself to soften the blow. I did want kids. I just did not think my body was capable. God placed a glimmer of hope in my heart, telling me I could be a mom. We trusted that. To this day, I still spend many moments in awe marveling at the ease in which I was able to become pregnant, twice. Nothing ever came easy. I expected pregnancy would not either. What a true blessing that took me by surprise. What did not come easy was finding information on becoming a disabled mom. The books that were out there had so many things in them that did not apply ...