Thursday, May 31, 2012
May 2012
While my faith may have been tested, I still believe God has a plan and purpose for each one of us. The following is taken from my friend Shawn Smucker's blog.
"The fire rages in our lives, and in its wake we are left feeling disappointed, bitter, angry or depressed. Or all four. Or something else. The landscape of our life begins to feel charred and dead. Worthless. Mordor-like."
Sometimes it takes the fire to purge our lives so new new life can begin to flourish. As I process what God's trying to show me through all this, I'm reminded once again that God does care and love us despite our inability to accept what we experience in this life on earth. So, go to hell you little devil, because I refuse to listen to you anymore.
If you would like to read more of Shawn's blog go to http://wp.me/p1AFbN-1gH
Thursday, April 26, 2012
April 2012
Another event was the Annual 5K Gordie's Run/Walk. A caring couple from church host this event to help raise funds to help me with wheelchair modifications and medical expenses.Thanks to all who participated. I am forever grateful for all the support you continue bless me with.
Perhaps the most exciting thing in my life at this time, is I found out I am going to have a grand baby in November! I am so excited to be a grand parent.
I posted some pictures for you to enjoy!
Tuesday, March 20, 2012
March 2012
Friday, February 10, 2012
January 2012
Right now my focus is to get well, regain my strength, and not grow weary in my walk with the Lord.
Thanks for your prayers
Wednesday, December 14, 2011
December 2011
I remember the first Christmas after my diagnosis was a sad time for me. The only thing on my mind at that point was how many more years I will get to spend Christmas with my family. Now I'm actually looking forward to this Christmas. As the years go by, I focus less about dying and more about living. I am fully aware of what this disease will do to my body, slowly rendering every muscle in my body useless, evenually leaving me paralized and unable to breathe, resulting in death. Until then, I intend to live and enjoy life as best as I can.
For some, the holidays can be a time of sadness and somewhat bittersweet due to the loss of a loved one, illness, or some other tragic event. My thoughts and prayers go out to those in that situation. I pray they will experience peace and joy during the holiday season, despite their situation.
One thing I learned, giving gifts is nice and a fun time with family and friends, but there so many around us that literally have nothing. How many of us need more stuff? That's all it is, stuff. Probably things we could do without. Why not bless those less fortunate and bring real joy to those in need. After all, Christmas is the time of year we celebrate the greatest gift of all, the birth of God's gift to mankind, Jesus the Savior of the world. So this year, don't forget why we celebrate Christmas and make this a time where we can give a gift to those that could truly use what most of us could do do without.
Hope you all have a blessed Christmas season a Happy New Year!
Tuesday, November 8, 2011
November 2011
I had a recent visit with the ALS clinic in Hershey, which I felt went fairly well. My breathing capacity dropped to 48%. They recommended nebulizer breathing treatments three times a day to help keep my lungs clear and help with phlem building up in my lungs. Seems to be working. All in all they were pretty pleased with my condition over all. I'm getting some modifications done to my chair.
Carla Whitley a long time friend of ours recently organized a walk in for the ALS Association in Atlanta where she lives. Emy was able to fly down to participate in the walk. Thank you Carla for doing this for me. Funding for research to find a cure for this dreadful disease is grossly underfunded compared to other diseases and every little bit helps.
Wednesday, October 5, 2011
October 2011
As for me, I am doing pretty well. With the cooler weather setting in, I need to take extra care not to get sick. Every day is a another day I am blessed with. As this disease slowly robs me of my ability to function, I am reminded to appreciate what little I can still do on my own. Typing is becoming quite cumbersome and time consuming. It just takes more effort to navigate around the keyboard. I'm constantly hitting the wrong keys due to the lack of control of my fingers. But I'm grateful that I haven't lost complete function of my hands. There is always something to be thankful for if you don't dwell on what you can no longer do. I'm trying to keep a positive outlook through it all. Your prayers, generosity, and support are greatly appreciated, thanks!
Monday, September 12, 2011
September 2011
Five years later, I was diagnosed with a disease I barely even knew anything about. Much like that day on 9/11, I was left with a sick feeling of hopelessness and despair. I knew my life would never be the same again unsure of how many years I had left to live. Most people are given three to five years after diagnosis. I have exceeded that by a year and a half.
My life has changed dramatically since then. First, I lost my ability to walk leaving me confined to a wheelchair. Then I noticed my fingers not responding, my speech began to sound slurred. now I can't speak at all, eat, have difficulty swallowing, droll, get my nutrition through a tube in my stomach, my arms and hands are weak making it nearly impossible to hold onto anything without dropping something. I require help with every aspect of my personal care. This certainly isn't the life I wanted to live but with God's help, I have come to terms with my situation.
Since my diagnosis, I came to realize we are not guaranteed tomorrow. Just like those that lost their lives on 9/11, they didn't go to work that morning anticipating to die on that particular day.
I have made the decision to live out the remaining days of my life knowing God has a plan and a purpose for my life whatever that may be. I still have much to be thankful for. I have great people surrounding me that love me and a wonderful family, wife, kids, wonderful daughter in laws.I have been blessed with the best caregivers anyone could ask for. They have almost become like family to me and am extremely grateful for the care they provide for me.
Psalms 73:26
My health may fail, and my spirit may grow weak, but God remains the strength of my heart; he is mine forever.
Tuesday, August 9, 2011
August 2011
This past week we went to Ocean City, MD for a week which was nice. The weather was good for the sun worshipers! Hot! It's always good to be surrounded with my kids and family. My wife, Emy did a good job caring for me without the help from our caregivers. I will be forever grateful for her love and support. The best moments in my life are when I'm surrounded by my family. Never take those you love for granted. Cherish every moment with them because you never know what the next day has in store.
Lately I’ve been feeling sad. I’m not sure I know why. Maybe it has to do with my progression and the reality of the effects are sinking in. But I think the biggest challenge for me right now, has to do with lacking the ability to engage in meaningful conversation with other people. It gives me the feeling of being alienated from the lives of my friends and the people I used to interact with. Even when I get out and around people, I still feel left out. There is no time to type out what I want to say to be involved in a conversation when I have something I would like to say. There are times I would love make a comment while driving along but I have to sit there in silence. I can't use my iPad while driving because my hands aren't very steady. I can communicate with my iPad with an app, but it's just not same. It speaks with a robotic sounding voice which doesn't really relay my true expressions. This has by far, been the most difficult aspect of dealing with ALS to date. I can't even begin to explain the isolation and loneliness it causes me to have.
Your prayers and support are greatly appreciated!
Saturday, July 9, 2011
July 2011

Summer seems to be flying by rather quickly. Before you know it, the leaves will be falling and another season passes. That's how my life feels at times. I recall as child, I thought my life would pass at a much slower pace. Nothing to worry about but do my chores and the rest of the time was spent playing whatever we could imagine and pretend to be. anything from cowboys and Indians to motorcycle racing on our bikes. Since we didn't have a lot of toys, we made up our own creative adventures. If only life were that carefree and innocent now As the seasons in our life come and go, things don't always go as planned. I had a mental picture of how my life would be. Boy, did that change. I sure didn't think it would turn out like it did. Many bumps and bruises along the way, a few detours, and disappointments, here I am at this stage in my life. I am living my life with an incurable disease called ALS. This certainly wasn't the picture I had etched in my mind.Tuesday, June 7, 2011
2011 ALS Walk
People tell me how much of an inspiration I am to so many people. I certainly don't feel like it. But when I think about others that have inspired me, I think I get it. To be quite honest, I'm only doing what comes as a natural thing for me to do, and that is to trust God and let him have his way in my life.

I often picture it this way. I'm like a little boy holding on to my Fathers hand walking along and looking up at him, asking why did this happen to me? He looks down at me, smiles, and says to me, trust me son, everything will be alright. Content with his answer for now, we continue walking hand in hand. I have come to the conclusion I don't have to know all the reasons why things happen, but simply realize God has everything under control because that's what he said. One day, it will all make sense and we will be grateful for the lessons learned.

Tuesday, May 3, 2011
Some Thoughts About Easter
There have been times I questioned how God could allow some of his children to suffer, when there are those who despise God and seem to live healthy prosperous lives. God promises us our rewards in heaven while they enjoy their rewards here on earth.
Regardless of my my disease, I can say God is good and just. After all, he suffered more than any of us will ever have to. He gave his life so that you and I can have salvation from our sins. That is why his love for us is so amazing! There is absolutely nothing we can do on our own to receive God's amazing grace. He gives his grace freely to all regardless of our past history or how good we think we are. Like the story of the prodigal son, he is anxiously waiting for us to come to him no matter how dirty we are from the filth and slop of this world.
I love the song amazing grace that saved a wretch like me. It just resonates with me.
As for me physically, I'm doing about the same as the last report, other than that, my speech is no longer understandable and my fingers and hands are becoming weaker.
I'm trying to enjoy each day and make the best of my situation.
Friday, April 15, 2011
Dine to Donate
Thursday, March 31, 2011
Five Years Ago
Thursday, March 10, 2011
March 9, 2011
I would like to express my sincere thanks to the wonderful caregivers God has blessed us with. Irina is a special person with a heart of gold. She has a sweet caring spirit and is so positive about everything. She is very patient with me when I try to speak. Sometimes I think can read my mind and knows what I need before I even ask. She's also good for Emy. She provides her with encouragement and support. Not just a caregiver for me but also a true friend to
Emy. Trinity is one of the other caregivers. She does a good job as well with a light hearted attitude.
And then there's my wife and my sons and their wives who also take good care of me. I could not do this journey without them. I am truly blessed and I love each one one of them. I don't know what this year will hold for me but I know who holds the future and that's all that matters.
Friday, February 18, 2011
Febuary 2011
I am thankful for my family and the love and support they provide. I thank God for a wife that loves me and is always there for me. I know it's not always the easiest thing for her to deal with but she never gives up. My boys and their wives are a blessing as well. They help out when needed and are very faithful to spend time with us. God has blessed me with an awesome family and I want to say I love you all very much.
Tuesday, January 25, 2011
Today
which really doesn't make me feel very happy.
I hate this life with ALS
but I guess God knows what's best.
I'm trying my best to understand God's plan for my life
Why he would allow a disease that brings me so much strife.
I pray for healing but healing hasn't come
But I know he can do it, because he did it for some.
Sometimes I wonder does he even care
But because of my faith in him, I know he is always there.
There are times when I can't feel him, but I know he is near
that's when I reach out to him and know I have nothing to fear.
All things work together for the good
I want to believe that and wish I understood.
He wants us to trust and obey
and promises to show us the way
Today the weather may be dark and grey
but it won't be long till there will come a brighter day,
If we remain faithful to the end
with him in heaven we will get to spend.
So when troubles come your way
and there seem to be no answers when you pray
One thing I know, that certainly is a must
His ways are not our ways and in Him we must trust!
Saturday, January 8, 2011
January 2011
Christmas was a fun time with my family We exchanged some gifts and enjoyed the day together. What would I do without my loving family. The best gift they could ever give me, is knowing they have a heart to serve the Lord. They truly are a blessing! 



























