Good evening, another thing about not being able to get out of the house is no date night. My wife and I can't go out for dinner, a show or even to visit friends. Having ALS has really put a damp on or lives. Just things you take for granted, getting in the car to go out for dinner, run to the store or a visit to a friends house. I can't do anymore until we get a mobility van.
Thursday, March 16, 2023
Sunday, March 12, 2023
ALS and the loss of travel
Happy Sunday all. Having ALS really sucks, because now I can't leave the house because I can't get in our truck. We have a carrier on the back for my wheelchair, but I can no longer lift my leg high enough or stand on my weak leg to support myself. I tried two weeks ago now to travel to a doctor's appointment and had to be placed on the ground by my wife and 911 had to be called to lift my butt back into my chair.
We have started a go-fund-me to try and raise some money for a mobility van, because they are so expensive even if we trade our truck in it would not cover the cost of a decent van. Not being able to travel out at all sucks. I can't go to the store with my wife, out to eat with out granddaughter, taker her to the park or anything. It really put a damper on life to be stuck at home all the time.
If you can donate it would be appreciated from the bottom of my heart! God bless everyone!
my go-fund-me is: https://www.gofundme.com/f/help-me-with-my-fight-against-als
Friday, November 18, 2022
Good morning and happy Friday,
I have not written in awhile, due to being busy and upset about having ALS, it is not for the faint of heart as my muscles continue to weaken. My left hand/arm is about useless now, I cannot tie my shoes, put on my socks and struggle with many things I always took for granted like opening a zip lock bag, or even a box of cereal.
I have lost my driving privilege's as I blacked out and fell down about 6 stairs at a customers house while doing an estimate. Scared the homeowner as well as my wife. My watch called her after my fall but as soon as she answered it hung up this happened a few times before she called back and the homeowners answered. I won an ambulance ride to the hospital and a 4 day stay, and to this day no one call tell me why I blacked out. They did a CAT scan, an MRI, a doppler on my heart and my carotid arteries, as well as an EKG. Still no answers, also they had me wear a heart monitor for 30 days to see if my heart was the problem, but no new is good news as I have not heart back from cardiologist. I hope to find out more on my next visit to cardiologist.
Sunday, April 25, 2021
Diagnosed with ALS, Lou Gehrig's Disease on February 25, 2021
I have recently been diagnosed with ALS, it is affecting my left arm and hand.. I have lost strength in my left arm and hand.. I have no fine motor skills in left hand, I have a very hard time gripping it items, and cannot even hold up a foam plate with a tortilla shell on it. It is very sad, it makes me mad and frustrated that I cannot do thing easily, like pull a zipper or open a zip lock bag. Getting dressed is a challenge most days and putting on my boots can take a few minuets.. This disease sucks and it will eventually take my life. Average life expectancy is 2-5 years after being diagnosed.. I hope I last longer than that.. My wife is taking this very hard, and is very upset about it.. It is a hard thing to think about and deal with right now.. More to come soon...
Friday, December 25, 2020
Merry Christmas everyone.. I hope you and your family are doing well during this crazy year... The woo Han flu that has effected thousands of people is sad. We are struggling during this lock down of restaurants, and other eating and drinking establishments. It is unbelievable that you can go to Wal-Mart, or other stores but they are limiting out-to-eat or dine-in restaurants. What are your thoughts on the lock down? Should we reopen our country or keep it locked down?