Ailsa has such a positive attitude, I see myself in so much of her story. I have a goal to follow her example, accepting the hand life has dealt me with grace and dignity.
It is pretty easy to get in myself into a pitty pot as I am faced with new and different challenges daily. One thing about ALS, every day you wake up is a surprise, some days good, some bad. I try to find one blessing in every day and as I look around me it’s not hard.
I also miss the simple things like cleaning, cooking, driving, singing and dancing. I especially miss being able to get up and go anywhere, anytime I want, saddened as it further adds to the loss of my independence. I try to focus on the things I can do, sharing stories like Ailsa’s and never losing hope. I too am hanging on, waiting for that elusive cure.
Thanks Ailsa, for your inspiration.
“When you come to the edge of all the light you know, and are about to step off into the darkness of the unknown, faith is knowing one of two things will happen: There will be something solid to stand on, or you will be taught how to fly.”
“Too busy to be afraid”… Those words sparked my interest, Tim has ALS. He is truly an inspiration to anyone who is challenged with an incurable disease. As the fear of the unknown haunts my every waking hour, reading stories like Tim’s gives me renewed hope. Former Titans linebacker Tim Shaw is facing life with ALS
Check him out on Facebook https://www.facebook.com/TimShawOfficial/?fref=ts and Twitter https://twitter.com/TShawsTruth he is one amazing individual. Even a tough football player like Tim, faced with the increasing difficulty of once simple tasks, has an unbelievably confident attitude that keeps him grounded, embracing the triumphs of even his smallest accomplishments. I want to be like Tim.
Give a Girl the right shoes, and she can conquer the world. ~Marilyn Monroe
This story is an example of just one of the many struggles that I can relate to… I love shoes! I now have many pairs I cannot wear anymore because they are heels or simply just too hard to get on and off my feet because of the weakness in my hands.
Like Tonni and Wes, I also went on a trek for cute shoes that weren’t high heels, flip flops or slides, and have found there are some really adorable footwear choices out there that I can wear without fear of falling or getting stressed out because they are too hard to get on. Vionic has some really cute strappy sandals and Skechers Go Walks come in fun colors and styles, both are super comfy. So far, I have bought Vionic Rest Paros Strappy sandals, Skechers GOwalk 3 Pulse Women’s Walking and Performance Women’s GOwalk 3-Digitize Walking (shown above). Fighting the constant battle of tying shoe laces also sent me on another venture to the find any easy alternative. I tried a pair of the elastic no tie shoe laces but my hands are too weak to hold the shoe open and get it on my foot. Zubits Magnetic Shoe Closures (also shown above) were the perfect answer to that fight. I got a set for each pair of my shoes with laces from Amazon and absolutely love them.
The installation can seem a bit confusing, here is a great how-to video:
This is an incredible story.
Her determination is truly inspirational.
PCEye Amazing Technology
As I started losing strength in my arms and hands, it was getting increasingly more difficult to use my big clunky hair dryer, so I ordered this little baby. When it came in the mail, I was concerned about it’s size and strength to dry my hair, but the Berta 1000 is awesome!! It dries my hair in less time than the monster 2.4 pound hair dryer I was using. It only weighs 10 ounces and has a nice long cord. It’s all about the little things that make my life easier. Plus, it just happens to come in my favorite color…Pink! LOVE IT!!!
I have learned two important lessons since being diagnosed with ALS; 1) You have to keep moving (stretching and exercise are mandatory) 2) More is not necessarily better (don’t wear yourself out, it doesn’t help). This was one of my first additions to the 2X a day stretch regimen I do daily (this is non-negotiable for me). Stretching is vital as muscles get progressively weak and fatigued. The calf muscle is one that can get very tight and makes already difficult walking an even bigger challenge. I used the calf stretch wedge in PT and my husband Randy, a very talented woodworker, built me one to use at home. We adjusted the plans a bit from what I found online. You can get the non-skid tape at Menards or Amazon. I actually ordered only a few
and Amazon sent me a big roll by mistake. I will send strips (as long as they last) to anyone who has a need, just message me where to send. Randy will also build a wedge for anyone, $20 plus shipping cost or we can email plans (contact us, firstname.lastname@example.org). Anyone who has tight calf muscles will benefit from the calf stretching wedge no matter what the cause. Good article about tight calf muscles, http://bit.ly/1YMORzd. I stretch both legs at a time for about 1-2 minutes. When it comes to stretching, more is definitely better, and it feels awesome!