Sunday, March 04, 2018

Walking on sunshine?

Walking, Stumbling, Tripping, or Falling

     Well, this article was a bit of a struggle. It was mainly a bunch of charts and statistics that deal with walking and MS. It was really really REALLY boring. But I did manage to glean one good gem from the nine pages of research and findings.
     It was consistently found that persons with MS are more often not active enough outside of regulated, light routines to be able to feel the full benefit of in their walking. This came as stark wake up call for me. I started off this year meaning to do more of my physical therapy routines more consistently, but I have not stepped them up enough. This article has inspired me to do more. 

See you next week. 

Sunday, February 25, 2018

Sometimes, repetition isn't so bad

     Every six months I have to go through a six hour infusion.
2nd Poem:
(dumb as the first, just a little bit longer and MUCH worse)
Anticipating Rituxan
It is time again for an infusion.
My next appointment approaches in days,
Hoping to slow this diseased intrusion.

Up before the sun, and in seclusion,
In the car by the light of the moon's rays,
It is time again for an infusion.

Avoiding the rush hour confusion,
My trek goes through many familiar ways:
Hoping to slow this diseased intrusion

At Shepherd I am met with inclusion,
Greeted by smiles and friendly displays.
It is time again for an infusion.

Checked in and ready for the perfusion,
The 'pre meds' put me in a slight haze-
Hoping to slow this diseased intrusion.

Six hours later, there's one main conclusion:
Never surrender! For, I am always:
Hoping to slow this diseased intrusion.
It is time again for an infusion.

Monday, February 19, 2018

Just Triceps Something New

Triceps

     The triceps really aren't that exciting. They're often overshadowed other muscles. Think of the stereotypical gym scene from a movie people: running, benching, flexing, and such. But, over the years, this MesS has shown me just how important this group is. From getting into my rollator's seat, to getting off of the commode, or getting out of bed, my arms are seemingly in a constant workout mode, and the group does the most are the triceps. So, here's a brief rundown of what I do on Mondays, Wednesdays, and Fridays: 2 sets of 10 reps for each arm using blue (8 lbs.) resistance band. 
     At first I didn't have any resistance bands and just used a simple, three pound hand weight. When my physical therapist showed me how to use resistance bands it went much more fluidly. The bands are what I use now and in addition to being lighter in weight, there are other bonuses as well. It's less stressful when I fall, being easier to pull myself to my feet. Getting from my rollator to the toilet is easier because there is less trembling as my triceps are better at helping me keep still. The best result, however, has to be from being able to cook. As a career fat guy, cooking being curbed due to my inability to use a knife was a real downer. But now I am seeing some ability coming back.
All in all, it's tough, frustrating, but possible!

Monday, February 12, 2018

A basket? No, how about a skillet?

Baked Omelette Pie

     In keeping with my attempted resolution to drop gluten, at which I failed last night by having a piece of pizza, here's a wonderfully complex, but workable, recipe. Here is a link to the original recipe. This recipe calls for a cast iron skillet, but if you don't have one, a regular skillet can work, but be sure that it is able to be used in an oven up to 350° F (175°C). Below is my version of it with accommodations for this MesS.


Ingredients

1 large baking potato
6 eggs
1 teaspoon salt
1/2 teaspoon ground black pepper
1/4 cup chopped fresh parsley
2 tablespoons olive oil
1 onion, chopped
1/4 cup chopped red bell pepper
1/4 cup chopped fresh mushrooms
1/2 cup chopped ham
1 tomato, sliced
1/4 cup shredded Cheddar cheese

     I know it seems like a lot to do just to make something for breakfast, but I do have a few 'short cuts' that might make it easier to make it. 😏
  • Instead of a large baking potato, consider a Yukon golden, or red skinned potato. They're smaller, cook faster, don't need to be peeled, and taste MUCH better.
  • Instead of cracking six eggs, which for me is enough work to need a nap on some days, consider "Egg Beaters," or some other alternative. They have an added bonus of being a little healthier too.
  • Slicing tomatoes always gives me fits. Trying to hold the tomato, slicing through, and NOT squishing it is never easy. Sometimes I just use canned tomatoes, or even sun dried. But be careful, with sun dried tomatoes a little goes a long way.
Directions
  • Bring a medium pot of salted water to a boil. Add potato and cook until tender but still firm, about 15 minutes. Drain, cool, peel and slice.
  • Preheat oven to 350 degrees F (175 degrees C). Beat together eggs, salt, pepper and parsley.
  • In a cast iron skillet, heat olive oil over medium-high heat. Saute onion and red pepper until soft, then stir in mushrooms. When mushrooms start to shrink, add the chopped ham, potato and tomato slices. Pour in the egg mixture; gently stir to combine.
  • Sprinkle cheese on top of eggs and place skillet in preheated oven. Bake until eggs are firm, about 10 to 15 minutes. Allow to cool briefly before serving.
It tastes wonderful, and leftovers make a good brunch or snack cold right from the fridge. Now, for some cheesy egg puns. 😜

"I went to the store today and bought some really oddly shaped eggs.
Now I can't find them.
I think they've been mislaid."

"What day to eggs hate the most?
Fry-day."

"How many French eggs do you need?
One egg is un oeuf."

"I was walking past the store today when I saw a sign saying, 'All items one-third off.'
So I bought a dozen eggs.
Unfortunately four of them were rotten."

Monday, February 05, 2018

I am such a 'spaz'.

     Spasticity: a spastic state or condition; especially muscular hypertonicity with increased tendon reflexes. (Merriam Webster Online)

     Before this MesS became a part of my life, the word, "Spastic," only made me think of a cartoon character, nerdy gamers, and amped up tweakers. But, that view changed with my diagnosis. Yes, I still get a laugh over spasticity, but it usually comes at my own expense. For example, when my calf muscles and shins get spastic while I am sitting, my legs will 'bounce'. My four year old usually tries to dance along with the bass-like thumping that my heels make as they're slammed against the floor. 
     It can also be annoying. I have had my legs freeze mid step, sending me to the floor. At times my hand will enter, what is commonly called, "The Claw." When the claw hits, it is most often when I am trying to write, type, or even grab a glass or can. The result is usually a writing sample of the proverbial 'chicken scratch', a sentence that needed to be retyped several times, or a dropped drink. But, the most annoying aspect of it comes at night, when I am tired and trying to sleep. My legs will jump from a laying down position almost to a karate-like pose, often kicking my wife or launching me off of the bed. 
     In looking into spasticity, I discovered a wonderful article from the National Multiple Sclerosis Society's magazine Momentum. This article is a wonderful source about spasticity. The author covers examples, treatments, medications, therapies that help, and presents it all in clear and easily understood manner. She [Elinor Nauen] took a lot of the fears and worries had about spasticity. Here is a link to the article published in the 2010 issue of Momentum. If you would wish to read more about spasticity, then follow this link

Monday, January 29, 2018

I still don't know it

     As the first month of 2018 comes to end, I have tried to keep up with my resolutions, and so far, I think that I am on track. But, now there is one final step that is rather embarrassing. I decided to share a poem about MS of my own creation each month. I have created poems in the past, maybe even shared them, but these are newly created for this year. My goal is to have a collection of twelve new poems about my life with this MesS. So, here is the first:

Changes 
My world has changed, grown.
There's now so much more to see.
In a dream, I wander aimlessly
To make improvements on my own.

I have set goals, will work tirelessly
To see them finished.
But, my ability is diminished
By this disease-inspired melancholy.

I have lost so much, but will rebuild
With a new found desire to achieve.
Forcing myself, once again, to believe,
I dedicate myself to seeing this dream fulfilled.
-Josh Evitt (2018)                                     


Monday, January 22, 2018

Get Your Head In The Game

Meditation
Mindfulness
Introspection
     We've all heard about meditation and it's benefits to this MesS. But, I never really understood it, even now that I have started trying it. At the beginning of this year I started seeing a psychologist to help we with some building anger issues that began to creep out. 
  • Getting angry at the drop of a hat
  • Swearing A LOT
  • Catching myself saying the most hateful things
     So, at my wife's request, I began seeing a therapist and was introduced to the concept of, "Mindfulness." Yes, it pretty much is just guided meditation, but it is also really difficult to do with the end result being much more of a tolerable person. 
The steps which were presented to me are:
  • Find a quiet place
  • Focus on breathing
  • Empty thoughts
  • Eventually bring one's mind back to the present.
     This seemed all well and good until I tried it. I keep on spend the most time thinking, obsessively, about how much I've failed. I am going to keep at it, but not solo. I have created a playlist of just one song that repeats a few times. It's a song that is purely instrumental, calming. 
     I have also begun looking, my doctor's suggestion, at a website called Headspace. It's an interesting site, and if you're in my situation of wanting to practice 'mindfulness', then feel free to check it out.

Here is my 'mindfulness' song.

Monday, January 15, 2018

Bye-ceps

     Well, this past weekend was fun. Fun as in I slipped out of my shower chair, missed my handrail, and then sliced my toe open as my feet slid into the vent cover. But there was a silver lining to this embarrassing cloud. Beginning around December of last year, I noticed that my falls had become more frequent and more crippling. I began to accept that whenever I would fall that it'll now just take me anywhere from 2 - 3 hours to get back to my feet. Needless to say, apathy started to fester.
      But, after working with a really good physical therapist on developing a routine for falling, exercises to help bolster my wobbly legs, and ways to 're-wire' how my arms work, I have been able to improve my recovery time. A few weeks ago I had a leg-extension spasm, similar to the one that caused me to wreck my car, and fell out of my rollator's chair in the middle of the kitchen floor. I used my arms and pulled myself across the kitchen and into the dinning room. I was actually able to lift myself into a chair, I call it my 'fall chair', and rest until I could return to my feet and wall-walk back to my walker. Then, just a few days ago, I fell getting out of the shower. I tripped on my shower chair and gravity took over. But, I was able to crawl out of the bathroom to my bed and lift myself to my feet by 'climbing' up the bed. Then, today after my shower I was able to take a shower without needing to my usual routine:
  1. Sit on shower chair
  2. Move to toilet
  3. Lift shower chair into shower
  4. Reverse to exit shower
I was able to move my chair to the shower without stopping at the toilet and didn't need to use my chair to exit the bathroom! Physical therapy can help, and especially in this case: Biceps.
     I wanted to highlight biceps this time because mine are rather lacking. I use a walker in the house a large mobility scooter elsewhere. So, I have stopped needing my arms as much as I thought, but this year I am keeping up with my PT routine of working arms and I am noticing some improvements when I have to pull myself up to a sitting position or off of the floor. Here's the big secret: I don't do it every day. 
     Biceps fall on Mondays, Wednesdays, and Fridays. I only do two simple sets of ten reps on each arm. For weight, I started with a small, green resistance band, about 2 lbs. worth. Now I have begun using a tougher band, five lbs. resistance, and hope to eventually move to a 10 lb. weight. Who knows. 

Monday, January 08, 2018

Deliciously Vichyssoise

     In keeping with my attempt to lower the impact that I make on the ground, losing weight, I have embarked on a trial of going gluten free. Now, I am not severely going gluten free, as some have to do for health reasons (i.e., celiac disease). I am not going this extreme for two main reasons. First, I do not have Celiac Disease, so I do not have an aversion to gluten. Second, I know that if I try to go full blown, zero gluten I will: get bored, become frustrated, and then quit. But, I am going to try a gluten free recipe and share it along with any extrapolations I have come across or improvised.
     So, here is the first: Vichyssoise, or leek and potato soup. It can be a very simple or a highly complicated recipe, depending on how much of a stickler for following recipes you are.  Now, this might seem like it is very difficult, but there are some aspects that make it easier for those of us with limited mobility.

  • It only uses one pot. Since there is no grease to be drained, meats to be separated, or cooked things to add later, this entire recipe can be cooked in one big pot.
  • It is easy to supplement some the 'pricier' ingredients with just one simple one. See the notes in RED.
  • It tastes REALLY GOOD! - Fat guys know what tastes good. The proof is in the pudginess.

Ingredients

  • 4 tablespoons unsalted butter

  • 1 1/2 pounds trimmed leeks (Clean and slice a leek) I also add an onion, sliced, for extra flavor.

  • 2 teaspoons kosher salt, plus more to taste

  • 1 1/4 pounds Yukon Gold potatoes, peeled, cut into eighths (any potato will work, but Yukon Golds are the best.)

  • 3 cups chicken or vegetable broth, or more as needed to adjust thickness

  • 1 cup heavy cream
  • 1/2 cup creme fraiche
  • (to make it simpler, I just use 1-2 cups of buttermilk)

  • 1 pinch cayenne pepper (optional)
  • Chopped fresh chives for garnish
  • *An added ingredient that I also use is good cheddar cheese, grated and stirred into the soup while hot.*

Directions


  1. Melt butter in soup pot over medium-high  heat. Add leeks and salt; cook until leeks begin to wilt. Reduce heat to medium or medium-low and cook until soft and almost paste like, 30 to 40 minutes.
  2. Place potatoes in the pot; add chicken broth. Adjust heat so mixture simmers slowly. Cook until potatoes are soft, about 30 minutes. Puree mixture with an immersion blender or in batches in a blender. Whisk in heavy cream and creme fraiche. Heat over medium heat. Add more salt, if needed, and cayenne pepper. Do not boil.
  3. Serve with a drizzle of creme fraiche and a sprinkle of chopped chives.
Here's a video of a chef that really follows the recipe.

Monday, January 01, 2018

New Year and New(ish) Blog


        So, here is my first attempt at a second shot. I recently read an interesting article in the National MS Society's magazine Momentum that deals with balance issues and how to help with them. Now, balance is one of my worst symptoms, and I know that I'm not alone in that. So, I thought that I'd give a brief summary and highlight, what to me are, the most important parts. 
     First, the article gives a very clear explanation of how easily MS can sabotage balance. Basically, since balance uses so many parts of one's CNS (central nervous system), and MS damages the CNS the chances of causing balance issues is very high. The article then explains how physical therapy can help, but that is up to the patient and a doctor, or therapist, to develop exercises that fit one's own balance issues. 
     Next it mentions a thing called, "Vestibular Rehabilitation," which seems that it might work, but, since it focuses more on inner ear complications with balance, would only work for a very small subset of patients with MS. It also briefly mentions using a device that is a type of treadmill that makes one feel lighter, the Alter-G.
     But, the most interesting part, as well as one that I am going to try to implement for myself, was to combine four different types of exercises: breathing, stretching, relaxation, alignment. I plan using these four, along with an already prepared regimen, set up by my physical therapist, to help me maintain and hopefully improve my current balancing issues.


     I am not going to sugar coat this.

It's going to be tough

But, I am going to do it!