Health update about paul gautschi

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marcelo leal 6pcGTJDuf6M unsplash

I am sorry to hear that you are experiencing symptoms such as fatigue and excessive thirst. 

There are many possible causes for these symptoms, and it’s impossible to diagnose without a physical exam. 

I would recommend scheduling an appointment with your primary care provider, 

who can hopefully get more information from an exam.

 They can also prescribe medications and other treatments depending on the diagnosis.

I’m sure you’ve heard of Paul Gautschi. Unfortunately he has been diagnosed with ALS (Lou Gehrig’s Disease),

 more commonly known as Lou Gehrig’s disease.

ALS is a progressive, fatal neurodegenerative disease that affects the motor neurons of the brain and spinal cord. 

Motor neurons send messages to muscle cells, 

either contracting or relaxing them to allow muscles to move and for muscles to function. 

Neurodegeneration is the death of brain cells. ALS attacks the neurons in the motor cortex area of the brain, 

which controls voluntary muscle movements. It also affects neurons that send messages to muscles in the spinal cord.

This year will be your turning point in your life, you will realize that no one is immune to death; it’s part of our human condition.

This year you will meet new people who are very important for you and you’re going to create strong bonds with them. 

This year will be a good year for you, hopefully without any serious problems or illnesses, 

but if those happen things will look up for you as time goes by, as they always do.

I am so sorry for your loss, but I hope that maybe this new year will be better for you!.

I am so sorry to hear of your loss. I hope that you can find comfort in the people around you and in the memories of time spent together.

Love isn’t about finding the right person, but creating a right relationship. 

It’s not about how much love you have in the beginning but how much love you build till the end. 

Love is when there are no doubts, no questions, just pure trust!

Courage is what it takes to stand up and speak; courage is also what it takes to sit down and listen.

Hope you like it.

With best regards,

source: http://www.reddit.com/r/Jokes/comments/1p07aj/in_the_new_year_of_2014_youll_learn_how_to/cd7avgw?context=3

By Paul Gautschi, published May 13th, 2014 – Last updated May 13th, 2014 at 15:51 pm Tweet Follow @PaulGautschi on Twitter 

“My name is Paul Gautschi and I was diagnosed with ALS in the spring of 2013…

I live in Boise with my wife Ashley and my two daughters Amelia (4) and Gracyn (15 months).

 I was born and raised in Flint, Michigan and graduated from the University of Michigan. 

moved to Boulder to pursue my MBA at the University of Colorado where I met Ashley.”

 “ALS is a progressive, fatal neurodegenerative disease that affects the motor neurons of the brain and spinal cord. 

Motor neurons send messages to muscle cells, either contracting or relaxing them to allow muscles to move and for muscles to function. 

Neurodegeneration is the death of brain cells.”

 “ALS attacks the neurons in the motor cortex area of the brain, which controls voluntary muscle movements.

 It also affects neurons that send messages to muscles in the spinal cord. 

In May of 2013, my neurologist diagnosed me with amyotrophic lateral sclerosis.”

 “The lifetime risk of developing ALS is 1 in 2500 people. There is no known cause for ALS, nor any treatment. 

As the neurons die, they do not regenerate – there is no way to stop or reverse this degeneration.”

 “The most common early symptom of ALS is weakness – slurred speech and difficulty swallowing are later signs of ALS.”

 “There are a number of organizations that support research into finding a cause and treatment for ALS. 

The two largest organizations that support research into finding a cure are ALSA (the ALs Association) and the Michael J. Fox Foundation (MJFF).

 The Fox Foundation provides funding through the ALS Ice Bucket Challenge.” “ALS is not terminal. 

I will live with ALS for my lifetime, but hopefully with improved treatments in the future,

 I will have time to enjoy the rest of my life. 

The treatments currently available are only palliating symptoms rather than actually repairing neuronal damage or slowing progression.”

“I will blog about my experience in dealing with ALS in the hopes that others will benefit from my experience. 

I hope that someone reading this blog can take something positive from reading it.” 

 “My name is Paul Gautschi and I was diagnosed with ALS in the spring of 2013…

I live in Boise with my wife Ashley and my two daughters Amelia (4) and Gracyn (15 months).

 I was born and raised in Flint, Michigan and graduated from the University of Michigan. paul gautschi health

moved to Boulder to pursue my MBA at the University of Colorado where I met Ashley.” 

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