Georgia lady faces ALS with grace, hope

March 4, 2015 - als

ATLANTA –
Jennie Fountain is behind during a Emory ALS Center for checkup, a small on-edge. Fountain, who is 57, says “Today was a small scary. we was endangered about my breathing.”
 
Her respirating is okay, about 98%.  But it was here, 3 and half years ago, Jennie got a news, from neurologist Jonathan Glass. Fountain remembers,  “He said, You have ALS. And we was like, How do we know?  Because it was that matter of fact.”
 
Dr. Glass, who heads adult a Emory ALS Center, says,  “There’s no violence around a brush with this, it’s not fair.  People wish to know, and they should know.  There are dual things we tell them. we contend series one, we have this disease. And series two, we’re going to take caring of you.  And those are a dual things they need to hear.”
 
ALS, a engine neuron disease, gradually destroys a haughtiness cells that control a muscles. There is no cure, and it’s opposite for any person. It’s enervated Jenny’s mouth and neck muscles and her hands and arms.

The zealous skier and ALTA tennis player, was in her mid-fifties when she started seeing it was apropos tough to speak. The symptoms reminded her of an ALS studious she’s worked with as a respiratory therapist 30 years earlier.
 
Jennie’s father Laurence says, “She had a hunch.  we remember we were sitting examination TV one day, and she was afraid.  She was saying, “I wish it’s not what we consider it is.”   Jennie says, “You always think, “Why me?” But each time we do that, we also follow it adult with, “Why not me?”
 
Jennie says a hardest partial is how most ALS steals divided from you. She has always been active and healthy, and there are so many things she can no longer do.  It’s a story maturation in a FOX strike play “Empire.”  Fountain says, “Oh, my God, we adore that show! It’s great!”
 
In it, Lucious Lyon, a song noble during a tip of his game, unexpected is faced with his possess mortality.  He’s diagnosed with ALS, told he has about 3 years to live.  To Jenny, “Empire” feels real, it gets ALS. And yet she would never never have selected this path, she’s beholden for Dr. Glass and his team.

“Who know what’s ahead, and can expect and beam her.” Dr. Glass says, “She’s still means to swallow, she’s still means to eat, she’s progressing her weight.  That’s good news.  But what we unequivocally have to watch out for is her inability to swallow. She competence choke, she competence rise pneumonia.”
 
Dr. Glass is a ALS researcher.  In one of a studies he’s operative on, surgeons are injecting branch cells directly into a spinal cords of people with ALS, to see if a cells can delayed down a disease.   So far, 30 patients have undergone a initial surgery.  And

Glass says patients – like Jennie – pull him to work harder.  He explains, “I’ve been doing this a prolonged time, and people ask me what I’d do if we got sick.  we have no idea. Until you’re on an aeroplane that’s about to crash, we don’t consider we know what you’re ostensible to do with that.”
 
At home in Smyrna, Jennie Fountain chooses to concentration not on what she’s lost, though what she still has.  She says, “I am dynamic to do all we can for as prolonged as we can.”

App users click here for some-more images and video

source ⦿ http://www.myfoxatlanta.com/story/28263926/georgia-woman-faces-als-with-grace-hope

More als ...

› tags: als /