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We used to watch Network TV.  Those were the days. Turn on a favorite show and fast forward through the commercials.  Always trying to keep in pace with the rest of the family to avoid spoiler conversations at the dinner table.  Now we binge on Netflix after our terror of a 2 year old is passed out from her cyclone of destruction. As we fit 3 episodes of a show into our hour block of quality time, we too try not to pass out ourselves.  One of our favorite shows was This is Us. Just try to get through an episode without bawling your eyes out...I dare you. It was real, it was raw. It tackles issues that not everyone has went through, but still remains so relatable, you swear you know each and everyone of the characters.  My father-in-law could never remember the name of it, and once referred to it as Here We Go. It stuck as an inside joke with us for years.

This show reminds me that every family is unique in it’s story.  We all experience love and loss, highs and lows. We all fall down.  If I were to put my own families’ story out there, what would it look like to you?  You probably wouldn’t relate to a lot of it. Forgetting a feeding tube when you go to the restaurant or trying not to shock yourself (again) when plugging in your husband isn’t the most relatable story.  However, This Is Us...literally. Over the course of the next two weeks, I want to share with you our story of love and loss, our ups and downs. Let this series illustrate that even though we are all different, deep down we are all the same.  So, as Ken might say...Here We Go

A History of A Life Story Foundation


We are immensely proud of all that we've accomplished. Here is our journey in a snapshot. A key pillar of our mission is to empower work that results in effective treatments, and ultimately a cure for ALS. In 2019 3 potential treatments made it to Phase 3 Clinical Trials. That's more progress than the past 10 years combined. For as far as we've come, there is so much work yet to be done. Join the fight - tell a friend, make a donation, start your own fundraiser, like our Facebook page... there are so many ways to get involved. Thank you for joining our mission over the years, and thank you for all the ways you continue to support A Life Story Foundation.






May is recognized as ALS Awareness Month


Note from Kevin


May is almost over, so that means that ALS Awareness Month is too. It's always nice to see a bump in action around a topic that is all too familiar to so many of us. I think it's so important that we use this new found momentum as a springboard for the year ahead. There's been more significant advances in the past year than the previous five combined on the drug development scene!Heck, former president Barack Obama tweeted about ALS yesterday, underscoring the critical urgency to continue until we "win this fight"!


Please help us keep marching and rolling forward! 



Kevin, Shaina and Elliott




The Facts of ALS - as of May 2019



For our Caregivers:

Trach Care - 101


As ALS progresses, breathing becomes more labored. PALS have the options of using a BiPAP machine, or a ventilator with mask that assists in pushing the air into the airways, or a tracheotomy. 


It has been two years since Kevin underwent his tracheotomy. 


A tracheotomy is a permanent option to assist in the breathing of PALS. An incision is made into the windpipe, into which a tube is inserted. Air is then pushed through the tube, with the use of a ventilator, directly into the windpipe.


As with any surgical procedure, special care is needed with the trach tube. Kevin's caregiver, Sue, makes sure to have all of the supplies nearby for his trach care. These include a trach care kit, six cotton swabs (in addition to the two in the kit), gloves, 4"x4" gauze pads, new dressing for the trach (or "pants"), hydrogen peroxide, and a new collar. 


The first few steps Sue takes are setting up the supplies. She removes the tools located inside the trach kit, but leaves the two cotton swabs in one tray and adds the additional swabs, leaving four in each section of the tray. From there, she mixes a half and half mixture of distilled water and hydrogen peroxide. Sue adds distilled water to one section of the tray, and the water and hydrogen peroxide to the others. 


Next, Sue puts on her gloves to remove the old dressing and collar from the trach. She pulls the balloon out of the tube to check the pressure - an important step, because this balloon prevents any air from escaping through the upper airway. 


The gauze pads are then dipped in the distilled water and used to wipe any drainage and crusties away from the stoma, or opening where the tube is inserted. After wiping away, Sue clears around the stoma with the water and hydrogen peroxide mixture, swabbing away from it, with a maximum of 3-4 swipes per cotton swab. She then takes the cotton swabs in just water, and repeats the steps. 


Ensure to dry around the stoma, always wiping away from the stoma. Sue then puts the new dressing and trach collar into place and disposes of any waste. 


Thank you to Sue for shedding light on one of the parts of Kevin we see every day, but may not know how to tend to! 



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A Life Story Foundation is a 501(c)(3) organization.

ABOUT US

A Life Story Foundation’s mission is to raise awareness, innovate and implement new education and outreach programs, and create action to discover effective treatments, and ultimately a cure for ALS.

Contact

Email: JSWAN@ALSFTEAM.ORG

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