ERIN'S CAMPAIGN FOR KIDS
Super excited that the KY Family Career and Community Leaders of America is considering Sepsis awareness as their 2017-2018 community service project. This would include over 150 chapters and 4500 students from all across the state who would be raising money and awareness of Sepsis, especially in children.
Sepsis Alliance is a charitable organization run by a team of dedicated laypeople and healthcare professionals who share a strong commitment to battling sepsis. The organization was founded in 2007, by Dr. Carl Flatley, whose daughter Erin died of sepsis when she was 23 years old.
Sepsis Alliance was created to raise sepsis awareness among both the general public and healthcare professionals. Sepsis awareness can and does save lives, yet only 55% of American adults have ever heard the word. Sepsis Alliance also gives a voice to the millions of people who have been touched by sepsis – to the survivors, and the friends and family members of those who have survived or who have died. Survivors and those left behind often feel as if they are alone.
If anyone needs help with how the site works please email me or call and I will walk you though it.
I have posted on a couple websites about why cant the patient and/or caregiver be informed about the possible complications to come months and years later. I understand there are some legal battles and several reasons why it cant happen. But why cant the patient and/or caregiver be informed its possible they might develop PTSD or an anxiety/panic attacks. It doesntt have to say they will be its possible and things to looks for. Its not for any particular medical condition but for long term ICU care there will be some things that are different for you years later. From everything I have read about PICS (Post ICU Syndrome) things tend to be a little different for some if not most people. Just as HIPPA was formed why cant something be formed for a more informative way (video or pamphlet) to patients before they are released.......Just a RANT
I had to add some comments about my app verses other similar apps on the about page in BLUE. All of the others use an ipad which a lot of people don't have and cost money to download. Mine is totally free.
Had to add Dr. Ashley Montgomery's picture to the home page. She is a huge part of my recovery and will always be family.
On the home page I couldn't help but to give a shout out to my critical care DR. Ashley Montgomery.
Just as a friendly reminder I removed Weebly from the site. So now its just www.ez-caregiver.com
Would anyone care to post an opinion if this site or app is any benefit to the medical field. I would appreciate any feedback.
The Read More section has been updated with a little more information of why I had Sepsis and ARDS.
Just added a donate button that goes to help pay for some of my cost for working on the website, traveling, medical, and to keep the site up and running. I hope you find the site useful and if need any help please contact me.
I added a new mobile app to the EZ Caregiver page. Would appreciate some feedback.
Just do a search on the Google Play store "EZCaregiver" and it should show up. I do not have on itunes at the moment but can still go to the website and do same thing.
App has been published so hope gets approved and will be able to find on your android phones!!
A retired engineer that had to quit work due to traumatic health issues and want to share and help others