How to Help

As you probably know, Karen is recovering from a double lung transplant. For a more detailed description of The McGinnis Family and everything they have been through, please see their story on the gofundme site, which is linked on the right of this page. If you would like to help, please see the list below of things that would really help them during this difficult time:

1. Thoughts and Prayers - This is most important to the family and they really appreciate everyone's thoughts and prayers! Please leave a comment on the blog for Karen to read!

2. Food - On this site is a link for the food calendar. There are no allergies and the only food that is not a favorite for all of them (but some of them do like it) is seafood.

3. Other Gift Cards - If cooking is not your thing, they would always be happy to have gift cards. The gas costs are piling up as the kids drive back and forth to the hospital. Grocery store gift cards and gift cards to places like Walmart or Target for household items would also be very much appreciated.

4. Monetary Donations - the GoFundMe site is also linked on the side of this page. They have recently found out that insurance isn't covering Karen's last hospital visit, which is costing more than $17,000! Also, they will be eating a lot at the hospital over the next several weeks and that money can add up as well. --If you would like to donate something but can't get it to their house (or mail it), please let me know and I would be happy to pick it up and deliver it to the family! stacey.grote@huschblackwell.com

Please see below for updates on Karen's progress. Go Karen, Go!

Tuesday, February 3, 2015

Update from Mike, 2/2


After a long night and morning, Karen's heart settled back into normal sinus rhythm at about 5:30am. Finally I felt comfortable enough to get some sleep. Thank you to Matt our nurse, who our daughter Morgan thought was extremely cute, and a very helpful short doctor who I can not pronounce his name. They stayed close by the entire time helping to get Karen's heart beat back to a regular rhythm.
The doctors came by late today, which was great because it gave Karensome time to rest. Well the doctor's attitudes definitely mellowed a little into a more cautious, but still pushy care giver. The objective is still clear and remains the same. Karen has to get off of the ventilator entirely and the longer it takes, the more difficulties present themselves. However, there is a fine line between pushing someone with the focus being on moving forward while also building confidence and achieving success at the same time, versus pushing someone with the only consideration being reaching the final objective. Everyone can not be pushed the same way. They all have the same objective, but they are not all clones of each other. Seeing success while also building confidence seems to me to be the path to take.
So today instead of setting the goal at 8 hrs breathing on her own, they instead set a more realistic goal of one hour, hoping to show Karen that she can do it by herself. After the other day Karen had no confidence in her ability to breathe entirely on her own. If we could get her through the hour. Then she could see that she can be successful. It seemed like the longest hour ever. Karen struggled from the first minute, but there was no way I was going to let her fail. So I was her cheerleader the whole time. Karen successfully made her hour on her own. Great job Karen.
Next she got on the teadmill and walked for a total of 16 minutes, with an occasional stop to rest, which was one minute more than yesterday. Karen was beat the rest of the night, but all in all it was a very very successful day!!!

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