Skip to main content

Lets go for a hike!

Steve, my mom and I decided to go for a hike this afternoon. So we piled into the jeep and headed to Little Cottonwood Canyon. We ended up at the Bell Canyon Trail. I was pretty stoked to see how well I could handle this trail compared to Mount Olympus. On a side note- My mom never leaves Gus Gus (Gus's extra LVAD computer and extra batteries) when we leave the house, even if it's only for 5 minutes. A little ridiculous if you ask me. So, Steve grabbed Gus Gus and up the trail we headed. We were about an eighth of a mile up the trail and BOOM!!! I literally thought Steve punched me or a big boulder hit me right in the chest. If you know Steve you know what it would feel like if he socked you in the chest. It startled me so bad. What happened was I received a treatment from my defibrillator which was implanted back in 2009. Steve called the LVAD 24 hour emergency number and got a hold of Genea the LVAD nurse. While Steve was on the phone my mom starts asking all the stroke questions and asking if I knew who my husband was and what her number was and so on. I told her I was fine! Genea said that the protocol is to come into the hospital, but she knows how much I love hospitals... NOT! So long story short- I will go in tomorrow to have them check my defibrillator and everything. So there goes comparing how well I do, I guess. I am feeling fine, it is crazy, they have told me for years that I would know if I received treatment and yup I sure do. Felt like a horse kicked me, or my stallion of a husband.
Well, I am ready and I want to thank all who have prayed for me. You guys are amazing!! :)


Here is my Driveline site without a bandage. LVAD nurses say it looks real good. 

Comments

Post a Comment

Popular posts from this blog

Chalk It Up as a Miracle.........

Some of you may know, but Ashley went through another Heart Transplant yesterday. After her first first new heart started to fail, we re-listed on the her on the transplant list immediately. We knew getting another heart would be a long shot, but we wanted the option to be there if a heart came available. Sure enough 18 hours on the list a second heart came available that was a perfect match for Ashley. Ironically, it took 4.5 months and then 2 hearts in the same week. We, including the doctors, are all chalking it up as a miracle. It was decided not to wait to see if the first heart would handle the load she would need but rather to move forward with the new donor heart. Going through a transplant a second time makes you really feel for the family who lost their daughter, sister, spouse and friend. We are grateful again for the family and the individual who choose to give life. We were in quite a predicament and feel only divine intervention could have provided a means out. Ashley is
7 comments
Read more

Stinking INR

Another day in this lovely hospital because my stinking INR will not get were in needs to be. INR means International Normalized Ratio, its a number that describes your bloods clotting factor. Doctors want my INR to be around 2.0 but I am stuck at 1.5, a normal person should be below 1.0. So the higher the INR the thinner the blood. Because I have an LVAD they are very picky about my INR because they don't want a clot to form in my LVAD. But, if my INR gets too high I bleed, so it's a fine line we are walking until I get my new heart. On a higher note, my mom and I did some crafts.... getting ready for Christmas and my baby boy Wrigley came and visited me, some of you are thinking Wrigley is a terrible child's name but he is actually my French Bulldog :)
5 comments
Read more

Stinking Breathing Tube!!!! Actually they are out!!! YAYA

Anywho the stinking breathing tube is still in, which makes it more than miserable for Ashley. She is so frustrated, can't talk, can't get anyone to understand what she is trying to say.  It's difficult to see her suffer like she has. The Dr. just told us it's not all just up to her, her lungs may just be that full of fluid that the oxygen saturation may just be low. They have gotten lots of fluid off her which is helping and we are hoping later today will be the day. It's going to take getting that out to  get her up walking and making leaps and bounds of improvements. We are calling today day 2 post surgery, she was on bypass through the weekend which did not put her ahead any, she had fluid on board already from the first surgery so now the fluid has basically compounded. 8PM Update- Breathing tubes are out, still on oxygen, much less irritated, she has one of her favorite nurses on tonight and we think another one of her fav's  will be working with her
2 comments
Read more