Followers

Thursday, April 26, 2012

Thursday, November 10, 2011

Reaching me

If you attempt to reach me, you will have to leave your email address. The way these blogs are set up, there is no way for me to know your email address. If you want me to respond to you, somehow you will have to leave away for me to contact you.
It is my sincerest desire to assist ALL who have suffered with this affliction. Please allow me to respond to your requests.
Lisa

Saturday, November 5, 2011

I am still here

I wanted to let anyone who has ever kept up with the blog know that I am still here. I have celebrated the 5th anniversary of my surgery tp/ict. Our lives this years have been so busy. My husband just finished his Masters in Nursing. He will sit for his NP exams very soon. My days were spent packing lunches, trying to keep up with the laundry and the house. For those with chronic illness, you understand how difficult minor tasks can be at times. Even though I did not earn an academic degree somehow I feel like I have accomplished something, by just doing what I have done. This self directed learning procees was so intense, he did not have time to focus on anything but school.
I make posts when I do to let those searching know that 5 years out, I am still here, enjoying my life. I don't want to give people false hope, I suffered for 10 long years waiting for something. I still have deficits, I still have pain, but this pain is controllable, the other was not. I still have times when I have to lay in bed which btw is my least favorite thing in the world, but that seems to be something that assists with the pain, so lay down I will do. I have survived long enough to see my only child marry, give birth.. twice. Hold two precious little girls who have their grandmothers eyes. What more could a person want? If you are on the fence deciding about surgery... don't wait another minute. Don't let pancreatitis steal one more minute of your life.
Yes, I check my blood sugars frequently, my last HA1C was 5.7 equal to that of a non diabetic. I also give insulin every night ( just to keep those little islet happy and snug as a bug in a rug in my liver) to answer the next question the amount Lantus is 3.5 ( yes I said 3 point 5 not thirty five). I purchase special insulin syringes that measure half units. I eat a lower cab diet. Carbohydrates are the building blocks we need to burn as fuel, so eliminating ALL carbs in not the answer, without some carb we burn muscle. I am here if there are any QUESTIONS that some may have. After reading my blog you have probably determined that I am a Christian. I will leave this post with this scripture.

19 This day I call the heavens and the earth as witnesses against you that I have set before you life and death, blessings and curses. Now choose life, so that you and your children may live 20 and that you may love the LORD your God, listen to his voice, and hold fast to him. For the LORD is your life, and he will give you many years in the land he swore to give to your fathers, Abraham, Isaac and Jacob.
Deuteronomy 30-19

Tuesday, August 3, 2010

My 44th birthday

Today is my 44th birthday. I have spend the last 3 days in bed. This has be happening quite frequently lately. I went to church on Sunday ( the first time in 2 weeks) I knew that I was getting really hungry, and I know this is not good, I was trying to get home to eat. Today is better than Sunday afternoon and yesterday.
I have survived longer than I ever thought. Each day is a miracle, soon I will be a grandmother again.

Friday, July 2, 2010

Chinese posts

I really don't mind if people leave comments regarding pancreatitis, but this is MY blog. It is rude to leave comments in another language, but to leave explicit content on a blog intended for people with a life threatening illness is another thing. Find somewhere else to post your comments, I won't tolerate this, I will pull this blog before I let this become a place for people to post what ever they want. It is simple enough to get a blog, why not get one and do what you want on your own. Enough said.

Sunday, June 27, 2010

Life goes on


It will soon be 4 years since I had surgery. The big question every one asks was it worth it. The answer is YES! Did it take away all of the pain, NO. That said, I have not woke up screaming in agonizing pain since the day of surgery. I had still had pain that made me cry and have felt pretty bad, but that pain is gone. Since my surgery, I have had chronically elevated liver enzymes. I was told that this would go away, it never has, occasionally they will get pretty high. There are times that I feel pretty bad, but I am able to eat some, which is a big deal, before I was tube feeding with no hope of ever eating again. My quality of life is better, I do get bummed when I have to spend my days in bed. I would say that I spend about 4-5 days in bed per month compared to getting dressed about 4-5 per month previously. The amount of pain medicine that I take has drastically decreased. No where on any of the journal articles that are posted does it say that people who have tp/ict receive complete pain control. If these articles are read, they will give a percentage of people who were able, most do NOT receive complete pain control. Most continue to live life with pain, and challenges. We were challenge prior to surgery. No one promised us life would be easy. We have God's promise, that he will always be with us, even to the end of the earth. I am counting on this, I have put everything on his promises. To date, he has never left me or forsaken me. Nor will he ever.

I have notice that there is a several Japanese posting going on the blog. I don't really know what this means and I will find a way to translate. I will assume that what is written here is good until otherwise determined to be something else. Just know that I am still watching and reading posts.

I hope this finds all with pancreatitis well ( as well as you can be with the beast within) just know that you are not alone. There are many fine yahoo groups that deal with the topic of chronic pancreatitis and I high suggest that you join them. I will NEVER forget the day I found one person who knew exactly what I spoke of when I talked about the pain. NEVER forget when I spoke with another woman who was getting the run around just because "women have a lot of abdominal pain that is never diagnosed" I was told this by a very respect physician at the Mayo Clinic in Minnesota, despite the fact that I had a documented known, visually seen annular pancreas from an open gallbladder removal. I was told "poor interpretation by your surgeon". No it was really there, causing a small bowel obstruction for me.

If one person learns that they can trust what they are feeling through these blogs then it will all be worth it. Don't let someone tell you what you feel, just because they have been to school for years, does not give them the ability to know what and how you feel. Be blessed and know that I read all comments. If you have questions ask them, I will get back with you.

Saturday, July 5, 2008

I wanted to add some pictures of my life here


This is a five generation picture. From lt to rt
Thelma Russell ( my grandmother) holding Madeline Riley Herth
Teresa Wolf ( my mother)
Lisa Atwell (me)
Ashley N. Herth ( my daughter)

About Me

I am a wife and a mom. I have 2 cat children that I adore. I suffered for 10 years with chronic pancreatitis. I suffered horribly, no one should have to live I like I did.