Health
Since 1995, Bob and I have loved hiking. At times we could not do much hiking, because we had important responsibilities elsewhere, but as much as we have been able, we have hiked. I have a treasure trove of pictures from our various hikes. They are all beautiful, and I wouldn’t trade a single one of them. They are the memories of those amazing times that we have been able to spend together. The peacefulness of those hikes cannot be copied in any indoor setting…nor would I want to. The fresh air, the birds and animals, the quiet, and the push on our bodies, all add to the feeling we get from our hikes.
Many of the pictures I have taken over the years, while wonderful, were not of the quality I had wanted. They were taken with my phone, and while they were great shots, I still could not get that elusive shot of landscape or wildlife. I knew I would need a better camera, but I hesitated because of both cost and bulkiness. Nevertheless, that elusive shot was always in the back of my mind, especially when it came to wildlife. I wanted to be able to get a shot of an animal or bird that looked like I was standing right there, next to it, and that was impossible with my phone…even though it is an iPhone and has a great camera…along with the dozens of apps I had tried, in search of just such a camera.
This year I decided that the time had arrived to get the camera that would do what I wanted it to do. It’s not the most expensive camera, but it has a couple of good lenses, and it takes good, high resolution pictures. I had played with it a little bit at home, but this vacation was going to really put it to the test. My hope was to finally get the kind of pictures that would be award winning…whether I ever entered them in a contest or not. With each hike we have taken my appreciation of this new camera has grown.
I have three more days of hiking and picture taking ahead of me before we head for home, and the possibilities are endless. I could potentially take some amazing pictures, and any 
one of them could be better than any I have ever taken. Still, I have to think that while the pictures I took of the Red Winged Blackbird were…less than amazing, the picture of the Downy Woodpecker, which was the first of those elusive shots, has more than made up for it. Yes, the pictures of us on the trails are great, and the bridge on the trail is very quaint, but it is the Downy Woodpecker that finally got me that elusive shot.
The excitement of having a baby is hard to contain. But, finding out that something is wrong is so completely opposite of that excitement, that it has the ability to make you feel like you are dying, even though you have none of the symptoms of impending death. Those feelings come from the unsure future that you and your baby now face. Your thoughts turn to wondering how you are going to deal with all these new challenges. This is where the parents of a child suspected of having Down’s Syndrome, or any other disability find themselves…and where my niece, Cassie and her husband, Chris found themselves two years ago…and Down’s Syndrome was what little baby Lucas was diagnosed with. I’m sure that Cassie and Chris felt all the normal fears, but they bounced right back and have proven themselves to be very capable parents. Lucas is a blessed little boy!
I suppose that you might think that this is a sad story of shattered hopes and dreams, but 
you couldn’t be more wrong, because Down’s Syndrome is what Lucas has…not who he is. There is no room for sadness in the home that Lucas shares with his mommy and daddy, because Lucas is a happy, smiling baby, who leaves no room for sadness or regret over what might have been. Lucas loves with all he has, and brings so much joy to his parents’ lives, that they simply can’t see how they could be any happier.
There is no sadness in this family because of Down’s Syndrome, because that is just not what defines Lucas. Instead, there are giggles and smiles. There are all the firsts that every baby has…first tooth, first time crawling, sitting up, and so many other milestones. It may take Lucas longer to do these things, but he will do them. There is nothing holding him back. People with Down’s Syndrome can and do live very productive lives.
There is no room for sadness in the home where Lucas and his parents live…because it is too full of love for sadness to have any space at all. Sometimes, people think that the parents of a disabled child are always thinking of their hopes and dreams, now all crushed into the dirt, but that just isn’t so. Lucas is making new strides every day. His future is as bright as his smile, that is filled with new little teeth. There is nothing standing in the way of success and a happy life for him and his parents. Today is little Lucas’ 2nd birthday. Happy birthday little man!! Have a wonderful day!! We love you!!
My father-in-law passed away on May 5, 2013, but my mother-in-law is doing ok. Alzheimer’s Disease has removed all memory of his passing. I know that many people look at Alzheimer’s Disease as being a cruel thief. I can agree with the thief part, in that it has taken her memory of recent events away, but cruel…maybe not. Her mind simply creates its own reality. In her mind he is not gone. He is at work or visiting the neighbors or out in the garage. Death means nothing to her. It has been the same with her parents, who have been gone for 28 and 23 years now.
I have long known that she lived in a world of make believe, but that fact never hit home as much as it did tonight, when Bob and I were out visiting her at the nursing home. She often speaks of those who are closest to her, and sometimes she speaks about you…to you, saying things like, “Caryn is going to be cooking dinner for everyone” when she is talking to me, or “Bobby is on his way to Grandma’s for the summer, to help with the cows” when she is talking to Bob. Corrie and Amy, work at the nursing home…at least in her mind, and my father-in-law is over by the telephone, so he will answer it when it rings. These were just a few of the recent things she has talked about, and things we are getting used to hearing.
Tonight…well, tonight was different. We were talking with my mother-in-law, and the conversation was following the normal lines…or at least, it was until it wasn’t. Suddenly she said, “Hun, can you help me get this afghan over to the sewing machine so I can finish it up.” She was talking to Bob, but to her, he was my father-in-law. At first we thought it was just a slip of the tongue, but then it happened again. She said, “Walt, you need to move that other sewing machine to the table.” We didn’t know exactly how to react. It was not the first time she had mentioned him, but it was the first time she spoke to him when it was actually one of the guys in the family. She thinks nothing of talking to him, but we know that he is gone, and the pain of that parting is still very fresh in our hearts 
and minds. We can’t be upset with her for what she says, because in her mind, it is reality, but to us it is make believe. Like it or not, we have to play along, because to do anything different is to make her relive his death over and over again.
I’m sure we haven’t heard the last of my father-in-law visiting my mother-in-law. Her mind will bring it up again, and it’s likely that her sons or grandsons will have to play the part again at some point. They will do it, as often as needed, because it is for her. They can do nothing else. They will play the part…so that she can keep her illusion that the love of her life is never far away.
A few days ago, I received an email from a man named Cameron Von St James. He had read my blog, and knew from many of my stories that I have spent much of the last 7 1/2 years being a caregiver. It doesn’t matter what the illness is, when the need is serious, caregivers step up to provide much of the day to day care for those they love. It is a sacrifice that goes above and beyond what many people are able to grasp, and one that is rewarding beyond what most people will ever know. Cameron knew that story as well as I did, and he asked if I might share his wife’s story of survival with my readers.
Cameron’s wife, Heather was exposed to asbestos when her dad worked in construction. At the age of 36, just 3 months after giving birth to their beautiful daughter, Lily, they would receive the terrifying diagnosis of…Mesothelioma. No one knew what the dangers were back then. Sadly, that is the case with so many dangerous substances. By the time we know the dangers, so many people are already affected, but with new research, staying hopeful and 
positive and with much prayer, more people are beating cancer. It is my belief that our faith in God and His mercy and love for us is vital. I am so pleased that Heather has been blessed with a great victory over a type of cancer that almost always carries with it a death sentence.
Heather’s fight began at almost the same time as my mother’s brain tumor, and my cousin, Jim’s fight with Mesothelioma. My mother’s story had a happy ending in that her cancer was confined to her brain only, and had not started somewhere else in her body, which would have been much harder to cure. It is rare for a tumor to be found only in the brain. Her doctor, an amazing faith filled man named Dr Mills, told us that we were blessed in that hers was “just a Lymphoma” and it should be an easy fix. While hers could not be removed by surgery, it was a very slow growing cancer that was gone after 3 treatments, and after 6 more for good measure, she was done. She has been cancer free since January, 2007, and we give God all the glory.
Like Heather, my cousin Jim, was diagnosed with Mesothelioma. His story would not have the 
happy ending that Heather was so blessed to have. Jim passed away in February 1, 2006…he was 42 years old, and he never knew how he was exposed to asbestos. He left a son, Cody, who misses him terribly, as do we all. While Heather’s story will not be able to help Jim, it is my sincere hope that it will help others like Heather and Jim, who have been affected by this terrible disease. Please watch Heather’s story and read Cameron’s Blog for Caregivers, and be sure to pass them on to your friends. It is the hope of the Von St James family that it “might raise awareness and support for people fighting illness, and the caregivers who fight alongside them.”
For the past seven and a half years, my life has been largely defined by a series of responsibilities known as caregiving. For anyone who has ever been a caregiver, even for a short time, it is easy to understand what that entails, and what it means in the lives of those involved. Caregiving is not a job that usually becomes less demanding as time goes by, although that is not an impossibility. While caregiving is not an easy job, I can tell you from my personal experience that it is a very rewarding job. It is one that places you in a battle for life…or at least a battle to prolong life. While it is rarely a battle you can win in the end, you do win in that those final years are made more comfortable for the patient, and filled with the knowledge that you love that person so much that you are willing to make this sacrifice for them.
Now, after the passing of my dad, the recovery of my mom, the necessity of placing my mother-in-law in a nursing home, because Alzheimer’s Disease no longer allows her to stay at home, and the passing of my father-in-law, I find myself no longer in the position of being a full time caregiver. Yes, I still have minimal responsibilities with my mom and mother-in-law, like doctors appointments and visits with them, which are very important to their emotional well being, but the main responsibilities belong to others or are no longer necessary. So, I find myself wondering what do I do now that I am not a caregiver? What is life supposed to be like now? This has been who I was for so long. It was even all I talked about sometimes, as many of my family members can attest to.
A part of me is still very tired. At times during the day, I feel like I could sleep for a month, and yet, I have trouble getting to sleep at night. A part of me is ready to get back out on the trails…walking and breathing in the fresh air, and yet a part of me feels like I just want to sit and do nothing. Maybe it’s an emptiness because of no longer being needed as much as before. It seems like concentrating is very difficult…unless it’s about why we lost the battle for life, or what we might have done differently.
I know that I will get used to having more time again. And as with my dad’s passing, I will come to know that you don’t get over it…you just get on with it. I will get used to not being a caregiver, but I know too, that I will never be the same person I was before. I can’t be. I have seen too much…learned too much…felt too much…know too much, to ever be the same person I was before. I have experienced the adrenalin rush needed to hold myself together during life threatening illnesses reaching emergency levels, and making the decisions necessary to treat loved ones who can’t speak for themselves. I have held their very lives in my hands, and been responsible for trying to bring them back. And, I have lost that battle…twice. I will recover from caregiving and I will get on with it, but I will never be the same. I don’t think it is a bad thing, and I would not change any of it, except the loss of my dads, but while I would do it all again, I know that I have been forever changed by this experience.
Today is my mother-in-law’s 82nd birthday. If you ask her how old she is, she will likely tell you that she is 65. Alzheimer’s Disease has taken away her memory of the more recent years, but she is still here with us, and that is a blessing. She was recently in the hospital, and the doctors did not expect her to survive that stay. Nevertheless, she fooled them, because they don’t know what a fighter she is. They said that she would not be able to swallow again, and that drinking water would be impossible. Now, she is eating and drinking and getting stronger every day.
When a person gets into their 80’s, you learn to cherish each birthday, holiday, anniversary, and basically every day, because you don’t know how long you will have them with you. And when they are sick, you pray that they will, make it to the next holiday, or until someone in the family can come from another state to see them. Each moment that they are sick finds you praying for just a little more time with them. You begin to understand just how precious life is…how precious each moment is.
This birthday finds us thankful that my mother-in-law will reach another year of age. The age of 82, is one that we would not have expected her to reach, just a few short weeks ago. Now, she will get to celebrate one more birthday with the great grandson, her first great grandchild, Chris, who was born on her birthday…a very special birthday present. She gets to spend one more birthday with my father-in-law, the love of her life, who himself is recuperating from pneumonia. She will get to spend one more birthday with her family, who all love her very much.
At the age of 82, we all know that this could be my mother-in-law’s last birthday. She has lived a good, long life, and she is getting tired. Nevertheless, we will rejoice in the victory that she has achieved. We will celebrate her strength to fight her way back from the brink. We will laugh and sing and smile with her in celebration of one more birthday, and just a little more time. Happy birthday Mom!! We love you!!
Sometimes, in the life of a child, a situation arises that brings out the extraordinary in that child. And even if what the child is doing, isn’t something so unusual, the actions of the child are still extraordinary. I have seen the extraordinary in all 4 of my grandchildren over the past 7 years of caring for 2 sets of their great grandparents, but this current situation is about my grandson, Josh. Josh is my youngest grandson, and he has been the one who has been able to help in the current care of his grandparents, because at 14, he is too young to have a traditional job. Tradition has certainly not played a part in the work that Josh does every week. Most 14 year old kids think only of playing video games or hanging out with their friends, but not Josh. He wants to go to his grandparents’ house every time he gets the chance. And he doesn’t just sit and visit, he wants in on the work…although it isn’t work to him…it is love for his grandparents.
Because, Josh has been more available to help in the care of his grandparents, he has had the chance to bond with them in a way few of the grandchildren have been able to do. His care and concern over their well being is so touching. Recently we had to put my mother-in-law, his great grandma in a nursing home, after she took a bad fall. It was the second of two falls in less than a week. Falls, are probably the worst thing that can happen to the elderly, but we were blessed in that she did not break a single bone. She did, however, tear the skin on her left arm badly. We took her to the hospital by ambulance, and from there she went to the nursing home. Josh wanted to know all about the nursing home. especially where it is. When his mom, my daughter, Corrie told him that it was in Paradise Valley, he said, “No, Mom!! No!! That won’t work!! That is too far from the hospital!! What if she falls?” Of course, once Corrie told him that there were nurses and 
CNAs on staff at the nursing home, he felt much better. He knew she was safe. He loves her dearly, and Josh has made her safety a top priority for some time now.
Josh comes with us to see his great grandma as much as he is able to, but now he has shifted his caregiving skills to his great grandpa. He is such a loving, caring boy, and his dedication to his great grandparents has endeared him to them all. He helps, my mom, his great grandma at church, to get up and get to her car, and anything else she needs, and he helps with the care of his great grandpa, my father-in-law, every chance he gets to get over there. I am very proud of Josh, and his caregiver’s heart.
Our nephew, Barry’s wife, Kelli has always been an outdoor girl. She loves hiking and long drives…going just about anywhere. Saturdays often will find them heading out for a drive, and posting pictures of the things they see on Facebook or Twitter. Kelli loves to travel and, while Texas is the place she likes the best, so far, you never know if, in their travels, she just might find a place she likes better.
During various vacations, Kelli and Barry have hiked in a number of places. On trips down to Colorado to visit her mom, they have hiked in the Rocky Mountain National Park. They have also hiked in the Black Hills, the Oregon Trail, the Big Horn Mountains, and many other places. A love of hiking and the mountains is something Kelli and I definitely share. We also share a love of beautiful nature scenes, and I have really enjoyed the pictures she has posted.
Kelli loves animals. She likes the wild animals in nature, and she loves her dog, Dakota, but the thing that surprised me the most is her love of donkeys. I can relate to that in that 
when we go to the Black Hills, one of the highlights of the trip is being able to see the wild donkeys there, but Kelli would love to raise donkeys. That is something I had never considered doing. Donkeys are so sweet though, and I think that would be a really cool thing to do, and I hope she will get the chance to make that dream come true someday.
Kelli has been a part of our family since she and Barry were married in 2004. They share so many common interests, and it seems like they have always been together. Today is Kelli’s birthday. Happy birthday Kelli!! We love you!! Have a great day!!
Alzheimer’s Disease is a mind thief, and when your loved one has been diagnosed with it, you find yourself thinking often of all that they have lost. You have to remind yourself to look at what they still have, which is hard sometimes. My mother-in-law is really a shell of what she used to be, and even though she seems happy with her life, I remember the things she used to do, such as knitting, crocheting, sewing, cake decorating, canning, baking, and raising her family. In her lifetime she made many people happy with the various things she made, and it is sad to think that she won’t be making those things anymore, even though she thinks she still does.
One thing that I have had to look back on, even though she will never do that again either, is her horses. My mother-in-law would have lived on a horse if she could have figured out a way. If she could have figured out a way to never get off, she would have done it. She owned horses with names like Molly and her colt Pie Face, Danny, and Twinkles. I don’t know who named the horses, but my guess is that it was her. There are a number of pictures of her with and on horses. And of course, her favorite shows are Westerns. I’m quite sure she can picture herself on the horses they are riding, galloping across the prairie. I don’t think she ever liked driving a car much, and she only did it when she absolutely had to, but a horse, she would had taken everywhere, if only she could have.
I agree with the research I have done concerning Alzheimer’s patients, in the you need to forget what they can no longer do, and focus on what they can, but I also think 
that sometimes it helps in their care, to remember what they used to be, because in so many ways, they think they still are that person from the past and they still do the things they used to do. They don’t know that they no longer do those things. I wish she could still be that person from the past, but since she can’t, I’ll just remind her of the days when she was a horsewoman…and a very good one.
Many people think that the elderly have nothing left to give to this world. They are pretty much done, and maybe even waiting to die, right? I couldn’t disagree more. I have been a caregiver since 2005, and while there have been challenges and sadness, the overall experience has been very rewarding. While there have been times when they are irritable, or even downright grouchy, I have found that if you will just walk a mile in their shoes, you will walk away with a new understanding of what they are going through and why they might have mood swings.
I have also found that if you take the time to listen to things they have to say, you can learn a lot about their lives while you are caring for them. These people have live in times that we have no idea about, and listening can teach you a lot about the past…a past that is your heritage. So many of my stories have come from just such talks about days gone by, and I will be forever grateful for having been given the opportunity to hear about it. All too soon, these people could be gone, and with them go all the stories they have stored in their heads. If you have that opportunity, I strongly recommend you have a talk with your parents or other aging loved one so that you can see what it would have been like to walk in their shoes.
Last night and this morning, I found out what it really is like to walk a mile in their shoes, when I experienced a headache that just would not go away, and would not allow me to even think much. My neck was out of place, and after my Chiropractic 
appointment, I felt much better. Still, it was an eye opener for me, because the one thing a caregiver can’t do, is feel the pain of their patient. For days now, I have been and probably will continue to try to minimize the back pain my mother-in-law feels in an effort to get her to continue to walk. She experiences pain in the low back and would love to get out of walking, which is something I can’t allow, hence the need to minimise. I doubt if she will believe me when I say the it is not so bad, but with Alzheimer’s disease, she will also not remember it later….a very good thing. Nevertheless, I will do whatever I can to minimize it, because after the horrible headache I had last night, I can honestly say that I have walked a mile, or maybe two, in their shoes.
