It is Christmas time! Christmas is for families to celebrate being together. Many from all over the world will celebrate the birth of a very special baby! Adults look forward to having time off and winding down for a bit. We look forward to spending extra time with one another. We look forward to the activities that come with the holiday. Everything about Christmas lights up our senses. Christmas is for everyone but it is especially for kids. For children, Christmas time is magical. The anticipation that it holds for them is both precious and a provider of priceless memories.
I have made it clear in my previous blogs that I love kids. Equally, it could be said that I love people with special needs. I also have come to love children and young adults with rare diseases. Mainly, there is a community that I care about. That is the families and their children that make up the Batten community. This doesn’t mean that there aren’t others. I love little warriors in general. Anybody that knows me personally, knows that I love my son Benjamin to the moon and back. He is a really special guy. Benjamin has two brothers, and they are very special as well. They are special in the normal sense. Both are successful in their own way. Daniel is the oldest and Kenny is the middle son. Benjamin is our baby at age 27. We always have joked that we wanted a girl on our third try but got a Benjamin instead. I am so happy that we did. He brings so much joy into our house. Dad is getting older and more sentimental as time has gone on. This is all being fed by following kids with Battens but it has always been there in relationship to Benjamin and those that are like him.
Is Benjamin responsible for my sensitivity to the people in the rare disease community? Does my involvement on social media with the Batten community make me appreciate my special needs son more? The answer to both questions is a big YES. It is because of the fact that I have a sensitivity to special needs people that I am also sensitive to Batten warriors and other warriors that are like them. I have shared Benjamin’s life with others on social media and the outpouring of love towards him has touched me. This has increased my appreciation for those who battle Batten Disease, as well as, other types of little warriors. I see the love that some people have for Benjamin and it makes me love my son and those that are like him all the more. Benjamin’s story is a big part of who I am as a person. His story though, begins with that of another. Both stories are about people that are a gift to me.
There was a little girl that lived in the state of Oregon in the USA. Her parents loved her and of this there was no doubt. She had dark blonde hair and big brown eyes. She looked so sweet and her appearance held no deceit. She really was just like that. Although her parents loved her they were unable to care for her in the way that was needed. Sad as it may have been, she had to be placed in foster care. So it was that she appeared on the front door step of a home belonging to a minister and his family. The family was large and there was so much need already. There was, however, no way that she could be turned down once her appearance was made known. She became one of seven siblings and she would grow up in a very happy home. Within all those years spent with her adopted family there were no doubt truckloads of priceless Christmas memories. This because after all, Christmas is for kids and those that are like them! Although life had its struggles for her she would go on to overcome and achieve. She had many things that she enjoyed as she grew. One of the most important of which was being with and caring for children. That is where Benjamin’s story begins because his story begins with his mom’s story. That being Rosemarie Jean, or as she is better known, Rosie! That she happens to be my sweet wife is no accident!
Does that sound a little bit like a fairy tale? I am sure that there are many that have stories of their own to tell. Like I have already stated, all of my kids are special to me but Benjamin is special because his needs are special. His story comes out of my wife’s own special circumstances. That is why I am including a few of her details. Rosie grew up on the Oregon coast and then central Oregon. I grew up in California. In San Jose to be exact. We met each other while serving on active duty in the Navy. That was all the way near New Orleans Louisiana at NAS New Orleans. She caught my eye and that was it. To this day she is my best friend and it was 37 years ago that we met. Just like most any couple we wanted to have a family and so we did. You could tell that our first son Daniel was brilliant from a very young age. He is a successful IT professional now. Daniel’s middle brother Kenny is highly intelligent as well. He is self employed and does quite well. Trust me when I say that they do not get their intelligence from me.
Benjamin was born on April the 4th of 1990. We had moved from San Diego to Gilroy California and that was where Benjamin came into this world. He was born at South Valley Hospital. It never dawned on us that we might become parents to a special needs person. My wife’s biological mother was affected much like Benjamin would turn out to be. We however, were fixed on the fact that both his brothers were fine. Whereas Benjamin’s older brother Kenny had met or exceeded all his milestones, Benjamin did not. He was sick a lot. In fact, it wasn’t until we were told about a special baby formula that he began to get better. Constant ear infections and congestion were the biggest concerns at the time. He was just slower in everything that he did. Slow to pick his head up and to sit up on his own. He was slow to stand up and slow to walk. He would need a wheelchair to get around. We received help from Shriner’s hospital in attaining custom AFOs for ankle support and this helped him to learn how to walk. They did for us what our private insurance often failed to do. In the course of time we would become aware of the fact that Benjamin was developmentally delayed. That is, in fact, a big part of his condition to this very day. While being seen at Shriner’s hospital, he was seen by a geneticist who would do testing to determine a diagnosis. While she found evidence to suggest that Benjamin has a degenerative disorder, she could never give him a diagnosis.
Benjamin would have his first seizure when he was about nine months old. That was a complex or grand mal seizure. These days they are well controlled by medication but the amount that he needs would be of concern to most parents. Which is worse? The medication or the seizures? Along the way, he has experienced, grand and petit mal seizures, as well as absence seizures. One type, which name escapes me, involved him starting out in a deep belly laugh. He would then go into a grand mal. We love to laugh together but in that case you had to be careful. At age seven Benjamin Had an incident that landed him an extensive stay in the hospital. He aspirated into his lungs. He was taken by ambulance to the hospital and then life flighted to another facility that provided the care that he needed. The doctors said that he couldn’t be any sicker and we have never come any closer to losing him. Benjamin is a gift. I know that Aspiration is a common problem with children that have certain variants of Batten Disease. We understand but we would never compare our situation with someone in the Batten community. Your plight is as rare as the disease itself and you have our love and respect in the biggest way.
Over the course of time, Benjamin has been placed in several classifications by school systems and county programs. Cerebral Palsy, Neuromuscular disorder to name a couple. He is Autistic for sure and he functions at different levels in various areas of development. He is mostly non verbal but uses a combination of signs and single words. As time has gone on, and his weight has increased, he has become unsteady on his feet. He has issues with his equilibrium. You can sense his frustration at times with his inability to control his body’s function. He tends to get over stimulated and excited at times. This is revealed by a violent form of rocking and flailing of his arms. He can also use these same gestures to show happiness and excitement. There have, for sure, been problems along the way. There have been challenges and concerns. Only God knows how long we will have him. Benjamin is a warrior of a rare kind but his longevity is as unknown as his disorder. My son is a gift.
One thing was evident through all of this. That is that Benjamin has his mother’s sweet disposition. Many times, people that have met him talk about what a sweet spirit he has. I know one thing. Mom and dad are crazy about him. Yes, it is true. We should be enjoying the benefits of an empty nest. The benefits of having him in our home are to us, so much greater. Benjamin is his mom’s mini-me even though he now towers over her. I call them the twins or ‘My Two Faces’. We are very closely knit together. Can you tell?
Yes it is true that I love kids. I love kids and I also love those that are like them. The biggest and most present characteristic of Benjamin’s disorder is the fact that he is developmentally delayed. When it comes to his development he is varied in how far he has advanced in any particular area. One thing is for certain. He has kept his childlike innocence for a lot longer than a normally developing person would. Oh yes, he can get his grouch on, but there usually has to be a reason for it. When he is in a good mood, which is most of the time, he is oh so sweet. He loves to smile and his smile is infectious. The two of us are especially close and there has been tons of laughter while spending time together. Some of the best pictures have come as a result of dad making Benjamin laugh. I couldn’t imagine him missing from my home and so this makes me think of all of you who are missing a loved one. You may be one of the many that have lost their young warrior to Batten Disease. I could be talking about someone like my friend JoAnn Caudle who lost her special needs son Tommy to cancer. Whoever you may be, it is my heart’s desire that you would find peace during this holiday season.
Just like any other one who is childlike, Benjamin enjoys the wonders of Christmas. When the decorations go up, the anticipation begins. Benjamin has a room full of toys and many of them come from Christmases past. It seems that most of the time the toys just sit there unnoticed. He loves buses and stop signs more than anything. I had bought him a toy city bus one year and I thought that he would absolutely love it. He opened it and just set it off to the side. I was like oh well, I tried. You know what though? He came back to it and he often keeps it on his desk right where he plays. He is aware of things but you cannot always tell. He will take it with him from time to time. Benjamin has a lot of school buses. He rode on them frequently when younger, so thus, the fixation. There is an end table and a chair in his little playroom or ‘man cave’ as we like to call it. I like to eat my breakfast in there early before going to work. It is always dark when I go in and I have to feel my way through to the end table and the lamp that is on it as I go to put my cereal bowl down. Sometimes the little table has a lot of toys on it and I will think that my wife has rearranged things. I will mutter something under my breath but as It turns out it is actually Benjamin that is responsible. He is paying attention but you would never know. That is an aspect of his autism and his delay. One year, I was thinking to myself that he had enough toys and that we should only get him clothing and other things for Christmas gifts. As he finished opening all of his gifts he looked at me and said the words ‘toys’. My heart sunk within me. In his deep voice he said ‘toys’. Christmas is for kids and those that are like them. Benjamin, you will always get toys on Christmas from now on. I promise!
When it comes to Christmas, I love to give gifts. In fact, I love it more than anything. I can’t think of much that I would want for myself except to help others. I wish I had more to give. Well, maybe a new laptop would be nice. Ha ha! Anyway, this year we will send out something for our kids that are away. Benjamin will have presents by the tree on Christmas day. As far as me and Rosie, we don’t plan on doing anything much for each other. We will, however, be sponsoring a child. We will be doing this through an organization called Mito Wishes Upon A Star. Each year they help find sponsors for children with Mitochondrial Disease. My dear friend Christen Brawley has done an excellent job of finding sponsors and we decided to help. There is one other person that we have in mind and there could always be last minute additions and changes in plans.
The idea for this particular blog entry came as a result of a chat that I had with my friend Donna Brown. She is one of the many friends that I gained through following a special little girl named Ali. Most anyone that follows kids with rare diseases knows who Angel Ali is. Ali, of course, had Batten Disease but has since made her home in heaven along with the many others (Batten Disease really isn’t that rare). At it’s height, Ali’s page hosted 134K likes. That is a lot of people. It is not a contest to see who has the most likes on their Facebook page but there is something that I would like to point out. If a 134 thousand people are out telling all their friends about Batten Disease, that creates a lot of awareness. Not only did it create a lot of awareness but it also created a lot of friendships that have endured. There are a lot of people that I really care about whose friendship with me came about because of Ali and her mom, Donya Catlett. One such friendship is with Donna.
Donna has created a page and an organization through Facebook called Teddy’s Angels. I was so pleasantly surprised when I learned about all that she is doing in the way of spreading awareness about childhood cancer and rare diseases like Battens. She has created characters using costumes that she uses for getting the message out to others. She goes out in public places and spreads awareness to people who do not yet know. Donna gives talks to children at the schools in her area. Her husband is a truck driver and they have placed Teddy Angel’s ribbons and logos on the truck. This helps them to spread the word wherever they go! Donna has also raised money directly to give to families whose children are battling cancer. You go girl!! This Christmas she and her team have set a goal of sponsoring 85 children to receive a Christmas gift. Last time we talked, she was oh so close to achieving that goal. How cool is that! After all, Christmas is for kids and those that are like them. Donna attributes the inspiration that she received for doing all of this to following two special children. One with childhood cancer and the other with Batten Disease. The child with Batten Disease was none other than Angel Ali or Ali Vise. Ali was loved by so many people, one of which was Donna. Like so many others, she had a dream of meeting Ali in person. That dream became a reality when she, along with her husband Jeffry, attended an event put on by Ali’s mom, Donya. You can only imagine that being a very special meeting for Donna and in fact that is what she would tell me. Meeting someone who is so loved and followed by so many is a great privilege and it comes to very few. When it happens you know that you are experiencing something special and it often times can have a profound impact on you. Much of what Donna is doing is being done because of an angel that she met who had Batten Disease.
There are a very few things in the way of material objects that I would like to have as a gift. I really receive so much more by doing for others and seeing the joy that comes to those that gain from something I was able to do. My writing is really for others although I have received so much by doing so. So I want to acknowledge that like Donna, my life was changed because of Ali’s life. It has been a gift given to me. It didn’t happen on Christmas although it may be one of the best gifts that I have ever received. Ali’s image has adorned our home during every Christmas since we first became aware. I started to follow Ali in what had to be the year 2013. It was through a series of Facebook pages that I was led to Ali’s Angels. Up to that point, I didn’t know what Batten Disease was. I had heard it said by others that when it came to Donya and Ali, it only took one look and you were done. I can testify that to be the case because the same thing happened to me. Now since that time, there have been other Batten warriors and their families but it all started with Ali and her family. It was through Ali that her grandparents received the sweetest nicknames. Donald and Doris Catlett became Papa Cat and Nini Cat. I just thought that the entire family was so neat. I was taken by Ali’s plight and the sacrifices that were being made on her behalf. I read every post and made comment. Like so many others, I did my best to get to know Donya and her family on the deepest level that I could from across the country and I tried to help in every way that I could. I started writing posts on Facebook about Ali and Donya and it showed people how we felt as a family. I can remember people making comments about the posts as if to say, wow, who is this guy? The same type of feelings that I have shown in my blogs about Batten families first existed in those posts about Ali and her sweet family. It was in those original posts that I discovered that I love to write. Like Donna Brown, I felt like I needed to meet Ali and so in June of 2014 we would make the trip.
I have shared that the trip to meet Ali was made in conjunction with the opportunity to dive an underwater memorial that is dedicated to a Navy SEAL who gave his life in service to our country. His name is Adam Brown and he was from Ali’s hometown of Hot Springs Arkansas. It was actually through Adam Brown and his memorial, named Fearless Rock, that I learned about Ali and Batten Disease. That has always amazed me. My perspective and motives in life were all changed by these events. At the time we were selling a rental house. I had to plan the trip and take diving lessons while staying well during cold flu season. Everything had to go according to plan and it did. In all our years of
marriage we had never been on a long distance vacation but we were going to Hot Springs. It was Benjamin’s first and only airplane ride. We told him that he was going on the ‘bus with wings’. He did a great job and we were so proud of him. It was exciting and there are so many details that we could share. You will often hear people talking about Christmas being a magical event. In fact it is. Especially if you are a child or one of those that are like them. Meeting Ali and her family was a magical event for us and it was one of the greatest gifts that we ever could have received. It was Donya that told me that I should blog about the event. This has led to greater understanding about expressing myself through writing. It was only a lunch date but the time spent was priceless. The love that Donya had for Ali was even more evident as we met in person. Ali was flawlessly cared for and was in fact pure perfection. The conversation was rich and the memories will always be sweet. It is hard to know what impact the event had on Benjamin but it is very clear that it had a profound effect on me.
This is my Christmas blog! One of the best gifts that I have ever received is having my perspective in life changed. Coming to the realization that it is not all about me has changed me. It is so much better if we are in this world to help others. Especially if we are talking about Kids and those that are like them. Especially if we are reaching out to those that need extra attention or a source of encouragement. That is why I so enjoy being involved in the Batten community, as well as those communities that are like them. Being a servant to my son has taught me much. Being a part of his story and sharing it with you means a lot to me. I look forward to what is coming up in this blog and I’ll do it for as long as I am able. I so appreciate the families that have allowed me to write about their precious warriors. Batten Disease is not that rare, is it? I have written about a family from Newfoundland and one from South Africa. Maybe the sweetest one of them all comes from Plymouth in the UK. Greece and Turkey are the homes of two really good friends that care for wonderful warriors. My Royal Family lives in England and of course there have also been many families here in the USA that have placed their trust in me. All of their stories have been written in the blog because I have been allowed to do so. All of them are special to me. So this is my Christmas blog. It has been written at Donna Brown’s request because she is honoring my Benjamin as one of her little warriors for Teddy’s Angels! After all, he is little at heart. We have included both of our families meeting Angel Ali because her sweet life has impacted both of our lives in a very big way. I hope it makes sense to you. I have stuffed this blog like a Christmas stocking. Packing it carefully with a lot of different things. Please remember that you are important to me and please remember this…. Christmas is for kids and those that are like them. It is, however, a time for us all!
From the Lopez family
Greg, Rosie, and Benjamin
Is it them or is it us? Is it the feelings that they produce in us or is it that there is something truly special about them? I think that the answer has to be all of the above. It is them, but they also do something to us. Once you give a little piece of your heart to these kids and their families, they come close to taking all of it. Let it happen!
I would like to welcome to my blog Sanfilippo families, as well as, families in other MPS communities. I am grateful for every opportunity to write about those who battle an MPS disorder. This, of course, alongside their special children. This is a labor of love that is extended to each one of you! Scroll down to see MPS family titles.
Highlighting a previous blog that might interest you:
Forever Royal - The Final Version
One child in a family with a rare disease is a challenge. What if there is two? Heartbreak multiplied you pick up the cause and do your very best to make a difference. That is how a normal family becomes Forever Royal ...
Take the titles listed below and go to month and year listed in the archives.
January 2017 -
*The Story Between The Lines
February 2017 -
*I Know Just Where You Are
*My Kind Of Royalty
March 2017 -
*The Caring Type
*Face to face: A Fairy-tale
April 2017 -
*No Ordinary Love
*A Rare Friendship
May 2017 -
*Tyrell and The Rare Love Story
June 2017 -
*Seth and The Healing
July 2017 -
*Little John and The Reason
*Sands and The Scottish Princess
August 2017 -
*A Rare Kind of Devotion
*The Giggle Box
September 2017 -
*Sweet Montanna and The Status
October 2017 -
*The Blog About My Blog
November 2017 -
*Lydia, I Love You!
*Kayden And The Change In Plans
December 2017 -
*Those That Are Like Them
January 2018 -
*Nora Skye - I Know Just Where You Are
*Brock and The Priceless Memories
*Jamesy Boy and The Treatment
*The Priceless Princess From Beyond
*Forever Royal - Part One
*Forever Royal - Part Two
*That Kind of Love - Conner's Story
*What I See (She is a Butterfly)
*No Longer Alone - Kristiina's Story
*Things We've Talked About - Oscar's Story
*The Reason Why - Hannah's Story
*Kayla's Perfect Princess - Breanna's Story
*Where Do I Go From Here? - An information only blog
*Warriors Unaware - Mia and Kaleb
*Her Little Story
*Someone Like Raelynn
*Forever Royal - The Final Version
*Awfully Beautiful - The Life of Noah and Laine
*A Lifetime of Love - Tegen's Destiny
*Forever Beautiful - Gabi's Story
*The Miracle Baby - Amelia's Story
*Dylan's Life - A Small Town Story
*Princess Grace and the Challenges
*Anything for Tessa - Her Story
*Haley Bug's Battle - A Family Story
*Journey Unexpected - The Rich Family
Sanfilippo Syndrome and other MPS family titles -
*The Beautiful Light of Haidyn Grace
*Any Distance Traveled - Reagan's Story
*The Missing Someone - Kiernan's Story
Archives - Use title listed above with the applicable month and year.
Highlights from the beginning of gregster60.com -
Benjamin's Daddy - March and June of 2016 - Revised May 2017. Titled Benjamin's Daddy Revised.
My Fearless Adventure - April and May of 2016
A Different Type of Warrior - January 2017
Larry - February 2017