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Tuesday, April 28, 2026

Explaining My Love for Spanish

I figured that it was time to give all of you dear readers an explanation for my love for the Spanish language. I did not start off being bilingual. However, through many years of struggle, learning street Spanish, taking a smattering of formal classes and being married to a native Spanish speaker.

I naively thought everyone would be bilingual in Colombia. I only had one year of required high school Spanish so I knew basically nothing. I remember landing in Bogotá and being shocked by the fact that almost no one spoke English.

I remember failing to tell my bank that I was in Colombia and they assumed that I was a scammer so they blocked my access to all of my debit and credit cards. Luckily, a nice store owner took pity on me and after I explained my situation, he let me use his phone for free to call the one person whom I knew at the time who spoke English. He was nice enough to come pick me up and let me stay with him. 

I also remember for about the first six months of living in Colombia, it seemed like everyone spoke 1000 miles per hour. It took me about six months to get used to it. I remember once having to buy packing tape for a move. I went to the local shop and I asked for "cinta" (tape) and I said it about fifteen different times, in fifteen different ways before the lady understood what I was saying.

I have always had an accent when speaking Spanish. I think that I always will. However, I consider a foreign accent as a badge of honor. It means that you can speak a language which is not your native language. Now that I have been affected by facial paralysis, it is harder to understand me sometimes. However, I am very lucky that throughout all of my brain surgeries I have not lost my ability to understand Spanish. 

I learned Spanish at first, only to survive and not starve. This was well before I started to really enjoy being bilingual. I remember being recently arrived to Colombia. I went to the local grocery store and I bought what I assumed was chicken. However, it was super cheap. I was excited to get such a discount. I went home and cooked it in a stew. I spit it out immediately and didn't finish it. I found out only later that what I had bought was the gizzards or innards of the chicken. 

Even after all of these years of speaking Spanish, I still struggle with some things. For example por vs para (the two forms of the word for) and ser vs estar (the two forms of the verb to be). Ser being a permanent action and estar being a temporary action. I also struggle with the imperative, which is how you give commands in Spanish. Another thing that I struggle with is era vs estaba. Both words mean "was" but in different context. 

Every word in Spanish has a gender, male or female. The general rule is that if the word ends in A it is female. So, you use la and if it ends in O then it is male. So, you use el. However, there are many, many exceptions. For example, you would say, el mapa (the map) not la mapa. As far as I know, the only way to learn these exceptions is to memorize them. 

There is a governing body for the Spanish language. They have established all of the rules for the spelling, pronunciation and grammar of the language. In general if you can say it, you can spell it. In this way it is much easier than English. If you have a doubt about something, you can look it up officially. There are not a ton of unwritten rules and customs like in English. 

I also like the fact that you can combine some words in Spanish. For example, contigo (with you) and conmigo (with me). I also think that supuestamente is easier to say and spell than using the English equivalent of supposedly. 

I have heard various reports that people are being targeted for deportation only for speaking Spanish. This is racist and illegal. It is un-American and it makes me sad. Many immigrants don't teach their children their native language because they want them to be more "American". I think that is a big mistake. 

Jenny and I are raising our daughter Eliana Valentina to be bilingual and proud of it. I speak to her exclusively in English and Jenny exclusively in Spanish. I remember when Eliana Valentina was about 2.5 years old she went through a phase where she was constantly saying cacas (poop). She got a rise out of Jenny and I so she kept saying it. Even after we informed her that it was not polite to do so. I remember telling my parents about it on a video call in English since they don't speak Spanish. I figured that Eliana Valentina was too young to understand what I was saying, or that she was not listening. 

However, she came up to me with her hands on her hips and she defiantly said to me in perfect Spanish, daddy I will never stop saying cacas (poop). It was then that I knew instantly and without a shred of a doubt that my daughter Eliana Valentina was fully bilingual and English was no longer my secret language. Luckily, she has had a much easier time learning English than I did learning Spanish. I don't think that being bilingual has harmed or slowed her development in any way. In fact, I think it has benefitted her. I know that it will benefit her going into the future. I wish more people would become bilingual. 

I will end this by saying that just as in English, every different country has their own version of Spanish. Learning Spanish in Colombia is like learning American English and learning Spanish in Spain is like learning British English. So, now I can speak both flavors of Spanish. Interesting cultural note, in Colombia everyone says me regalas (give it to me as a gift) even when they fully intend to pay for the item. However, in Spain if you say me regalas then you are literally asking to get something for free. So, that was the first thing that I had to unlearn when I moved to Spain. 

I am still learning even after speaking Spanish for 14 years. I don't consider myself fully bilingual and I expect to be learning something new about Spanish my whole life. However, after 14 years I am fairly fluent and I can get what I need. It is pretty rare that I am unable to get my point across. 

Til next time, Tyler 


Friday, April 17, 2026

Gratitude

I have mentioned this before but I thought it was worth mentioning again. I am grateful not to have a degenerate medical condition. I am very lucky that I will not continue to get progressively worse. In fact, my current situation is the opposite. I will continue to improve with time and effort.

I think of people like the famous scientist Stephen Hawking, who by the end of his life could only move one cheek muscle which was connected to a computer that spoke for him. He was lucky though, there are people who have locked in syndrome and they are unable to communicate at all. It would be pretty terrible to be trapped in your own mind and unable to communicate. 

I have both speech and mobility issues. However, I am not paralyzed thank God, nor am I mute or in a coma. I have family and friends that love and support me and I have a beautiful wife and daughter. I cannot do everything that I once did. My life is hard in many ways. I would not wish this to happen to my worst enemy. I am still reasonably independent though. 

However, I still have a lot of life left ahead of me hopefully. I am thankful for everything that has happened to me. I have learned a lot from all of it. I am blessed beyond measure everyday that I have the opportunity to wake up again.

Til next time, Tyler 

Saturday, April 04, 2026

April Update

Not much new to update you on for April. However, in the gym I am up to 150 lbs on the ab machine, 25 minutes on the treadmill (5.0 incline and 1.7 speed). On the water wheel (a machine used to strengthen your arms, I am on level 17/20. On the elliptical machine I am up to 32 minutes without stopping. I can do nine laps and I can do one lap in 2:58. I have gone 2.15 miles.

All of this working out is getting me into the best shape of my life. My 71 year old father works out along side me. There is no guarantee that all of this exercise will help me but it certainly can't hurt me. My dad is getting into shape with me.

In addition to working out six days a week with my dad, I walk for an hour a day, Monday to Friday with my mom (using my walker) up at the local basketball court. I have started practicing with a traditional walker without forearm support. I am up to 30 minutes a day with the new walker. It is my goal to transition to using a cane. I don't expect to ever walk again totally unassisted. If I can't use the cane successfully, then I will use the traditional walker.

I am still looking for a job online and teaching English to some students in Spain. In the little freetime that I have, I watch TV or read. I also visit my family and friends. The girls get here in June, so I am excited about that We have a lot planned for Jenny and Eliana's visit.

That is really all for now. Til next time, Tyler 

Sunday, March 22, 2026

Positivity

Many people admire my positivity in the face of all these health challenges. A common question that I get, is how do I stay so positive?

There is no magic bullet. I have been given a difficult hand to play in life. However, things could be much worse for me. I am not sure or in a coma nor do I have a degenerative medical condition.

I am blessed to know that if I put in the time and effort, that I will continue to get better. I am far from being totally independent, I do have to deal with limited mobility and speech issues but I am at the point now where I can generally do almost everything in my daily life for myself. I have come a long way in the past six years.

Every day that I get the chance to to open my eyes, I make a deliberate decision to stay positive. My only other option is to fall into another depression. I would go into a downward spiral, losing my progress and motivation. I don't want to go back to that.

I am very lucky to have supportive people in my life. Including my wife and daughter, my family, my extended family, Jenny's family and my friends. I would be doing them all a disservice if I just gave up. 

Getting back to normal life won't only be a benefit to me. It will also allow Jenny and Eliana to get back to normal life as well. They deserve it as much as I do. None of us asked for any of this, but they have both been amazing. 

I have been affected by all of this for all of my daughter's life. She doesn't know me any other way. However, I am lucky and blessed that she loves me just as I am and she doesn't treat me any differently than any other able bodied father. 

That is all for now, Tyler 

Sunday, March 15, 2026

March Update

We are now March, it's time to catch up on my progress.

Monday-Friday I'm walking an hour with my mom using my walker at the local the basketball court. 

Monday to Saturday I'm going to the gym with my dad and exercising 2 hours a day. 

I'm also looking for a remote online job. I'm doing English classes for 3 online students (they're in Spain). 

I've seen family and friends in my short time.

I'm looking forward to the girls and their visit.

Really, I have only just noticed one big change so far. I can move my arms and legs so much better. Everything is coordinating so much more naturally. I'm in better shape in general. I can really notice muscle.
I have also been visiting a chiropractor to get adjusted and taking a daily creatine supplement. I don't know if any of this is helping, but it certainly is not hurting. 

Til next time, Tyler 

My Health Anniversary

I don't know exactly when I went into the hospital for the first time but I do remember that it was in March of 2020.

For those of you who don't know, I was born three months premature back in 1984. I was born with a medical condition called hydrocephalus (water on the brain). It meant that my body was unable to drain fluid off of my brain naturally.

To combat this, the doctors installed a pump on my brain that was connected to a tube that went into my stomach and released the excess brain fluid there. Everything worked like a charm. Other than the doctors having to extend my shunt tubing when I was 13, I had no other issues. 

That is, until I was 35 back in 2020. I always knew that one day my shunt could fail. It finally did fail in 2020 due to the plastic becoming too old. I never expected all of these problems but I am lucky and blessed to have the support of my family and friends and I know that things could be much worse.

Back in March of 2020, I was hospitalized in Pamplona due to my shunt failure. I had a total of six brsurgeries;ies, first they tried to repair my original shunt. They couldn't because it was too old. I ended up with facial paralysis and damage to my fourth ventricle in my brain. This was due to the increased brain pressure. Your fourth ventricle controls your speech and balance. Hence my current issues. The facial paralysis also affected my speech.

I was put on a liquid/pureed diet due to the facial paralysis. I also had to have thickener added to my liquids. I still have to have thickener to prevent the liquid from going directly to my lungs. I lost a ton of weight on that liquid diet. Luckily, now I can eat any solid food that I want. 

In 2023,the doctors in Pamplona were out of ideas. After enduring six brain surgeries I was really no better. It was then that I found out about a wonderful doctor named Dr Poca in Barcelona. I ended up getting transferred there.

I ended up having six more brain surgeries. By this point, I had two shunts. One shunt is dedicated only to controlling the fourth ventricle. The issue that I was having previously was that one shunt would work and the other would not. Dr Poca gave me two shunts that can be adjusted via magnets. Thereby, avoiding another brain surgery only to adjust the pressure. Additionally, the shunts that she put in have a technology that allows them to talk with and synchronize to each other. Avoiding the issue I was having before of one of the shunts working and the other not. In addition to all of this, Dr Poca found and removed an old piece of shunt tubing from my stomach lining which was causing me to vomit constantly and lose weight.

This has been a long, hard road to recovery which I never expected. I am forever grateful to Jenny and Eliana Valentina for always being there for me. In addition my parents, extended family and friends have all been great. 

Due to the damage to my fourth ventricle, I will never again be able to walk totally unassisted. However, being able to transition to using a cane, or worst case scenario, a traditional walker will have me over the moon.

In addition to everything else, the increased brain pressure damaged the optic nerves in my eyes. I have needed glasses or contacts my whole life. However, now due to one of my pupils in my eye being twisted and off centered due to the increased brain pressure, I can no longer drive or wear contacts. I don't miss driving though! 

The doctors injected Botox into my eye to try to straighten it. However, it only worked temporarily. Now the doctors tell me that they can do an additional surgery to straighten my pupil, but it will be only cosmetic, it won't improve my vision. So, I am thinking that I won't bother with it. Having the twisted pupil does affect my balance but over the past few years my body has learned how to deal with it. My vision is bad, but OK with glasses. My balance is slowly coming along. It is annoying having bad vision. However, I am thankful not to be blind. 

I wouldn't wish this on my worst enemy. However, I consider myself lucky for the shape that I am in. Things could be much worse. I am lucky that I don't have a degenerative condition. With time and effort I will only continue to improve. I am currently back home in Texas until the end of August. I am walking daily with my mom up at the local basketball court, using my walker. 

Every afternoon, I go to the rehab gym in Nocona, Texas for a 2 hour workout with my dad, we alternate between leg days and arm days. Additionally, I am still practicing my speech daily with my AI apps and I am still teaching English online to 3 of my students from Spain. Once a week, I have a session online with a memory specialist back in Spain to work on my short term memory.
So I have been staying busy! This has been a long, hard journey for the last six years and counting. However, I consider myself a lucky guy. I wouldn't change anything even if I could. If you are reading this, I love you and I am thankful for your support.

I have what amounts to a traumatic brain injury. The doctors tell me that it will never fully heal. However, with time they expect the undamaged areas of my brain to take over for the damaged ones I am seeing slow, small but steady progress. I can handle having limited mobility or speech issues. However, having both makes life difficult. I would love to get to the point where I have either speech or limited mobility, not both things. Obviously, having neither of them would be ideal. 

I want to be employable again. However, due to my mobility issues, an at home job would be best currently. Due to my speech issues, having a job where I don't have to talk to anyone is ideal. So far I am not having any luck with my job search due to my requirements. 

Jenny and Eliana Valentina have both been amazing. I couldn't ask for better support. I have been affected by all of these health problems for the entirety of Eliana's life. Sadly, she doesn't know me any other way. At least Jenny got to know me before all of this happened. I want to fully be a part of Eliana 's life without having to worry about my limited mobility or speech issues. She worries about me a lot and she is always willing to help me out. However, I want her to have a normal childhood, not to worry about her dad. 

Me getting as close to a normal life as I can will allow Jenny and Eliana to return to normal life too. That means any improvement that I can make will not only benefit me, but them also. So that is basically my update and my goals. 

Til next time, Tyler 

Sunday, March 08, 2026

My Exercise Routine

I figured that it was high time to put my exercise routine here in order for everyone to keep me accountable. My overall goal is not to walk totally unassisted, which is unrealistic unfortunately. However, I do want to transition to using a cane. Or worst case scenario, a traditional walker without forearm support.

To accomplish this, I am walking an hour a day with my mom (using my walker) and I am going six days a week to a local rehab gym with my dad. Below, I will post my workout schedule. 

Workout Schedule

1. Treadmill-30 minutes 
2. Water wheel-30 minutes 
3. Ab machine-100 reps
4. Stationary bike-30 minutes 
5. Rope pulley-25 reps
6. Leg press-50 reps
7. Arm and leg machine-30 minutes 
8. Elliptical machine-12 minutes 
9. Leg extension machine 25 reps

Monday 
1. Treadmill- 30 minutes
2. Water wheel -30 minutes
3. Ab machine - 100 reps
4. Arm and leg machine - 30 minutes
5. Elliptical machine - 12 minutes
Total workout time - 1hr 52 minutes

Tuesday
1. Treadmill - 30 minutes
2. Water wheel - 30 minutes
3. Ab machine - 100 reps
4. Rope pulley - 25 reps
5. Elliptical machine - 12 minutes
Total workout time- 1hr 32 minutes

Wednesday
1. Treadmill - 30 minutes
2. Water wheel - 30 minutes
3. Ab machine - 100 reps
4. Leg press - 50 reps
5. Elliptical machine - 12 minutes
Total Workout Time- 1hr 32 minutes

Thursday
1. Treadmill - 30 minutes
2. Water wheel - 30 minutes
3. Ab machine - 100 reps
4. Leg extension machine - 50 reps
5. Elliptical machine - 12 minutes
Total Workout Time- 1hr 32 minutes

Friday
1. Treadmill - 30 minutes
2. Water wheel - 30 minutes
3. Ab machine - 100 reps
4. Stationary bike 30 minutes
5. Elliptical machine - 12 minutes
Total Workout Time- 1hr 52 minutes

Saturday
1. Treadmill - 30 minutes
2. Water wheel - 30 minutes
3. Ab machine - 100 reps
4. Bicep curls - 25 reps
5. Elliptical machine - 12 minutes
Total Workout Time -1hr 32 minutes

Total weekly workout time - 6 days. 9 hrs and 52 minutes weekly

In addition to all of the workouts, I am doing my speech therapy daily. I am trying to beat this facial paralysis. Because it will be easier on me to have either limited mobility or speech issues but not both of them. 

I hope all of this effort is going to help me reach my goals. I am doing this not only to benefit myself but to benefit my family as well. Now, you can keep me accountable. Even though none of this is ideal, I still consider myself a lucky guy. 

Til next time, Tyler 

Thursday, March 05, 2026

In defense of anti depressants

I have talked about this various times before. However, I can't remember specifically blogging about it. I am on a mission to de stigmatize antidepressants and getting mental health help if you need it. I would write this a million times over again if I knew it would help someone who is struggling. What follows is my experience and yours may differ.

I grew depressed a few years ago when I was sick and hospitalized. I never considered ending my life thank God. However, I was absolutely numb. It got to the point where I didn't even care if I lived or died. 

Nothing brought me joy or anger or frustration or anything. I didn't care about myself or my family or friends. I had so much to live for but I had lost all of my motivation. The only reason I even opened my eyes was because it was an automatic reflex from my body. 

It was around this time my wonderful general doctor in Spain prescribed me an anti depressants. I am forever grateful to him for going the extra mile and caring about me more than he had to. He would call up to the hospital weekly to make sure that I was taking it. 

I don't agree with anyone's decision to commit suicide but I do now understand wanting to end the numbness. Being on an antidepressant (which I am no longer taking) allowed me to have normal human emotions again.

I came back to reality from the edge. I found my joy and motivation again. I was able to realize how lucky I am to have the wonderful family and friends that I do. 

I took joy in hearing my daughter laugh, talking about boring daily stuff with my wife or even getting annoyed or angry. Just remember, if you are reading this and struggling, it is not a sign of weakness to ask for help, talk to a professional or get on an antidepressant. You have a lot to live for. You would be ending your pain by committing suicide but the pain would only be beginning for your loved ones and friends left behind.

Edit: I have recently done some research. I was just curious as to why some people choose to end their lives after being put on an antidepressant. The medicine is supposed to make you less suicidal not more. However, interestingly my research has shown me that depression affects your energy, drive and motivation. I can certainly relate to that feeling. 

The depressed person may want to kill themselves but they lack the motivation to actually do it. Luckily, for me I was completely numb emotionally but I never considered actually killing myself. The antidepressant first restores the person's motivation and then it gets rid of their suicidal thoughts. 

So, the most dangerous period of time for some depressed people, is that small window of time where people who are taking antidepressants, is when they are motivated enough again to actually kill themselves and they still have the desire to do so. 
If this helps even one person it will have been worth it. 
Til next time, Tyler 

Thursday, February 26, 2026

February Update

Now that I have been back home for roughly a month, I figured it is time to give everyone an update. My overall goals remain the same. I want to improve my balance and overall independence, thereby giving Jenny and Eliana a shot at returning to a normal life. 

I want to transition to using a cane. Worst case scenario, I want to be able to use a traditional walker (without the forearm support). I know that it is highly unlikely that I will ever be able to walk again fully unassisted, due to the damage to my fourth ventricle. However, I will be over the moon to get to the point where I can walk using only a cane. 

To accomplish my goals, I am walking daily with my mom at the local high school basketball court, using my walker with forearm support, for an hour daily. Then, in the afternoons after lunchtime, I go with my dad up to the gym and we exercise for two hours daily. We alternate between arm and leg days. Once this is all said and done, I will get both of my parents into good shape. 

In addition to all of my exercise, I am still doing my speech therapy and I have registered with the Texas Workforce Commission, looking for a remote job that I can do from home. I am also staying busy reading and watching TV series. I am also still teaching English to three of my students from Spain, online from here in Texas. 

Jenny and Eliana Valentina will be here to visit me in mid June until mid July. We plan on seeing and doing a lot. I will be here in Texas until the end of August. In my little spare time, I am visiting family and friends and eating good Texas food. That is all for now. 

Til next time, Tyler 


Friday, January 30, 2026

I made it home

I thought I should update this and let you know that I made it home safely. This will be short and sweet. However, I will be home until the end of August. Right now, we are just trying to stay out of the ice and snow. I am looking forward to seeing Jenny and Eliana Valentina in June.

I am also happy to be home and I am available to see family and friends. I am looking forward to working hard and hopefully regaining some of my mobility and independence. 

Til next time, Tyler Horton 

Wednesday, January 21, 2026

My trip home

I figure that now is as good a time as any to let all of my dear readers know that I am heading back home to Texas with my dad on Tuesday the 27th.

I will be back home until August 31st. Of course I will try and visit with everyone, but the primary purpose of this visit home isn't social. It is to train hard and hopefully make progress with my mobility and speech issues. 

Now that I am 41, I am not getting any younger, nor are my parents. This may be my last chance to make meaningful progress. Due to the damage to the 4th ventricle in my brain, I am under no illusions that I will ever be able to walk again totally unassisted. 

However, it is my goal to get rid of the wheelchair and walker with forearm support. I want to transition to using only a cane. Worst case scenario, I want to move to using a traditional walker. I will be returning to Spain August 31st. The shape I return in, is realistically the shape I can expect to be in for the rest of my (hopefully) long life. I will be returning to Spain with my mom.

Jenny and Eliana Valentina are both coming to visit me in July in Texas. I hope that we can have a good time. I look forward to seeing all of you soon. My parents no longer live in Little Elm, they moved to Saint Jo Texas. However, I hope to visit my last remaining grandma and all of the family and friends that I can. 

It will be hard being away from Jenny and Eliana Valentina. However, I don't want to be a burden on anyone. Nor do I want to live my remaining life with both a speech and mobility disability. I can deal much easier with one disability instead of two. Three of my clients (students) of English will be continuing English classes online with me while I am in Texas. This will be good for my pronunciation practice and a way to stay busy. 

Jenny and Eliana Valentina both deserve a chance at a normal life and they won't get it until I do. I still consider myself lucky to be in the shape that I am in. I am not bedridden or in a coma. I still have a lot of life left to live even if it is not as easy as before. I am also grateful for the amazing support of my family and friends and Jenny's family. I couldn't do this without them.

Next time I write you it will be from Texas. Til next time, Tyler 

Sunday, December 28, 2025

My year in review

Now that we are (almost) in 2026 I thought it might be nice for me to do a quick review of my 2025.

Overall, I have had a good year. When we went on our week long European cruise (with my in laws and Ana and Fran) in addition to Jenny, Eliana and myself. I had a terrible time. I got what I assume (I never got tested) to be covid. 

I was sick as a dog. I barely left the ship's cabin. In addition, everyone else got sick as well. Once we got home, I ended up getting hospitalized for a week. Luckily, I was able to recover from my illness and had no lasting issues. 

I got the chance to spend time with both of my parents in person here in Pamplona. That was nice. Coming up, we will have my birthday and Jenny and I will celebrate it one of our anniversaries (the civil wedding). In addition, we will be celebrating new years eve. Eliana is growing like a weed and just celebrated her 5th birthday. I can't believe how fast time flies!

At the end of January, I will be going back to Texas for a while to focus on my physical recovery. It is my goal to be able to walk with the assistance of a cane. Failing that, I want to be able to transition to a traditional walker. No more wheelchair or walker with forearm support. 

I will miss Jenny and Eliana but they will be coming to visit me in July. I am not getting any younger nor are my parents. This could be my last chance to make meaningful progress with my mobility and speech issues. 

Overall, other than getting really sick on the cruise, I have been holding steady and slowly but surely making small progress with my speech and mobility. I am still going to my physical therapy 4 times a week and teaching English online to work on my pronunciation. 

I am a lucky guy and grateful for all of you and every day that I have above ground. There are others out there who have it much worse than I do. 

Til next time, Tyler 

Sunday, November 16, 2025

Outliving Others

This one will be short and sweet. I am only 40 years old but I have already outlined seven of my friends (that I know of) plus Jesus and all of the 27 club. I have certainly had my fair share of health issues over the past five years but I consider myself a lucky guy and very fortunate to have the support of my family and friends. I hope that I still have a lot of life left to live, even if I struggle with speech and mobility issues. If you are reading this, know that I am thankful for you and I love you. I am grateful for every day that I have above ground. 

Til next time, Tyler 

Thursday, November 06, 2025

My selfish blog

I have spoken at length about all of my health issues over the past five years but today I wanted to step back and selfishly congratulate myself.

I still have a long way to go to get back to normal life after surviving 12 brain surgeries and one failed eye surgery. I would not wish this on my worst enemy. This has been a extremely difficult, slow and a long process not only for me but also for my family and friends.

I am extremely grateful for the love and support that I do have. While I didn't ask for or expect any of this my family and friends didn't either. I am extremely grateful to them all. I am a lucky guy who has the love and support of my wife and daughter, my parents, brothers, extended family and friends and all of Jenny's family has been great as well. They never asked for this either. 

While I do have speech issues, mobility issues and issues with my short term memory, I have come a long way in the past five years and hope to continue progressing towards eventually getting back to normal life. Jenny and Eliana deserve nothing less for all that they have given me. 

I went from being 100% dependant on others for everything in my daily life, to now less so. I am still more dependent on others than I want to be, due to my speech and mobility issues but I am not paralyzed thank God and I still have a lot of life left to live.

I went from losing weight until I weighed almost nothing, and being on a total liquid diet to now being able to eat whatever I want. I have spent roughly nine months of my life in the hospital cumulatively over the past five years.

However, since my wonderful doctor in Barcelona managed to fix my two shunts in 2022, I have not needed to have another brain surgery. Hopefully, I am through the worst of it now. I still need to use thickener with my liquids due to the facial paralysis affecting my swallowing. I also need a wheelchair or walker to get around. However, these limitations are manageable and could be much worse. 

I still have a long road ahead of me to get back to normal life but I will continue my daily speech therapy and going to my physical therapy 4 times a week to work on my balance issues. Additionally, I have returned to teaching English online, not to make a ton of money but to improve my speech. My life is not ideal but, it could be much worse. I am thankful and grateful to everyone for their love and support and while I am not fully independent, I am not paralyzed or in a coma either. I do not want to be dependent on others forever nor do I want to be a burden to anyone. I want to return to being a normal husband and father.

That is all for now. Til next time, Tyler 

Monday, October 20, 2025

My blog anniversary

I started Traveling with Tyler when I left the United States on November 4th 2009. I only planned to go to Australia for a year and then return home. Sixteen years later I now live in Pamplona Spain.

I write less now than I once did. I also travel less. However, I am grateful that I have been able to keep this up for sixteen years and counting. I hope my future descendants will enjoy reading this. When I was little, my dad used to tell me a story every night before bed, from his childhood. 

I was fascinated by his stories and I secretly worried that I would never have any good stories to tell my future kid(s). I was wrong though. 

As of 2025, I have been to 47 different countries and lived and worked in seven. I married a Colombiana and we have one beautiful daughter Eliana Valentina. I have had enough adventures to fill a book. I have even written my memoirs.

I have certainly had my fair share of health struggles over the past five years and I wouldn't wish that on my worst enemy. However, I have an amazing group of family and friends and I consider myself very lucky. 

I wouldn't change anything even if I could. I still have a lot of life ahead of me even if I can't do everything that I once could. I am much better off than some other people. I am not paralyzed or bedridden.

You never know what life has in store for you. Take every day as the gift that it is. None of us know how long we have.

That's all for now. Til next time, Tyler 

Monday, September 08, 2025

My mom's visit

Well my mom has come and is now headed back to Saint Jo, Texas. We had a great time seeing her. I am very lucky to still have both of my parents and they are still in good enough health to come see us. It is a long, multi step journey from Texas to Pamplona Spain. I am lucky and grateful that they are still willing and able to make the trip.

I am not sure who had more fun, Eliana Valentina or my mom. They both had a ball together. Luckily, my mom still has a lot of energy because my daughter will take it out of you! It was a pleasure getting to see them spend time together. They sure do love each other. Eliana loves all of her grandparents and her great grandmother.

We got to disconnect for a few days go camping (in a handicap accessable cabin) in Asturias, Spain. It was very nice and fun. We had a great time. It was much more enjoyable than our cruise. We had no bad luck or sickness.

We also got to go to the lake and puttered around Pamplona. We were busy nearly everyday. My mom will be returning here to visit us in Pamplona in January. Then, I will be going back with her to Texas for a visit. It will be good to see everyone back home. 

I am not 100% health wise. However, I am stable for now and doing much better than before. I still consider myself a lucky person and things could be much worse. I will continue looking for work, my daily exercise and speech therapy. I will continue teaching English online as well.

I may have limited mobility and speech issues but I still have a lot to live for. I am a lucky guy and I have an amazing family, in laws and friends. I couldn't ask for much more. 

Til next time, Tyler 

Sunday, July 20, 2025

My Mindset

Today I noticed on Facebook that it is my third anniversary of my release from the hospital in Barcelona. I still have a long way to go but I have come a long way in three years. I am nowhere near as independent as I want to be, however I can do most of the daily responsibilities of life on my own without assistance.

I would not wish my current condition on my worst enemy. I can't do everything easily and automatically anymore. I have issues with my speech and mobility. However, things could be much worse. I am not bedridden or paralyzed. I still have a good quality of life and I can do a lot even with my limited mobility. 

I am grateful and very thankful for the support that I have received from all of my family and friends. I especially want to single out Jenny, Eliana, my in laws and my parents and brothers. I couldn't do this without any of them.

Here is to hoping that I can continue my progress slowly but surely. I hope to get back to normal life sooner or later. I want to have normal speech and mobility again. However, even if I never do, I am happy with the life that I have. I have been blessed with amazing family and friends. Hopefully my shunts continue to function and I can continue focusing on my physical recovery. 

I am still working on my physical recovery. I am going to physical training 4 days a week. Additionally, I am teaching online to work on my speech. I am still looking for full time work. Either in person or online. 

Til next time, Tyler 

Monday, July 07, 2025

Something that I want to remember

I am only putting this in my blog for posterity.

I know that I have talked about this a lot recently, however I strongly believe in being open about your mental health.

I was put on an antidepressant for a while, which I thankfully no longer need.

However, I am very thankful for modern medicine. One pill daily took away my emotional numbness and gave me back regular human emotions.

Luckily, I never thought about ending my life. However, at the worst of my depression, I only opened my eyes because it was an automatic reflex and I wouldn't have cared had I died. Luckily, I made it through that. 

I would encourage anyone that is struggling with depression to talk to your doctor about possibly being medicated. It was a great help to me.

Something amazing

I was just thinking today about infant mortality. So I decided to ask Google Gemini the following question : Tell me the percentage globally of children in 1900 who died before the age of 5? This was the response: The percentage of children globally who died before age 5 has seen a dramatic decrease from 1900 to 2025.
In 1900:
 * While precise global figures for 1900 can vary, historical data suggests a very high child mortality rate. Some sources indicate that nearly two out of every ten children (around 20%) died before reaching their fifth birthday. Other estimates suggest that around 40% of children perished before age five in the period leading up to the early 20th century. For infant mortality (deaths before age 1), rates around 165 per 1,000 live births were reported in 1900.
In 2025:
 * The global under-5 mortality rate for 2025 is projected to be around 24.99 deaths per 1,000 live births, which translates to approximately 2.5%.
This represents a remarkable reduction in child mortality over the last century, primarily due to advancements in healthcare, sanitation, nutrition, and access to vaccinations and antibiotics.

I also learned that the scientists predict that globally 99% of the children will reach the age of 5 by 2100. That is great news. Humanity in general really can do great things if we can stop trying to kill each other and hopefully we don't create a technology that we can't control. In 1850 the oldest woman in the world was 100. Today we are routinely living into our 80s and beyond. We have come a long way with modern medicine and sanitation.

That is all til next time, Tyler 

Sunday, June 22, 2025

Thankful

I know that I have said this before but it bears repeating. I don't have an ideal health condition, I am more dependant on Jenny and Eliana than I want to be. I would not wish my current health condition on my worst enemy. However I have come a long way in the past five years. My condition could be much worse. I still have a decent quality of life and I hope it only improves.

Thank you to Jenny and Eliana for putting up with me. Thank you to my parents for always helping me out even in the hard times. Thank you to all of my extended family and friends for their unending support. 

I never asked for nor expected this. However, I am dealing with it the best way that I can. I hope that I don't have to go back to the hospital and that I will continue to recover. I will continue trying to motivate myself to get better physically and mentally. I am hopeful that I will be able to start working again soon and will be be able to financially take care of my family. I am tired of being a burden to Jenny and her family. 

Well this is all for now. Til next time, Tyler