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Special Needs

7 Valuable Things I Learned Raising a Child On the Autism Spectrum

January 10, 2025 by Julie Leave a Comment

Little boy in pirates outfit

My son was diagnosed with Autism when he was five years old. At the time, they called it Asperger’s, but they have since stopped giving that label. If he had been diagnosed today, it would be as autism spectrum disorder (ASD) level 1. Getting the diagnosis is a blessing. We were then able to learn how to help him.

Fast forward, and my son has just turned 18. He is officially an adult, finishing his senior year of high school. Looking back on his childhood, I can think of all I have learned from raising him. Having a child on the spectrum is so different from raising any other child. And my child on the spectrum is different from any other child with autism. What works for some won’t work for everyone, and as a parent, you are always trying to figure out the best way ahead.

Raising a Child On the Autism Spectrum

Creativity in parenting is a must!

There have been so many times when I struggled to figure out what to do next with parenting my son on the spectrum, but then a creative idea would come to me. And a lot of times, it would work.

Parenting a child with autism is a lot of pivoting from the norm and figuring out what works. When my son was younger, he would do almost anything for a Skylander. I have many memories of us in Toys R Us and him picking out a new one he had earned. It made him so happy, and they made great rewards for him.

Routines Routines Routines

Finding a good routine was also a must. But knowing that sometimes we would have to move away from it and planning ahead for that was also helpful. When my son knew what to expect, it made things so much easier. Even today, he always wants to know what the plan is.

Things Change

When my son was in elementary school, I worried he would always struggle with what he was working on. He had a lot of trouble in school, which was wearing me down. But what helped was hearing from parents of older kids on the spectrum and how they were doing as teenagers and young adults.

Kids on the autism spectrum learn how to handle specific challenges over time. Things are still hard for my son, but he is mature enough now to know he isn’t going to be having daily fits about them anymore. One of the most complex parts for my son is not having a say in his daily life or schedule. But at this age, he has much more control over his days.

Kids Will Shock You In a Good Way

We went to Disneyland in October of 2022, and my son, 15, wanted to take off by himself. I was pretty sure he was capable, but I worried about him. I told him to check in with me every hour. And you know what? He did amazing. I was so proud of him. Kids with autism will shock you and make you proud every day.

Pushing Them vs Helping Them

Over the years, one of the trickiest things for me is balancing pushing him out of his comfort zone or giving him the extra help he needs. It isn’t always so obvious what to do. And I know I have made some mistakes when it comes to this. But finding that balance is essential. It is good to push them so they can grow, but you also want to be aware that sometimes, that extra help is precisely what they need to get through something.

Tuning Out The Noise

Whenever autism comes up, whether online, in person, or even in the news and media, there are always different points of view. What you should use for therapy, what labels should be used, and what you should do for your child.

I have gotten a lot of advice over the years. Some of it was pretty good. Some of it was not. You have to be strong and stick to your guns sometimes. Not everyone is going to understand your path.

My Child is On Their Own Path

When my son’s senior year began, we started getting emails and mailers from colleges around the country. Colleges that he would never be interested in. Colleges that share all about campus life and all they offer. Colleges that maybe I would have wanted to attend at that age.

But my kid is on his own path, which looks different from the traditional path, and that’s okay. However, sometimes I have to fight feelings of jealousy over it. But I must remind myself that this transition to adulthood, his college experience, and everything after will look slightly different than the norm, which is okay.

Getting an autism diagnosis for your child can be challenging to take in. What will their life look like? 5 years? 10 years down the road? But it’s one of those things where you have to try your best, research, advocate, and, ultimately, know that you are doing what you can for your child.

You love them, you will help them, and you will meet goals, even if they take longer than you thought they would. There is something so unique and beautiful about raising a special needs child. I have learned so much over the years, and I hope he always knows how much we love and support him, even into the adult years.

7 Valuable Things I Learned Raising a Child On the Autism Spectrum

Filed Under: Asperger's, Special Needs Tagged With: aspergers, Autism, parenting, Special needs

Great News! EFMP Will Be Standardized Across All Military Branches

June 27, 2023 by Julie Leave a Comment

Great News! EFMP Will Be Standardized Across All Military Branches

Have you heard of EFMP? EFMP stands for the Exceptional Family Member Program. This program is an enrollment program that works with different agencies, both military and civilian, to make sure that military families with special needs can receive the support they need at their duty stations. EFMP is the reason you may or may not be able to be stationed in certain locations.

Active duty service members are required to register for EFMP as well as making sure their status stays updated. This is to make sure family members are able to receive the right housing, education, medical care, and personnel services that they need.

Being stationed in a place where you couldn’t receive much-needed therapy can be a problem. While this does sometimes complicate issues when it comes to where a service member needs to go for their career vs where a family can go to get services, EFMP can be a good thing to make sure family members get exactly what they need.

Up until recently, each service branch had its own regulations and guidelines when it comes to EFMP. However, the DoD has made some changes to standardize the EFMP program. This is much needed and should have been done a long time ago.

Who qualifies for EFMP?

Military families who have any emotional, developmental, physical, or intellectual needs that require any special treatments, therapies, education, counseling, or training qualify and need to sign up for EFMP. If you are on OCONUS orders, you will need to go through EFMP screaming. My son and I had to do this before we did a PCS to Germany. At the time we didn’t have any diagnosed special needs and weren’t aware of any, so our doctor filled out a form saying so.

What will the changes in EFMP look like?

According to Gilbert R. Cisneros Jr., Under Secretary of Defense for Personnel and Readiness, “Service members can’t focus on the mission when they have concerns about a family member’s health or education needs. Enrollment in EFMP provides families access to critical services and support, no matter their service branch or location. We will continue our work to enhance EFMP to better serve our military families.”

The DoD Office of Special Needs is enhancing the Exceptional Family Member Program to help improve the experiences of military families in every branch in the following ways:

  • Medical services will coordinate the documentation of the special needs and the family’s enrollment in the EFMP. Identification and enrollment will be standardized.
  • Each branch will use the same criteria when it comes to the assignment process. You will also be told what the reason is if you are declined a location.
  • Family members will be able to connect with resources that can help. EFMP Family Support providers will help with this.
  • There will be guidance and transparency when it comes to disenrollment. The disenrollment process will be standardized.
  • There will be revisions when it comes to respite care, such as a consistent number of hours across the services and covering adult dependents who are eligible for respite care.

You can read more about this on the DoD Press Release page.

Hopefully, these changes will help improve things for EFMP families. Not being able to find the care that you need when you or a family have special needs can be frustrating, especially when trying to balance that with the military lifestyle.

Filed Under: Military Families, Special Needs Tagged With: Dod updates, EFMP, military families, military spouse, Special needs

When You Have Special Needs Kids With A Spouse In The Military

March 14, 2016 by Julie 2 Comments

Having special needs kids adds an extra level of stress and hardship to a family. It simply isn’t easy when you have kids that require a little bit more help than others. Add military life onto that and sometimes it can feel like too much.

When You Have Special Needs Kids With A Spouse In The Military

We didn’t know we had special needs kids when my husband joined the military in 2005. Our son was 13 months old and it wasn’t until he was about 2.5 year’s old that he was diagnosed as developmentally delayed. We were in Germany at the time and my husband was deployed.

Our 2nd little boy was diagnosed with Asperger’s at the age of five in 2012. We were at Ft. Campbell when this happened.

I am not sure what we would have done if we had known we would have two special needs kids during our time as a military family. Would we have decided it would have been too stressful? Would the benefits we knew we would receive cause us to join anyway? It’s so hard to say.

Over the years I have experienced what it is like to solo parent with special needs kids, to have to figure out who can watch my son when I don’t have family close by and how to make it through the unpredictability of this type of life with kids who don’t quite understand what is going on. It’s difficult and even though my husband is not active duty anymore, I am still trying to figure it all out.

When you do have special needs kids in the military, you need a good support system.

You will need people in your life you can call and depend on. Some days will be very difficult and knowing you have someone to call, even to just talk to is a must. If you don’t know anyone local, find someone you are close to that doesn’t mind a phone call every now and then. Just talking to someone who loves you and your children can help you get through a difficult period. Stay away from people who are just going to judge you. They are not worth your time and you shouldn’t spend too much energy worrying about what they are doing.

When you are married to someone in the military, there will be times that you have to be a solo parent, special needs or not.

It is so important that you take care of yourself during this time. Look and see what they have in your community or what you can do to help yourself. It might not be an easy thing to do and each person is going to have to figure it out but is so important. Even if it means taking a bubble bath after all the children are asleep, or binge watching a tv show or going to get coffee with a friend when everyone is at school. Find something to help you focus on yourself, even if it is just for ten minutes a day. You are a caregiver and all caregivers need breaks now and then.

You also need to make sure you are receiving the right benefits for your child. I was so thankful that when my son was first diagnosed with Asperger’s that we were able to start ABA therapy right away. This is a very expensive therapy but luckily Tricare paid for most of it. You need to be aware of changes with health care for your special needs child. They don’t always cover everything you need and sometimes you will have to fight for it. Sadly, some military benefits get taken away and that can hurt your special needs child.

Find other moms of special needs kids to connect with, either in person or online.

Being able to talk with others trying to raise their special needs kids in the military lifestyle is going to be good for you. You can vent together and help each other out. Some people know more than you do about the hurdles you might have to jump over in order to get what your child needs. EFMP, ABA, IEP, 504, etc, there are so many terms that are hard to understand. Talking to others who have been through it can help you understand more about the special needs military world and can become your support system.

Don’t let having special needs kids scare you if you are also a military spouse. Know that you are not alone and there is help out there for you. Know that you will have challenges but you can make it, one day at a time if you have to. Don’t forget about your own needs and find some good friends to support you.

Have you struggled having special needs children while having a spouse in the military? What have you done to make things easier for your family?

 

 

 

Filed Under: Military Life, Special Needs Tagged With: military life, Special needs

Christmas With A Child With Autism

December 11, 2015 by Julie 1 Comment

Christmas With A Child With Autism

Christmas With A Child With Autism

Christmas can be a stressful time of year for anyone. Christmas with a special needs child can add another layer of things to think that. As a mother of a child with Autism, Christmas has had to change a little from what I would thought it would be… (read more)

Filed Under: Asperger's, Special Needs Tagged With: asperger's, christmas

What You Need To Know About IEP Meetings

August 25, 2015 by Julie Leave a Comment

What You Need To Know About IEP Meetings

Thank you so much to Meg from MilKids Education Consulanting for this wondering guest post all about IEPS! As a special needs mom I have been to a lot of these types of meetings and they can feel so scary. There is a lot to know about them and this post gives any special needs parent a good idea about what to expect.

The elusive IEP, or individualized education program, is a tough beast to pin down. It comes in so many different forms, with literally infinite varieties. It looks different every single time, understandably it is a challenging thing to fully grasp.

Luckily, you have an expert IEP tracker on hand to tackle all of your questions and concerns.

First things first: what in the goodness is an IEP. Basically, it is a plan to help students who fall into one or more of 13 specific disability categories. That disability or disabilities also has to adversely affect that student’s academic progress. This plan specifies what kinds of services, like OT, PT or speech, the student qualifies for and what kind of academic program would be best.

The academic program explains where the student will be taught certain subjects: in the regular class with or without modifications, in the regular class with an aide, or in a separate smaller group with a special education teacher. A student could receive instruction in any or all of these places.

So, now that that’s out of the way. Let’s get to the nitty gritty, from a teacher’s point of view.

I want to help your child. I want to help him get the broadest, best education possible. But that education is different for every single kid. Might some kids go to Ivy League colleges and be elected president after receiving special education services? Sure. Might other kids have the goal of learning to dress themselves or use the bathroom appropriately? You bet. Most students in the special education system will fall somewhere in the middle.

Part of the process of special education is getting real with yourself and your expectations for your child. This will be hard. I understand. We all want our kiddos to achieve at the highest level, graduate from college, get married, have an awesome job, and raise a family. Unfortunately, for many severely disabled children this might not always be possible. It is a challenge to let go of those dreams, and create new ones. I once had a parent of a severely autistic student, who needed help bathrooming in the third grade and was working below a first grade level, ask me if I thought he might be a good candidate for a college that specialized in educating students with specific learning disabilities. That kind of disconnect between what your child is actually doing and capable of, and what you wish they were able to do, is extremely dangerous mentally, emotionally, and to your role as a parent.

Once we are all on the same page in terms of the child’s ability and reasonable expectations, we can proceed to the discussion of services, modifications, and accommodations. Let me be clear, these services are not intended to fix your child or to magically make your child excel at something that is currently hard. They are designed to help your child grow, to achieve at her highest level possible. This won’t happen overnight, or maybe ever. An accommodation or modification doesn’t mean the work is easier or graded differently. It means that the work has been adjusted to best meet your child at her educational ability right now.

One of the big things that we hear in IEP meetings is homework. Homework does not stop because of an IEP. It might be shortened. It might be different than the rest of his peers. It might even happen every other night. But there will be homework as determined by the teaching team, in consult with the special service providers.

The other thing we hear a lot is about specifics. Lots of IEPs are worded vaguely. They have to be. Teachers need to be able to adjust education tactics mid-year, while still progressing toward a specific goal. For example: Using a teacher created tool to monitor work progress, Johnny will complete 75% of his assignments in a given grading period on time. The quantitative part at the end is pretty specific: 75% of assignments must be on time.

The teacher created tool is where a lot of people get hung up. Many parents, and teacher, want a specific tool to be written down. Like this: Using a work assignment checklist (see attached), Johnny will complete 75% of his assignments in a given grading period on time. But this way would be a disservice to the child and the teacher. Let’s say that right now, X method is working to get Johnny to finish his work. But in a month, he’s no longer responding to this. If it is written into the IEP, it cannot change.

Let me repeat: IF IT IS WRITTEN INTO THE IEP, IT CANNOT CHANGE.

Not without a meeting to discuss new findings, rewrite that particular goal, and assess how other goals might be affected. That’s a lot of hassle over wording. In other words, let the teachers have the freedom of flexibility to change the program while still meeting the goal.

Let’s look at it this way: what if you had to create a nutrition plan that would last you all year. In order to change that plan, you needed to convene a meeting with your doctor, nutritionist, personal trainer, and the head of your doctor’s practice. In September, you really like mangoes. So you wrote them specifically into your plan: will eat 3 mangoes each day. But in December, you got really sick of them. If they are written into your food plan, you must eat them. How much better would it have been if you wrote: will eat 5-6 fruits or veggies each day. Now, you are working toward the same goal (eating healthy fruits and veggies) while still allowing yourself to be flexible in what you are consuming.

Once everyone agrees on everything, or agrees enough that the document can be signed, the meeting is over and the IEP is “live.” That means from this day until one calendar year from now, this is the IEP that rules the roost. It dictates everything about your child’s day in school: who he sees for the core subjects, what special services he is receiving and how often he gets these services, testing modifications or accommodations, and his academic placement (inclusion, general education, or substantially separate).

Now, you need to monitor to make sure that all of these things are happening correctly all of the time. Might a few slips happen? Of course! Teacher are, believe it or not, human. We get sick, have a meeting that can’t be rescheduled, or need to swap a schedule around sometimes. But if your child’s services are being provided correctly the majority of the time, that’s great!

As a parent, monitoring what is going on with your kid in school is super important.

You need to know. Here’s the dirty secret schools won’t tell you: they are routinely understaffed or staffed to just meet the needs of their kids.

Paraprofessionals have ultra tight schedules. They work with Child 5 from X-Y, then move to classroom 123 from Y-Z. They rarely get breaks, they juggle different grades, different children, different schedules. I know. I did this. It is hard. And they are paid unbelievably poorly. Schools hire just enough to cover the students that absolutely MUST have an aide, with very little wiggle room.

Special service providers, like PT, OT, and Speech, also have very tight schedules. They must see a large caseload of children with all different disabilities over the course of a 40 hours week. All of the children have a different number of hours that must be provided, and many see more than one specialist. It is common to see OT and PT on many IEPs since they often teach similar skills. In addition to all of that time, students must still receive core instruction, go to their PE and arts teachers, and eat lunch.

Schools do not hire extra PTs, OTs, SLPs, or paras. They hire just enough to meet their needs based on the data from the prior year and the students who enroll over the summer. What does this mean for you? Scary things.

Let’s say that your child has previously been able to keep up with the work, but this year is completely unable to do so. He’s in a class without a para or a co-teacher. Even if the special education teacher and the general education teacher agree that this is a child who would benefit from an aide, he probably won’t be getting one.

If at any point you feel that your child’s needs aren’t being met, or the learning environment is no longer appropriate, you can request a meeting to discuss outplacement. Outplacement is when the school district pays for your child to be educated in a private school that specializes in what your child needs. This happens ONLY when the least restrictive placement cannot be provided by the school system. Sometimes, schools might bring this up, especially if a child is a danger to himself or others on a very regular basis. The most important thing to remember is that a school cannot place your child anywhere without your consent, and your consent may be withdrawn at any time.

So, after all of that, I hope that IEPs are somewhat more clear. There are a lot of parts to the federal and state laws that govern special education. There are exceptions and loopholes, and there are many, many pages of forms that are required to be filled out and steps to be followed before we arrive at a completed IEP.

Even with all of that, it is worth it. It is worth the fight by parents and teachers of children to ensure that each and every child is getting the education he or she richly deserves.

Meg FlanaganMeg Flanagan is a special and elementary education teacher who holds an M.Ed in special education and a BS in elementary education. In addition to classroom experience, she has also worked in private tutoring and home schools. Meg is passionate about education advocacy for all children, but especially for children with special needs and children of military and state department personnel. You can find Meg online at MilKids Education Consulting, as well as on Facebook and Twitter.

Filed Under: Special Needs Tagged With: military children, Special needs

Back To School With Special Needs

August 5, 2015 by Julie 2 Comments

Back To School With Special Needs

Back To School With Special Needs

Summer is almost over for us. The boys go back to school next week. My son with Asperger’s is going to start 3rd grade! I find that a little hard to believe. It seems like we were just getting ready for him to start kindergarten. What a nervous mom I was that summer. We were working with our ABA therapists to get him ready for school. He had been in preschool but kindergarten was something else. We were able to get a schedule of what his school day would like ahead of time and went over it with him.

He started school and that year was challenging. He started 1st grade and that was another challenging year. The summer before 1st and 2nd he really matured a lot. He was not the same kid when he went back to school. 2nd grade was a lot better but still had its challenges. We went from having to worry about him acting out to worrying about getting him to do his work. That was a big change because it involved two different things. He was not acting out as much which was great but he was refusing to do some of his work. It wasn’t that he couldn’t do it, but he is a bit of a perfectionist, so if he didn’t feel like he was doing it 100%, he would freak out and not want to do it at all.

We are working with a good team at his school. A few of them have known my son since he started at the school. It is one reason we are still in Tennessee. I worry that when we move, we will have to start over a bit and that scares me. Right now it is working and I don’t want to mess with that at the moment. Although I do know that there are plenty of resources for kids with Autism where we are planning to move to.

As we get ready for third grade I am feeling pretty positive about it. I have seen him mature a bit over the summer. He is no longer acting out just because someone does something he doesn’t like. He still does this sometimes but not like he did. I can tell he is really working on that. He is being more helpful around the house too. Things just seem a little more calm which is good.

So as we look into starting third grade with Asperger’s, I am excited about the year. However, I know there will still be challenges. He might not want to do all his work, and we will have to find a way to make sure he does and starts to understand that he needs to get it done. He might not get along with everyone in his class. He might wake up one morning and decide he does not want to go to school that day. I am trying to prepare myself for however the year is going to go.

Having a child with Asperger’s is challenging in so many ways. But we just have to work through them. I am glad I have a good team of people we are working with to help my son have a good year. It will be challenging at times, we will have a lot of IEP meetings and there will be a lot of tears on my part I am sure. But it will all be worth it so that my son can get a good education and can learn about how to do well in school.

Do you have a special needs child getting ready to go back to school? What are your biggest fears about it?

Filed Under: Asperger's, Special Needs Tagged With: asperger's, Special needs

How I Am Helping My Son With Asperger’s Through Summer

June 4, 2015 by Julie Leave a Comment

Asperger's

Having a child with Asperger’s means summer can be quite a challenge. There will not be school and a regular routine so you have to make one. There are a lot of activities for kids but they might not be right for your child. It can be difficult to decide what to do.

I have come up with a few things to help this summer. My son is eight and if I let him he would spend the entire summer playing video games. I have to really try hard to get him interested in other things.

1) Pool time. He told me he loves the pool. So that was part of my reason for getting a pool pass this year. We can go whenever and stay for however long and it is fine. We can go almost everyday. He will also do swim lessons in July.

2) Daily chore. I require my boys to do a daily chore during the summer before they can play any video games. This works really well for my son with Asperger’s and he is usually the only one of my three to ask about the chore vs me telling him. I base the chores on what needs to be done around the house. Does the living room need to be picked up? Can you help me with the dishes?

3) Snacks. My son is a very picky eater and I learned that I need to make sure I have a snack for him that he will eat. While my other two will pretty much gobble anything down that I pack I have to make sure to include something he will actually eat. If I don’t, he gets a little grumpy. Not full on meltdown mode but still. It just makes things easier. I pack snacks and drinks every morning so we always have something on hand when we go places.

4) Days at home. This is a hard one. He craves a full day at home when he doesn’t have one for a while. I get it, I really do. I somtimes need that downtime as well. I am trying to balance that one out with daily activities outside of the house. I think my plan is to stay home on some days when we don’t have plans and the weather is bad. This will help him and help me handle him a little better.

5) Listening. As you probably know, when someone has Asperger’s, they tend to talk about what they are into all of the time. I am really trying to listen to my son this summer because he gets really excited about certain things and I want him to know that I care. It’s hard sometimes because I am not always interested in what he is interested in but I am trying my best to listen and hear what he has to say. I also ask him how he is feeling about the week. It gives me a good idea of how he is doing and what type of mood he is in depending on the types of activities we did.

What about you? Do you have a special needs child home for the summer? What are you doing to help them during their time off from school?

Filed Under: Special Needs Tagged With: asperger's, Special needs

When You See A Child Throwing A Fit

May 18, 2015 by Julie 2 Comments

When You See A Child Throwing A Fit

 

When You See A Child Throwing A Fit

The other day there was a video being posted online about a boy throwing a tantrum in the car. Although I thought it was a little odd that they were filming and not pulling the car over, I felt sympathy for the kind of fit the kid was having.

It was the kind of fit I am familiar with.

It was just like an autistic fit.

Maybe it wasn’t. Maybe the kid had no behavioral issues and was just acting like that to get his way. But maybe not.

But the thing that really struck me was the comments people were making about the kid. About if he were their son his “butt would be beat” or how their own child never would have been allowed to act that way. It gave me insight into what people could be thinking if I was out in public when my son was having a similar fit.

But it also made me feel like people just don’t get it. That they don’t understand what it is like to have a child like that.

I know for me that anytime I am anywhere and see a child with a similar fit my thoughts immediately think there is some type of special needs going on. That is based on my own experiences and what I have had to deal with.

I know that others don’t think that way and have their own opinions about the subject.

As a special needs mom I have learned to ignore a lot about what people say concerning my child. There is ignorance out there and there is acceptance. I try to surround myself with people who get it and who are not going to judge.

I really do wish that instead of assuming a child needs harsher discipline that people would take a step back and remember that most moms are doing their best and there are certain issues that some children have that cause them to act in certain ways.

That although it might not seem like it, that child could be improving. That they used to throw 5 fits a day and now they are down to 3.

That the mom was up all night because the same child doesn’t sleep and gave in when she really probably shouldn’t have. Because that happens sometimes.

That the day was going really well until something small set the child off and their parents are still learning how to handle what is happening to their son.

That the parents are still trying to wrap their minds around a diagnosis that they never saw coming.

That the fit you see is not quite as loud and harsh as it used to be and that the parents are thankful for that.

That the parents are working with professionals about how to figure out what to do next with their child.

There are so many reasons why that child is throwing a fit at the moment. You just never know what someone else could be dealing with. Give them the benefit of the doubt, offer help if it makes sense to and just be a bigger person then one that assumes they know what is best for someone else’s child.

All of us special needs moms will with thank you for it.

Filed Under: Motherhood, Special Needs Tagged With: motherhood, Special needs

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About Soldier’s Wife, Crazy Life

 

Welcome to Soldier’s Wife, Crazy Life! I am so glad you are here.

My name is Julie and I first became a military spouse in 2005 when my husband of 3 years re-joined the Army. Then, in 2014, he joined the National Guard. In January of 2024, he retired from the National Guard after 21 years of service.

During our time in the military, we got to spend 4 years in Germany as well as Tennessee where we now call home.

We have three boys and have been through four deployments together.

I hope that you can find support for your own deployments, PCS moves, or anything else military life brings you through my articles and social media posts.

 

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This website uses cookies to improve your experience while you navigate through the website. Out of these, the cookies that are categorized as necessary are stored on your browser as they are essential for the working of basic functionalities of the website. We also use third-party cookies that help us analyze and understand how you use this website. These cookies will be stored in your browser only with your consent. You also have the option to opt-out of these cookies. But opting out of some of these cookies may affect your browsing experience.
Necessary
Always Enabled
Necessary cookies are absolutely essential for the website to function properly. These cookies ensure basic functionalities and security features of the website, anonymously.
CookieDurationDescription
cookielawinfo-checbox-analytics11 monthsThis cookie is set by GDPR Cookie Consent plugin. The cookie is used to store the user consent for the cookies in the category "Analytics".
cookielawinfo-checbox-functional11 monthsThe cookie is set by GDPR cookie consent to record the user consent for the cookies in the category "Functional".
cookielawinfo-checbox-others11 monthsThis cookie is set by GDPR Cookie Consent plugin. The cookie is used to store the user consent for the cookies in the category "Other.
cookielawinfo-checkbox-necessary11 monthsThis cookie is set by GDPR Cookie Consent plugin. The cookies is used to store the user consent for the cookies in the category "Necessary".
cookielawinfo-checkbox-performance11 monthsThis cookie is set by GDPR Cookie Consent plugin. The cookie is used to store the user consent for the cookies in the category "Performance".
viewed_cookie_policy11 monthsThe cookie is set by the GDPR Cookie Consent plugin and is used to store whether or not user has consented to the use of cookies. It does not store any personal data.
Functional
Functional cookies help to perform certain functionalities like sharing the content of the website on social media platforms, collect feedbacks, and other third-party features.
Performance
Performance cookies are used to understand and analyze the key performance indexes of the website which helps in delivering a better user experience for the visitors.
Analytics
Analytical cookies are used to understand how visitors interact with the website. These cookies help provide information on metrics the number of visitors, bounce rate, traffic source, etc.
Advertisement
Advertisement cookies are used to provide visitors with relevant ads and marketing campaigns. These cookies track visitors across websites and collect information to provide customized ads.
Others
Other uncategorized cookies are those that are being analyzed and have not been classified into a category as yet.
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