Showing posts with label obstacles. Show all posts
Showing posts with label obstacles. Show all posts

Tuesday, July 7, 2015

Two Years Ago Today

Two years ago today, Jaymeson and I suffered from Carbon Monoxide (CO) poisoning while I was 36 weeks pregnant with Tatum. Jaymeson and I have been through a lot the last 2 years during our recovery, and still have a lot to go through. A lot of it is unknown at this point, but it is there.

I didn't think today was going to feel much different than any other day. But, I woke up this morning, moved the laundry from the washer to the dryer, heard my sweet baby boy shout "Mom! Get out?" from behind his bedroom door, and I burst into tears. I opened his bedroom door and I saw his sweet, perfect, little face laying on his bed just staring at me. I picked him up and held him close, kissed his face a million times, and whispered "I love you so much" in his ear over and over again. He even whispered "love you much" back. He will never understand the magnitude of my love for him. He will never fully understand what it meant to save his parents lives before he was even born. And I will never forget that I could have lived my life without him in it.

Jaymeson and I often lay together after the kids go to bed and just hold each other and reminisce about our lives and our story. This one comes up often as we talk about the changes that we are each going through and how they effect ourselves and each other and our families. It's still so unreal to both of us. It's like it was all a dream. I can't even explain it. We lived those moments, we are still suffering from the experience, but somehow it just doesn't seem real. 



I heard on a song on the radio recently that reminded me of how I feel currently. I hate when official music videos ruin the song. So here it is with just the lyrics,


And all those things I didn't say
Wrecking balls inside my brain
I will scream them loud tonight
Can you hear my voice this time?

This is my fight song
Take back my life song
Prove I'm alright song
My power's turned on
Starting right now I'll be strong
I'll play my fight song
'Cause I've still got a lot of fight left in me

Starting today, I will let go of what's gone, appreciate what still remains, and look forward to what's coming next.

Don't know what I'm talking about? Look here and here for a recap.

Tuesday, January 20, 2015

Things you don't say to someone with a TBI

What is a TBI (Traumatic Brain Injury)? Well, google defines it as "an insult to the brain from an external force or substance, possibly leading to permanent or temporary impairment of cognitive, physical, and psychosocial functions, with an associated diminished or altered state of consciousness."

This could mean anything, right? A car accident, a sport accident, falling down the stairs, physical abuse, lack of oxygen to the brain, etc...

Being someone who has experienced a TBI (lack of oxygen to the brain through Carbon Monoxide poisoning), I have experienced the frustration of feeling as though no one understands what you are going through, and feeling as though you have no support. It's true, it's close to impossible to understand or truly support someone who is experiencing a trial that we have not been through ourselves. But as good friends, neighbors, and family members, we try to be there for those we know that are experiencing something difficult.  

I was thinking about those posts that you see about what not to say to certain people experiencing certain things (ie; What not to say to a Pregnant Person, What not to say to a Stay at Home Mom, etc), and decided to come up with one of my own regarding TBI's. Mostly because it's a way to get my frustration out about it without offending anyone directly. I think it's good to be aware of these things, because you never know who you may come in contact with who is suffering from a TBI. Remember, TBI's almost always show no physical signs and can be hard to detect.

For background on what I am reffering to, click here or here.

So, with the help of brainline.org, here is my list of 10 Things Not to Say to Someone with a Brain Injury

1. You seem fine to me.

"The invisible signs of a brain injury — memory and concentration problems, fatigue, insomnia, chronic pain, depression, or anxiety — these are sometimes more difficult to live with than visible disabilities. Research shows that having just a scar on the head can help a person with a brain injury feel validated and better understood. Your loved one may look normal, but shrugging off the invisible signs of brain injury is belittling. Consider this: a memory problem can be much more disabling than a limp."

I have experienced this on countless occasions. In a way it is nice to hear, but more often than not, it is belittling and frustrating. Yes, I am happy that you can't tell by looking at me that I function a lot less normal than I used to. But also, that doesn't make me feel very validated in the changes that I am experiencing. In fact, it makes me feel like you don't believe that what I am going through is really anything at all. It makes me feel like the 2-3 doctor/therapy appointments I go to every week are considered pointless, when in reality they are changing my life.

 

2. Maybe you’re just not trying hard enough (you’re lazy).

"Lazy is not the same as apathy (lack of interest, motivation, or emotion). Apathy is a disorder and common after a brain injury. Apathy can often get in the way of rehabilitation and recovery, so it’s important to recognize and treat it. Certain prescription drugs have been shown to reduce apathy. Setting very specific goals might also help.

Do beware of problems that mimic apathy. Depression, fatigue, and chronic pain are common after a brain injury, and can look like (or be combined with) apathy. Side effects of some prescription drugs can also look like apathy. Try to discover the root of the problem, so that you can help advocate for proper treatment."

I have never experienced someone telling me that I am lazy. If they had, they probably would have been knocked to the ground because I am the very opposite of lazy. In fact, I have been accused, by at least 2 of my doctors, of taking on too many responsibilities and inhibiting my recovery. However, I have definitely felt a lack of interest to do things, including spend time with my friends, lack of motivation to do the things that need to get done, including laundry and dishes, and lack of emotion about things that matter, including arguments that Jaymeson and I may get into. I have also felt the guilt that goes along with that. I think the best thing to do is to push me a little bit. It's good for me to get out of the house and spend time with friends, or not give up on my regular responsibilities, or to force myself to care about something when I know I don't want to. So don't take no for an answer... unless I have a really good excuse.

 

3. You’re such a grump!

"Irritability is one of the most common signs of a brain injury. Irritability could be the direct result of the brain injury, or a side effect of depression, anxiety, chronic pain, sleep disorders, or fatigue. Think of it as a biological grumpiness — it’s not as if your loved one can get some air and come back in a better mood. It can come and go without reason.

It’s hard to live with someone who is grumpy, moody, or angry all the time. Certain prescription drugs, supplements, changes in diet, or therapy that focuses on adjustment and coping skills can all help to reduce irritability."

I have heard this one quite a few times myself, and to be honest with you, I can't blame them. I am more of a grump than I have ever been. But that doesn't mean I like it, or I want to be that way. I believe that it is mostly because my brain is not able to handle as many things as it used to. So, while I look like I'm angry or not having fun, my mind is probably just preoccupied with other things that I am not realizing where I am. I have also been accused by a therapist of not living in the moment. That's actually one of the main things I am working on right now. Living in the moment and not letting my brain wander and missing out on regular every day occurrences because my brain is "out of this world". 

 

4. How many times do I have to tell you?

"It’s frustrating to repeat yourself over and over, but almost everyone who has a brain injury will experience some memory problems. Instead of pointing out a deficit, try finding a solution. Make the task easier. Create a routine. Install a memo board in the kitchen. Also, remember that language isn’t always verbal. “I’ve already told you this” comes through loud and clear just by facial expression."

I have never been told this out of anger, but I have been told similar things in a joking, nonchalant manner. Something along the lines of being frustrated because I didn't hear them the first time, or that I asked them the same question multiple times. Again, for me, it's a multitasking thing. If I can't focus on what you are saying because I am preoccupied with something else, chances are I have no idea what you said. In some of the therapy that I go to, I am learning ways around this. Such as, taking notes, asking you to repeat yourself, asking you to slow down, etc. Some of them are working, and some of them still need some work. 

 

5. Do you have any idea how much I do for you?

"Your loved one probably knows how much you do, and feels incredibly guilty about it. It’s also possible that your loved one has no clue, and may never understand. This can be due to problems with awareness, memory, or apathy — all of which can be a direct result of a brain injury. You do need to unload your burden on someone, just let that someone be a good friend or a counselor."

This seems like something very harsh to say to someone who is struggling, and I personally haven't heard it so I don't have much to say. So... just take note.

 

6. Your problem is all the medications you take.

"Prescription drugs can cause all kinds of side effects such as sluggishness, insomnia, memory problems, mania, sexual dysfunction, or weight gain — just to name a few. Someone with a brain injury is especially sensitive to these effects. But, if you blame everything on the effects of drugs, two things could happen. One, you might be encouraging your loved one to stop taking an important drug prematurely. Two, you might be overlooking a genuine sign of brain injury.

It’s a good idea to regularly review prescription drugs with a doctor. Don’t be afraid to ask about alternatives that might reduce side effects. At some point in recovery, it might very well be the right time to taper off a drug. But, you won’t know this without regular follow-up."

I am not currently taking any medications, other than good ole' birth control or some sort of antibiotic to fight off whatever sickness has invaded my body. I have personally made a solid effort to try to resolve my impairments on my own instead of relying on medication to make it happen. I believe that I will be stronger in the end for it, and that I will have less chance of relapsing if I can learn to deal with this myself. Sometimes I do feel like I need something and that I can't do it on my own, so I understand completely how the statement above can be very frustrating. I know how it feels to not want to do any of this anymore and just give up. Some people have less will power or are less stubborn than I am, but the medication thing is definitely a reality. 

 

7. Let me do that for you.

"Independence and control are two of the most important things lost after a brain injury. Yes, it may be easier to do things for your loved one. Yes, it may be less frustrating. But, encouraging your loved one to do things on their own will help promote self-esteem, confidence, and quality of living. It can also help the brain recover faster.

Do make sure that the task isn’t one that might put your loved one at genuine risk — such as driving too soon or managing medication when there are significant memory problems."

I am guilty of trying to control too many situations, even before the brain injury. I feel capable of doing most things thrown at me, and as a result of that, I sometimes don't trust others to being able to appropriately handle things (at least the same way that I would). I have a hard time allowing people to do things for me unless I know that it is so so simple that they can't screw it up or it's something that I just don't want to do. But even now, I'm learning that it's important to do things for myself to help rebuild those skills that I lost. Yes, I need to give up more responsibilities sometimes, but I don't need to hand off the responsibilities or even part of the responsibilities that I have chosen to take on just because I may be a little slower at it than I used to be. Practice makes perfect, and that is true in the recovery process. 

 

8. Try to think positively.

"That’s easier said than done for many people, and even harder for someone with a brain injury. Repetitive negative thinking is called rumination, and it can be common after a brain injury. Rumination is usually related to depression or anxiety, and so treating those problems may help break the negative thinking cycle.

Furthermore, if you tell someone to stop thinking about a certain negative thought, that thought will just be pushed further towards the front of the mind (literally, to the prefrontal cortex). Instead, find a task that is especially enjoyable for your loved one. It will help to distract from negative thinking, and release chemicals that promote more positive thoughts."

Literally, this is the hardest thing to do. "Think positively." Yea. Sure, I can think to myself that I am lucky to be alive, or I'm lucky to not have as many issues as this other person. But to actually be able to think positively in the midst of a real struggle, is sometimes extremely difficult.

 

9. You’re lucky to be alive.

"This sounds like positive thinking, looking on the bright side of things. But be careful. A person with a brain injury is six times more likely to have suicidal thoughts than someone without a brain injury. Some may not feel very lucky to be alive. Instead of calling it “luck,” talk about how strong, persistent, or heroic the person is for getting through their ordeal. Tell them that they’re awesome."

This is the number one thing that I hear. And honestly, it doesn't really bother me. It actually makes me feel special. It's true. I am lucky to be alive. Jaymeson is lucky to be alive. And Tatum is lucky to be alive even more! I haven't experienced any suicidal thoughts or similar, thank goodness. Sometimes I do feel like I can't do this anymore, or I can't deal with that anymore.  I understand why someone would have those terrible thoughts. It is beyond frustrating not being able to live and act and be the same person you have lived your whole life being. Having to completely restructure yourself, by no choice of your own, is not an easy task.

 

10. Take your time -- we are not in a hurry.  

I took one out that I felt didn't really apply, and added this one. People who have experienced a TBI often are not as quick as they used to be. Saying "Take your time, we are not in a hurry", while very considerate of you, also makes us feel like a project or incapable. We know that we need to take our time in order to effectively do something. We know that you are waiting on us. We know that you can probably do it faster. Although it may be a considerate statement, think about how you would feel if you were struggling to do something you used to be able to do just fine and someone telling you to take your time because they aren't in a hurry. (You know, because if they were in a hurry, you better not be taking your time.) Don't you think you'd feel a little unnecessary pressure? Maybe I'm crazy.

 

11. And as an added bonus... Are you sure your doctors know what they are doing?

This one I also added myself, and is my favorite. And by favorite, I mean least favorite. No. I have absolutely no idea if my doctor's know what they are doing. They are just my doctors, who specialize in what I am going through. They are just changing my life, little by little, every time I see them. They are sometimes the only support that I have. They only studied exactly the treatment that is recommended for me for several years of their life. You're right. They don't know what they are doing. Ok... lots of sarcasm. But really, I'm not a doctor. So I guess I don't really know. I just know what has been recommended for me and my family, and what is helping us right now. 

 

I'm lucky (or unlucky) because my husband was also exposed to CO poisoning at the same time. So even though he may not be experiencing all of the same side effects that I am, he understands that I am different and that I am going through changes, and it may be awhile before I can adjust enough to feel comfortable in my own skin again. It also makes our relationship a lot harder than it used to be sometimes. We are both going through so many changes, and sometimes you just want consistency. Sometimes it's frustrating if the one thing you are supposed to count on (your spouse) is not always capable of being counted on due to their injury. Jaymeson and I are both loyal and determined people, and I have no doubt that we will make it through this and be stronger in the end. So, maybe we are lucky. :)

A short update on each of us: I am still going through Cognitive Rehab and Counseling. I am progressing on up the "scale of recovery" and things are going well. I definitely have my hard days, and some very hard days. But I am grateful that I am near specialists who can help me, and that I am able to get the treatment that I need. I really don't like the person CO has changed me to be. I really hope someday I will get back to who I used to be before, but I don't know if that's a reality. Jaymeson, due to work, has not been able to start his recommended treatment yet. We are hoping that he will be able to work out a schedule with his office soon that will allow him to get the treatment he needs regularly. Tatum is perfect, almost. He has had some kidney issues, that may or may not be related to the CO poisoning. (More likely that they are considering the kidney issues he had just prior to birth and at birth.) We are treating it as it comes, and hopefully we will have more answers soon. Other than that, he is perfect. He is developing just how he should be, and he is the light of our lives!  

Someday, when I am in a better state of mind, I hope to create some serious awareness for CO poisoning. It may be a few years before I am able to do this, but it is something I want to do and feel strongly about. I will use this blog to follow our progress sometimes, but I am always open to talking to people about it. Sometimes it's hard, but that's good for me. So, if you have questions, feel free to ask. And for now in terms of awareness, if you don't have a CO detector in your home... GET ONE. Seriously. Here is a link for one. :)  




 

Thursday, January 17, 2013

NuMom2Be

At my very first prenatal appointment, I saw a sign on the door of the bathroom for a new mom study. Requirements were that this had to be your first pregnancy or you have had no more than 2 miscarriages under 20 weeks, and you had to be in your first trimester. So I thought, sure why not? I looked into it, and was chosen to participate.

It is a University of Utah study, called NuMom2Be.

The purpose of the study is to find out why so many first time pregnancies have complications or turn to miscarriage. You have one appointment per trimester, where they run tests, do a pelvic exam, and an ultrasound (3D during 3rd trimester). Then at delivery, they take samples, and wah-la! I'm done.

Did I mention this is all free, and I'm compensated for my time?

The coolest thing about it is that I get 3 extra ultrasounds that I wouldn't normally have. Yesterday was my first appointment, at almost 12 weeks.

 
Baby at Almost 12 Weeks







Baby is certainly starting to look like a baby. We still think it's a boy, and it's looking like he's going to be tall like his Daddy and big sister. Also, baby is growing pretty fast, because my due date has changed 3 times! First it was August 7, then based on the growth of the baby it was August 4. As of yesterday, the due date is August 1.

I have mixed feelings about the due date moving up, because I want the baby to come to us as soon as possible (healthily), but also, I have this weird thing about wanting to not have a baby-baby on our first wedding anniversary. I guess it would be ok, though, if the baby came early enough before our wedding anniversary, that I could go out with my husband and celebrate while not looking like a whale. (not likely)

Sometimes I get sad when I look at my facebook cover photo and think, "I'm never going to be that skinny again." At least, my genes are against me. Boo.

Back to the point of this post, the appointment was cool. It was at the IMC hospital, where I plan to give birth. Which is also the hospital where Jayah was born. It went just about how my 6 week appointment was. They took some blood from me, I did a urine test, pelvic exam, and an ultrasound. I also spent close to an hour doing an interview with the Research nurse. Basic questions about my overall health. In depth questions about my family health history, and even more in depth questions about my eating habits in the months prior to my pregnancy.

The bummer thing is that all of this information is anonymous. I am just a 10 digit number. So I'll never get the results of any of my testing. They also keep samples of everything they take from me for future testing. You know, in case they find any correlations with anyone else.

I was worried that Jaymeson wasn't going to be able to make it to my appointment (because his work sucks), but luckily he was able to get there right on time. We are 3/3 on appointments with Jaymeson. Hopefully we can keep that track record going all the way through pregnancy.

One (cool) thing that I learned through filling out questionnaire after questionnaire, is that my mom had the Rh Factor Issue as well, which resulted in 4 of her miscarriages. Her blood type is O Negative, as well as 3 of my other siblings, which could be the only reason why we survived to full term. Which is also weird because normally you get the blood type from your father, and my dad is not O Negative  Luckily, that was 20+ years ago, and technology and medicine is much more advanced than it used to be. Maybe I will be able to have other babies after all. :) That is, if I feel like I can survive pregnancy/child birth a second time.

Another (not cool) thing that happened at my appointment, is that my records are under a different name. So when they printed my ultrasound picture for me, it said Heather Cheney. Gag. Luckily, the Research nurse was nice enough to black out the name on the photos for me. :) So now I need to go get my Roush License ASAP, so I can get in there and change my name with the hospital. I don't want to see that ever again, especially on my ultrasound pictures! Does the whole name changing process ever end?

Next study appointment is in March, where they will confirm the sex of the baby. We will have our normal appointment a week or so before that one, so it really will just be more of like a confirmation. But still cool!

I want to thank all of you for your comments to my previous post. I love reading everyone's opinions and it has definitely helped me to consider things I probably wouldn't have normally considered. I am always open to opinions of others. Like I said before, I am very uneducated on all things baby-making, so I appreciate all the help I can get! 

Saturday, August 18, 2012

My Happiness Project.

I have found myself lately being fairly depressed while I am at home and Jaymeson is working late. Life is hard when the only person you want to spend every second with, has to spend most of their seconds somewhere else.

I don't really have any hobbies, all of my friends live everywhere EXCEPT within a 40 mile radius of me, I hate our house (we are moving soon) so there are no projects there, and I'm tired of spending so much time on the couch, watching movies. I want to GET OUT and do something!

Today I was google-ing "Things to do to make you happy" and came across this website...

Click Here

...and decided that for the next little while, I am going to leisurely complete every single one of these tasks, on my own, while Jaymeson is at work. Starting today. And to make it even more difficult, I am going to do them in the order they are listed. I'll keep you updated. :)

Eat that, unhappy Heather!

Tuesday, July 3, 2012

A friend of a friend...

I realized something rather interesting at my Bridal Shower this past weekend.

There was a variety of people there, most that didn't know each other. As friends were introducing themselves to one another, the subject of how they knew me came up. Probably close to half of those girls there knew me as a result of my ex husband.

There was an old coworker of his.
An old friend of his sister's.
One or two good friends who took me in during my separation.
His old mission companion's wife.
His best friend's brother's wife.
A roommate from just after my divorce. 
The bridal shower even unknowingly took place in a home that I spent the summer of my separation learning to sew in.
Heck, I only know my fiance because of him!

As I heard the laughter of everyone's crazy story on how they know me, someone mentioned to me about how I must have gotten the friends in the divorce. As funny as that is, I think it is true! Mostly I don't talk to anyone I knew from when I was married, but those that I do are mostly mutual friends of ours that have stayed close to me and have supported me in my efforts to restore my life.

I am so grateful for the love and support that so many people have shown me going through my divorce up until finding the man of my dreams and marrying him for eternity. I know I couldn't have done it without so many of them, and I am so grateful that God has blessed me with some beautiful people to share my experiences with.

Guess I definitely got the better end of the deal.

Wednesday, January 11, 2012

What I wanna know is...

...how in the world can anyone claim that any sort of physical relationship, with someone besides your spouse, while you are still married, is NOT cheating?

Right?

So, I had a little fall out with my ex today. Lovely. We rarely talk to each other,  and when we do, it is always very cordial, to the point, and then goodbye. Now, this little gem from my past is getting married in a few weeks. One, it has come to my attention that certain members in his family have that strange idea that I want to keep him from getting married. And two, the same certain family members seem to be in denial of a few facts from our marriage.

Someone that I really look up to, who also happens to be a member of that family, told me her story shortly after my divorce. It's very personal, so I will not share. But basically, she was very much wronged by someone very dear to her. She hid it for so long, for fear of what people would think, fear of doing the wrong thing, and fear of hurting someone's feelings. She held it in for so long, that it eventually became unhealthy for her. The wrong-doer eventually passed away, and she finally realized that she did not need to hide the truth any longer. It wasn't that she needed to make sure to shout to the world what really happened, but that she needed to respect herself, her health, and her future relationships by "owning up" to the truth. She told me her story so that I would know that someday, I would be there too.

There's something about owning up to the truth with yourself, and with others, that is healing. And after this little falling out, that's where I am today.

I have said it before, and I'll say it again. I do not agree with divorce, in almost any circumstance. But in mine and my ex's case, I do. That was a hostile marriage. It was unhealthy, and unhappy, and going to take more effort than it's worth to make it work. We both could have done things differently, but ultimately it was his decision to get divorced, and despite all of my efforts, there was nothing I could do to change that. I believe that he expected marriage to be something very different than it is, he expected things from me that are not realistic, and he didn't expect to have to share his life with someone else, or to have anyone to be accountable to. To be frank, he was not ready to be married. He longed for the single life, and he managed to find a way to experience it although, we were still married. A decision had been made, the papers were signed (or soon to be signed), but we were still married. (FYI: A marriage is not a marriage when you sign the marriage license. It is a marriage when you sign the marriage certificate. Then, and only then, is it legal. Same with divorce. A divorce is not final once the motion is filed. (Although some people like to use that as an excuse.) A divorce is final once it has been signed by the judge. Then, and only then, is it legal. Take that up with God if you have any questions.)

With that being said, my divorce was the hardest thing I have ever gone through. I went through Hell and back, and recovery was hard. But I made it through quickly, and I have been so grateful to not be married to that man since. There have been times where it has been hard. Not because I wanted to be with him again, but because it's hard to go from being married to being single all because of one piece of paper, within a matter of minutes. But overall, all of that pain was worth it.

He is getting married very soon, and I couldn't be happier for him. I don't know who he is now, or if he is ready for marriage this time, but that's not my concern. Sometimes I hope that poor girl that he met online is smarter than I was, or that things will be different for them. But I really do not care either way. If they make it work--great! If they don't--well... great! It does not matter to me. Believe me, if it did, you all would know about it. I am in a very happy relationship with someone I never would have found if it weren't for Jon, and I am grateful for Jon for that. But I wouldn't have things any other way. So...congratulations to both of them!

Maybe Zac Brown could tell it a little better?



Does that resolve anyone's concerns?

In 2 days, it will be one year from mine and Jaymeson's 2nd first date. In about 2 weeks, it will be one year from our first kiss. And I am so happy! Jaymeson and I have been through so much together. We both came out of very hostile, unhealthy, and unhappy marriages, and we found each other. We were friends, helping each other heal for about 6 months, and then it just clicked. Out of nowhere, we couldn't get enough of each other, and then we started dating. And that's the way I've always wanted it. We started out as friends--best friends. And that developed into a strong and successful relationship. We are celebrating his 26th birthday this Friday, as well as the anniversary of our 2nd first date, and I am so excited!

If there is still any doubt about the way that I feel, feel free to direct yourself to my pictures. You will never see either me, or Jaymeson happier, than you do in those pictures.

Speaking of Zac Brown... his concert is next weekend! Woot!

Tuesday, September 20, 2011

Tuesday the 30th

On to more serious thoughts...

For those of you who can't read that:

"The time you invest to deeply understand the people you love brings tremendous dividends in open communication. Many of the problems that plague families and marriages simply won't have time to fester and develop. The communication becomes so open that potential problems can be nipped in the bud."

My parents are divorced, I'm divorced, and because I'm divorced, a lot of people that I know are divorced.

This "Habit for Highly Effective People", I believe, could save marriages.

If you look back on all the relationships you know of, of people that are divorced... I bet communication was one of the top causes in their divorce. I know that when I first got divorced, a good friend of mine was preparing a lesson in Relief Society and she wanted to know my thoughts on "characteristics of successful relationships" and that was the first thing that popped into my head. Communication.

Now, Heaven knows my divorce was caused by much more than miscommunication, but I firmly believe that if we had communicated properly with each other, a lot could have been avoided.

In my relationships with my family, friends, roommates, people at work, and even with Jaymeson, I've noticed the difference in communicating issues and solutions when they come about, instead of letting them fester and blow up days later. It's ALWAYS a good thing, and it's probably saved a lot of my relationships with people.

I'm obviously not a pro at it, but I'm working on it. And I know and value the importance of it.

Just passing along some knowledge... :)

Tuesday, September 13, 2011

Bless the Broken Road.

Thank you to Rascal Flatts for inspiring this next blog post.

Jaymeson and I had the opportunity to go to a Rascal Flatts concert this weekend with some of our friends. (They were amazing, but that's besides the point.) We had a good time, we laughed, we sang, Brandon almost got beat up, and I won a huge beach ball from the radio station. :)


But I think the most important thing I (re)learned this weekend, was that everything happens for a reason.

While Rascal Flatts was singing their famous song "Bless the Broken Road", Brandon snapped this picture of us:

(Its obviously been photoshopped cuz I'm cheesy, ok?)

When I saw this picture, and heard the song, all I could think about was God really did bless my road. I've been hurt. Seriously hurt. By many men, family members, friends, lots of people. But everywhere I've been is exactly where I should have been. And everywhere I'm going has everything to do with the road God blessed me with. Looking back on all the pain, I wouldn't change it for the world.

I used to always tell myself and everyone else that Jon was an answer to my prayers. He magically appeared into my life right after I ended a very long and hurtful relationship. He swooped in and swept me off my feet, and because of him, I easily healed and moved on from that relationship when it otherwise could have been a very long and hard process. When I first got divorced, I spent a lot of time angry at that thought. How and why would God put Jonathan into my life to help me heal from my previous, devasting relationship and then turn around and hurt me worse?

Two reasons:

1. I did need Jonathan to help me heal from that relationship. But also, I believe the heartbreak of that previous relationship helped to prepare me for the hurt that would come from my marriage. Jon helped me heal from that relationship, and in turn he helped me to know how to heal from our relationship.

2. Jonathan led me to Jaymeson. Weird, right? Jaymeson and I know each other through a very twisted, complicated string of people. But without my marriage to Jon, I would never have known Jaymeson. And my broken road, has thus far, lead me to him.

I learned a lot down this long and crooked journey (Whoops, popped into Bachelor mode for a second. When does the next season start anyways?) that I've been on. I learned to love unconditionally, I learned to allow myself to cry (well, almost), I learned to be honest with myself, I learned to trust, I learned to be independent, I learned to give myself completely, and so many other qualities I hope to continue in all of my relationships. But most of all, I learned that God is with me the whole way.

I don't know where Jaymeson and I will go, but I do know that because of him I am a better person. And because of me, he is a better person. We fight and argue and bicker just like every other real relationship, but we also laugh and cry and dance and love together. We teach each other, we help each other, we have learned so much about ourselves and each other and relationships that if we do not end up together, we will be one hundred times more prepared for our "soul mate" (if you believe in those) than we would have been otherwise. We each are in the place that we need to be, and for what ever reason, we need each other now. And I'm grateful that my very broken road led me straight to him.

:)

"It's all part of a grander plan that is coming true."

Saturday, April 30, 2011

Day 22 - A picture of something you wish you were better at.

There are a few things I can think of.

One.













Cooking. I just wish I could cook. I could make my own meals, not have to go out for lunch at work, save lots of money, have parties. Ah, it would be amazing. My mom is an awesome cook. And my sisters are pretty good too. How did I miss that?!

Two.













Working out. I wish I had the desire to get up off my butt and get to the gym, for anything other than tanning. My roommates, and my boyfriend, are all really good at going to the gym. I should follow in their example. But then there's the whole idea of what the heck do I even do at the gym? Ugh.

Three.



















Public Speaking.

I do not like the lime light. I admire people who can just stand up in the center of a crowd and say whatever they want without feeling and/or looking like an idiot. I guess that's why I love to write?

Day 23 - A picture of your favorite book.