Tag Archives: sleep

Focusing on the grace…not so much the race

17 Jan

This is a post I’ve wanted to share for a long time. I’ve written probably fifteen iterations of it over the last few months and every time I let fear win…I delete…I walk away…I keep it to myself.

I’ve not landed on a word for 2020 yet. I had one last year…I’ll probably decide on one this year, but it’s something I do with prayer and intention…but I can tell you that a theme I keep hearing in music, in scripture, in prayer and in life – is SHARING. So, I’m going to DO THAT. When I feel something resonate with me that I hope can help others, I have a natural inclination to want to share it. So here it is today:

Having something wrong with you that others cannot see is a struggle. When I show up at Bible Study with my hair curled, a dress on and my shoes actually match…you don’t know that I had to wash my hair the night before because there’s no way I can wash, dry and fix my hair without a break in between. You don’t know that I had to pick out my clothes the night before to make it easier for myself the next morning or that I decided against makeup because holding my arms up for extended periods of time makes me exhausted. You don’t see the tears I cried last night because I didn’t feel like cooking dinner for my family because I knew it would wear me out and that a bath would be out of the question….because even that is tiring. You don’t see the depression that cycles from missing out on life events…the anxiety that comes with planning anything – literally anything – because I am afraid that when it rolls around I will be too fatigued to show up. You don’t see the worry that comes from letting people down and fearing that they won’t give you grace – again.  You don’t see the disappointment from getting excited about getting out and doing something but then it’s “one of those days” and there is NO way you can make it out of the house….and quite frankly, the bed.  You don’t see the way I miss the race of deadlines and a work family and last minute presentations.

Chronic fatigue syndrome is a THING.  It is one of MY things and I have truly tried to own it.  To just live with it…to give MYSELF the grace that I’d extend to any of my loved ones.  To pace myself. To do what I can and focus on THAT.  Focusing on the things I can’t do…the things I run out of steam for…the things that do not get crossed off of the list? That leads to frustration, shame and sadness.  Which puts me in a funk…which leads to a depressive state…which….are you seeing a pattern here?

When you see someone with a cast or a sling or hear them coughing or see visible scars – is your inclination to judge them or feel a certain pang of hurt for their illness/injury?  Just because all scars are not visible does not mean that we don’t all have them and need that sympathetic/empathatic smile you’d give someone that you knew was going through something based on their appearance.  I have to tell you, I barely made it through this afternoon.  I overcommitted myself this week and I was struggling this afternoon.  Once I had the chance, I got comfy and I slept for HOURS. I needed it. It didn’t mean I am lazy or worthless or unproductive.  It meant I was taking care of a need.  I needed rest.  But don’t think I didn’t go to my calendar, make a line for rest, draw a box AND CHECKED IT OFF.  Focus on what you CAN do, friends.  It makes a world of difference.

*******SIDE NOTE TANGENT BELOW*******

While I’m at it…a reminder…check on your friends.  The sick, the well, the strong, the weak.  The busy, the bored, the employed, the retired, the traveling, the homebodies….ALL THE PEOPLE.  Ask how they are…and listen to the answer.  And y’all…if someone asks how you are, TELL THEM.  I don’t know about you but I mean it when I ask someone how they are really doing….I want to hear the truth.  I don’t want to a hear a standard answer or a flippant reply.  I want to know HOW they ARE….how can I be praying for them….have the prayers I’ve been praying been answered?  I value my friendships…I value my prayer time…and I want to be sure that my friends know I am praying for them with intention, as specific as possible and as often as I say I am.

Heart Broken Week (Pt. 4)

27 Dec

I said I’d update after Mike’s appointment and I promise I meant to right away but……Christmas!  Whew!  What a busy and amazing and wonderful and blessed time of year….but….busy!  🙂

His appointment was A LOT.  I had several questions, naturally.  He had a few too….but he let me go first!  (He is SO smart, y’all!)  I had some small questions about his new meds and new diet and exercise….but my biggest, scariest, most important question was…..how likely are we to go through this again?  I know there are no guarantees and that there are so many variables that are involved but I also know that many health conditions or episodes are likely to happen again once you have had them once.  I wanted to be realistic and knew that the answer might be one I didn’t want to hear but I needed to know.  She gave me the best answer EVER.  Through a lot of technical reasons (lack of blockages in his other arteries, success of the stent, etc) and historical data….she says it is very likely that this could be an isolated incident!  Of course, that all depends on him taking his meds correctly, exercising regularly, eating balanced meals, decreasing his stress and addressing his sleep apnea.  That is a long list of things to do, yes…but I think he is more motivated than ever.  He detests the thought of a C-PAP machine but he has promised to try it.  (He’s been kicked out of the sleep lab before hahahahaaha – y’all he’s kinda hard headed and every machine he’s tried has not been a good fit for him.)  He had just started to exercise more regularly and has an amazing friend that is willing and a such a blessing to us that he will help him in that area.  The food is my area since I cook for him and he has promised to be more open-minded about trying different things (fruits and veggies are a big deal and he hates about 99% of them).  He also has committed to taking a lunch every day and actually getting out of the office.  His Dr has had several conversations about this with him and how important it is for him to take a brain break.  He is also going in later than usual so he can sleep a bit longer and THAT is a blessing to me (and also is going to take some getting used to as that was a good thing for me to get up early and get my Bible time in…so I have to figure out how my day is structured when I get back home!).  The hospital we use has a great cardiac rehab program that he will be taking advantage of and I am happy that he was open to that immediately.  He already has an appointment with a sleep specialist so we are on our way to a healthier (and hopefully less dramatic) 2020!
We are currently in NC visiting our families and enjoying this season.  It has been great to rest the last two days…since leading up to Christmas is a bit of a crazy time….and we have done just that.  Mike is still a bit tired and the Dr says that is normal and expected.  He played golf yesterday locally though and said he felt tired towards the end of the round but that he never felt “winded” as he would have normally.  THAT is such a blessing to hear!  I am telling you, God can make any situation GOOD.  I am so thankful that Mike is feeling better, is heeding the warnings and is listening to the team that is caring for him.
Again, I cannot say enough thank yous to all of you who have been praying for him (and me too) so faithfully.  We feel the love and we are so grateful.
I’ll update again in a bit once we have more information on the sleep apnea because I know that will make him feel so much better if he can get GOOD sleep!!  Hope each of you had a Merry Christmas!!!

Heart Broken Week (Pt. 3)

17 Dec

That was scary, y’all.

Though I have heard all the words that revolve around heart attacks and heart issues, learning about them through the lens of how they affect my husband has been quite an experience. I think in Part 2 I left off with us getting home on Thursday. I think we both slept SO hard that night. Post-hospital exhaustion is so real!!

Mike listened to the advice of the physicians and took it very easy over the weekend. No working, no lifting, just lots of rest and fluids. I was very proud of him for being a good patient. He can be very hard headed in case that was not obvious to y’all by now! 😉

Monday was a big day! He went back to work…but instead of getting up at 4:50 and leaving around 5:45 or so he got up around 6:30 and left around 7:20….which of course changed my schedule around but soooo worth it if it alleviates some stress for my sweet hubby!

I took him lunch around 11:45 and he sat in the car with me to eat for about 30 mins…not talking about work but just chit chatting about kids and our upcoming trip home to NC and how he was feeling. No rushing to get back in the office, just enjoying the time together.

MJ had a basketball game that was earlier than normal and he met us there a few minutes before 4 pm so his day was short. It was probably the perfect scenario for the first day back from his episode last week. The Lord really worked that out for him….not a stressful day back at all. So many of his work days are and I am so grateful that the Lord saw fit to spare him in countless ways!

He has been SO tired. Exhausted, really. I am not sure if it’s the meds, the after effects of the trauma and emotions and lost sleep or the return to work yesterday but he was asleep by 8 pm last night! I had to wake him up to take his nightly medicine with some toast! His wrist was sore last night, likely from using his laptop keyboard – and it’s his right hand – and he’s right handed…so I sort of expected that. The site of the entry looks fine – so thankful for that! He has had ZERO chest pain since before the stent. Other than a mild headache he has really been amazed at how he feels!

We have had so many conversations about how the whole thing went down last week and there are so many ways that we can see how God shaped and orchestrated the days leading up to THE DAY. There are ways that we have both been blessed by family and friends and strangers that I can’t even recount them all. There are new fears and new worries, yes. But there are also renewed promises and faith and knowledge that through it all, we were blessed.

I can’t thank everyone who was praying for us enough. I heard from people far and wide and we felt your prayers. We felt peace. We felt love. I am so incredibly grateful.

Mike’s follow up appointment is tomorrow and I sure hope they are ready for me…I mean him! LOL Let’s just say I.HAVE.QUESTIONS. This post heart attack life is going to be different….we are going to learn from it and we are going to move forward with renewed hope that we can make it through anything with faith and with one another!

I will update again once we have that appointment with any new information that we learn and I am certain I’ll have more thoughts and emotions and yes…probably more questions!!!

Weight Loss Chronicles ~ TOC

24 Feb

I cannot tell you the number of times that I have been contacted by a friend from high school, a neighbor or a perfect stranger to ask for help as they decide whether or not to take the plunge and have Weight Loss Surgery.  It can be SO intimidating and stressful throughout the process and especially when thinking of maintaining a new life and a new relationship with food.  I am always SO happy to help and always direct them to this blog as well as my Instagram feed for WLS (username:  rnyftw) but I have noticed how hard it is to go back and reference each stage of my journey so I thought I’d link it all here to help anyone (and myself!) who may need to see a specific one:

WLS Chronicles – The Decision

WLS Chronicles – The Initial Visit

WLS Chronicles – Pre-Op Testing

WLS Chronicles – Pre-Op Diet

WLS Chronicles – Surgery Day!

WLS Chronicles – Post-Op Diet (Days 1 -3 Clear Liquids)

WLS Chronicles – Post-Op Diet (Days 4 -13)

WLS Chronicles – Emotions

WLS Chronicles – HELP!!! (links to apps, and support talk)

WLS Chronicles – Post-Op Diet (Days 14 – 20) ~ Semi-Solids

WLS Chronicles – Post-Op Diet (Day 21/Week 4 – Day 41/Week 6) ~ Soft Foods

WLS Chronicles – Post-Op Diet (Day 42/Week 7 – Three Months Post-Op)

WLS Chronicles ~ Week 14 Update

WLS Chronicles ~ Dining Out

WLS Chronicles ~ Maintaining

I hope that makes it easier for everyone to reference the stage they are looking for!  If you have ANY questions beyond what I’ve blogged out, please please please reach out to me!  My email is mrsjmejones@gmail.com and I truly do enjoy helping others in their journey as well!

 

Inzombia

14 Sep

That word mush of insomnia and zombie has probably been coined already….and I’m probably late to the party…but it’s the only thing that sums up my life right now!

Between menopause (from ovary removal 6/22) and pain in my LLQ (that’s left lower quadrant if you’re blessed to not have to know these abbreviations) that is from something like endometriosis on my colon OR a femoral hernia OR an alien abduction…I am soooo sleepy.  All day, every day, I could sleep.  I wake up to fetch MJ from school, take her to school, go to doctor appointments, and cook/eat.

I feel like this should be a sponsored post from Hallmark Movie Channel, Hallmark Movies & Mysteries, and Lowes Foods To Go!!

I am hoping to hear from some tests and to get a CT scan scheduled immediately to confirm my Dr’s latest theory….but until then, I have a mystery in Eden Lake to solve!

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