bloggingchronic illness

Regrouping: A Quick Life & Blog Update

A Quick Life & Blog Update

Before I give you a few blog updates, I just wanted to share a quick story I posted on my personal Facebook wall yesterday:

I had an interesting experience of Walmart of all places today. As many of you know, I spend the majority of my day house-bound if not bed-bound. This has been a little better week so today, I was able to leave the house for the second time this week (look out world!). As I was getting ready to check out, I noticed an older lady behind me with her cane in her cart and she just looked tired. I told her to go ahead of me and she just looked so relieved. As she unloaded her cart of TV dinners and various types of juice, she proceeded to tell me that she had finally had someone come over to sit with her husband who has severe Alzheimer’s and dementia but only had a short amount of time. As she unloaded her cart, she said that she was no longer able to cook full meals like she would like because she’s afraid of leaving the stove plugged in as she’s afraid her husband would turn it on and cause damage. She was constantly worried about him running off or getting himself hurt. You could tell that it had been quite some time since she had had any time for herself. It broke my heart. As she was checking out, I overheard her talking to the cashier. She told a little bit of what was going on and how she was so thankful that I had allowed her to go ahead of me in line and how much it helped her. She said there were so few nice and courteous people left in the world any more and how thankful, blessed, and overcome with gratitude she was. All because I let her go in front of me in line at Walmart. My hips were throbbing and I was in so much pain but something in my heart told me that she needed to go before me. Once she told me her story, it took everything I had not to break down. The most simple thing can make the biggest impact in someone else’s day. I’m not sharing this as a pat on the back to me but as a reminder to myself to do it more often. You never know how much a simple act of kindness can change someone’s day (or life).

It was definitely a very powerful and moving experience. One of those types of experiences where you feel like you need to take your shoes off because you are standing on sacred ground. God gave me such a powerful reminder today that life is so much bigger than me and even when I feel like I am drowning in my own problems, there are always people suffering more than I am. My husband came sympathize with her more than I can on the struggles of being a caregiver but before she left the store, I just wanted to chase her down and give her a huge hug. Then I realized she may have thought I was some kind of major creepo. Maybe I should have done it anyway. Sometimes its the most simple things that are the most important.

With that being said, I wanted to post a quick life and blog update. I really want to get back to the roots of A New Kind of Normal. I thought last year was hard but this year has proved to be even worse and I have felt so lost. I felt like I have just wandered in circles. I’ve tried to come back to posting but each time I’ve done so without a plan in mind so in all of my posts, its apparent that I am just wandering in circles and that is SO not what I want for this space. I want A New Kind of Normal to be a place of inspiration, encouragement, support, and most of all empowerment but in order for that to happen, I first need to feel inspired, encouraged, and empowered.

I am going to take the next week and a half off from blogging in order to get myself organized and my content structured so that this blog can go back to being what it was made to be. I am going to be reading, researching, and finally putting all those blogging boards on Pinterest to good use! I am also in the process of renovating our office/guest room/beauty room so I will have a space where I can truly feel inspired so that also has me really excited! There will definitely be a big reveal when everything is ready!

Things here at A New Kind of Normal will kick back up in May. Sharing Our Spoons will be starting up again so May 3rd will be the first post where we can share our goals for the month. Check-ins will take place the first Tuesday of every month as a way that we can support one another to be the healthiest versions of ourselves possible on all fronts. I am also restarting sharing the stories of our fellow spoonie warriors as a part of Sharing Our Spoons which will be featured once a month so if you are interested in being interviewed and sharing your story, please shoot me an email!

My goals are to post four times a week with Tuesdays being directly chronic illness/health related; Wednesdays will be Chronic Style days; Thursdays will be geared more towards home and family life; and Fridays will be focused on faith and emotional health. As you can see, I really want to hone in on this idea of holistic health and taking care of ourselves as a whole. When you are chronically ill, so many times there is always the bulk of focus placed on our physical health when there is so much more to us than that. I want A New Kind of Normal to become a thriving community of the most bold and vivacious spoonies anyone have ever met.

I am excited and already feeling empowered just by writing this post and I am hoping that you understand and that you too will feel excited and empowered about what is coming ahead. While I will not be posting here until the first of May, I can still be found on social media (Instagram, Facebook, and Twitter).

I am now also on Snapchat (@anewjamee) but I am still trying to get that one figured out! If you have any tips on getting the hang of it, please let me know! And friend me:

Snapcode for ANewJamee - Snapchat

 

I hope this post finds you all doing well! In the next few weeks, if there is anything that I can be praying for  you about or helping you with, please let me know! We can become stronger, inspired, and empowered together! I love you all and I truly mean that!

chronic illness

No Dreams of Sugar Plum Fairies: Chronic Illness, Anxiety, And Insomnia

We all know that the holidays can be stressful (especially with chronic illness). Traveling, baking, shopping, and crazy family can take regular stress and anxiety up to an 11 for a healthy person. Add it all it on top of illness and it becomes a whole new brand of crazy. The message of Christmas is not the same was what the media and marketing would like us to believe but the exact opposite. The message of Christmas is peace, not busyness. It is a message of hope, not stress. It is so easy to get mixed up in the craziness and mess out on the message, meaning, and purpose of the gift that was given to us in the form of a Savior.

Why am I talking about Christmas in February?  Because it was during this season, instead of being filled with hope, I was filled with despair. Instead of breathing in the peace of the season, I felt like I couldn’t breathe at all.

Chronic Illness, Anxiety & Insomnia
What kicked off the chain of events I don’t know. I cannot think of any one thing that started it. I cannot think of anything that stressed me out beyond my max. Honestly, at the start, I don’t remember feeling stressed at all but, oh, how that would change.

For the last several years, I have struggled with getting enough sleeping (not only quantity but quality). Most anyone with chronic illness can probably agree with me that even when you are out of your mind tired and beyond exhausted that sleep can be hard to come by. It can be difficult to get comfortable enough to fall asleep. It can be difficult to stay asleep without pain waking you up. Sleep is supposed to be refreshing, rejuvenating, and healing but that isn’t always the case. Thankfully, up to this point, there were medications that helped overcome these hurdles.

I’m not sure what happened. The trouble started about a week before Christmas and with every night that passed, it become increasingly more difficult to fall asleep (even with treatment). I found myself spending most of the night staring at the ceiling instead of the back of my eyelids. I didn’t feel manic but it was like my body would just not shut off. It was like I was currently plugged in. At the beginning, I didn’t feel like the reason I couldn’t fall asleep was become my mind was racing. I know that feeling and this wasn’t it.

Anxiety has definitely been a struggle. It was always an on and off battle but after my bowel obstruction surgery, it became an ever increasing struggle. I am terrified, TERRIFIED of having another obstruction. We know that scar tissue is there and we know that it is causing a problem with pain and function of my GI system. Because of my obstruction history, I am considered too high risk to go in preemptively to remove it so I feel like we are just waiting for a repeat performance and that scares the heck out of me.

So while I have felt increasingly anxious, I did not feel like that was what was keeping me up at night. My mind was not saying, “I’m terrified of another obstruction or emergency surgery.” It was saying, “Why the heck aren’t I asleep?” At least that is what it was saying at the beginning.

By December 23 I wasn’t sleeping at all and I mean at all. Not that I just wasn’t getting quality sleep but I was literally not sleeping. My mind and body were just on constantly. I couldn’t even nap during the day. It was absolutely the most miserable feeling I have ever experienced.

With every night that passed, things began to shift. My anxiety became magnified and any hint of depression became a billboard. I was constantly on the verge of tears and I became hypersensitive to light, sound, and touch. It is impossible to enjoy the fun of Christmas with family when you feel like you are in a hole. It is impossible to embrace the peace of Christmas when it seems like you have lost the understanding of the concept. It is impossible to sing “O Holy Night” when your nights have become a living hell.

My body and my brain began to do crazy things. We know that the long term side effects of not getting enough sleep can increase your blood pressure, your risk of developing diabetes or other chronic health conditions, and memory loss to just name a few but the side effects of sleep deprivation are downright scary. Your cognitive function becomes impaired such memory loss inability to concentrate. You become more emotional, irritable, and unbalanced. Mentally, in addition to increased anxiety and depression, you can become flat out delusional. You can begin to hear and see things that aren’t really there. You can experience sleep paralysis (which you know if you have every experienced it, it can be terrifying).

Personally, I didn’t hear anything but by night 7 or 8, I felt like I was seeing shadows. Probably the most scary experience was one night towards the end of this awful experience and I was laying in bed one night with my eyes closed and I opened my eyes to see what I could only describe as the shape of a grim reaper above me. Again, I want to be 100% transparent in sharing my experience. It was terrifying. I began to scratch/cut myself on my arms and upper legs not to hurt myself but in attempts to find something to break the anxiety. Something to break the cycle. I was desperate. I would stare at the medicine cabinet and wonder how much I could take to knock me out without going too far. I know I was on the brink but thankfully I had enough insight left to recognize it.

My parents had taken Abby to the beach with them the day after Christmas so she was not here during most of this ordeal thankfully. John was obviously aware of what was going on but on December 30th, I disclosed everything. The scratches. The urges. He held me tight and the next morning, he called my doctor’s office (which of course had been closed during to this point during this ordeal because of Christmas – holidays are a bad time to lose your mind) and we headed to the emergency room.

In addition to the psychiatric rundown, they also did blood work to make sure there wasn’t something physically wrong, like a chemical imbalance or a vitamin deficiency, that could be the problem. After the initial rundown of questions, they gave me a small dose of medication which unfortunately lost its benefits as soon as they sent in the nurse who butchered my veins before finally successfully drawing blood. I hate having beyond crappy veins.

I was cleared physically and deemed not a threat to myself or others psychologically so I was sent home with a three day prescription to get through until my doctor’s office reopened after the new year. I can proudly say that I was not awake to see the ball drop and ring in 2015 because, hallelujah, I was sleeping. SLEEPING.

It was amazing how much of a difference just that one night made but recovery was definitely a process and the experience was definitely a wakeup call. When my doctor’s office reopened, she referred me to a psychiatrist. It was time to give myself and my family a better life by finally getting my anxiety under control. Whether or not, consciously my anxiety kicked off this chain of unfortunate events, I have allowed it to consume much of my life already. I accept the reality of my life with chronic illness and the fact that uncertainty is a part of the gig but I also want to accept that I don’t have to let that control my mind. I want to be able to exhale and embody the peace Christ has to offer. I want to be able to let go versus constantly carrying that weight around.

Today I had my first appointment with my psychiatrist and while the drive there nearly induced a panic attack (I hate driving in Charlotte) but it was definitely a great experience. She was very knowledgeable about endometriosis and chronic illness and in addition, recognized the depths of how it impacts every impact of your life. As crazy as it sounds, I have heard so many doctors, real doctors, blow off endometriosis, fibromyalgia, and other chronic illnesses as not a big deal or easily “cured” or handled. When she said, “people just do not understand the gravity of endometriosis, how it works, and the damage it causes and if they did, there would be more focus on finding the cause and how to treat it.” I could have kissed her. Then she stated how Lupron was an evil drug and never, ever be used. Can we give this woman a medal?  This is coming from a psychiatrist, not a gynecologist or women’s/pelvic health specialist. Maybe we should start giving awards to awesome medical professionals as a part of the Blogging for Endometriosis Awareness campaign.

In short, this experience was pure hell and I would never, ever wish it on my worst enemy but like all things in life, great and positive things can happened as a result if we allow them to. I am now working to make major steps to move forward and hopefully by sharing my story of chronic illness, anxiety, and insomnia, I will be able to help someone else do so as well. I will keep you informed on how my anxiety journey continues and how things go now that I am working with a psychiatrist (and we are adding a therapist to the team). I whole-heartedly believe that chronic illness is holistic and affects every aspect of your health (physically, mentally, emotionally, etc) and therefore I whole-heartedly believe that it should be treated holistically.

Do you battle anxiety (or depression) and have any remotely similar experience as a result of how your anxiety/depression manifests? What have been the things that have helped you the most get a grip on it?

 

chronic illness

Longing for Sunshine

The weather this past month has been mostly clouds and rain. Besides the effects that rain has on my joints, I have definitely noticed how it is more greatly affecting my moods.

In the midst of life’s challenges I try to keep a positive outlook and feeling the warmth of the sunshine on my face goes a long way in helping me feel as though I can overcome the hurdles of chronic illness.

The last several weeks, however, the sun has peeked through less and less  and I feel as though I have less and less wind in my sails. My pain levels have also been up so I am not sure if my disposition is more directly tied to pain levels or if it is a combination of the two.

The sun make an appearance this morning, albeit a short appearance, but the few moments I was able to take a walk in the sunshine I could feel a change in my thought patterns. As the clouds have rolled back in, I have once again found myself melancholy.

I have so much to be thankful for and excited about in life but lately I am finding it more challenging. I know that there is a time for every season and some seasons in life will be more challenging than others.

Spring is still five weeks away so in the meantime I will keep dreaming of warm sunshine and afternoons spent on the backyard swing.