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Charlie’s Legacy: Grieving The Loss Of A Pet

Charlie's Legacy: Grieving The Loss Of A Pet

 

Not a day goes by that I don’t grieve the loss of Charlie. It will be two months next week since we lost her and just the thought of it brings tears to my eyes. She was my constant sidekick and my ever faithful shadow and to not have her with me is like a piece of me is missing. For 12 1/2 years she was my best friend and I try to count my blessings in that we had her in our family for so long and she lived a full and spoiled life for 14 years. I am so, so grateful that we celebrated her birthday with a bang as she started to decline a month later. Thankfully, her decline was swift so she didn’t have to spend a lot of time in pain so for that I am grateful but if we could have had her 1000 years, I would have wished for 1000 years and a day.

She was just a perfect dog. She was very gentle and quiet spirited. I had written a post on the power of pet therapy and I wish I had known more about it early on as she would have been the perfect therapy dog to visit nursing homes and hospitals because of her gentleness.

She never tore anything up except her bed or her toys. She would destroy her bed but even in her young years, she never destroyed anything in the house (her floppy-eared companion, on the other hand, destroys everything).

She loved hanging outside and enjoying a cool breeze. John and I took the girls (Charlie and Chloe) with us on our first family vacation after we were married to the Outer Banks. The house we rented was on the sound side and the porch was gated so we just left the front door open and Charlie practically lived out on the porch, soaking up the breeze.

She was just amazing. There just isn’t any other way to put it. She was a huge part of this family and we all feel her loss. Chloe mourned for weeks. She still looks for her but she isn’t quite a mopey as she was those first weeks. Abby will come up and sit on my lap and whisper in my ear that she misses Charlie. We made a stepping stone (we used this kit from Hobby Lobby) and buried a box with her collar, letters and our favorite memories so being able to see it helps. There are many times that I have went out and there to talk to her like I would if she was here. I know one day we will be together again.

Charlie's Legacy

 

Helpful resources for grieving the loss of a pet:

Rainbow Bridge – This is an amazing resource. The “Rainbow Bridge” poem is beautiful and they also have grief support resources, a community, and ways to memorialize your pet.

10 Tips on Coping With Pet Loss – This is article provides great advice for moving through the grief process and the website also has many resources such as helping children cope with the loss, creating a memorial, and deciding when is the right time to get a new pet.

Coping with the Death of Your Pet – The Human Society is obviously a great resource to keep bookmarked when you are a pet owner but they also provide a lot of advice and resources for dealing with grief after losing your pet.

What Not To Say to Someone Grieving A Pet – Goodness knows as with any life experience, you get bad responses from well-intended persons. They want to help but they just don’t know the right things to say. I hear it every day about chronic illness but you also hear it after losing a pet and every time I hear “Why don’t you just go get another one?” I wanted to scream. My Charlie isn’t was a thing to be replaced. We will likely adopt another dog but in time. This is a nice article to read and yell at the computer “I know, right?!” Definitely a must read.

Dog In Mourning: Helping Our Pets Cope With Loss – Like I said in my post, all members of our family grieved the loss of Charlie and that included Chloe. I knew she would grieve but I didn’t realize just how hard it would hit her. It makes since as for her 8 years of life, she has always had Charlie so to be without her was a big struggle. This article gives great advice on helping your pet cope with loss as it can help you identify the signs that your pet is grieving and ways to help.

I hope these resources can help you with grieving the loss of a pet like they have been able to help me! If you have recently suffered the loss of a beloved pet, you have my deepest sympathies!

chronic style

My Very First Beauty Favorites Video!

As I have stated, the last several weeks have been challenging and three things have helped keep my sanity: my family, music, and makeup. I have spent probably way too much time watching beauty videos on YouTube but it has been a really great outlet and I have loving learning and trying out new products and new looks.

While I don’t think I’m quite at the point of filming tutorials, I did decide to jump in with both feet and film my first beauty favorites video! As a reminder, I am new to the whole video thing so please have patience as I figure out setup, lighting, and editing. I will definitely work on getting videos shorter as well. I feel like I cut out a lot of products but either I didn’t cut out enough or just talk way too much. I guess we all have to start from somewhere!

Here are my favorite products from January 2015:

List of products mentioned:

Boots Botantics Rosewater Toning Spritz
Eva*NYC Therapy Session Hair Mask
Hard Candy Sheer Envy Illuminating Primer
L’Oreal Infallable Pro-Matte 24h Foundation
Real Techniques Expert Face Brush
NYC Blush in Taupe
NYX Simply Vamp Lip Crayons
NYX Wonder Pencil
Rocksbox (Use code JAMEEBFF when signing up to receive your first month free!) *This is a referral link but not sponsored or affiliate.

Favorite YouTubers mentioned that you have to check out:
Leighannsays: http://www.youtube.com/leighannsays
ThaTaylaa: http://www.youtube.com/thataylaa

Let me know what you think of this video thing! Is this something you would like to see more of (both beauty and spoonie related)? If so, what are some things you would like to see?

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?