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Bulldog Sweatshirt & Floral Print Flats: On A More Serious Note

Let me begin by saying that this post is of a more serious nature than normal and since this is a style blog…

THE STORY

…I won’t be at all offended if you skip over this and head straight for the shots of my fabulous bulldog sweatshirt (and my fabulous actual bulldog who is making a guest appearance today). Those of you who have been with me for awhile know that I rarely never really get too personal around here. Although I do post photos of myself for all the world to see, I’m still very private by nature both in real life and on the blog. The thing is, I have felt compelled for awhile now to write about this both to explain why my posts have maybe been rather lackluster and sporadic recently, and also to share a little bit about something most people probably don’t know a whole lot about. Chronic Fatigue Syndrome…ever heard of it? Well, I have it.

I cringe to even use that name because it’s really quite demeaning and a substantial understatement in regard to an illness that is very, very real. It was just recently renamed SEID or Systemic Exertion Intolerance Disease which really isn’t much better…that just sounds like an uber creative way to say lazy. The sad reality is since people who are living with it don’t look sick and they aren’t dying it isn’t taken seriously.  Most people who have heard of it seem to think things like “Take a nap” or “Go to bed earlier” or the even better “You’re just lazy”.  Here’s the thing, if you truly have it throwing more sleep at it doesn’t fix it. And while it’s thankfully true that I’m not dying, it does do serious damage to my quality of life.

I was first diagnosed about 13 years ago. I underwent every type of medical testing known to man; some of it excruciatingly painful. Trust me, if anyone ever offers you a spinal tap, take a pass on that…I’d rather birth a whole litter of babies than go through that again. In any case, due to the facts almost every test came back normal with the exception of brain lesions that showed up on my MRI, and I exhibited every single symptom, I was diagnosed with CFS (or SEID if I’m bein’ trendy). The first few years were utterly awful. I couldn’t function for more than a few hours a day. The exhaustion is not the normal “I’m so exhausted from a long day at work” exhausted. I can’t even describe it; I wouldn’t be able to remain awake if you held a gun to my head. The all over body pain and  headaches were horrific, I gained 20 pounds because my metabolism ground to a halt,  and I think the worst part was how badly my brain was misfiring (in the CFS world it’s called brain fog). I had sticky notes all over the place at work because I couldn’t remember even the simplest things. It didn’t matter if I slept 4 hours or 18 hours (that’s not hyperbole I actually did sleep 18 hours once), I felt like I hadn’t slept at all.  Since there is no treatment for it, you can only take medication to manage the symptoms. My doctor had my on a stimulant to keep me awake and I downed over the counter medication for the pain. Eventually after several years, the symptoms eased up enough to where I could function relatively normally without medication. That’s sometimes the case with CFS; there are bad periods and somewhat not so bad periods.

I’d been doing pretty well for the last 7 or 8 years, but for whatever reason about two months ago it returned with a vengeance. Hence, the 10 pound weight gain I was complaining about recently. I blamed it on the Oreos, but I knew the real reason. I was just trying to avoid it. It has gotten progressively worse to the point I often have to take a nap during the 40 minutes at the end of the day between when the kids leave and when the teachers are permitted to leave. If I don’t, I run the risk of falling asleep on the short drive home. I’m in so much pain that wearing anything but flat shoes is impossible. My supervisor brought me some paperwork the other day that required my initials. I put the pen to paper and could not remember how to write my own initials…I ended up printing them. That was a fun little moment of terror and embarrassment all wrapped into one package. I made a joke out of it, because seriously, what else could I do other than cry? I’m on the couch by 6:30 and on the weekends I’ve been averaging 12 hours of sleep at night. I’m not trying to be melodramatic, but when you hit 50, you realize that you can’t be wasting entire days of your life either asleep or so out of it you’re barely coherent. I finally broke down and went to my doctor Tuesday and thankfully she put me back on medication to help me function more like a human being. I just started it today, and I’m hopeful that it will at least improve things enough that I can be myself again until the symptoms ease up and I don’t need it anymore.

Please know that I am not looking for pity. That’s the last thing I want. I merely wanted to explain why my writing has not been up to par and in many of my photos I’ve looked dead on my feet. I thought about taking a break from the blog, but I truly do love it so much and I’ve grown to really care about so many of you and I love the interaction. I miss being me, and this is one thing that helps me feel like myself. Rest assured, even if I’m not commenting a lot, I do try to read your blogs as often as possible. I also hope that if you’ve managed to slog through this rather lengthy post, you walk away a little bit better informed about something that is misunderstood by so many.

 

IMG_6687 IMG_6670  2015-04-01

Sweatshirt: JCPenney (No longer available);  Pants: GAP (Old);  Shoes: Target

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déjà pseu
9 years ago

Debbie, I’m so sorry you’re having to deal with this. I’m glad to hear there are some meds that help, and appreciate your openness. I think it helps others who might have the same issues to know they’re not alone, and that there can be some relief. Cute bulldog, and love the sweatshirt!

Maricel Edwards
9 years ago

Ah, if I take a break from blogging for a mere Spring Break excuse, you can definitely do so for such a harrowing condition. Take care of yourself, my friend. That’s cold comfort and won’t ease the physical pain and stress, but know that you have people in your camp cheering you on. And that bulldog is super fab! <3

Suzanne
9 years ago

Eeek. We have more in common than I’d ever have guessed. I’m so sorry you are in a flare right now. Once you get into a bad cycle it is so very hard to climb out of it. I sure hope the meds help. I’ve had Fibromyalgia for over 26 years now. Before they even knew what it was. I was told it was “all in my head” by a quack Dr. in Quebec. Thank heavens I had already been diagnosed by a real Dr. in Alberta. I just looked it up and Fibro and SEID are very similar. I… Read more »

JJ
JJ
9 years ago

Oh my! (that’s all I can say right now)

I can comment on your super cute outfit though…It’s super cute! :o) I just love how you brought out the Pink of the bulldog’s tongue in the rest of your outfit!

JJ
http://www.dressupnotdown.blogspot.com

Erin
9 years ago

Oh my friend! What a soldier!!! So sorry you have to deal with this BUT I have to say you look AMAZING (as always!) and hand,e it with such humor and grace!!

renae
9 years ago

hi Debbie! You don’t look like you have gained weight. Sorry you are going through this. Sure hope this new medication is super helpful. Medicines are amazing and some are not. Must take an estrogen blocker but it causes osteoporosis, which I already have. I asked to be on an alternate one. Man, horrible hallucinations with that one. Is it worse osteoporosis or can’t stop having mean people lunging at me in my sleep and disrupts my sleep to where I’m useless the next day. I feel for you, my friend. It was just the other day, I was seeing… Read more »

Dawn Lucy
9 years ago

Gosh, I never would’ve guessed, Debbie. I’ve often admired how you teach and still manage to post great fun looks every day. I hope the medication helps and you start to feel like yourself again. I can’t imagine what that would be like. The only thing I can compare it to is depression, which I’ve suffered from in the past. It’s another illness that people don’t understand too well. Take care & we’re all rooting for you.
Adorable sweatshirt, Dear!

Thanks so much for sharing with FUN FASHION FRIDAY!
OXOX
Dawn Lucy
http://fashionshouldbefun.blogspot.com

Jess
9 years ago

Hi Deb I am sorry to hear of your chronic fatigue. Having Ehlers Danlos Sydrome, I can totally relate to fatigue. I have to rest more in the afternoon and even more. I know about CFS and I know that there is lack of education with people. I understand this too,. I do hope that the medication helps you as fatigue can be debilitating!I wish you well. Msg me anytime! On your outfit! I love the pup sweatshirt, i want a shih tzu one!! The shoes I had tried on too, so I love those, pretty pastel colors. jess xx… Read more »

Kiki
9 years ago

You look fab in your bulldog sweatshirt!! How cute.

And as for tiredness…I have heard often of the syndrome, but only in recent years. I guess it’s because they only started taking it seriously in recent times.
I truly sympathize. One of the side effects of my condition (thyroid problems) is extreme tiredness so I now at least that aspect of it.
My best wishes to you. Don’t bear yourself up about what other people think and don’t be too hard on yourself. 🙂

Shybiker
9 years ago

So sorry to hear, Debbie. I’ve had clients with CFS who struggled with diagnoses and treatments, so I know how difficult your situation is. Wish you the best.

Claire
9 years ago

Hi Debbie, I am sorry to hear it has flared up again 🙁

You look lovely as always, you are such an inspiration :):)

Loving your bulldog sweatshirt and of course you lovely bulldog :):) thanks for stopping by and take care. Happy Easter..

idu
idu
9 years ago

Oh no! So sorry you are having to deal with this. I sure hope the meds kick in and are effective. You look wonderful in the face of all that. Kudos girl. http://fashionablyidu.blogspot.com/

Rachel
9 years ago

What a cute sweatshirt, love how you paired it with floral flats.

http://www.racheldinh.com

Jeannette
Jeannette
9 years ago

Dear Debbie, I read the entire post and I am so glad I did. I don’t really want to say I am sorry for you… why? because I know you are going to go through this quick and successfully and I believe everything in our lives happens for a reason and make us stronger. Reading your post was meant to be for me. Three weeks ago I had an MRI of the brain done that came back with lots of brain lesions. The first diagnosis I got from the radiologist was Multiple Sclerosis. I was in total shock when I… Read more »

Nikki at Bedazzles After Dark
9 years ago

Debbie – I am sorry to hear about your SEID. It sounds like it can be pretty frustrating, especially for someone as active and on-the-go as you. I think you still look great! And life’s short – eat the oreos! P.S. TOTALLY in love with that sweater and your flats. If you have to wear flats, at least they’re totally adorable! Hope you get to feeling better soon – or at least like yourself again.
xoxo,
Nikki at http://www.bedazzlesafterdark.com

Enter my Mint Julep Boutique giveaway here!

Rachel
9 years ago

Thank you for sharing this. I have a friend that has CFS as well and she had people from her personal trainer to close friends tell her she was just lazy and while it hurt her she was bound to do something about it. Now she is an Advocare consultant and while it may or may not be a sells pitch somehow she is doing a lot better and has more energy, plus she exercises more. I am sorry the past years and past few months have been rough. I like your shirt and flats by the way, such a… Read more »

Monika Faulkner
9 years ago

Major kudos for keeping up with your fab outfits and your blog posts, dearest Debbie; struggling with an illness (especially one that most people just don’t “get”) is never fun…but doing something you really love can hopefully make up for some of the sh*t you’re dealing with right now. Your bulldogs, by the way, are too cute for words…both the one on your sweatshirt, and ESPECIALLY the honest-to-goodness live one sitting next to you!! XOXO

http://www.StyleIsMyPudding.blogspot.com

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