woman lying on bed in messy room

My House Is a Mess Because I'm in Pain, and That's OK

10k
10k

Reality check: my house isn’t featured in those design magazines.

And unfortunately, I don’t think it ever will be. I would love for it to be one of those kinds of homes, though. You know… clean. I’m sure we would all love a home like that, right? Bright. Inviting. Spacious. Maybe I’ll have a home like that one day. But for now…

My house is a mess.

I can tell you right now that if you were to come over, you will find dishes in the sink, jackets thrown over the sofa and cat toys everywhere. Even if I had been expecting you, my house would be in the same state. You may think I’m just lazy. When you see me, you see a healthy looking 20-something stay-at-home-mama. You may even think that I’m incredibly lazy because it’s not as if my child is a toddler who needs constant care. My son is 12 years old. He walks to and from school by himself. He prepares his own breakfast and heats his own lunch for school. But something you don’t see…? Something you don’t realize is that…

I struggle. Every. Single. Day.

You can’t tell by looking at me that I have had seven diagnoses since September 2015: one dermatological condition, four spinal conditions, anxiety and clinical depression.

You wouldn’t know that:

– I was one semester away from graduating from my registered massage therapy program before I had to go on this medical leave

– I have seen six specialists to try and find the correct diagnoses

– I have a “little pharmacy” in my bathroom for the collection of medications that I have to take and that I get a blood test every month to make sure that my medications aren’t affecting my liver

We’ve all been there are some point – quick to judge until we realize that there are conditions that are not visible to the naked eye. Just because someone doesn’t look like they’re struggling or suffering, doesn’t mean that they aren’t.

So why is my house a mess?

The simplified version: my back hurts.

The not so simplified version: the conditions that I was diagnosed with causes me great back pain. So much back pain that I have to lay down multiple times a day to get the pressure off my spine. I was advised by my doctor to not get a job where I stand all the time. In all honesty, that advise kinda sucks. It’s not as if my back only hurts if I stand for long periods. My back also hurts when I sit for too long. So pretty much… laying down is the only pain-free position for my back.

Let’s go a bit in-depth, shall we?

The least worrisome of my spinal diagnoses are degenerative disc disease and scoliosis. I mean, we’re all going to get DDD at some point in our lives and my degeneration is still on the mild side. I have an s-curve scoliosis – that means that it affects my entire spine.

My last two diagnoses are a bit more complicated and they’re the ones that affect me the most. I was diagnosed with bilateral spondylolysis and spondylolisthesis.

Spondylolysis is a defect in a part of your vertebrae. In my case, I have a fracture on either side of one of my vertebrae. How did it happen? Beats me! *shrugs* It’s usually caused by high-impact sports. I don’t do sports.

Spondylolisthesis is when one of your vertebras slip forward in relation to the others. There are four grades – a grade per percentage affected (grade 1 = 0 to 25 percent, grade 2 = 26 to 50 percent etc.). The higher the grade, the higher chance it will start affecting your nerves (…because it’s getting squished). I have a grade 2… it’s getting there.

The combination of those four conditions makes me feel like I’ve got a load of bricks on my shoulders no matter where I go.

The pressure on my spine is intense. I can only walk one-third of a kilometer before I feel it. It hurts to bend my back… so maybe you can see where I’m going here. What requires bending when taking care of a home? Silly question, I know. But honestly, my spinal conditions affect a lot of things in my life.

– I can’t lift anything heavy… it’s added weight to the bricks I’m already carrying

– It hurts to do the laundry. Switching the clothes from washer to dryer… ugh.

– It hurts to load and unload the dishwasher. Repetitive bending? No, thanks.

– Vacuuming puts a lot of pressure on your low back, even if you don’t realize it. I do. It hurts. So I can only vacuum a little bit at a time. One section a day.

– I can’t walk or stand for too long. Necessary things like grocery shopping, I need to brace myself for. No, really. You see me pushing a cart? It’s probably because I’m using it as a walker.

Actually, speaking of bracing. I have a back brace. I also have a knee brace because the whole ordeal is starting to have some effect on my knees. Lucky me.

So that’s why my house is a mess.

It used to bother me. It took a while for me to accept that I can’t function the way I used to. It’s either I clean my house like a mad woman and then be out of commission for days or… I clean what I can – when I can – so that I am still “useful.”

So what’s with the sweats?

I’m a homebody. I love to stay home. I go out if I have to… you know… grocery shopping and the like. But if I have a choice… I’ll be at home. There is no need to “dress to impress.” I live in my sweats because it’s comfortable. Imagine being in pain and uncomfortable. Not pretty. No thanks. I’ll pass.

Truth: I love my sweats.

So please don’t judge me. Don’t judge my messy house. It’s messy because I don’t want to be down for the count. It’s messy so I have the capacity to take care of everything else. It’s messy not because I’m lazy, but because I’m in pain.

We want to hear your story. Become a Mighty contributor here.

Lead photo by Thinkstock Images

10k
10k

RELATED VIDEOS

TOPICS
JOIN THE CONVERSATION

The Challenges of Being a College Student With Chronic Back Pain

18
18

Let’s be honest: living a life of chronic pain in college is hard. Trying to explain yourself to everyone around you. Always having a condensed version of your story ready to explain to whoever asks. Hoping they will accept your story with an open mind and a kind heart. Knowing that half the people you tell will say that their back hurts sometimes too. It is hard to be kind in explaining that although sometimes their back may hurt, yours is constant.

When I wasn’t in college I was able to separate myself from my back pain. It didn’t have to be the center of my being. But now that I am away, my pain has taken on a new life. I can’t shove it in a closet and forget about it.

People greet me and ask one of two questions. The first is: “Where were you yesterday?” This question is generally asked by people who don’t have a clue about my pain or have forgotten my pain was a thing. Every time this is asked my response is either that I was at the doctor or that I wasn’t feeling good. I don’t have the energy to tell them that my back was hurting so much I couldn’t sit through class or that I was going to my third doctor appointment that week.

The other question I hear is: “How are you feeling today?” While I am grateful that they remember what is going on in my life, all I want is to be “normal.” I want to go back to being the person who could shove their pain to the side and forget it is there.

I am still in the beginning of my chronic pain journey. For this I am thankful, but also frustrated. I am still trying to find a doctor who will validate my pain and stop pretending it is in my head. Because of this I am struggling to validate my pain and health issues with campus access programs. One of the hardest things I have done while at college was apply with the disability program. Not long ago I was a teenager leading a typical life. Now, just a few years later, I am a 19-year-old applying for disability and sitting in waiting rooms with people more than three times my age. The amount of times I hear “Girl, you are too young to have a back problem” makes me want to scream.

But regardless of the frustrations of my situation, I remain hopeful. Hopeful this doctor will do something, hopeful I’ll find relief, hopeful I will get through this semester.

In the same sense, I am incredibly thankful. I am thankful for the doctors and nurses and therapists who are trying to help me, thankful for my incredible roommate who always wants to listen and thankful that I know I can get through this.

Stay thankful and keep hopeful and you can get through anything with a smile.

We want to hear your story. Become a Mighty contributor here.

Image via Thinkstock.

18
18
TOPICS
JOIN THE CONVERSATION

The Decisions I Have to Make on Christmas Day With Chronic Pain

63
63

It’s Christmas Day! For most people this stirs excitement for the upcoming events of the day. Family time, the scents of the tree, carefully chosen gifts, fresh baked treats and our favorite dishes for the big meal of the day.

For me, I think first about how dressed up I will get. Will I spend the extra effort to curl my hair and dress up my make-up? Fancy festive clothes or comfortable clothes? Do I push the envelope and try to wear some heels even though I know I shouldn’t? They would look better than flats with my cute outfit though. (My first anxiety episode usually kicks in right about now.) I give up and go with the more comfortable clothes because if I’m going to be in pain most of the day, why add to it by wearing uncomfortable clothes.

Running late, due to all the “rest breaks” I had to take while getting ready, we hurry to load the car with all the gifts and food and drive 30 minutes or more, depending on traffic, to our first destination. Do I take a pain pill now or do I wait until later in the day? If I wait till later, I can at least enjoy part of the day without being in a hazy fog. Although, if I wait too long, then my pain will rule the day and I won’t enjoy anything. I try, I really do, to enjoy the festivities. All the while, I’m trying to hide how bad I’m hurting or going outside in the cold air to try and soothe another anxiety attack without anyone noticing or commenting.

Now, how many houses do we visit? Do we focus on one side of the family today and try (knowing someone will get their feelings hurt) to move the other half of the family to Christmas Eve or the day after Christmas? Or do I push myself to go to both places in one day? Fight through the pain and anxiety attacks, knowing I will get no sleep that night? How long do we stay? Can we move things along without looking like that’s what we are trying to do? Not because I don’t want to spend time with everyone but because the less time I’m there the sooner I will be in the comfort of my own home. Then I can start dealing with the physical/mental aftermath of the day’s events. Tomorrow will be filled with pain meds, guilt, more depression and laying around while the acute pain runs its course.

Meanwhile, the frustration of my family shows on their faces or in their comments. The questions of “Why don’t you just have surgery?” or “Have you tried doing _____?”(cue filling in the blank with just about any suggestion you can imagine). Or, my favorite, “Hope you feel better soon.” I grit my teeth every time I hear that one! Even though I have explained to them numerous times that I won’t ever get better. I will always have pain. The degree of pain may be “better” on some days, but I will never see “before back pain” comfort levels ever again. I get their frustrations – believe me, I do! Yet no one is more frustrated about it all as much as I am. Dealing with chronic pain every day is more than frustrating; it’s debilitating. Physically and mentally.

All of that being said, last year my husband and I spent Christmas Day at our house, just the two of us. We split our time up between each side of the family. Doing the day before with one side and the day after with the other side. We asked them to please understand. Even though I am close with my family, I must say it was one of my favorite Christmas Days ever! We took our time waking up, had a nice breakfast, turned the fireplace on and relaxed all day. We enjoyed each other with no stress. We reflected on our past year and looked forward to the years to come with hope. Christmas music on in the background, we fixed an easy Christmas dinner for two. Then we opened our gifts and drank some wine in the dark with nothing but the Christmas tree and the fireplace adding a soft glow. It was wonderful and romantic.

Can we with get away with making this our Christmas tradition from now on without upsetting the family? I don’t know. Understandably, I can already picture the looks of disappointment and the sad tones in their voices. It is wonderful to be loved so much! Besides the fact that it kept me from pushing myself past my “comfortable point,” it was a more meaningful Christmas Day for my me and my husband. I finally enjoyed Christmas for the first time in forever because there was no stress, no toes being stepped on and no big mess to clean up! This also made the days leading up to Christmas more enjoyable because I knew exactly what the events of the day would be. For the first time in years I looked forward to Christmas Day with excitement instead a cloud of dread and depression.

I guess those of us struggling with limitations should try to make Christmas the best it can be for ourselves. We can try to include the old traditions, but we won’t always be able to make everyone happy and we need to be aware of our limits. So, while I stress over what I am going to wear on Christmas Day and where we will spend it this year, I wish you all a holiday season filled with comfort, peace and happiness!

We want to hear your story. Become a Mighty contributor here.

Image via Thinkstock.

63
63
TOPICS
JOIN THE CONVERSATION

When a Nurse’s Compliment During My Procedure Changed My Life

18
18

As I sit and write this, my back pain in flaring up. Just sitting in a computer chair makes it feel like my back is on fire. Let me explain about my back: I have two pinched nerves in my neck, mild degenerative disc disease in my thoracic spine and a bulging and herniated disc in my lumbar spine. So when I say my back hurts, I mean my entire back.

After years of putting up with this pain, I finally found an amazing pain management doctor who suggested getting an epidural for my lower back pain. An anesthesiologist sedates you for the procedure so you have to get a ride home from the hospital. I’m not sure why, but I hate asking people for rides. Because I live with chronic pain, I fight to stay as independent as possible. Asking for rides reminds me there are times when I absolutely have to depend on other people to help me.

After my first epidural I decided to do some research to see if there was a way to avoid the sedation. During my research, I discovered sedation could be optional for my next procedure. I was so excited when I read that. As a person who doesn’t like to ask for rides or get sedated I thought maybe I could avoid both. When it came time for my next epidural, I asked my doctor if I could try the procedure without sedation and he agreed. I was familiar with the procedure because I had it done before, but I was concerned about the amount of pain I would be in. Along with the epidural I was also receiving trigger point injections for my neck.

On procedure day, I was still a little nervous about the pain. They had me lie on my stomach, and they put an oxygen mask in my nose. Between the staff’s calm voices, the oxygen and knowing some pain relief would be coming soon, I really started to relax.

Once they confirmed with me I wasn’t getting sedation, the procedure started. There was no turning back now. As the epidural needle went into my lower back, I felt the medicine being pushed in – a weird sensation I would describe as liquid being forced into your body. But there was no pain. At all. Just the prick of the needle. I got really quiet and the nurses kept asking me if I was OK. Between the oxygen and the sensation of the needles, I was actually calm. They took my blood pressure during the procedure and it was lower than when I got there. That is how relaxed I was. The nurses started telling me I was so brave. Someone also said there are grown men who skip sedation and are screaming in pain during the epidural. I loved hearing all this encouragement. Once the epidural was over, my doctor moved onto trigger point injections. Even after multiple needle sticks, it was a very peaceful experience.

The entire staff in the procedure room was kind and supportive. Then came the words I will never forget. One of the nurses, Julie, said to me, “You’re an Amazon woman.” It was in reference to the fact that I didn’t get sedation and made it through the procedure without complaining. Having had chronic pain for almost seven years makes me feel weak. On my worst days, just getting out of bed seems like a monumental task. It is also frustrating when my mind says, “Go” but my body says “Oh, heck no.” Having Julie say those words to me was so empowering.

Now when I think I can’t do something or am struggling with even a simple task, I say to myself, “You are an Amazon woman,” and it gives me the drive to push myself. Julie changed my life that day. To have a total stranger see I am strong despite my unrelenting pain made me want to be an example to others – to tell them “Yes, the pain does suck, but you are so capable of being strong.”  I try to encourage others the same way Julie encouraged me.

And let me just take a minute to mention how awesome my pain management doctor is. It took me years to find such a kind and caring doctor who believed I was in pain. I know many people who had to search for years like I did to find the right doctor. If you are still searching for that great doctor, don’t give up!

I have the same procedure done every three months to help with my back pain. I actually look forward to going because I know pain relief is coming. But I also get to see Julie and the amazing staff in the procedure room who tell me how strong I am – a reminder that I am an Amazon woman!

Image via Thinkstock Images

18
18
JOIN THE CONVERSATION

When I Realized Labels Can Enable My Children With Special Needs

383
383

Many parents are scared of “labels.” So scared, they don’t pursue a diagnosis for their child because of the fear their child will forever be defined by their diagnosis.

I understand this fear. I once shared it too.

There is a reason we did not initially share our daughter’s Asperger’s diagnosis with her, or with too many people around us. We were scared she would be defined by her diagnosis – forever limited by her label. In fact, I once wrote the following:

I am trying to remain positive and focus on what we can do next to help her, but I am worried about “the label.” With our son, the label that came with the autism diagnosis was welcome; it helped us obtain funding and assistance for him that he needed. He clearly has special needs and I have never hidden them from his teachers, friends or family.

My daughter is different. She doesn’t appear to have any special needs, and while a label might help the school obtain extra aide time, a label can also imply certain expectations of function and behavior. I don’t want her to be judged by the fact she has Asperger’s – I want her to be judged on what she can do as an intelligent, funny, affectionate, unique little girl.

She may be known by a different label today, but to me she is still my little girl from yesterday – and I will always love her, just as she is.

I wrote these words nearly exactly 5 years ago. I’m not sure when my thinking changed. But it did. Slowly and irrevocably.

I think a lot of the change came when I fully accepted the diagnosis myself. For a long time I unconsciously thought the diagnosis, and the label that came with it, was indicative that something was wrong with my child. I never said this aloud, and I never even consciously gave it a lot of thought at the time, but looking back, I can see that was my headspace in the early days.

Now I see the spectrum as a wonderful place of clever thinking, innovative ideas, boundless creativity and unique perspectives. There is nothing wrong in any of that. It is just a different way of thinking and viewing the world.

Yes, there are challenges with an autism diagnosis – I live with them every day. However, now I’ve come to accept my children for who they are, the challenges are less daunting. I realize the challenges are tied innately to the way they interact in the world around them, and I can usually do something to help them.

I’ve since come to realize that a diagnosis, and the label that comes with it, should not be viewed in a negative way at all. Instead of defining someone and their abilities, I believe a label actually enables and empowers.

A label provides access to help, support and assistance. Without a diagnosis, people cannot receive funding to help meet the costs of care. They cannot apply for assistance at school. They cannot receive benefits they are rightfully entitled to. A label allows them to access the help and support they need.

A label is the key to understanding and acceptance. A diagnosis and a label can provide answers and promise help. As I’ve described above, the label, even though I feared it, allowed me to fully accept my children’s conditions and understand them better. We have a far better relationship now there is a label to explain their needs and requirements.

A label is a sign of action, representing the first step in moving forward. Seeking a diagnosis and a label is a proactive step, recognizing there are unique difficulties and making a move to address them. Once the diagnosis and label are accepted, it is far easier to move on emotionally and make real progress – believe me.

A label allows people to find their tribe and their community. A diagnosis helps families congregate – to find others in a similar situation. There are support groups, in real life as well as online, which can only be accessed with a diagnosis. A label provides entry to these groups and also represents a common link, bond and connection.

A label can help people take ownership of their condition. Many people come to accept their diagnosis and feel a sense of pride in their label. My kids are proud to be on the spectrum. They relish “being different.” For them, it’s a source of pride and it’s helped develop their self-esteem and self-respect. They know they are different and they are OK with that.

In the end, a label is just a word. A way to categorize similar things. Yes, words are powerful. They can cut, wound and stab just as deep as any weapon. However, words can also be owned. They can be claimed. They can be reformed and remade.

We all have the power to reclaim the meaning of the word “label.” We can change the negative connotations associated with it. We can recognize it for what it is – an enabler.

We can all do our part to change the way labels are seen in the future. We owe it to our kids, our families and our communities to tackle the word head on and not let it stare us down.

We shouldn’t live in fear or avoid a diagnosis and the label that may come with it. We should be doing everything we can to identify our kids’ needs and doing everything possible to address them. Because how can we help them if we don’t know how?

That’s why I truly believe labels don’t define. They enable.

383
383
TOPICS
,
JOIN THE CONVERSATION

Finding Self-Confidence Through Physical Fitness as a Person With Cerebral Palsy

454
454

Hi, my name is Tiffany Eickhoff. I’m 28 years old and from Saint Louis, Missouri. I was born with cerebral palsy.

Two years ago, I made a drastic change in my life. At that point, I was just graduating college and was at a very unhealthy weight. I got to the point where I couldn’t walk or stand for long periods of time without my body hurting. With my whole life ahead of me, I faced the fact that I needed to improve my health and give myself a chance to live the best life I possibly could.

A few weeks after I graduated, my health journey began. I started working out a few days a week in a group fitness class with trainers and a few days a week on my own. I also took a huge leap by completely changing my nutrition. I gave up soda and now lead a paleo lifestyle. My diet consists of lots of veggies, protein (mostly meat), seafood and fruits. I cut bread and fried foods from my diet and eat very little dairy. Every once in a while I treat myself, but I feel so much better now. It’s all about striking a healthy balance.

Tiffany Eickhoff.
Tiffany in a 5K.

While these changes to my lifestyle took time and perseverance, my quality of life is much better as a result. Over the past 21 and a half months so far, I have lost 70 pounds. I am down to only having to walk with one cane and rarely ever use my wheelchair any more. I even raced in my first ever 5K on November 14th of last year, and completed my third 5K on April 2nd! The positive impacts have also been reflected in my mind and spirit, giving my overall self-esteem and confidence the boost it needed. Now, I’ve gotten into fashion and enjoy putting outfits together and taking more pride in my appearance. I also gained the courage to start learning how to drive again and got my driver’s permit.

Being healthy is a lifestyle for me now. I realize it’s a process, and take it one day at a time. I keep getting stronger every day and continue to reach for higher goals that allow me to live life with greater independence. Next up, I want to complete a half marathon, marathon, and triathlon. I am currently learning how to drive with hand controls, and hope to get my driver’s license soon. Eventually, my goal is to live completely on my own and totally support myself. Life is about the journey. I am confident, driven and determined that the sky is the limit for me!

Editor’s note: This post is based on an individual’s experience and should not be taken as medical advice. Please see a medical professional before starting any diet or exercise program.

This story originally appeared on Miss Amazing’s Musings.

454
454
JOIN THE CONVERSATION

Real People. Real Stories.

7,000
CONTRIBUTORS
150 Million
READERS

We face disability, disease and mental illness together.