Showing posts with label chronic pain. Show all posts
Showing posts with label chronic pain. Show all posts

Thursday, September 19, 2019

What you don't see


Me at my last pain management Dr apt.  My pain was at a 10




 In honor of pain awareness month and suicide prevention month, I want to talk about what you don't see from those in your life living in chronic and intractable pain. 
My family are the only one's who get to really see my pain.  I only share photos of myself on the good days.  Am I prideful? Yes!  But mostly I just don't want to bring others down by sharing my misery.  I don't like to talk about pain.  It takes so much from my life in the first place, I don't want to give it any more attention or energy.  But, I felt compelled since it's pain awareness month to share my heart on this subject. 

Me on a very severe pain day

 Pain is invisble and subjective.  It is not only difficult to explain but hard to quantify.  The pain scale helps us a lot to be able to gauge where we're at.  But given how subjective pain is, not everyone's "10" is the same. 
What about the days when we're out looking "normal" but gritting our teeth through levels of pain that would land normal people without pain in the ER?  And why is this even important to talk about?  I feel it's important because 100 million plus people suffer with chronic pain & a subset of that population suffer with intractable severe pain, ".
     "Intactable pain is described as “pain that is excruciating, constant, incurable, and of such severity that it dominates virtually every conscious moment, produces mental and physical debilitation and may produce a desire to commit suicide for the sole purpose of stopping the pain.” In the authors’ clinical experience, bonafide IP patients suffer profusely and are fundamentally bed- or house-bound in the absence of intense medical management."https://www.practicalpainmanagement.com/resources/intractable-pain
 I live with Intractable pain. 



  Someone you know likely suffers in chronic pain and I have lost count of the people I know that say at least someone in their life either doesn't believe their pain is that severe or they don't understand.  It strains relationships to the point that many lose those relationships.  I know people who hide it altogether because of the stigma associated, so they suffer in silence. 




Which leads me to my next point, life is not meant to be lived alone.  People need people.  When relationships are strained the risk of loss and therefore isolation increases exponentially.  With pain being so common this really is something that should be discussed because there is such a stigma associated with chronic pain.  Most people who've never experienced long term pain don't understand the concept of how if affects your life living day in pain day out, or even just on a regular basis.  It makes it really hard to understand what you can't relate to.  I get it, even as a RN and before my pain journey even began I couldn't fathom having to live in pain that didn't relent.  It broke my heart for those people, but since I didn't understand it, what more could I do?



What I've learned from living in constant, daily pain for 10 years is that it is so important to try to help our loved ones understand our struggles.  Just like that saying, "everyone is fighting a battle you can't see,"  pain is one of those for many people.  Just as communication is crucial to the health of relationships, understanding someone else's experience is just as important in my opinion.  I am blessed to have an amazing husband who supports me and loves me regardless of the limits pain has on me. He is my rock and tries hard to understand. I'm blessed to have children who are compassionate and understand my limitations. I'm so grateful for the support of other family members.  I'm blessed to have friends that try hard to understand, and have stuck it out with me despite how I may not be the most fun friend since this is a part of my life 24/7.  Having said that, I have experienced difficulties like anyone else living in chronic pain has.  I have been blessed in the sense not many people openly doubt me or suggest that my pain isn't real.  There have been very few actually that have suggested that, but I realize that was out of complete ignorance and I really do forgive them.  Have I lost friends and some family members, yes.  But what I've gained is substantially better & I have support.  Unfortunately, for many others, they are not so lucky.  They've lost spouses, family members, and friends and that shatters my heart to pieces.  I realize not everyone is as lucky as I am so that is my heart behind sharing this with you.  



None of us who live in pain asked for it.  And I've yet to meet someone who would choose this lot in life.  Are there people who make up pain to get pain pills  yes, but they are fewer than what is being reported.  Are there people who make it up for sympathy or exaggerate?  I'm sure there are, but I've yet to meet one.  And it is really difficult to get good pain management anymore, you have to provide imaging and all sorts of documentation that your pain is real, which is good in my opinion.  Though I realize it hasn't always been this way.  It is now.  At least in the state and states of friends I know living with pain and they are spread all over the country.  





So why do I share all this.  What is my point?  What you see is usually me made me up and smiling.  That is not the regular and I feel like it's being disingenuous of me to not share that what it takes to get me to be able to get to those points is a whole production in itself.   I have to plan to rest up for said event, often times I've got to shower one day and wash my hair the next, and usually style my hair the next day.  A lot of resting in between has to happen.  I have to time the medication just right and because of the current climate I don't get the amount of medication that keeps my pain levels managed.  Therefore I have to try and plan around after I've taken my meds and be done before they wear off.  There is a ton of spacing out activities so I can get it done.  Do I have to wear makeup, no but I do that to feel somewhat normal and like "me".
My Mom took this picture of me waiting for my Dr, my pain was a "10"
What you don't see is my Mom driving me every couple months to my pain management Dr where I pee in a cup to prove I'm taking my meds as prescribed and try my hardest to explain to him my pain levels. What used to be a "10" (natural childbirth), is now something I live with regularly.  My pain stays at a 
"8", but reaches a 10 more than I thought possible. And there's absolutely nothing that can be done that I'm not already doing.  

You may see me wearing makeup and looking somewhat put together.  But what you don't see is that 90% of the time I'm doing really good to bathe and change my clothes.  I slap some make up on to try to hide that pain and cheer myself up.  If I allowed myself to look the way I feel all the time it would bring me down.  This is a means of self care for me. It's worth the price I pay to feel somewhat "normal" even if only temporarily.



What you don't see is that there is no more house cleaning days.  I do what I can which isn't much and my kids and husband have to help with the rest (which I hate btw...so much guilt).  I used to have a day every week where I deep cleaned.  I prided myself on the fact that you could eat off the floor.  No more of that... What you don't see is the only meals I can cook for my family is a meal I can dump in the crockpot.  And it is challenging to find meals that will taste good and are somewhat healthy.  Thank you cream of chicken soup!  There's nothing wrong with that, it's just I used to love making my family healthy meals.  I used to love spending hours planning and prepping.  I know, weird.. I used to love working out, I'm talking for hours.  I LOVED IT.  Not just doing stretches in my bed.  I used to love taking my kids on dates and going out with my husband.  I used to love getting together with girlfriends & visiting family. I used to love serving sex trafficking survivors and serving at church.  I LOVED, LOVED LOVED my  job as a nurse. It is my passion. These things happen very rarely now.  And not one day goes by that I don't pray God heals me so I can go back to work, back to living, that I can live life the way I long to so I can be there to the fullest for the people I love.  I maintain my licensure in the hopes that I will be healed enough to the point I can go back  to work. My dream is to finish my Masters.  Daily I pray for that and all the aforementioned to be restored.  What you don't see is that pain has taken so much from me that I refuse to give it any more attention.  It's like the criminal who stole someone I love and I grieve for the life I had.  I don't want it getting any more of my life. I won't give it anymore attention.   



But what I will do is share what you don't see in hopes that maybe it'll help someone else see all the things it steals.  All the ways it affects the lives of those you know, just in case you're having a hard time understanding.  There's no shame in that by the way.  I can't imagine understanding it either if I didn't live it or live with someone who did!!  I do hope my tone comes across as helpful and not critical, my heart is to help spread awareness.  Those of us in the pain community are already suffering and we need all the awareness & support we can get.  That's why I share.  Nearly every day, someone new in the pain community is contemplating taking their life, ending their suffering.  They're tired, tired of living a life they didn't ask for and being judged for it.  Tired of not being able to go to the Dr and get the medication they need to have any quality of life.  If you only knew some of these stories... it would surely break your heart.  And this is me being very real, but I have been where they are.  My family and faith saw me through the darkest days of my entire life where I chose to stay because I had too much to lose.  But I totally understand those that are too tired to fight anymore.  It's a fight that feels at times pointless. "Since there are 41,149 suicides every year in the U.S., according to the National Center for Health Statistics,  it’s possible that many of these suicides are driven by pain. Not proven fact, but plausible hypothesis. This would suggest that perhaps as many 20,000 or more Americans a year with chronic pain kill themselves, which would be more than the government’s tally of 16,235 deaths from prescription opioids every year."https://www.psychologytoday.com/us/blog/nation-in-pain/201511/chronic-pain-and-the-risk-suicide

“Approximately one-third to three-quarters of people with chronic pain experience moderate to severe depression. Patients with depression experience increased pain because of overlap in the two affected systems: pain reception and mood regulation. Both depression and chronic pain share some of the same neurotransmitters and nerve pathways. So pain is worse, function is poor, response to pain treatment is diminished and their prognosis is worse until they can get their depression under better control.”5https://www.ableto.com/resources/why-chronic-pain-causes-fatigue-and-depression/
  
We need your support and understanding or willingness to understand now more than ever!!  So my main reason is sharing for those lives that are suffering with little to no support.  Because every life is precious, right? 



If you read all of this I thank you from the bottom of my heart.  Truly.  I know this isn't a comfortable subject and life has enough ups and downs without adding anymore voluntarily.  So truly, thank you.  Just know that I appreciate you more than you'll probably ever know.  Here are some suggestions on how to help if someone you love lives in pain. 


Tuesday, July 23, 2019

Traveling with chronic pain/illness & my 20 travel essentials





Last week we went to Six Flags & Hurricane Harbor in the 100 degree heat of the TX sun.   My son specifically asked for this for his birthday so I was bound and determined to make it happen.  The whole trip was a big production.   I was exhausted and hurting severely before we even left our house, not a good sign.






 In the back of my mind I was wondering if it was a good idea, but alas my tenacity kicked in.  And I want to share my experience since I know especially during these summer months a lot of us Mama's are faced with similar situations.   
For the 4 years before this & off and on for many before, I was confined mostly to my house making it to very few things, much less family fun things.  Holidays, birthdays, outings, church, events you name it I missed out on so many things.  Many times I cried about missing out on precious family memories or not being as big of a part as my heart longed to be.  But this trip turned all that around for me. I hope that by sharing it will encourage you as well. 

First of all I made sure to stock up on medications, all of them, the heavy hitters and everything in between including my supplements & oils.  I brought.it.all. Not only can the heat make me faint, fall, vomit, and increase my pain, but it also triggers migraines. Plus I can't physically walk well because of my balance issues. Thank you EDS, CCI, & AAI!!  So I researched park accommodations & discovered that for less than what I could rent a wheelchair at the park, I could rent a power scooter from a medical supply store here in my state, and no one had to wear themselves out pushing me(I can't push myself because of my weakened upper body strength and tendinitis in my forearms)!  I was all over it. I ordered a pack of cooling towels  a case of Smart Water, and bought this sweet misting fan that literally may have saved my life.  There are several other things I brought along which I've linked below with prices and where I bought them. 




 The first day we decided to go to Hurricane Harbor since there's water and I would presumably find a shady spot and be wet so what's the big deal, right? WRONG. So WRONG.  Somehow I forgot about the collar I wear 24 hours a day not being able to get it wet. So we looked into renting a cabana but it cost more than our hotel stay, hard pass.  We ended up renting a tiny little tent like apparatus that fit 2 chairs under neath...barely. I was excited as I plopped my bag down and went to try to find a comfortable resting position. Until 30 seconds later when I realized somehow the temp in this "shading tent" was at least 10 degrees hotter than actually sitting in the sun. I turned my little misting fan on and that puppy was like a dream, for a while anyway. I was still dripping sweat down my back and glistening all over in a very non attractive way.  My face looked like I dipped it in highlighter because of all the shine! But, I was there, so that was all that mattered.  I plugged my noise cancelling headphones in, turned on my Audible book and set out to just relax. It was enough of a distraction that I was okay to stay there for a bit.
I was just praying my hubby and kids wouldn't come back or at least my daughter who is scared of most slides, as the temp would surely increase 100 more degrees.  Also, I was hoping they were having so much fun they'd forget I wasn't there enjoying the slides with them. Plus, I knew if my son saw I was uncomfortable that he wouldn't enjoy himself but it would be impossible to hide at this point.  Thankfully they stayed gone a while and I was able to keep this routine up. I was about to take a sip of my water when that was hot like I'd microwaved it for tea when they returned with arms full of icees.  No thanks, hot water for me since I have sensitivities to sugar, flavoring and corn syrup.  The brief enjoyment was not worth the price I'd pay later.  I also forgot to bring a portable cooler....nice one! This story doesn't end well so I'll save you the dramatic ending and say that unless you have breeze, cold fluids, can get in the water, have the ability to ride a power scooter or wheelchair (if you have trouble walking),can re-wet your towel every 10 min or more, or if you have orthostatic intolerance, heat intolerance, and increased pain levels with heat/activity that I don't recommend an amusement park in the dead of summer (my tenacity is sometimes can be a huge weakness!)  This all probably seems pretty obvious but I was just naive enough to try it.

 I ended up passing out in the car for 2 hours with the AC on high, slamming cold water and still holding the fan on me because my body temp would.not.go.down. The heat exhaustion was real y'all!! I was pretty discouraged considering Six Flags was our destination the next day.




The next day however, was so much better that's why I share. Firstly, the park was big enough to accommodate my scooter, and I could use all of my gadgets from the day before AND find multiple open shaded areas. That made all the difference.  When I exert myself even by standing it takes a lot out of me and increases my pain.  I think that's another reason it hit me the hardest at Hurricane Harbor because I was not only overheated but either having to move to stay cool or walking.  With the scooter I had none of that nonsense.  I was also able to keep my water cold because I could bring more inside.  It did help that the park had multiple shaded areas, misters, and places to sit too. I really didn't even need my misting fan the whole time, and it was just as hot as the day before. That really stood out to me too because it encouraged me how much those changes and accommodations made a difference. 




 I of course wasn't able to ride any rides but I was THERE.  So, that was many answered prayers and meant the world to me and my family. We got there about 11 and all of us made it to 5 when my son was the one begging to go!! 

 The worst part of the whole day was when we stopped to eat lunch. I hate being the center of attention, but I'm used to getting a couple curious stares from people just being in the collar.  Well, that was magnified 100 times when we entered or I tried to enter the packed restaurant in my big 'ol power scooter.  My husband went to clear an area for me and I'm trying to communicate with him from across the restaurant that I'm just gonna park it outside.  He was not having it though.  I was literally at the table with the people next to the door, so so awkward for all.  I am holding up the keys assuring him it would be fine and he's waving in big motions for me to just come through. People were having to move to make room for me, my kids looking on in horror from the line to order.  It probably looked like we were arguing. Y'all it was up there with one of the most embarrassing experiences I've had! Not because of the scooter, I was grateful for that, but just the squeezing it into this tiny, full restaurant.  Too much, for me anyway.  I believe we'll bring our own food next when/if we go back for fall break. That little break though was a enough to cool us off, hydrate us all and get through the rest of the day where my son got to ride all he wanted to ride.  And I got to have some fun with my daughter who isn't a huge fan of rides.  





Steven and Jeremiah on a ride








I got to take all the pics some of us Mom's like to  take when their kids are on a ride, it was grand!  And I was so excited that it was him that actually begged to leave, not me! The best part was getting to be THERE.  GETTING TO BE THERE THE WHOLE DAY!!!!  It meant the world for real to all of us.  And I know this isn't possible for everyone but it just reminded me of all the progress we've made with my condition over the past year and that anything is possible. No matter what you are facing today, there is always, always hope.  So Getting to go on this 3 hour road trip both ways, 1 1/2 days of amusement parks and all of the family fun time we were all starved for, was more than a hundred answered prayers, it was a  dream come true.  Where so many times before I felt like a failure as a wife and mom, a burden and just a big let down. I left TX feeling like a victor.  CHALLENGE WON!!!! 








 I just wanted to share that because I remember how I was always looking for any glimmer of hope from others living with these challenges and I would hope to find someone with a similar story, and I did.  I'll never forget it, reading a  woman's story many years ago about her progress with the right treatments. It set my decision to persevere and continue searching for answers in motion.  So, today I'm hoping and praying that if you are reading this, & you're in a dark  season, that awful hopeless place where you're wondering what the point of it all is since you're not able to live your life the way you'd always envisioned it, that there is hope.  Our stories may be different but please just remember there is always hope, and that no matter what circumstance or situation you are in, you are loved and needed in this world by someone, just how you are, despite any and all limitations.  I hope you know that in the deepest part of your being and that you are encouraged by being reminded of how important & loved you are!


Here is a list of the products that are my travel essentials and a few I'm adding in for next time. I did not get paid by Amazon to suggest these products, I just have used and love them, but if you use the available links to purchase I may get a small percentage. 

1. HEADPHONES: https://amzn.to/2YedSgn

2. Mini fridge (to keep my headache hat, water or meds cool).  I found this more effective than a regular cooler with ice: https://amzn.to/2SDQ8Nl

3. PEPPERMINT OIL https://www.amazon.com/gp/product/B0062C2IKA/ref=as_li_tl?ie=UTF8&camp=1789&creative=9325&creativeASIN=B0062C2IKA&linkCode=as2&tag=jennyhart-20&linkId=7d40f7025f2143447fd0f4efde255517

4. Sea Band: https://amzn.to/2Y16O7q

5. Cooling Towels: https://amzn.to/2LDp5Rz

6. Misting fan: https://amzn.to/2K2tBWw

7. Medication organizer: https://amzn.to/32HYk3T

8. Tranquility essential oil(because car rides make me anxious): https://amzn.to/2JNIflw

9. Headache hat: https://amzn.to/2K0pLx8

10. Sunglasses: https://amzn.to/30QgDSz

11,  Eye mask: https://amzn.to/2JZH1CD

12:  sweat pants: https://amzn.to/32NbcWj

13. weighted lap blanket: https://amzn.to/2LDQW4d

14. Emesis bags: https://amzn.to/30Su9oI

15. Bag hanger(use for purse and also trash): https://amzn.to/2XWqsl0

16. Orthopedic seat cushion: https://amzn.to/30YbtnL

17.  Essential oils travel diffuser: https://amzn.to/30NTsrW

18. Travel AC adapter: https://amzn.to/2Yfbce8

19. Ice/heat packs multi-sized: https://amzn.to/2Y19Ick

20.  Head relief essential oil blend: https://amzn.to/2YeJi1U