Health Update

A ” Why Me” Moment

It is the third day in a row of feeling worse than the prior day, despite rest. I can’t do much except lay here and think. Even that can be challenging thanks to POTS depriving my brain of blood. I don’t usually gripe about being sick. However, I’m having a day where I just need to! I wasn’t going to post my thoughts. There are people out there dying that would happily trade places with me. What I need to remember, as does anyone else suffering from anything, is this… Just because someone else is worse off than you, doesn’t mean your suffering doesn’t matter, or that you should be grateful you only have – insert issue here. I chose to post because I want other people to know that it’s okay to have “why me” moments. Just don’t let them turn into days and weeks. That’s how people become bitter and stop appreciating what they still have left. ((Fun fact, pessimists die, on average, younger than optimists.)) So, I’m going to vent, but that doesn’t mean I have no hope or am walking around an angry girl… It means I’m human and am just having a rough time today.

The only activity where I am not acutely aware of my symptoms, is sleep. So, not counting sleep as an experience, I do not remember what it feels like to enjoy something without simultaneously being in pain and battling all of the “thinking issues” my brain not getting blood creates. I want to eat without having to consider the correct amount of food to eat so my blood doesn’t all go to my stomach to help digest, leaving my body even worse off with circulation problems. I want to go one week without feeling nauseous. I want to wear sundresses and show off my legs rather than having them covered by compression stockings. I want to tell Jake to go take a nap while I go to the park with Emma. I want to stand in a long line with passing out not even crossing my mind. I want to do things for my parents other than saying thank you. I want to be able to have a busy, exhausting day, and wake up the next morning refreshed. The idea people can do a lot, sleep, and wake up fine is astounding from where I’m sitting. I want planning my wedding to sound fun rather than exhausting.

It is terrible having my dreams kept at bay, not due to lack of ability or desire, but because I spend everyday sick. Since I was a teenager, I knew I wanted to go into a helping profession. I worked really hard throughout college to gain experiences and become better in my field, all while being sick. I see situations that I know I could help make better if only I wasn’t sick. I have so many ideas that I’d love to still have the ability to put into action.

All of what I’ve said explains why I have “why me” moments from time to time. However, none of this is the worst thing about having a chronic illness. The worst part of being sick is not feeling like my relationships are reciprocal. My friends and family give me so much, and I can’t offer much in return other than gratitude. I used to be the one running errands, helping clean, figuring out stuff, but now I am not. I used to be known for sending thank you cards for the littlest things. Often, I spend my last bit of energy trying to do something I know will make someone smile because I can’t stand not being able to give back. When I think of what I’ll do when I’m better, one of the first thoughts is always doing nice things for all these people. I also have a tough time with how sad my being sick makes everyone. I wish I could get better so all of you guys could be ecstatic at having some good news about me.

Maybe someday some good will come of my being sick. It will allow me to understand the people I help more. Maybe I’ll even end up with helping people with chronic illness as my purpose. I don’t believe everything happens for a reason. So in this “why me” moment, I come up with this answer… There is no reason as to why this disease chose me. It really could happen to anyone. So please don’t make my mistake. Appreciate your ability to go out into the world, enjoy your daily life, and chase after your dreams.

My “why me” moment is officially over. Time to push out the negative thoughts and focus on the positive. I’m going to be sick regardless of if I go through each day angry versus happy. Why not choose positive and happy?

24 thoughts on “A ” Why Me” Moment

  1. You bring joy and pride to our lives just by being you, sick or well. Love is reciprocal and can’t be measured. Remember when Maw would worry we were doing too much for her and she was too much trouble? No one ever felt that way, I’d have to remind her of all she had done for us. Right now you need to accept more assistance than you can give, but all of that balances out over a lifetime. Besides, who’s keeping track?

    • I’m keeping track! You never once have made me feel like a burden or that I am not doing enough. I must be pretty awesome if just my existence is enough 😛 haha

  2. i can really identify with this post. i love that you acknowledged that just because someone is worse off, doesn’t mean our suffering doesn’t matter. i think that is so important to remember – we shouldn’t feel guilty for talking about our suffering.

  3. We love you and love being able to do any little thing to help you! You have always gone out of your way to help everyone. If you refer to yourself as a burden again I will smack you, sick or not! :-)

    • I said I don’t like not being able to return the favor. I know I’m not a burden. I also know I was sort of insinuating that, soooo I suppose the smack is warranted. 😊

  4. Jackie, you are loved so much and so many prayers are being said for you. You gave all of us a wonderful gift saturday by being there for the Mamer Christmas. I know how hard it was for you to travel 2 hr. to get here but for us to all be together was wonderful. Im so sorry you are paying for it now. We love you

  5. Thank you for this post. I also agree with your comment about just because there are people worse off doesn’t mean what you’re experiencing is any less significant. It’s still real and you’re still allowed to have “why me” moments. It’s human nature I’m sure xx

  6. I often wonder why my partner puts up with me and *how* she can be happy with me when I’m so sick. I often ask her and she says ‘Even at your sickest, my life is better with you in it.’. I have trouble grasping this, but I believe her. I guess maybe it’s the same for your family and Jake?

    • I think you’re right. If any of my family or friends were going through this, I’d scold them for ever thinking they were a nuisance. In my heart, I know they all feel the same about me. There’s just that tiny little devil on my shoulder who starts talking sometimes!

  7. Hi Jackie, Thank’s for visiting and commenting on my blog. Good to meet a fellow Potsie.
    It is very tough to have chronic illness. This post echoes so much what I think and the fight to remain positive despite it all.
    On the sleep thing; Have you ever dreamed you were in pain? I have a few times- especially migraines that sneak into dreams. That’s the one time pain really does annoy me- because sleep should be an escape lol.

    You’re the same age as my oldest son. I pray none of my kids get this.
    Take care x

  8. Pingback: The “Why Me?” moment. | Thinking Love, No Twaddle

  9. You deserve all the things people do for you. You would be the first one to do things for them if the tables were turned. Just seeing your smile is payback enough for now because we all want to pretend you are fine. Just like your mom said it all balances out in the end. It is an honor to be your substitute grandma. Thanks for adopting me. Love you

  10. Hi Jackie! *waving* thanks for checking out my blog! :)
    What you deal with is terrible and no one would wish any kind of illness on anyone. But unfortunately we have no control over these things. You have a beautiful positive attitude and that’s brilliant! I too are focusing on the positives this year…on wards and up wards we both go!! Hugs Paula xx

  11. So very well said Jackie. I’m usually very positive and talk up my disease and treatment and how it’s going. I try to focus on the positives that are happening and not the negatives. But thank you for reminding me that it’s okay to acknowledge and not always feel like I have to hide how I am feeling (past few weeks have been horrible). The day you met me (and also the following day) I was having lots of “pissy pants” moments. Glad to know I’m not alone!

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