Appts everyday this week. My full time profession. 😬
And being a mommy…😁
And then there’s my Chronic Cough hanging on for dear life…
Today’s exciting episode…
Yesterday’s exciting episode…
My Botox is helping. Summer is a BAD season for Migraine. So much heat (100’s everyday) and with heat comes the constant change from AC to HOT and back again. My head…my head. Yesterday was not a happy head day but I was able to keep it tolerable pain levels. Today, I’ve already had to triptan and it still hurts like a mother. I have big plans to make and freeze breakfast burritos with my Nick. It’s 16:50 and I’m stuck in bed. Maybe we can cook together in another 30 min… Maybe I’ll be stronger and in less pain then?
To my brothers and sisters fighting the warrior life everyday, I send strength and love. To my true friends who don’t necessarily understand it all, but support me, I send love and gratitude. To those who think less of me or judge me and my life based on their ignorance, I say fuck off.
Weep not for roads untraveled
Weep not for paths left alone
‘Cause beyond every bend
Is a long blinding end
It’s the worst kind of pain
Give up your heart left broken
And let that mistake pass on
‘Cause the love that you lost
Wasn’t worth what it cost
And in time you’ll be glad it’s gone
Weep not for roads untraveled
Weep not for sights unseen
May your love never end
And if you need a friend
There’s a seat here alongside me 💔
I love this piece:
Nobody is “normal.”
Everyone is unique.
That said, long-term illness can change a person; it can change your mind, your emotions, your perspective, your way of thinking… (to say nothing of your body).
And the places in your mind that change can be impossible to perceive; what is caused by the physical (hey come on, literal viruses and bacteria in our brains) or the changes that come from long-term isolation, suffering, frustration, loneliness, abandonment, hopelessness…. (trust me, even with the deepest introspection, lines are blurry).
So when you are in this bubble of misery and feeling desperate, many of us reach that crossroad decision of whether to reach out publicly or not. Now, some do so all the time and some seldom do so. I want to share with you, the healthy person, the “normal” person, what may be going on in our heads and where the need to reach out comes from. Because to you, (sometimes frequent) posts regarding how someone is feeling physically and mentally can come off as:
Or “_____” fill in the blank
And honestly maybe some people with chronic illness are. But I am asking you to consider grace, and here is why:
Imagine you are living a fairly normal active life; you work, you socialize with friends a few times a week, maybe you are also busy with kids. You do stuff! You go out to movies, you eat out at restaurants, you meet friends for coffee, you have a lot of human interaction at work, you sometimes take day trips or mini vacations, and your life may not be perfect or exciting, but it is full.
One day your body starts to betray you. Suddenly all the daily things that were no big deal become as hard as lifting heavy boulders. Your entire body is tired, tired to the point it feels like you have lead in your veins. You swear Earth’s gravity just dialed it up a notch as you struggle to go up the same staircase you have been bounding up the last five years.
You start sleeping a lot more, so much more that you start to feel guilt over your “laziness.” Even after a full night’s sleep your body starts to shut down in the middle of the day and you need to nap. The thing is all this extra sleep doesn’t help and you are just as tired and fatigued when you wake up in the morning as the night before. Even worse, you feel hungover, even without alcohol: toxic, heavy, foggy, headache, basically like sludge.
So of course you pump yourself full of caffeine because you have a life and things to do… only the caffeine is a quick fix that doesn’t last, so you have more. After a few cycles of this you start to blow out your adrenals, and things get worse…. You start to feel like you are letting the people in your life down as you can’t be there for them in the capacity you were only a short while ago. Oh, and did I mention the pain? You are dealing with pain that has no business in your body at your age! You feel old and achy. Joints and tendons, muscles and tissues that you never even “felt” at all before, are making their presence known by infusing non-stop pain.
Along with all of this (and a myriad of other symptoms I could mention) is the fact that your mind and your thinking are as foggy as your body. You know that feeling when it’s past your bedtime and you feel your brain trying to shut down for the night? How everything becomes difficult if you are fighting sleep? Trying to just finish that chapter, watch the last 10 minutes of that movie as your brain wants to sleep… Now it feels like that all the time, all hours of the day as your brain is constantly trying to go down as you are trying to get it to go up. Every waking moment is a battle.
Normal conversations become difficult because it feels like you are fighting through fog to both process what you are hearing while trying to formulate the appropriate response. You never knew until now that it actually takes energy to communicate and be with people. You frustrate yourself as word recollection fails you and you can’t seem to formulate articulate conversation.
As time goes on all this takes a toll and you start saying no to things. The energy it takes even to get ready, drive places, prepare for things… becomes too much, and you start having to pick and choose what you are able to do in a day, or even in a week or month as things get worse.
You start realizing that every activity also requires recovery time, and one afternoon out may mean you need two days in bed afterward.
Your world grows smaller.
As time goes on mentally and emotionally you for through all kinds of cycles that can be up and down and all around. These can swing extremely even over the course of one day from crying to anger to apathy.
At first all the people in your life are supportive, but as time goes on and you don’t get better, and you have seen this specialist, and that specialist and tried every suggestion of every caring friend from acupuncture, to massage, to “this amazing doctor that helped my friend who had the same problem!” you have read every article ever sent to you on any condition that even sounds similar, you have done crazy alternative things you would never have thought you would ever try…
But slowly friends start to drop away, check in less and less, and stop inviting you to things because they know you will just say “no.”
Life moves on without you and as the years go by your world gets smaller and smaller and smaller until you find you are alone most of the time.
You probably at this point have little to no money because it’s been spent trying to figure out what’s wrong with you and/or trying to get better. You also probably either can only work very little or not at all, and if you can work it drains you so much you have nothing left for any semblance of a life.
Remember when I mentioned the muddled place of your mind and your emotions caused by both the physical and psychological? This is where you are now. You may feel desperate and sad and lonely. Since you don’t see people in person so much anymore you might reach out to your friends online; both your real-world friends and your friends who you met in chronic illness forums and such.
So I am speaking to you, “normal” person, who I love and admire. When you see this chronically ill person prolifically posting, “wanting attention,” talking about what they are going through very publicly, and (sometimes) going into TMI territory… know that this did not happen overnight. This is the same person you know and love and they are beyond desperate to be the person they once were.
They may post because:
They want fellowship,
They want friendship,
They want to both hear and be heard,
They need a sounding block,
They want to feel normal,
They don’t want to disappear and be forgotten,
They want to have a glimpse of normalcy and online may be all they have,
They don’t see people much face-to-face so “Face”-book is their life.
Hear me now as I write this for my sick brothers and sisters: Everyone needs people! When you are sick and isolated, online is your people!
I don’t believe we are grand-standers or attention getters (at least not most of us). I think we are people just like you whose lives have changed and been shaped by illness and circumstances. All we want is to be normal and healthy. We may covet the little things that most people take for granted, even just taking a walk on a sunny day.
One more thing I want you to know: Worry about the chronically ill people who don’t post and instead stay quiet. They may be experiencing everything the communicators are but internalizing their pain versus reaching out.
It’s about having an outlet, versus internalizing everything. Isolation, versus reaching out. Honesty, versus putting on a happy face. I have seen too many of the “quiet one’s” obituaries online. Please also know the anxiety a person may go through on what to post and what not to post. It is so hard to judge because (especially) on a bad day, perspectives may be askew… and the reactions from people can also vary greatly.
You get the positive feedback from the chronic illness community: “Thank you so much for sharing, I am not alone.” “So glad to hear another person’s perspective.” “Thank you for being honest and blazing a trail for others that will come behind you.” This community supports you and your difficulties as you support them. And this is a safe and honest place to be raw and real in your times of pain.
But, you also may get the negative reactions of people who think you’re a drama queen, or are sick of hearing about your pain, or… (see list at beginning of post). So you may get the negative feedback, or the stony silence of family members, or the snubs and shuns of people who used to support you.
In closing: why am I posting this? I will tell you it’s not for attention or sympathy. I want to give a voice to the silent struggling ones. I want to advocate for those whose families don’t believe them. I want to open a window into a world (I hope and pray) you will never experience so that you can have a better understanding of your sick friend or family member. So consider grace and understanding first when encountering someone who has been struggling for a long time. We have so much to learn from each other.
This made me sad to read. Half alive. I cannot post something so depressing on my wall. Not today.
So I want to publish a funny too… Which is a better representation of the me.☺️
Today…my head hurts. And my sacroiliac is ridiculous. Shocker. I’m battling hypoglycemia as well. And I don’t know why. Preparing for my wee trip. Rest is a huge part of my prep. One more doc appt tomorrow before I go. I’ve had to postpone some appts because of the timing. This causes great stress for a Chronic Half-Life.
I can do this. It isn’t all about me.
One thing is a given: I will NOT go to the emergency room for a migraine. Never. I will die at home or someone will have to physically drag me in. I won’t go.
Migraineurs are treated like crap in ER’s. Drug seekers, complainers, etc.
One time in 2008 after a 6 day migraine, I went in. This was months after I’d been kicked out of a neurologist’s care with her dismissive: “There’s nothing more I can do for you.” Thanks Jeanette Wendt.
My primary was doing her best to handle my chronic migraines.
I just could not get the sucker to break. I was vomiting (I never vomit) and did not know what else to do. Friends of ours watched all FOUR of our kids for almost SIX hours while Marc took me in. Our kids were 5, 6, 8, 10 years old. That alone was unacceptable to me. How could I leave my friends with ALL those young children for so long?? There are just some things that are out of bounds. And leaving my young children for someone else to take care of was one of those things. I did not ask my in-laws and I would not have asked my parents.
My parents watched my kids for 5 days in 2009 while my husband and I went to Cabo for our 15th wedding anniversary. The first thing my mother said when we returned was: “Never again.” Awesome grandparents.
Anyway, the ER did not make me wait. They took me right back after a quick triage. They got me a bag of fluid, some reglan IV and some Dilaudid IV. I was chatting to the nurse in the dark room when she was administering meds. Marc was by my side, holding my hand.
When she began pushing the Dilaudid, I stopped talking immediately and tears ran down my face, I chocked a cry.
The nurse freaked: “Are you ok???”
I said, “There’s been so much pain. For so long. And the Dilaudid – it’s taking it away.” And I cried and cried.
“Oh, thank God,” she said, “I thought maybe you were having some kind of reaction.”
Which I was: Relief, finally.
It was an excellent ER visit. I left with my pain at a 3. The physician suggested it was time to find another neuro. And I agreed. I went home, Marc picked up the kids, I took an imitrex and slept til the next day. I was better.
I learned 2 things: ERs are NOT the place for migraines and I was exceptionally lucky to receive such quick, non judgmental, and excellent care.
My new neuro asks that I call the office on day 3 of a difficult migraine. She will administer medications IM. Or, she will write orders for infusions of mag, Depacote, torodol at an infusion center.
But what I really know is this: every migraine eventually goes away. It’s just a matter of time. So why not wait it out at home…in my bed. I don’t want to go anywhere. Least of all an ER.
So when I was struggling yesterday…and there’s this thought that goes through my head: Maybe I should go to the ER? You know my migraine has taken me to a dark place. A fear-filled, dark and scary place of desperation.
But I didn’t go. Of course. There’s this medication called phenergen that is one of my rescues. Not only is it an antiemetic with pain relieving properties, it puts me out. Almost always. I can count on Phenergen for the Mini Coma that can take me to the next day. The Next Day…where hopefully, the pain is less intense.
I’m at the Next Day. Caught in the bathroom. Day after migraine from hell. I’ll just stay here all day. My husband is being not nice (probably cuz I asked him to get up @10:15 AND change the dog’s water bowl!) and I have my phone. So I’ll just have a little toilet command center day.
In-laws are in town with cousins – staying at a big lake house 20 min away. And I’m missing it all.👍