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Heather Loeb

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All the writing I did about Isla’s gifted and talented scores got me thinking about the idea of success and what that means for me.

When I was younger (high school-ish), I would’ve told you being successful was having a good job, being well-off and married. I thought my parents were successful, which they are, so I intended on emulating their lifestyle. But when I did go out into the “real world” after college, I couldn’t hang. I got a job hundreds of miles away, working as a reporter to a mid-size daily newspaper, the Corpus Christi Caller-Times. I missed my family, and even though I made friends, it was still so hard. My depression worsened for one, probably from being away from home and stress of my first job. I got in trouble a lot for calling in sick (either depression or migraines), and I ended up quitting just short of a year. I quit journalism too, even though I thought being a journalist was my calling. I felt like a loser, and I was really anxious and embarrassed about the whole thing.

I eventually got a new job where I could use my writing skills, but I still mourned the idea of not being a journalist.

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I never found another job that made me feel as good as writing for a newspaper did. After a few years of working various jobs, I stopped working all together so I could get healthy enough to have a baby. People judged me for not working, but to be completely honest, it felt amazing to get that pressure off me. I did become healthier and had two beautiful babies within two years. I still haven’t gone back to work, and I like it that way.

When people ask me what I do for a living, and I say stay-at-home mom, it sometimes stings but I think that’s because society has conditioned us to believe that success only lies in one’s occupation. And for a lot of people, that’s true. But not I. It never occurred to me back then that that a job is just a job — it’s not who you are. And just because I don’t have one (that pays) doesn’t make me less of a person.

But it’s not about a job, house, how much money you have, etc. For me, it’s about happiness and being fulfilled. I was never the brightest, thinnest, most athletic, most ambitious person. I’m not even sure I’ve been the best at anything, and I say that not fishing for compliments but to proclaim that I might be mediocre in many ways but I’m also exceptional in others. I celebrate the fact that my life doesn’t have to parallel my parents’ or anyone else’s. I celebrate my strengths, even though they may not match others’. God made me the way I am for a reason. And you, too.

Success should look different for everyone, because we’re not all the same. We don’t have to be. We don’t have to join the rat race, either. All those “flaws” I thought I had before aren’t flaws at all, and I should celebrate them because they make me, me. I don’t get paid, but I write everyday and blog about a topic that I’m very passionate about. It makes me happy, and hopefully, I’m helping others in the process.

I will remember this about my kids as they grow up and try to figure out life as they know it. And I’ll support them, no matter what success means to them. Just like my parents did with me.

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Earlier today, I was writing a piece for my kids’ preschool, and I wrote something that I’ve never really discussed before, at least here on my blog.

I talked about how my depression and anxiety weren’t that bad until I had children. That it wasn’t lost on me that after I had kids my brain changed drastically and my depression worsened. But at the same time, my heart opened and I felt love that I’ve never felt. Sure, I experienced pain that I’ve never felt before too, but oh my god, the happiness and love that I feel when I’m with my kids is so amazing and just indescribable. It was some weird trade-off, I guess. And I’m here for it.

I also talked about how Isla sometimes is anxious. It isn’t surprising given my history with anxiety but it sure is painful to see her struggling or in a panicked state. She could just be an anxious child or she could just have common, every day 6-year-old worries. She’s too young to diagnose, and I hope she doesn’t have an anxiety disorder at all. Eli, either. Of course, I don’t want my kids to go through what I’ve been through. But just in case, I’m ready for it. I know how to navigate mental illness, believe me, and I so wish that I had the knowledge and resources when I was 12 that I do now. Early intervention is so important.

Now that I’m in a better place, I can say that every terrible thing I’ve felt and gone through has been worth it. It’s so worth it if I can be with and enjoy my kids. The meds, the psychiatric hospital, the panic attacks, ECTs, suicidal thoughts — it’s all worth it. Maybe it’s easy to say this while I’m not experiencing a depressive episode. But it needs to be said, I feel. I need to express just how grateful I am for my family, especially my kids and how they’ve shaped my life. Yes, my life would be dramatically different had I not had kids, but screw that idea of “what could have been.” My life, despite my illnesses, is so good. And again, I’m so thankful. And if I have to endure hell sometimes, so be it. Every depressive episode or panic attack only makes me stronger. My kids will see that, and it’s OK that they see me suffer and cope. They’ll see my resilience and perseverance.

And maybe that’s why I had to go through all that I did — to help one of my children go through the same. If that’s the case, it’s been more than worth it, and I’d do it all again. As a parent, I’ll always want to help my kids (read more here) and even remove all the roadblocks in their life, but I know it doesn’t work like that. But I can help. I’ll always be there.

Maybe my kids are just fine and I’m making too much out of nothing. Maybe I’m supposed to be blogging about my experiences to help others. If that’s the case, if I’ve helped even one person, it’s all been worth it.

It’s all been worth it, no matter what the case. I’m a better person for what I’ve been through, and all I want to do is make someone, anyone, feel that they are not alone. That their feelings are valid. That they are worthy and important.

And even though my brain tells me the opposite, I’d like to believe all that, too.

Maybe if I say, “It’s all been worth it” enough I’ll believe it. Maybe I can believe that I’m worth it.

It’s all been worth it.

And I’m worth it, too.

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I don’t have much to say about this past week, other than it was OK. It went by quickly, which is good because I’m been anxious about receiving the scores of my daughter’s gifted and talented test. I thought they’d send them out, and I got so worked up about it that I called to office only for them to tell me they’re not sending out the letters until this upcoming Friday. That sucks, because we’re supposed to be leaving for Dallas that weekend for Spring Break. Oh well, I can’t do anything about it, and I know that worrying will only hurt me. So, I’ll try to let that go, lol. But I did talk to two other mothers who both told me they were constantly checking their email for the results, so I’m not alone.

I’m looking forward to our trip to Dallas to see my parents. We haven’t traveled in a long time, and it’ll be nice to get a change in scenery. I’m hoping to see my best friend, too but I don’t know if it’s in the cards.

Anyway, that’s it for me. This week I’m going to focus on decluttering, so I’m not so anxious and writing some more. I hope y’all have a great week. If you’re so inclined, please say a prayer about Isla’s scores. It’s important to me and my husband.

Stay in the light, my friends.

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Just Say No

by Heather Loeb

I don’t like saying no to my kids, big surprise, right? In the past, I haven’t wanted to hear them scream, whine or cry because I didn’t say yes. It makes me uncomfortable when they do that, and as you know, I hate being uncomfortable. So, if the kids wanted junk food, I’d say yes and if they wanted some kind of new toy, yes again.

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Then it dawned on me — I got everything I ever wanted growing up (which I’m grateful for) but I never learned how to work hard for anything, and I don’t want that for my kids. I had no work ethic, and I never learned struggle or how to cope with it. Already, my kids are privileged and spoiled. They are accustomed to the finer things in life, and the last thing I want them to be are entitled assholes when they grow up. You see — I don’t need to be in the business of saying, “yes.” I NEED to say, “no,” because I want to raise them to be healthy adults. It’s not going to hurt them to hear, “no,” and it’s not going to hurt me, despite what I’m feeling at the time.

The consequences of not saying, “no,” are dire. I’ll admit that I’m not a healthy adult, but let me be clear — it’s not because of anything my parents did or didn’t do. My shortcomings are due to crappy genetics, crappy coping skills, among other things. But they’re there. I don’t want my children to suffer the way I do now. For example, I have an eating disorder — I don’t take care of myself the way I should by eating healthy; instead I binge eat when I’m stressed — alas, a crappy coping skill. I’ve also never had a job for more than three years. I’m dependent on my husband, which isn’t necessarily unhealthy, but I’d like both of my kids to be financially independent and have a good worth ethic.

I’ll confess that sometimes I feel like they’re getting the short end of the stick by having a severely depressed mother. Buying them toys, clothes and other crap is probably me trying to compensate for being ill. But logically, I know that material things don’t matter — experiences matter. Teaching them how to be healthy matters. Showing them how to overcome adversity matters, and I can do that. I’m resilient and scrappy, two traits I want them to have, too. I may not be the healthiest, but being sick all the time has made me stronger. I hope that’s what my children will see — that even though I suffer with a chronic, invisible disease, I still show up to fight….for myself and my family.

Ann Landers said, “It is not what you do for your children, but what you have taught them to do for themselves that will make them successful human beings.” She’s not wrong.

And that’s what I have to remember every time I say no. I’m not depriving them of anything — I’m shaping them into good people (I hope). I also need to remember this when I don’t feel like taking care of myself, because they’re watching and learning. It’s up to me to model healthy behavior, as hard as it is.

Parenting is hard. We all mess up and think we’re not good enough, me especially. Then I remember how Isla collected more than 1,000 toothbrushes for the homeless because she was worried they didn’t have money to brush their teeth. I recall how Eli puts his hand on my face and tells me he appreciates and loves me. They’re loving, kind and a product of their environment, which I’m extremely proud of. Learning to say no will be hard but it will definitely help in shaping them into healthy adults. I truly believe that.

And while I’m at it, maybe I can be shaped into a healthy adult, too.

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Millennials and Anxiety

by Heather Loeb

I was on the phone with my mom yesterday when I brought up one of my cousins and how she too struggles with severe anxiety. Hers is so severe that she has had to drive herself to the ER because of panic attacks. Then my mom mentioned two other cousins who suffer from anxiety. My mom and I joked about how so many of us had anxiety and said that if she had mentioned having a headache or being nervous about something, she would be told, “You’re too young to have headaches or be nervous.” Basically, she and her seven other siblings would’ve been brushed off or told to suck it up. Not because her parents were mean or anything, that was just how it was back then. Because of this, my mom’s generation didn’t talk about feelings. I guess they bottled it all up or coped in other ways.

I had joked about it, but it got me thinking: why are so many Millennials (those born 1981 to 1996) so anxious? Why do (most) of us feel free to share their feelings and struggles when our own parents were taught not to? Do we overthink things? Am I overthinking this blog?

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I don’t think so, lol.

Fun fact: Anxiety wasn’t even officially recognized as a condition in the Diagnostic and Statistical Manual of Mental Disorders (DSM) until 1980, so I get why there’s resistance among older generations to acknowledge it as a real disorder/disease, but it now affects more than 40 million Americans — it’s a serious and widespread disorder.

The American Psychological Association reports that 12 percent of Millennials have officially been diagnosed with an anxiety disorder—almost twice the percentage of Boomers who have been similarly diagnosed. The Blue Cross Blue Shield Association also released a report in 2018 that showed that diagnoses of mental disorders had risen dramatically by 33 percent since 2013, and millennials make up 47 percent of that figure. 

“Millennials have seen two major economic collapses, higher rates of divorce among their parents, a skyrocketing student loan crisis and a widening gap between the rich and the poor,” according to culture critic Kalev Rudolph.

Byrdie.com says, “While every generation tends to believe that they lived through the hardest times, the spike in anxiety levels among millennials shows that they are indeed going through more periods of stress than generations before them.”

When talking to one of my besties, she mentioned that watching the shuttle explode in Kindergarten changed her, as well as watching the Twin Towers fall in high school. Understandably, it takes a toll. Some people may roll their eyes at what I’m saying because people say that Millennials are weak and spoiled. And while I personally can’t dispute the spoiled part, I can dispute the weak part. So many of us were taught to keep things inside and not be vulnerable, but also many of us have embraced being vulnerable and authentic in what we feel and struggle with. That’s not a weakness — it takes a very strong person to share her struggle and be open about what she’s going through.

It wasn’t easy for me to “come clean” about my major depression, anxiety disorder, eating disorder, personality disorder and suicidal thoughts. It wasn’t easy, because the stigma of depression and (other mental disorders) is still very prevalent in the U.S. That stigma is what kept me quiet during my struggles, which only made it worse. It’s lonely when you’re fighting a disease you can’t talk about with anyone. And now, people congratulate and sing my praises because I do share so much — and I’m beyond grateful for that. But it shouldn’t be that way — everyone suffering with depression or another mental disorder should feel supported and free to share their experiences.

So, no — Millennials aren’t weak, and Boomers/Gen Xers aren’t stronger for keeping their problems to themselves. I acknowledge that those generations were taught to “suck it up” and keep it to themselves. That’s what they knew and how they coped. I don’t mean to sound condescending, but they didn’t know any better.

But now, we know better — we’ve evolved…not as much as I’d like, but we’re getting there.

It’s not a coincidence that so many of my female first cousins suffer from severe anxiety. Obviously, there’s a genetic component but what else is at play? Personally, my parents never told me to suck it up or not to be honest about my mental disorders. But somewhere along the way — and I suspect it’s the true for my cousins — we were taught to aspire to a certain image (i.e. being skinny). I know this to be true because I’m not the only one in my family with an eating disorder. Also, that ideal didn’t include admitting to mental illness, eating disorders, suicidal thoughts, etc. I suspect that’s why I stayed quiet about my issues so long. I can’t speak for my wonderful cousins.

It’s nice to know that I’m not some genetic anomaly (although that could be debatable), because it can be so lonely to fight anxiety alone. I’m in good company — my cousins are all successful, kind, empathetic, loving women who fight just as hard as I do on a daily basis. I so badly want us to come together, share our experiences and support each other.

That’s the hallmark of our generation — strength and empathy.

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Not So Fun Times in Texas

by Heather Loeb

We live in Corpus Christi in South Texas. Because we’re a South Texas coastal town, we don’t see much cold weather. Not like we have this past week. Temps have been well below freezing, then it rained. Ice was on the roads and pipes burst, making our water undrinkable. We haven’t had any power since Monday at 4 a.m. It’s actually like this in most of the state. And it’s been a complete shit show.

Mentally, I was doing OK, despite having been locked in my house with my kids all week with nothing to do. Despite not being able to go anywhere. Despite having power in only parts of the house (which is better than most, believe it or not). That was all until yesterday. Yesterday morning, I found myself losing my temper more with the kids and generally was in a pissed off mood. Then I got word that there would be no school for the rest of the week, which I expected but dreaded. My kids have been fighting all week long, and I just have no more to give today.

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This week has just been shitty for millions of Texans. As I was talking to a friend about it, she said something along the lines of, “I am not good in these situations where nothing is routine or normal at all.”

And, boy did I feel that.

I too am a creature of habit. I get bent out of shape when even the slightest thing is off about my routine. I don’t like the unexpected. Hell, I don’t even like surprises most of the time, even if they’re good. When the pandemic hit last year, I thought I was going to lose my mind every single day. And yes, I did eventually adapt and we started a new routine. But with this shit this week, I have not adapted. I don’t enjoy sponge baths, I don’t enjoy having to entertain my two small children every minute of the day and I don’t enjoy being trapped inside the house (we can’t even take a car ride because of the icy roads). But this isn’t because I’m a creature of habit — this is because of debilitating anxiety.

My anxiety (a product of Generalized Anxiety Disorder) is more than a little nervousness about some things — it exhausts me, it makes me think worst-case scenarios about anything and everything about my life and it gives me panic attacks. That’s normal for me, in normal situations. In situations such as the one we’re in now, it’s so much worse. Little things, like repetitive noises and messes, send me over the edge. It’s hard to calm down once I’m already triggered, and it’s really hard to keep my composure in front of the kids, which I do attempt. It affects me mentally and physically. I’m exhausted and very tense. I’m so tired and frustrated, that I said “fucking” in front of the kids and my mother in law. My kids have definitely expanded their vocab this week.

I know it’s temporary and will all be over soon, but it doesn’t change how I feel. Some things are just harder for people with anxiety. I don’t wish it on anyone.

I had such high hopes for this week, because it’s my birthday week. Now, I’ll be lucky if they get the power back on by Saturday, lol. But I do know that it will all be OK soon. School will start back up Monday, and things will get back to normal. I’ll appreciate the structure and routine so much more than I did before.

If you have a loved one with anxiety, ask how you can support them. Avoid statements like, “calm down” or “don’t worry.” I always feel misunderstood and brushed off when my anxiety is met with statements like that. An anxiety disorder can be quite debilitating and should be considered serious. I have friends who have had a panic attack and had to go to the ER it was so bad.

I hope you are all warm and safe. If you’re not, I’m saying prayers for you.

Stay in the light, my friends.

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I’ve Gained 26 Pounds

by Heather Loeb

Last Friday I had an ECT treatment. I hadn’t been there in four weeks, so they asked to weight me (to calculate how much anesthesia I get). Usually, I avoid the scale. The number shouldn’t matter to me, but it does. Big time. I looked down after I stepped on the scale, and I was shocked. I’ve gained 26 pounds since the pandemic — 26 POUNDS! I’m almost 200 pounds, which I swore to myself I’d never be again. I mean, who has weight loss surgery and doesn’t lose the weight? Me, apparently.

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I have all the reasons in the world to lose weight and be healthy, mainly my kids. I want them to see me be healthy so that they can be healthy. I want to lose the weight because I want to live a long time. It would benefit my mental health greatly if I maintained a healthy lifestyle. But I don’t.

Even after my ECT, while feeling happy and more stable, I had the intense urge to overeat and binge. And I did. The ECT is supposed to reset my brain. Last week, I was so depressed and even had suicidal ideation, so I needed the ECT. But the ECT can only take me so far. I’m responsible for making health decisions for myself. And I need to hold myself accountable. At some point, I have to make the effort to be healthy without expecting something or someone else to help me.

I don’t know what drives me to overeat or binge. It sort of makes sense when there’s conflict in my life, and I feel the need to be comforted by food. But right now, there’s no conflict in my life. There’s no logical reason for me to shove food in my face. It bothers me so much that I don’t know why I binge, and I’m not sure it would even help if I did know. It’s just frustrating. And I know it’s a hard time because of the pandemic, but we’re not getting back to any kind of “normal” I know any time soon. So, it has to be now. I have to make changes now. But honestly, I don’t know if I will. I don’t know what it will take.

I bought a treadmill that will be delivered this week. I bought a food journal to help me track my water and meals. I have a brand new pair of running shoes to use for exercise. Conditions are favorable for change. My brain, my stubborn brain, is the only thing holding me back. Even now, as I’m typing this, I want to eat, to be comforted. To lose myself in the taste and texture of something delicious. I fear my urge to escape the real world will be permanent, as it manifests in other ways, too like abusing my anxiety meds. And again, I don’t know why or what I’m trying to escape. I have a great life — better than most — and I’m so grateful for everyone in my life and everything I have. So, I really can’t tell you why I want to escape.

At one time, I thought it was emotional pain that was holding back — trauma from my past. But I feel like I’ve dealt with that. I’ve talked to my therapist about it extensively. I wrote a blog about it that I will never share. I got if off my chest, but still the pain resides. At least, I think so. Why else would I be trying to fill this unrelenting void?

I so want to be able to wake up in the morning and not immediately think about what I’m going to eat. To plan my next meal, as I’m licking off my current meal’s crumbs from my lips. I live meal to meal, snack to snack, and I hate it.

I hope this week I can make changes to my daily life and incorporate healthy habits. I pray for strength and guidance. I pray for what feels like a miracle.

Next week is National Eating Disorders Awareness Week. It may not seem like a big deal, but there are 30 million Americans who suffer with an eating disorder. There are so many people suffering right now, who are suffering more because of the pandemic. Only 1/3 of people receive help for their eating disorder. Eating disorders have the second highest mortality rate of any mental illness, with nearly one person dying every hour as a direct result of their eating disorder.

If you are struggling with an eating disorder, please know that you are not alone. It’s a challenging time for us, but it’ll be OK.

We will be OK.

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I’m proud of myself this week. I had to move up my ECT (to this past Friday) because I quickly became depressed after the last one, which was four weeks ago. I hate getting them, but I knew I needed it. I went into survival mode last week (and had to cancel plans) and made it to Friday.

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I was more nervous about this one, but I don’t know why. When we got to Laurel Ridge, I started pacing in the waiting room. Luckily, there was only one girl ahead of me, so I didn’t wait long. But when a bed was available, the nurses couldn’t get my IV in. This made me incredibly nervous. I was afraid that they would do a bad job with the IV, then I wouldn’t get all the anesthesia I needed. I know that’s not likely, but that was the thought racing around my head. One of my favorite nurses finally got it, but to be honest I had shed some nervous tears. I tried to chat about my kids to take the focus off, and it helped.

When I went into the room, everyone was really nice and accommodating because of my anxiety and I had a good seizure — 72 seconds long. I was told the shorter the seizure, the better, but looking at my records, all my seizures are kinda long, over a minute. One was two minutes long — after that seizure, I was doing very well and was able to go nine weeks without an ECT. So, who knows. I am keeping a notebook where I’m documenting my symptoms a week leading up to an ECT and immediately after. I think it would be helpful to find patterns or correlations.

Enough about that. My birthday is this coming Saturday, so I’m looking forward to that.

That’s really all I got for now. Y’all have a good week, and stay in the light.

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Cancelled Plans and Spoons

by Heather Loeb

I’ve had to cancel plans with three different friends this week. I HATE cancelling plans — it makes me feel so guilty, because I feel like I’m letting my loved ones down. I know I can’t help it — and my friends are very understanding — but I still feel guilty and less of a friend.

At least now I can tell them the truth — I’m too depressed to leave the house. Before I went to The Menninger Clinic, I didn’t tell the truth, and I probably seemed like such a flake who didn’t care about spending time with her friends. But now, I’m honest. I said that I was having intrusive thoughts about suicide (not suicidal thoughts per se) and I just didn’t have the energy. I call it survival mode. You see, I’m getting an ECT treatment on Friday, so I just have to make it until then. The ECT should reset my stupid brain and maybe I won’t be so depressed and fatigued. I’m hoping that I won’t have as many migraines after this treatment, too. For some reason, my migraines have ramped up the past few weeks, and it’s been really annoying. I hate being limited by my illnesses, and on that note, I’m reminded of an article I read about the Spoon Theory by Christine Miserandino, who suffers with lupus. She writes about the physical and mental toll an invisible, chronic illness can take. And I relate.

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While describing what it’s like to have a chronic illness, Miserandino grabbed spoons and used them to represent finite units of energy. Healthline.com writes this of Miserandino’s theory, “Energy, for many of us with chronic illness, is limited and depends on many factors including stress levels, how we’re sleeping, and pain. Miserandino then walked her friend through the friend’s normal day, taking spoons, or energy, away from the friend as the discussion went on. By the end of the day, her friend wasn’t able to do as much as she wanted. When she realized Miserandino went through this every single day, her friend started crying. She understood, then, how precious time was for people like Miserandino, and how few ‘spoons’ she had the luxury of spending.”

I feel this in my soul. Especially right now. I have to save every waking minute in order to do what is absolutely necessary, what I deem necessary, at least. This includes taking care of the kids and all their needs. This, to me, comes first. My remaining energy, if you can call it that, goes to taking care of myself. Many people would argue that it should be reversed, and I don’t totally disagree, but this is how it is right now. I hope to change it, because I know you can’t pour from an empty cup, and if I don’t start taking better care of myself, my cup will stay empty. I’m working on that, too.

It dawned on me this week that I could probably space out the ECTs more if I just put in the hard work of self care. I don’t mean getting a massage every week, although that would be nice right now, but I mean taking my medicine as I should, taking breaks and eating healthier. And actually sitting and exploring my emotions instead of burying them then stuffing my face. That happens a lot, almost every day. I also would like to increase my therapy sessions to twice a week — I have a lot to do, lol.

That’s OK though. I’m worth the work; I just need to remember that every single day.

Thank you to my friends who were so gracious about me. cancelling on them. I love y’all and appreciate your support.

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  1. It feels like you’re dying — When I get a migraine, I have awful throbbing pain about my right eye that wraps around my head and sometimes goes down my neck. I get dizzy, sometimes I can’t see that well out of my right eye. I throw up. And sometimes my abortive meds fail and there’s nothing I can do except wait for my neurologist to call me back with ideas. It’s scary when I can’t manage my migraines, so I deal with fear and panic on top of the physical symptoms.
  2. People think I’m faking — Like with other invisible illnesses, people assume you’re faking and have no sympathy whatsoever.
  3. Doctors and other medical staff have thought I seeking drugs when going to the ER — When my abortive meds fail, I can’t get a hold of my doctor and the pain is severe, I have to go to the ER for treatment. I have been accused of trying to score drugs. Once, I went to the ER and I told the doctor I couldn’t have NSAIDs, which is true, so the doctor goes, “OK, so you’re here for narcotics, then?” It was embarrassing and frustrating, because I was in so much pain.
  4. I cancel a lot of plans with friends — Migraines spring up fast, and while my meds work quickly most times, I still don’t feel well enough to hang out or go anywhere. I’ve had to cancel on my friends a lot, and I know it hurts their feelings and makes them feel like I don’t want to be friends. Most of my friends now get it, though.
  5. I missed a lot of work (when I did work outside the home) — When I was working, I had to call out sick A LOT. Like I said, migraines can come on quickly and my meds don’t always work. Sometimes, the migraines last for days (called an intractable migraine). Not only did it piss my bosses off, it made my co-workers resent my absences because they had to pick up the slack. And if you can’t see the illness manifest physically, it’s hard for some to understand.
  6. The medicine is sometimes worse than the migraine — Right now, I take Imitrex when I start to feel a migraine coming on. Sometimes, it works with little side effects and others it’s just as bad as the migraine itself. It feels like my brain is leaking down the back of my head and neck. It makes me nauseated and very fatigued. I don’t know why I feel such severe side effects at times and not others. It’s frustrating, but I’m going to try a new medicine called Ubrelvy.
  7. I can’t wear my hair in a pony tail or put anything on my head –– This is not a huge deal, but when I have a migraine, I can’t wear my hair up or wear a buff (to help dry my curls) or have anything touching my head at all. My scalp is so sensitive that even water in the shower can hurt.
  8. I can’t sing — This might seem odd, but I love to sing. I sing all day long, which seems to really aggravate my kids. But when I’m sick with a migraine, it hurts so badly to sing, which makes me hard for me to put Eli to bed because he requests lots of songs. If I try to sing, the throbbing becomes way worse.
  9. I can’t always be there for my kids — Sometimes, I’m just down and out. I can’t get out of bed, which leaves my husband to pick up the slack. I hate not being able to play with them or spend time with them, especially because they don’t always understand why I can’t. It’s hard, and I have a lot of guilt about it, but it is what it is.
  10. I get migraine “hangovers” the next day — After a migraine, I feel like crap. I’m very fatigued, I can be irritable and each of my limbs feels like it weighs 700 pounds. Sometimes, my brain feels foggy, too.
  11. The medicine can be expensive — The new medicine that I’m going to start costs $1,000 per month. That’s not a typo. I have a savings card, but I’m not sure how much that will actually knock down the price. The thing about this drug is that there are no side effects — I was able to try some samples a couple months ago and I didn’t experience a single side effect and it worked quickly. I’m looking forward to using them, and hopefully, the savings card will help a lot.

If you suffer from chronic migraine, that means you can have 15 or more migraines in a month. That’s a lot of pain and time missed with family and friends. It’s not fun. Thankfully, after I had kids my migraines got a little better but they can still wreak havoc on my life. And one thing I didn’t mention — and probably the most important — is that having so many migraines adversely affects my mental health, and so many people don’t think they are related.

If you know someone struggling with migraines, ask how you can help and don’t ever judge!

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