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anxiety disorder

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I started a new preventive migraine medication about a week and a half ago (Topamax), and it has not gone smoothly. It’s an older pill, with a lot of side effects. I’ve been on it quite a few times before but have never experienced this many effects.

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First, there’s how carbonated beverages tasting like crap. Fine, who really cares? Then there’s indigestion – another slight annoyance. Then my eye constantly twitching. Also, I can’t sweat when my body temperature rises (say, when I’m doing karate) so I have to take lots of breaks and drink A LOT of water. More annoying. There’s major fatigue and tiredness (I took five naps in one day). Brain fog. Memory loss. My thinking is very slowed. Diarrhea. Oh, and there’s a weird taste in my mouth. Fine.

None of this would matter to me if I hadn’t just have started karate. I started training because I thought it was cool watching my kids. I wanted it for me. I was pumped. I wanted to be physically fit. Then I had to switch to this medicine. I lost my confidence. How was I supposed to tell my instructors — hey I can’t sweat so I have to leave the floor to suck down water every five seconds on top of hey I have retrograde amnesia and also I can’t retain a lot of new information so I need to do private lessons, too. I got issues. And those issues are only mine, I’m sure. But I’ve always hated having them. Some of of exclusion keeping me from being like the others. Keeping me from being healthy — that’s what it is. I’ve always hated hearing, “OMG, you’re so unhealthy. You take too many pills. You’re too young to be this way, etc. “

Cringe.

But I tried to keep my instructors up to date. I tried explaining the best I could. I tried to hang in there until I couldn’t possible go any more. I took my water breaks then got back in there. I wanted to more, yes. But I did enough, and sometimes, that’s what it takes.

That’s what it took yesterday when I earned my first stripe on my white belt. It was not given. It was earned, and I truly feel that way. I have loved getting every bruise on my body. I’ve loved every self-defense move. I’ve loved practicing every round kick (which I’ll continue to do). This is for me. And even though my kids were there (supposed) to be watching me, this was for me. I’m proud of me. But tell you the truth, I could have done without them saying, “Mommy is soooo slow.” or “Mommy is not doing that right.”

I did it the way I was taught and I did it to the best of my abilities. And I could totally kick both their asses, should it come to that. Totally kidding.

Another cool thing is that I see and feel my body changing. I’m getting stronger. I’m trying to condition every day — not to lose weight — but to make my training easier. It’s just going to get harder from here. I like the way it’s changing….how I’m changing. Physically and mentally.

If I can do all that I’m doing plus get a stripe while taking the medication from hell, my depressed, anxious, column-writing, retrograde amnesiac, migraine-having, no-sweating, no-Diet Coke-tasting ass can do anything.

Bring it.

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Limitations

by Heather Loeb

Before I realized I was out of survival mode and truly in recovery, I would always say to myself, “I have limitations.” And it was true, and maybe still is, but in the past few days I’ve noticed that I have moved past certain “limitations.” Some of physical barriers.

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For instance, I had a private karate lesson with my karate instructor on Friday. We have a test for a stripe next week, and I wasn’t feeling confident. It’s hard for me to keep up in class because there are so many people in there — beginners and advanced — and I just wanted to make sure I had everything down. I practiced my kicks and the mitt drills. I felt strong, and I’m truly looking forward to the test.

When I got home, I practiced my kicks on my punching bag, but it’s a little awkward because of it’s shape. I really have to pull my kicks high to strike. I digress. After that I wanted to work on my push-ups. I have very little upper body strength, only able to do push-ups on my knees. And barely able to do that. So I did that. And I did some against the wall. I figure I need to be doing push-ups every single day until I can do them on my toes.

The old, depressed Heather would never have cared about that, never would’ve challenged herself in anyway. So after the wall push-ups, I did some light weight lifting.

I then worked on my abs. Lately my abs have been on fire. I put my hands under my back and bottom and lifted my legs, I did the Superman pose, and finally, I wanted to try a sit up. I stalled awhile before attempting it because it has been years since I’d even tried. It was a daunting task. And I have limitations, right?

I tucked my feet under the couch and breathed in. I exhaled, pulled my ab muscles in, coming all the way up to my knees.

I DID IT!

I tried to do it again, but no dice. That’s okay. You gotta start somewhere. Really, you just gotta start. And that’s what I have done. I’m super excited to see where this takes me.

I love karate, and I feel stronger every class. Actually, I felt beat down after the last class, and I have the bruises to prove it, but I’m better than the class before.

I hate to quote Kanye, but I’m really harder, better, faster, stronger. One sit up, one lap, one round kick at a time.

Limitations can’t hold you back if you don’t let them.

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Just a few years ago I couldn’t get out of bed. I was consumed with depression and anxiety. I lied to my husband about being sick or having a migraine so he would take the kids to preschool for me. I couldn’t take regular showers or brush my teeth. I spent as much as my energy as I could on the kids, leaving me running on fumes.

I abused my anxiety medication, taking six to seven pills instead of the one or two I was prescribed. I binged on unhealthy foods, seeking comfort where I could. But it wasn’t real, just temporary, and after the binge was over I felt nothing but guilt and shame.

I was suicidal, and at one point, had a plan to die by suicide. The pain was relentless. My own brain betrayed me, telling me I should die, that I wasn’t worthy, and I would never feel better. My psychiatrist told me I had treatment-resistant depression and said most medications wouldn’t work. He didn’t offer any plans, solutions or other therapies. I didn’t think I would live to see my children grow up.

It was bad.

I was hospitalized in 2019 for all the aforementioned symptoms. I was there for only six weeks, but it still felt life-changing. I got on different meds, I did intensive counseling, I took classes on how to cope with my many diagnoses. I also started electroconvulsive therapy, which probably saved my life.

After I left the hospital it felt like I was walking on eggshells…or a minefield. I quickly realized that I would never be “cured.” This would be a lifelong journey for me, and that’s okay. I’ve accepted that.

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Fast forward a few years and here I am with my blog, with a column in the local newspaper, and I’m the Communications Manager for NAMI Greater Corpus Christi. I eat, sleep and breathe mental health, but in a good way. I share my story and hopefully help others who can’t be so open about their struggles.

I’ve become stronger. Just the fact that I’m able to look outside myself and try to do something helpful is a sign that I’m on the road to recovery. A long, hard road but one I’ve started on nonetheless.

What really strikes me as amazing is that I tried out a karate class. Last summer my kids started karate at Life Martial Arts, and I immediately fell in love with it. I toyed around with the idea of taking a class myself, but was too scared. Two days ago I did my first class and fell in love. Tonight’s class was harder but rewarding. I didn’t want to start karate as a way to lose weight or exercise, but I want my body to be stronger. I want to accept it as is right this minute, and I want to honor it. I also want self-discipline. Discipline is a huge part of karate (as I’ve learned through my kids’ classes), and something that has always eluded me.

When I came home from class tonight I was beaming. I know I’ve only had two classes, but that’s not the point. This means that I am physically and mentally healthy enough to do something that was completely healthy and fulfilling. I’m doing something for my self (#selfcare). I can still do hard things even though I’m 38 (still youngish).

I can do hard things.

I can put in the work to be healthy.

I can be in recovery from depression (and all the other disorders).

I can be happy.

There will be bad days, even in recovery, but look what I’ve already been through. I’ve come so far, and I’m so close to accepting myself and treating myself well.

But there will be good days, too. Like today.

Today my legs are jello after karate class, and my abs on fire. But I wouldn’t change it for the world.

It’s nothing in comparison to the joy in my heart.

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Vacation Heather

by Heather Loeb

Last week my husband and I took a trip to Turks and Caicos to celebrate our 10-year anniversary. It was totally amazing; I can’t wait to go back. It was definitely hard to readjust to our routine and structure today, but we did it.

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But I can’t stop thinking about the vacation. I’m not trying to relive it; I’m just going over how different I was there. I packed a different dress to wear ever day, heels and sandals. I did my hair and my makeup, something I rarely do in every day life. I was put together, chic, and most importantly, I was confident. So confident. I wore a different swimsuit every day, too. Including a two-piece. I didn’t use a coverup either, something I always do around pools/beaches.

I just felt so fantastic. I even drank a few daiquiris, something that rarely happens also. I remember telling David that Vacation Heather was fun, confident and relaxed. He replied that he loved Vacation Heather.

So I’ve been wondering — why can’t I be that version of myself here at home? Surely there’s a way to merge the two. I realize that it can’t be exactly the same. After all, I’m taking care of two children and volunteering for NAMI Greater Corpus Christi. I don’t get paid, but it IS work. Then there’s bills, taking the kids to karate and waking up at 5 a.m. just to list a few.

My husband also mentioned that when he comes home, I’m already in my sweats and he doesn’t get to see me in “real clothes.” I have to admit, that’s my favorite time of day: coming home after picking up the kids/going to karate and putting on my comfortable PJs or lounge wear. I have to balance this love with David’s need to see me in real clothes. I don’t want that to sound like he’s bossing me around or anything. I think it’s good that he sees me in nice clothes; I certainly like him when he dresses nicely.

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So today I wore a yellow blouse, jeans and nice sandals. I put a beautiful headband on, and I feel good…confident. But adding Vacation Heather is more than wearing makeup and dresses everyday — I need to alter my attitude. I need to relax, especially when it comes to the kids. I want to yell less and be more laid back. My depression and anxiety don’t make that easy, but there’s room to loosen the reins on everything, I think.

I will make an effort to look nice. I’ll put on a dress because it makes me feel light and sexy. I have to remember that I’m a human being, not just a mom in the trenches of parenthood. I’m more than sweatpants and PJs. I deserve to feel good about myself and to show off my personality. I’m more than my depression and anxiety. Sometimes I feel like I eat, breathe and sleep mental health and I get caught up in my conditions, treating them like a ball and chain I’m lugging around, but that has to stop.

From now on, I’m going to be me — the real me who celebrates herself, no matter if she’s on a tropical island or in Corpus Christi.

And I can’t wait to see it.

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Don’t Worry About It

by Heather Loeb

I hear these words far too much, and I’m here to tell you that if you have anxiety (multiple forms), you can’t help but worry.

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For example, I noticed that my left breast had a red spot and I could feel a tiny knot/lump. It hurt a little. This has happened before — I had to get a mammogram then a biopsy. Luckily, it was benign, but the radiologist told me that I should start getting mammograms because my breast tissue is so dense.

Looking back, it wasn’t a huge deal. Was I worried? Yes. Did I ruminate? Oh, yeah. And now that it’s happening again, it seems like my anxiety disorder is in overdrive. Since discovering it, I’ve Googled everything from “dense breast lump” to “lump in breast” and “breast cancer lump.”

I feel like it’s normal for me to do that, but then my brain takes it to another level. I start to think about getting cancer, and losing my hair, and radiation, and whether I’ll be able to work as I’ve been doing. I texted the picture of the red spot to a friend and kept repeating myself, “It’s probably nothing. It’ll be like last time, right?” Then I awaited her reply, searching for assurance. I did the same to another friend.

I realize that it is probably nothing, that I’m overreacting. I also know that my brain is an asshole, always exploring the worst case scenarios. This is what I hate about anxiety. It’s relentless. And what also sucks is knowing that there are people out there who can really tuck an issue away and worry about it later. Or not at all.

It’s important to know a couple of things: when someone has an anxiety disorder, they can’t control it. Also, it takes a physical toll.

The Mayo Clinic reports the following symptoms:

  • Persistent worrying or anxiety about a number of areas that are out of proportion to the impact of the events
  • Overthinking plans and solutions to all possible worst-case outcomes
  • Perceiving situations and events as threatening, even when they aren’t
  • Difficulty handling uncertainty
  • Indecisiveness and fear of making the wrong decision
  • Inability to set aside or let go of a worry
  • Inability to relax, feeling restless, and feeling keyed up or on edge
  • Difficulty concentrating, or the feeling that your mind “goes blank”

Physical signs and symptoms may include:

  • Fatigue
  • Trouble sleeping
  • Muscle tension or muscle aches
  • Trembling, feeling twitchy
  • Nervousness or being easily startled
  • Sweating
  • Nausea, diarrhea or irritable bowel syndrome
  • Irritability

Some people think that anxiety is “all in our heads,” but for me, and millions of others, it affects our everyday life and relationship to others. It’s difficult to deal with. It’s difficult to control with medicine. Believe me, I’ve tried. I even got addicted to Klonopin a few years ago. It’s pretty easy to do.

The Mayo Clinic also reports the following:

Generalized anxiety disorder often occurs along with other mental health problems, which can make diagnosis and treatment more challenging. Some mental health disorders that commonly occur with generalized anxiety disorder include:

  • Phobias
  • Panic disorder
  • Post-traumatic stress disorder (PTSD)
  • Obsessive-compulsive disorder (OCD)
  • Depression
  • Suicidal thoughts or suicide
  • Substance abuse

Unfortunately it’s not something that goes away. Learning healthy coping skills helps, as well as therapy. It can be manageable, but it’s still a major bummer to deal with it. To say the least.

My whole point during this rant is that I can’t control my anxiety. I try my best, I take medicine and I go to therapy but it’s still there. It’s like my brain just wont turn off. It’s non-stop intrusive thoughts, and I rarely get breaks. It’s just fucking dark in here, y’all.

I know there are others like me, and I’d just like to say that you’re not alone. I urge you to seek help, such as support groups and therapy.

I’d like to hear from you guys and ask what you do to manage your anxiety?

That’s it for now. Thanks for listening. Stay in the light.

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My Son’s Diagnosis

by Heather Loeb

In the past week my son has hit me twice and bitten me, bringing on a dark purple bruise on my arm. All were done during a meltdown. He screams and cries, indignant and out of control. The slightest thing can set him off.

Combined with his hyperactivity and lack of focus, I knew he had ADHD long before a psychologist recently diagnosed him last week.

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The doctor said Eli’s ADHD isn’t severe, just a “mild case.” It doesn’t feel mild, to me or Eli’s teacher, who has been so supportive through this journey. She told my husband and I that we should consider getting him tested late last year. I had already seen him in somewhat of a classroom setting and he couldn’t sit still. He didn’t look anyone in the eye because he was so distracted by the toys, books and desks.

I haven’t observed him in his classroom, so I don’t experience the worst of his hyperactivity. But I have witnessed his impulse control many, many times. I’ve been hit, slapped, screamed at and more. He blows in my face because he knows it will annoy me, but he apologizes for all of this behavior soon after he calms down.

I realize he can’t control it. He doesn’t mean to do it; he just needs to figure out how to control his emotions, which is hard for a 5-year-old, nevertheless one with ADHD.

It would be easy to take all of this personally. When his teacher first brought ADHD up, I felt terribly guilty. I was so sure Eli was experiencing this because of my diagnoses — two types of depression, anxiety and a personality disorder. I went home and googled it, sure enough ADHD kids often have mothers with mood disorders. Obviously I don’t want him to struggle with this. I’ve struggled almost my whole life, and it’s no picnic.

I know it’s not my fault, but it’s hard to shake the guilt and shame that all moms experience.

The only thing to do is learn everything I can, modify our parenting, consult experts and just accept it.

I have to accept it. I have to accept that both my children may have inherited the illnesses I have. It’s not my fault, it’s not my fault, it’s not my fault. It’s not anybody’s fault.

I’ll do everything in my power to learn more and help him.

But I need to remember: In order to help him I have to work on myself, make sure I’m not pouring from an empty cup. I have to provide structure and routine. I have to set boundaries and actually stick to them.

I’m in recovery when it comes to my mental illnesses. Recovery doesn’t mean I have to be perfect, just that I’m always trying to grow.

I imagine Eli and I will grow together, be stronger because of the paths we’ll walk.

I know in my heart that he’s still the same sweet, loving little boy he was before the diagnosis. He just has his moments.

Lord knows I have mine.

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Last week I did a ketamine treatment, the first in years. Before I was hospitalized at The Menninger Clinic in 2019 for depression and anxiety, I’d done about two or three but never felt better after doing them.

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I tried again last week because it’s easier for me to do ketamine treatments than ECT treatments, which I’ve been doing since 2019. Those are a pain; I have to drive 2.5 hours to San Antonio, undergo the procedure (which includes anesthesia) and then have my husband drive back home while I battled an inevitable migraine. I’m usually out of it for the rest of the day and some of the next.

I haven’t had an ECT in months, the most I’ve ever gone since being hospitalized, but I started recognizing some of the signs that I might need one. Enter ketamine treatment.

I was very nervous when I got there and as they begin to set up the infusion and IV. I was scared that I would feel out of control and that I’d be overwhelmed. I was sweating. The nurse could tell I was nervous so she stayed with me for a few minutes. That’s all it took, really. I started to feel the warm flush feeling of the medicine entering my body and I started to panic. It was just so overwhelming, so I asked the nurse to slow it down, which she did. After that, it was a gradual high and I didn’t feel out of my mind. I started laughing, saying “wow, I’m so fucked up.” She left the room so I could vibe.

Because the infusion was going slower, I was able to realize that I was “high” and able to enjoy it. I did inventory on my emotions and felt hope that this would help improve my mood. I wasn’t sleepy or tired, but I could tell my eyelids were at half mast (plus I took a picture).

I felt a feeling of euphoria and thanked God for all I was thankful for. I relaxed and explored any emotion that came up, which is cool because normally I swallow my emotions, never giving them any time or space.

Finally, as I did become sleepy, time was up. They took the IV out. They let me “come to” after about 10 minutes. I was a little tired for the rest of the day but wasn’t totally useless, which is good. That’s how the ECTs leave me.

I felt like the treatment worked right away but thought that maybe it was just a lingering feeling of euphoria. It has been several days now and I still have that feeling — that I feel good. That I’m thankful. And like it’s going to be okay. I’m so pleased with how it went and I’ll be doing five more treatments to do.

I’m just so thankful that I didn’t have to get an ECT. I hate anesthesia and memory loss. It’s just too much to deal with, so I’m really hoping I can keep up with ketamine treatments instead.

Here’s hoping.

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Good Vibes

by Heather Loeb
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It has been 14 weeks since my last ECT (electroconvulsive therapy), a milestone for sure. That’s the longest I’ve been able to go since 2019, after leaving a psychiatric hospital for depression and anxiety.

It makes me so happy because, frankly, I hate them. I developed a phobia to anesthesia last year and have panic attacks before treatment. For those who don’t know, ECT entails going under anesthesia then doctors induce a seizure. It’s usually a short seizure and they give me a muscle relaxant so I’m not thrashing around. The seizure sort of resets my brain. Doctors aren’t sure why or how exactly it works, but it’s very beneficial to people like me who have treatment-resistant depression.

I thought since it has been awhile since my last treatment that my memory would start coming back, but there are still huge chunks of my memory I can’t recall. It’s common for people to experience retrograde amnesia, but usually memories return.

Not only can I not remember things from the past but also it affects my short-term memory. I can’t always retain new information. It’s especially hard to follow recipes or instructions on how to do something. Now I need assistance from my husband when I’m cooking.

It’s also embarrassing.

I’ll meet someone and not remember we met. Or I’ve forgotten people who I knew. People come up to me all the time and ask how David is or the kids, and most of the time I just can’t place them so I try to hide it. Hopefully they can’t see it in my face.

Still, even with the memory loss, it’s one million times better than being where I was. I was so lost and unhealthy, relying on binge eating, abusing my medication, cutting and shopping to distract me from my pain. I was suicidal all the time. Somehow I was able to take care of the kids, but my health suffered greatly. The kids sucked up everything I had. I don’t regret going to the mental hospital at all.

I wrote about ECT and losing my memory for a mental health site, The Mighty, and some people — a lot of people — thought it was so horrible that I was risking my memories. They couldn’t comprehend it, but one of the best things about my memory loss is that I don’t remember all the ugly, dark parts of my illness before I went to the hospital. It’s a blessing, actually. What I do remember is so awful and sad. There’s no part of me that wants to relive that at all.

So while my memory (what’s left of it) is terrible and it can be embarrassing, I’m so fucking grateful for where I am. For my support system, all my friends and family members who stepped up and completely support me. For being able to find joy in the little things. For being able to enjoy watching my kids grow up. For laughing until tears come to my eyes. For the growth that I’ve seen in the past three years. I’m just so grateful. I’d do it all again if I had to in order to feel as good as I’m feeling now.

I know there’s always a possibility of a depressive episode recurring, but that’s why I’m doing the difficult work of confronting my demons and putting into place healthy habits. I have to walk a fine line in order to be healthy, and sometimes that can be annoying, but it’s so worth it.

For anyone struggling with their mental health, I see you. I pray you don’t give up, and I have to tell you that it gets better. It gets sooo good.

There’s great divinity in finding the light where it is dark. And I hope you find the light.

You can do it. I clawed my way back from hell, and I’ll keep fighting to stay where I am, every single day.

Thank you to all my loved ones (and even strangers) who have been rooting me on all this time. It’s a beautiful thing to receive that kind of support.

And I love you all.

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My Dead Body

by Heather Loeb

NOTE: This post was originally written last year.
TW: suicide, suicidal ideation, depression, self harm

Last month I was asked to speak at State Rep. Todd Hunter’s Suicide Prevention Symposium. I talked about the many times I’ve been suicidal, and I realized I’ve never told the story here. While it is painful at times to retell, I think it’s so important to talk about because so many people suffer in silence. The stats on suicide have gone up, and there’s no doubt in my mind that those numbers will double, maybe even triple, because of the pandemic. If you are struggling with suicidal ideation, please seek help whether it’s your doctor, a trusted friend or the National Suicide Prevention Lifeline at 1-800-273-8255. You are not alone.

Here is my story.

I was alone at my parents’ house, and my depression was out of control at the time. My parents had taken my kids to their lake house about 90 minutes away. I remember fighting on the phone with my husband, I don’t know what about. I hung up with him and I felt out of control, like my insides were trying to jump out of my body. I was pacing, sobbing and didn’t know what to do. I started to shake, sweat and suddenly I all I felt was pain. My brain was telling me to die by suicide* and I calculated how to die — I would overdose on pain pills that I knew were in my parents’ bathroom.

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I went over and over my plan, and I started to shake harder. I had to sit. I didn’t want to die, but my brain was telling me everything would be better if I did. And my family would be better off, too. I thought of my kids and the guilt overwhelmed me. Then I thought about my mother coming home from the lake house and finding my dead body. My dead body. Those words gave me the chills, and I cried harder.

I called my mom in hysterics. She tried her best to calm me down. I hung up with her and texted my best friend, who urged me to go to the nearest emergency room. I was really scared I would die, so I went.

When I got there, I whispered, “I’m suicidal.” And the tears kept coming. A nurse took me to a room, and asked me routine questions about my health, then my mental health. I saw a doctor, although I don’t remember our conversation. They left me in the room for almost an hour, waiting on transport to an acute psychiatric facility.

The men in the ambulance didn’t talk to me the entire ride. They joked and laughed from the front of the ambulance and then pushed me on a stretcher into the building. When I got inside, they asked me to change clothes into scrubs they provided, asked me questions about my plan to die and mental health history. I was taken to a room and told to go to sleep, it was late then. I had a roommate who I didn’t meet until the next morning.

I can’t say I received the help I needed while I was there; the doctor, a man, was rude and condescending and told me I couldn’t go home until he talked to my husband (who was in Corpus Christi at the time). Once he talked to David, he said I could go. The whole experience was humiliating, and I hope to never repeat it.

I don’t mean to discourage those who are suffering to go an emergency room — please do so if you are in immediate danger of killing yourself. My bad experience doesn’t mean you’ll have one. My point, and I could go on and on, is that the way we treat the mentally ill MUST change.

But I regress. I’d like to say that was the last time I was suicidal, but it was not. When it does happen, I know to text my best friend, to call the Lifeline and to reach out to my husband. Most of the time, I’m about to tell myself that those feelings are temporary, and that they will pass, as painful as it us at that moment.

Being suicidal is the scariest thing I’ve ever gone through — I feel severe pain, I wrestle with the idea that I’d be leaving my kids and family, then I feel extreme guilt. The guilt just makes me feel more out on control. It’s awful. Let me be clear: I hope to never hurt my children, family and friends because I’ve killed myself. I love them more than anything, but when I become suicidal, I obviously am not thinking clearly. The only thing I truly feel is to end the pain. I don’t even want to die, but I do so long to end the pain.

That’s why I can’t stand when people say that those who die by suicide are selfish. They weren’t being selfish; they just wanted their anguish and pain to go away. And it’s completely understandable, having been in that position myself.

Again, that’s why we need to talk about this and expel the myths and misconceptions. We need to be able to discuss suicide like it’s any other topic, because too many are dying. What’s scary to me is that it’s the 10th leading cause of death in the U.S. The CDC reports that someone dies by suicide ever 12 minutes. Even scarier is that more than half — 54 percent — of people who die by suicide have no known history of a mental disorder. This means that a lot of people are struggling, not disclosing they are struggling and killing themselves without reaching out. It comes from out of the blue. How incredibly tragic and painful.

So, let’s end the cycle. Let’s be open about mental illness and suicide and resist the taboo and social constraints that are clearly killing people. Because it’s only going to get worse, thanks to COVID-19 and the lasting effects of the virus.

It is beyond tragic when we lost someone to suicide; I imagine someone in crisis, feeling overwhelmed and in pain. It hurts me to think that one of their last thoughts may have been, “I’m alone. I am worthless. I’m better off dead.” And that they die not knowing how special and needed they are in this world. It’s painful to think about, but that’s what we must do in order to change things.

And we must change things.

If you are in crisis, please reach out. If someone reaches out to you, please be open and supportive. Offer to drive them to the emergency room, sit with them or give them the National Suicide Prevention Lifeline. Do your part. Show compassion. Give love and support.

That’s all I got.

*Instead of saying, “committed suicide,” please say, “die by suicide.” There’s a lot of judgement when you use words like commit and it implies that they are doing something wrong (like committing a sin) when really they’re sick and need medical attention.

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This past week went by so fast. I can’t believe Thanksgiving is coming up. but I’m excited. I’m even more excited to go get a Hanukkah bush (Christmas tree) with the kids and decorate the house. This is my favorite time of the year, and I’m really enjoying the cooler weather and holiday vibes.

In other news, I’ve been working on a new website for the past year or so and it’s finally going live this coming week. It looks good; a lot better than my plain blog now. I’ll announce when it goes live so you guys can take a look.

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I’ve been struggling lately, but I’m confident that I can push through without getting an ECT. We’ll see. I’m really trying hard to heal right now. I’m examining my core beliefs and trying to shed that person I became to survive to become a stronger person. A new, better version of myself.

I hope you guys have a great Thanksgiving. Stay safe and healthy, and as always, stay in the light.

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