The reality is it isn’t easy. By the time you’re actually approved for disability you’re usually destitute. There’s no other way to put it. Even if you get a large sum of back pay, you’ve exhausted your savings and built up so many medical bills and other expenses that by the time you see your check, it’s all but spent. Don’t get me wrong, I’m extremely grateful to be able to sustain myself with what I receive from social security. And to know that I can also write on the side and teach students in my spare time to keep myself busy when I’m feeling up to it makes me happy. But none of these things create a windfall for me. I’m scraping by every month and barely surviving. If it weren’t for my mosque supporting me with zakat (charity), and help from my ex-husband occasionally, I wouldn’t make it. The thing is I used to have money. When I was married, things were fine. Better than fine, actually. But getting sick ruined my finances. And I haven’t been able to get myself together ever since. It’s like I’m treading water every month. I’ve often mentioned my issues with eating and my disordered patterns, but frankly, sometimes I just don’t have the money for groceries. So I don’t eat, simple as that. Everybody I know on disability is in a similar position. No matter how much they receive. They all tell me that their initial savings went quickly and they have trouble managing on what they receive each month. It’s really challenging. But nevertheless, I am still grateful for the fact that I have health insurance and some semblance of a paycheck. Things will get better. They always do. And my writing has already been helping me so much lately. So I can’t complain. I just wish more people were understanding of my situation. It’s hard struggling in silence. I feel like I’m alone in what I’m going through, until I remember those dealing with the same situation. That helps me not dwell on my problems and feel so sad. I’m eagerly awaiting the day when I don’t have to decide between paying a bill and buying a meal for the day. Then I’ll be able to focus solely on my emotional and mental well-being, and spending more time with my kids. It’s coming, I can feel it… 🙂
I began thinking about applying for disability in 2012. I had lost my job after a bad manic episode. At that time my mom was battling inflammatory breast cancer as well, and my children had just returned from a four year stay in Senegal with their father’s family. Stressed out doesn’t even come close to my mental state at the time. I simply couldn’t work under those conditions. I couldn’t even get off my couch or take care of myself in any capacity. I had no concept of functional self-care in any sense and I was barely lucid. After my mom passed away in early 2013, I became completely unstable. I went into a psychotic depression, sleeping off and on for several months. I was paranoid and delusional. I lashed out at those around me, accusing them of the worst things imaginable. My behavior was almost unrecognizable, and yet no one suggested I go to the hospital or even to my psychiatrist to get evaluated. They just lectured me to get myself together and stop acting out. Days merged into nights and I never knew what time it was or even the month. I developed bronchitis and then pneumonia but I still never left my house. I was too psychologically unwell. My primary care doctor was able to get antibiotics to my house as she knew I’d never make it to the emergency room for treatment.
At some point that winter, I finally decided to contact an attorney to help me file the paperwork for my disability claim because I knew I couldn’t complete it on my own. I remember telling the clerk I felt so poorly that if someone offered me a salary to simply staple papers all day, I’d have to decline because I didn’t have the energy to operate the stapler. I just couldn’t do anything productive. Even breathing was painful. I wanted to die. It took me 2 long years before I was able to get a hearing with a disability judge. My case was denied twice before that time. It was decided that I was sick, but not sick enough for disability. So I wanted to plead my case in front of a judge to see what would happen. On the day of my hearing, I was extremely nervous. Someone offered me a ride to the courthouse, because by this time I had stopped driving. I didn’t live on my own anymore either; I was staying with a family friend until I got back on my feet. Losing my mom took everything out of me. I was a shell of a person. Going to the courthouse was scarier than I thought it would be. My social anxiety was raging that day.
When it was my turn to go into the courtroom, my knees turned to jelly. I thought I was going to be sick. My attorney escorted me into the large room and showed me to the table where I would sit for the next hour. There were several people in the room already: The judge, the court reporter, a spectator/another disability lawyer, someone reviewing my case, and then my attorney. It was overwhelming and frightening. I felt like I was on display and I immediately wanted to run from the room screaming. But I couldn’t. I felt trapped. I sat at the table and shakily poured myself a glass of water. But I was too nervous to drink it. My attorney sat at an adjacent table. The judge introduced herself and explained why we were all there. She tried to put me at ease but it only made my anxiety worse. She asked me to begin telling my story and explain how I had come to be hampered by my mental illness. She wanted me to recount what had gone on for the last two years. But what scared me was that she had my medical records in front of her. How could I possibly remember all of that? I started talking and began stuttering right away. I do that when I’m nervous. Everybody in the room looked at me, puzzled. That made me more anxious and I continued stammering. I couldn’t stop. It was hard for me to put together a coherent sentence. My attorney looked so confused. Just a few minutes ago I was speaking clearly and without stuttering. I could tell she didn’t know what had happened and if I was faking my stutter. I was so embarrassed, but I had to keep talking. It was excruciating. My face was so hot, I thought it would explode. It felt like I was talking for hours. When I was done, the judge asked me a bunch of questions. I felt defensive and angry. If my medical history was right there, why was I being cross examined? It made me feel like a criminal. I was sad and humiliated. Everybody in the room could hear my most personal medical details; the worst parts of my disorder and what it had done to me. I’ve never been so ashamed in my life. I knew the judge wasn’t trying to hurt me and yet I felt demoralized by her pointed questions. All this in order to determine if my mental illness was in fact debilitating and disabling. This wasn’t fun at all. When it was finally over, she concluded that my medical records supported what I had testified to and that she would make a ruling in about 6 weeks. My attorney said that was a positive sign that things had gone in our favor.
In the end, I was declared fully disabled and entitled to benefits. But the point of my story is that when I hear people speak disparagingly about those receiving help from the state, it traumatizes me all over again. That was one of the worst experiences of my life. It was bad enough to have to live like that for those years. In a fog of complete mental instability and confusion. But then to have to recount it in a room full of people as though I was on trial was something that hurt in a way I can’t explain. I don’t mind being disabled by my mental illness. But when I think about that day, I hate my disorder and what it’s done to my life. I hate that I had to tell a group of people about my illness in that way because it isn’t readily visible and obvious. That’s what hurts and shames me. And that’s what I resent about the disability process.
I was feeling vulnerable. I was feeling less than pretty. I was feeling old and worn, discarded by society somehow. I needed validation in that moment. I needed acceptance and maybe a bit of ego stroking. I’m human too, after all. But I was rebuffed. I was brushed aside like my feelings don’t even matter. That really hurt. I didn’t say anything though. I never do in those situations. I don’t feel comfortable expressing when I’m feeling like I need more from people. I’m embarrassed to be so complicated. And it hurts that being ignored makes me feel so deeply wounded and unaccepted. I hate this about myself. It makes me feel so exposed and raw. So easily able to be dragged over the coals of indifference at a moments notice. So I just sat there, in the dark, in my house. And pretended everything was fine. I laughed and joked like I wasn’t dying inside. As if I didn’t want to retreat to my inner most feelings cave and never come out. I willed myself not to simply disappear. I’m still fighting the urge. Part of me wants to write and get my feelings out, and part of me wants to run and hide in a dark corner where no one can ever find me. I want to hide in shame because I hate that I need validation from others at times. I desperately want this to change. And quickly so I never have to feel this way again. So I’m never having to force myself not to walk away from the world when I don’t get what I need. Being vulnerable like this feels like a curse.
People say the opposite of addiction is connection. I struggle with loneliness and a feeling of not being connected a lot of the time. I also have what is known as an addictive personality. So it doesn’t come as a surprise to me that I would have developed addiction issues and alcohol dependence at a point during my life. I talk about my mental health issues every day both online and in real life. But my emotional issues I don’t address as often. I believe those issues are at the root of why I struggled with addiction when I did. And why I have an addictive personality in general. It’s why I have such a deep feeling of loneliness even when I’m in a crowded room, and why even though I have such a tight-knit, loving family, I often feel starved for attention.
I remember times back when I was deeply entrenched in my alcohol dependence or stimulant addiction. I used because I was so very lonely and sad. I reached for the bottle and/or pills back then to stave off those feelings of soul crushing loneliness. I often drank or used when I was alone. That’s the thing about my addiction. I wasn’t as much a social user as I was a lonely user. That makes me sad when I think about it; even though I’m better now. I’m sad for that person and for who she was. And even when I partied with other people, I used to excess. I drank to a point of alcohol poisoning many times in my life. I’m not proud of that. And I used pills to a point where I was scared my heart would stop or I’d have a stroke. Repeatedly. But that didn’t stop me from using. I kept doing it over and over again, for many years. I needed to numb my pain. I still do in fact. I always will, I just have found healthy outlets for my needs. And I have learned how to control my appetite for those feelings. But it hasn’t been easy.
I spend time with my friends when I can, and I talk about my feelings with those who understand. Though that is a slippery slope in and of itself. Talking about addiction too much can make me want to use again, so I have to be careful. Being around people who use or used to is hard. Because I never know how well they are and if they will backslide. And I’m always one slip away from falling into addiction again. Alcohol was easy for me to overcome. I could fall back on my religion for help with my drinking habits. There was simply no justification for me to drink anymore and I really didn’t need it; even when I was manic. So I quit cold turkey. But the pills were much harder. I absolutely needed them for my medical condition of excessive daytime sleepiness and adhd. If I don’t take them I fall into an almost narcoleptic like sleep. It happens in the spring mostly but also it’s a function of my bipolar and depression issues. So I almost can’t escape using stimulants. My neurologist practically insists on me taking them, even though he knows I have bipolar disorder. So I have had to muscle through my addiction with them. Thankfully, I overcame it, mostly on my own. I’m proud and grateful for the work I’ve done, knowing that it came easier to me than for a lot of people. For that, I give thanks to Allah and I say many prayers of gratitude.
My loneliness comes and goes. But as I make more friends, I notice I feel more connected and less alone in the world. I think a part of me will always be lonely. That’s the little girl in me that just feels sad no matter what. I accept that. It’s just a part of who I am. Writing this has helped. And meeting new people online everyday has also been a blessing. I do believe that the opposite of addiction is connection. I am working hard at staying connected and staying addiction-free for the rest of my life. As I said the other day, I love my life now. I intend to keep it that way.
Hi, how are you? How have you been? I’ll admit I’m a little nervous writing to you because I don’t want you to think I’m asking to see you. And I don’t want you to think about me and decide to visit. I’m just not ready to be around you. But I did want to check in with you since you’ve been relatively quiet lately. If you recall, it’s been about six months since we spoke. Well formally anyway. I see your posts online from time to time but I never comment. I think we were last together at the hospital, right? That particular stay was a doozy! I hope I never go back. Remember that one girl who kept attacking everybody and calling us names? That was so wild.
So Ziprasidone and I are pretty friendly these days. I know how you guys feel about him, which is also why I’m staying away. But he’s good for me. I do miss our old friends though. How’s Elevated Mood doing? I hear she might be coming to town soon. I know she always heads this way in the spring for an extended visit. Ooh, maybe she’ll get to see the cherry blossoms this time. Tell her I said ‘hi’ if you talk to her. Out of everybody, I miss her the most. She can be a lot to take, but she doesn’t mean any harm. She just has a ton of energy. We always have fun when we’re with each other. I wouldn’t mind getting together with her for old time’s sake.
Hey, you know who I’ve been thinking about? Impulsivity. Man, we used to get into so much trouble back in the day! I’m so glad I’ve learned to love him from afar. But sometimes I like to reminisce about the things we used to do. If nothing else, to remind me what life used to be like before my health got better. Do you remember when he and I went to get matching tattoos? Goodness, it was like we couldn’t help ourselves. We just had to do it and nothing would deter us. I was shaking so much in the chair from all my nervous energy that the tattoo artist got upset. He said if I couldn’t sit still, he wouldn’t continue. Imp just laughed at me.
Afterwards I felt so ridiculous. And by then, Imp was nowhere to be found, as usual. I was embarrassed I’d let him talk me into getting the tattoo. What bothers me is I’m not even supposed to have those. It’s against my religion. But as soon as Imp started hyping up the idea, I couldn’t say no. And it came up out of the blue, so suddenly too. We didn’t think about the consequences or wonder if we’d regret doing it. This didn’t occur to either of us. All that mattered was getting that ink. To be honest, we’d been hanging out with that guy Compulsion too often back then, and we let him influence our choices. I think both Imp and I are pretty suggestible, if you ask me.
Oh my gosh, do you know what I did the other day? I decided to create a gratitude journal to remind myself of all the good things in my life that I’m grateful for. Oh BP, it’s been such a help. Every day I write about the things that make me happy and what I appreciate. You know they always taught us to do this whenever we’d go to the hospital. Well I finally got around to it. You should try it sometime. You’d love it! And maybe it will give you a better outlook on life.
Guess who I’ve been chatting with lately? Insomnia! Can you believe it? I know we used to hate each other. But we’ve since reconciled and we’re spending almost every night together. We laugh and carry on like two little old ladies. Her jokes about not sleeping are too funny. And she still loves to play pranks on me in the middle of the night, as much as she always did. That Insomnia is such a card! We really have to stop meeting up though, or I’ll get sick again. You know how that goes.
So I have to know, how’s BPD doing these days? Do you see her often? Has she gotten herself together yet? Last I heard she was ruining yet another relationship. I’m sorry to say it but I hope I never interact with her again. She and I do not get along. She makes me so mad, I can’t stand it. And we always bring out the worst in each other. It’s always all or nothing with us. Things are either great or horrible. There is no in between, it’s awful. She’s just not a good influence for me so I try to avoid her at all costs. And if you remember, I had to go to therapy partly because of her. I’m still salty about that. I’m not trying to shift blame or anything, but I can’t help thinking that if I’d never met her, my life would’ve been much less stressful and anxiety ridden.
Speaking of my cousin Anx, did you hear she had a baby? Yeah, she named her OCD. I’m not one to criticize name choices, but OCD? Ok, I have so many questions. Don’t tell my cuz 😉 But why that name? What does it even mean? That kid’s going to have a tough time in life with a name like that. Why OCD? Is it a family name? Is it symbolic in some way? I keep saying it over and over, letting it roll around on my tongue so I can get used to it. It just makes me feel so prickly inside when I say it. But I can’t stop. I’ve repeated it about 500 times now. OCD. OCD. Nope, I still can’t get used to it. It sounds strange in my head, like an echo and a hollow tinny sound all at the same time. Oh wait; I’m getting fixated again. Don’t mind me. You know I do this sometimes. It’s gotten better, but I still slip now and then. My brother Buspirone has been helping me overcome it. He’s been such a blessing. He has his moments, like everybody, but overall I’ve loved having him around. I wish I had told him sooner that I needed his help.
You know, Depression has been on my mind a lot lately. I can’t help thinking about him and wondering if he’ll ever get better. He just seems so lost sometimes. It’s like he lives in his own dark world where no one can reach him. I feel so badly for him. He brings everyone down with his misery, negative outlook and detachment, and he doesn’t even realize it. He’s a good guy, just misunderstood I think.
I guess you heard that Anger and I made up a few weeks ago. We decided to part ways for good, but in doing so I think we’ve reached an understanding. I’m so happy about it. I think he realized how he much he was hurting me and knew why we couldn’t see each other anymore. It’s really for the best. I sometimes get scared that I won’t find anybody else, but I’m trying to be patient. I don’t want to go back to him just because I’m lonely. It’s hard though. Being alone I mean. I can’t shake the fact that I’ll die by myself, with nobody there to notice. That thought bothers me all the time. People say ‘just be positive’. But even in doing so, I haven’t found anybody else that understood me like Ang did. A friend of mine always counsels me to accept things as they are and to look forward to better times. You know that girl Patience? The one everybody always talks about? Well she’s his best friend. I guess that’s why he’s always so calm and collected. Maybe I should meet her someday. She sounds lovely.
I’m not even going to ask about Grandiosity. He annoys me to no end. Always thinking he’s better than everybody and deciding he can do whatever he wants. He seems to think the world revolves around him. That guy is so obnoxious. And he makes me look bad when he’s around. I get sucked into his schemes and plans, and I forget who I am. But his presence is so intoxicating. You know how he is; charismatic and charming…until he completely alienates everybody with his over inflated sense of self. I’m sure I’ll run into him again soon. It’s inevitable.
Oh wow, I just realized this whole letter has been one big gossip session. Hey, maybe we both needed that. Anyway, I hope you’re doing well, BP. I don’t hate you or anything, but I need some space. I hope you can accept that. I know we’ll always be in each other’s lives. I just think it’s best if we limit our time together. Take care of yourself.
I’ve had migraines since I was a child. As long as I can remember I’ve been dealing with them. My earliest recollection is laying down in the nurse’s office in 4th grade, with one hand on my stomach and the other flung across my forehead and eyes. Even though it was dark, I could still sense light trickling in from somewhere. And it hurt. The nausea was excruciating and I just wanted my mom to come to the school and make everything better for me. That was the beginning of my long history with migraine headaches.
For years, those headaches were the only complaints I had. Being active in sports and social activities didn’t allow me to notice anything extra. But then I was diagnosed with ADHD, bipolar disorder, and anxiety. My life drastically changed. Things weren’t only different because of the mental health diagnoses. But I also had to adjust to how my mental and physical health were so intertwined; both symptom and treatment-wise.
It seems like everything about my illnesses and medication regimen intersects. Sometimes I feel like I’m running on a hamster wheel, trying to keep up with it all. if I get a migraine, I have to be careful which meds to take to alleviate it. The wrong ones can send me into a depressive episode. Or into mania. And just having the migraine itself is a threat to my mental wellness. If it lasts too long, I’ll get sick mentally. And the headache always brings a bout of anxiety and panic symptoms with it. Which is another assault to my system.
My body just can’t handle the weight of physical and mental illness together. It’s too stressful. So I’m always vigilant, making sure to take care of my neurological health so that I don’t have any mental side effects. It’s a unique and specific dance I do every day just to stay healthy. And it’s extremely exhausting at times. But lately, I’ve been well on all fronts, which makes me very happy.
Art therapy is widely known to be an excellent tool in alleviating stress related to mental and physical illnesses. But for me it’s specifically coloring as an art form that seems to have a calming effect. This makes it a wonderful coping mechanism. The American Art Therapy Association says, “A goal in art therapy is to improve or restore a client’s functioning and his or her sense of personal well-being” (arttherapy.org). When I was in the hospital we used art as therapy in order to learn how to relax and smooth the prickly feelings of anxiety. We had guided lessons with the therapist, who used soothing music as an adjunct to our drawing/coloring sessions. I enjoyed those times in the art room. I learned to channel my energy into something beautiful, and the repetitive motion of coloring gave me something specific to focus on, instead of my symptoms.
The therapists advised us to keep a small notebook and a set of coloring pencils with us so that whenever we felt anxious, we could use coloring as a coping skill. However one of the challenges that I ran into early in my recovery was the fact that anxiety doesn’t appear on schedule, in a neat and timely fashion. It can be extremely unpredictable, especially when you’re out in public. So as an alternative, I began to use coloring apps on my phone to achieve similar goals. No, it isn’t the same as using real paper and pencils. There definitely is a difference between technology and traditional coloring utensils. However, I’ve found this to be a suitable alternative that I can live with, considering I’m often on the go when I start to feel anxious or a when a panic attack occurs. So these kinds of apps have truly been a life saver for me. In addition, I tend to obsess over minute details, such as the paper getting wrinkled, and if my pencils are sharp enough. Not to mention what happens if I color out of the lines or create something that’s flawed. Because of my OCD and anxiety, there are times when the nuances of coloring will leave me with more anxiety than I began with. And for this reason, the exact nature of coloring using a tech gadget comes in handy.
I’ve used my apps when traveling, in crowded spaces when I felt overwhelmed, and on the bus. It would have been difficult to pull out a pad and pencils in these settings. Yet my apps did the trick. I know that coloring is only one of the many ways in which a person living with an illness can de-stress. And I also know that people may prefer old school methods rather than the new ones we have today. For me, this is the perfect blend of therapy and current trends. And I plan to continue using these electronic tools to help manage my anxiety.
I have a thing for numbers. I guess you can call it a strange sort of fascination. I don’t love math, but numbers themselves are fascinating. It’s how they interact that gets me. Combinations, coincidences, pairs, all of it. It’s part of how my OCD manifests. I get hung up on numbers in every facet of my life. For example, on social media I always check my followers versus how many people I follow. Not because I’m interested in how many there are, but because I’m addicted to the numbers in my count. I need to have things even. And I also have an obsession with odd numbers. Weird combination, I know. As an example, if I have 1443 followers and follow 774 people, I’ll feel off. Even typing that made me feel icky. I can’t handle seeing it. So for my social media, I’d have to then delete somebody to make the 3’s match. And it’s a constant challenge because people are always following & unfollowing one another. It never fails. As soon as my numbers match, someone gets added to or deleted from my count, and I have to start the whole process again. Sometimes I’ll notice that I’m coaching myself in my thoughts. I’ll say things like, “Ok I just have to choose 5 people to unfollow and then it’ll be alright”.
It happens in my religious life too. Such as with the Quran. In it, there’s a verse where God says He taught Adam the words to say (a prayer) to seek forgiveness. That’s in chapter 2 verse 37. Then in chapter 7 verse 23, there is a description of that very prayer. The circular nature of those numbers is amazing to me. It’s something I think about all the time. I repeatedly go back to those 2 verses to check that the numbers are still similar, even though I know for a fact that they are. I can’t explain it.
I can name countless other instances where numbers and counting play a big role in my life. But that’s just one facet of my obsessive disorder. Another thing I deal with on a constant basis is intrusive thoughts. Sometimes even in my sleep. Ever since I was younger I’ve had this problem. Like when I’m near someone on the steps, it scares me to death. Because out of the blue I often think, “what would happen if I suddenly pushed this person down the steps by accident?” Or when I’m in a moving car I’ll wonder what would happen if I suddenly jumped out. One time I did start to open the passenger door. It was almost like a compulsion. I couldn’t stop it. All of a sudden at the last moment I caught myself and jumped back from the door handle. I remember crying silently because I didn’t want my mom to know what had almost just happened. It was one of the scariest moments in my life.
Some of the other intrusive thoughts surround my relationship with my children. I’ve mostly had thoughts about what would happen if I didn’t feed them for a period of time. Or something of that sort. This all sounds absolutely horrible, I know. And I used to think I was a monster for thinking these things. But I couldn’t help it or stop it from happening. I used to cry, thinking I was a psychopath. It took years of me researching psychopathy and then finally getting my OCD diagnosis to realize that I wasn’t a monster; that I simply had a disorder, which was causing these thoughts.
Here’s a story which illustrates how harmful it can be to have this problem during a crisis. When my son was a baby, a fire broke out in my dining room. At the time we were living in a 2 bedroom condominium and the washer/dryer set was situated off the side of the dining room. In a small nook. I was sitting with my son across the kitchen in the family room. I could see the fire straight ahead. I realized it was coming from the cord plugging the washing machine into the wall, so I called 911. But at the same time I was having trouble collecting myself in order to leave the apartment. I kept thinking about what would happen if I left without my scarf on. I was in my pajamas and uncovered. And I thought something bad would happen if I left. Not in a religious sense at all, but in some other ominous way. It consumed me and I ended up literally turning in circles deciding what to do. I ran back and forth between my bedroom and the front door, filled with indecision.
I ended up unplugging the washing machine, on instinct, and the fire burned itself out. Later when telling the story to someone, she gasped. “You’d leave the house uncovered in that case!! She shouted. Of course I know that. It’s obvious. But that’s the problem with intrusive thoughts. You can’t just decide to shut them off. Even when faced with danger.
Fast forward to today. I’m so pleased that I’ve finally learned to take control of my OCD and begun living again. Even though what I’m describing doesn’t sound functional, it’s heartening to know that things used to be so much worse before I sought treatment. Now when those thoughts come, I can challenge them. And of course medication helps a great deal. Even when faced with symptoms I can’t quite manage, the time it takes me to recover and move on is much less. For instance, instead of spending hours correcting my social media numbers, I may spend only a few minutes. And when harmful thoughts come, I don’t take as long to ignore them. This is my life with OCD. A glimpse of it anyway. But it’s no longer my life ruled by OCD. And that makes me happy.
It’s only mid-February. Winter is here in almost full force in the DMV area. But I’m already looking ahead to spring. Not so much in a good way though. It’s more a feeling of dread. Mania hits me every single spring. No matter what I do. I can take all the vitamins and minerals that are supposed to alleviate mental health issues. I can fast or drink only water. Consume nothing but juices and berries, restrict carbs, and take my psychiatric meds…. nothing helps. And most things make it worse, so much worse.
One doctor finally explained that my circadian rhythm just doesn’t adapt well to the extra hours in the day. Well, great. I feel like the only person on earth allergic to sunlight in this way. Ok I know that’s not true at all. But when I’m feeling sorry for myself or hating my bipolar illness, it seems to be so.
It’s happened each spring since I was a teenager. As soon as the time moves forward an hour and I’m exposed to more sun, I have a pretty major episode. I’ve even started to notice physical changes during those times. My skin glows, my eyes and hair are extra shiny, it’s crazy. Sometimes my eyes actually turn more hazel than dark brown during spring mania. I remember having a kind of ‘glow’ when I was pregnant. This is like that glow, but on steroids. It’s that much more pronounced.
A good friend of mine commented on my change in appearance once during an episode. She said she couldn’t put her finger on it but that I looked noticeably different. Possibly younger, even. She asked what had caused me to radiate like that. She was suspicious, I sensed. She didn’t ask any more questions and we just let the uncomfortable silence hang in the air until I left. It normally would have been embarrassing but since I was in the throes of mania, I took it as a complete compliment. I thought everything was simply wonderful and I was happy everybody else thought so too.
One time in college during one such episode, I was racing to a job interview. And I do mean racing! I was going so fast that I sped past a cop while blowing through a yellow light that turned red. Of course I got pulled over. I remember the officer was so annoyed that I was in such a ‘good mood’. He kept trying to bait me into an argument about why I was going so fast. And he insisted on repeating that he should give me a ticket. I just kept saying, “Ok” to whatever he said, and smiling like I had gone mad. Finally he threw my license back at me and stormed off. To this day I don’t know if he understood what was happening or not. But at least I didn’t get a ticket.
I’ve recently begun to read articles about spring mania. I’m glad that others know what this is like, though I hate that we all go through it. Nothing good comes from my springtime mania, and I almost always end up in the hospital. The last major episode I had was when I went to Los Angeles one April to visit a relative. That was a mistake. Not the trip, mind you, but the timing. I should have paid more attention to my symptoms. By the time I got on the plane to LA, I was already fully manic. I know that now. When I got home, I’d stopped sleeping and eating. I had the inappropriate cravings I only get during mania. And my mood was off the charts. Needless to say, I had to get sorted out at inpatient. I’ve since learned that changing time zones during travel can cause a manic episode. Good to know!
I keep looking outside and seeing the gloom winter brings with it as an unwelcome +1. I know that we have a ways to go until the time changes and spring comes blossoming in. But I’m still preemptively nervous. I hope this time things go well and I am thinking positively. But I’m also prepared for what usually occurs. I don’t want to say it’s inevitable, but that’s how I feel sometimes. Here’s hoping the upcoming season only brings showers and flowers for me and those who experience spring mania.
How to stay well in the spring with bipolar disorder:
- Make sure to get plenty of sleep. Regardless if your body wants it or not.
- Eat a well-balanced diet. Food definitely plays a role in how our episodes play out.
- Take your meds exactly as prescribed and be sure not to skip any doses. *If you take medication, that is.
- Monitor any symptoms that may occur, as soon as you notice them. Then check in with your health care provider.
- If all else fails, and you end up getting sick, please be kind to yourself. Get the appropriate help needed for the situation and don’t get frustrated with any setbacks.