Living With Multiple Illnesses

Life is hard. It’s difficult to navigate without directions and instructions, you have to figure it out on your own. You can’t follow other’s paths, for their journey is their own. You have your own path to follow, carved by the decisions you make every day. What happens when you’re living with a mental illness? It makes life that much harder. What if you’re living with multiple illnesses? Then things really get interesting. You have to learn to distinguish the differences between your illnesses, and manage them appropriately on top of just existing. Many times, mental illnesses and physical illnesses overlap, exacerbating everyday life.

I live with many physical and psychiatric illnesses. Bipolar disorder 2 rapid cycling with mixed features, borderline personality disorder, PTSD, social anxiety disorder, ADHD, high functioning autism, generalized anxiety, fibromyalgia, early onset psoriatic arthritis, and irritable bowel syndrome. That’s to name a few. They make my life hell sometimes. Other times, some of them are like a blessing. It’s a double edged sword to handle, really. Over the years, I’ve noticed and recognized when my illnesses are working together against me. My bipolar and borderline are besties, as are my fibromyalgia and IBS. They hang out a lot, and when they stick around my other conditions come out to play. My ADHD runs rampant when I’m manic, and it makes an appearance during my depressive episodes. It’s always there, it just becomes prominent during episodes. My PTSD is a trickster, it likes to surprise me when I least expect it. My autism is always there, it’s my operating system. I like to say that autism is just a different operating system for the brain, I’m just like everyone else only my wavelength of thought is on a different frequency.

Bipolar disorder and borderline personality disorder. Two illnesses that are commonly diagnosed together and also commonly mistaken for each other. I was diagnosed with both on January 9th, 2012. I knew quite a bit about bipolar disorder but the BPD diagnosis threw me through a loop. I researched my illnesses and read as much as I could about them. Research is one of my obsessions, it’s an autism thing. I felt such relief when I received my diagnoses, it was like a huge weight had been lifted from my shoulders. For so many years I asked myself “What is wrong with me?”, I had mental illnesses that were unchecked and didn’t know it. No wonder I felt like I was off all the time. I have been on and off medications for over 20 years now (I’m 34 years old), and I feel most like myself when I am on medications. Without meds I feel like Jekyll and Hyde. I can’t control myself, at all. I don’t like how I am without medications and when I saw how it was affecting my marriage and my family, I made the decision to stick with meds. It has taken me a few years to learn the differences between my bipolar and borderline, some days I am left mystified as to which one is causing chaos in my life. It really sucks when both are actively messing with me. At times I can be extremely impulsive, which can be caused by both disorders. Something will set me off, and my moods will flip on me causing me to split on myself, then I become terrified that my husband will leave me because I’m unstable (thanks a lot BPD). The hypomania, I have to admit I love being manic for the most part. I love feeling hyper and happy, and productive. I feel grateful for not being depressed. There is a downside to mania, though and it isn’t pretty. The impulsive out of character behaviour, the rapid mood swings and irritability, the racing thoughts and discombobulation. Not to mention the manic spending sprees, I’m so bad for that. Also there is the inevitable crash into depression that brings anxiety. I never know when the crash will happen so I get anxiety over waiting for the other shoe to drop. I’m not a big fan of mixed episodes, which is too bad because I get them on the regular. Mixed episodes are where you get symptoms of both depression and mania at the same time or as part of a single episode. My episodes vary, where I will have mental symptoms of mania and physical symptoms of depression, and vice versa. My depressive episodes are influenced by my fibromyalgia, which is a whole other basket of not so goodies.

My fibromyalgia affects me on a daily basis. I never know how I will feel when I wake up, much like my BPD and bipolar. Some days are worse than others. I can go to sleep feeling happy and fine, and wake up with strong pains radiating throughout my body. The weather seems to influence my fibromyalgia, severe and sudden temperature fluctuations in particular. Flare ups are no walk in the park, they can last for days if not weeks. I noticed over the years that a fibro flare up will almost always cause a bipolar depressive episode. It’s depressing when the weather is nice and you want to go out and enjoy it but your body has other plans. The worst days are when I’m bedridden. During a flare up I’ll have great difficulty walking, getting dressed, and feeding myself. Forget about regular housework. It’s a huge blow to my productivity when a flare up occurs. I’m a housewife and stay at home mom; I keep the household running and when I can’t do it that falls onto my husband’s shoulders, and he already works full time. I feel useless and worthless during flare ups, like I’m a burden to my family and friends. I don’t want my husband to have to come home and do all of my work too, that isn’t fair to him. Then the depression creeps in, and boom. Depressive episode. Some days it gets so bad that my husband has to come home from work and take care of me, which means taking care of our three kids as well since I’m bedridden. It breaks my heart when I am physically unable to pick up my baby and hold him because the arthritis and fibromyalgia in my hands and arms render them useless.

My ADHD is always around, but during episodes it likes to mess with me. It puts a kibosh on my hyperproductivity during manic episodes, it makes me wander around my house aimlessly. I daydream when I should be working, my thoughts race so fast in my head it’s dizzying. As much as I try to stay organized, I horribly fail. It stresses me out when my forgetfulness takes its toll on my household. I’ll get caught up in housework and forget to start dinner. I’ll make shopping lists and forget them at home. I try to multitask and get distracted by something and then forget what I was doing. I get confused between my ADHD and my mania at times, the symptoms are very much alike and it’s hard to differentiate between the two. I’m still learning to do so.

As I mentioned earlier, my PTSD is a trickster. It always catches me off guard, which sucks because I am hyper vigilant. I’ve learned most of my triggers but maybe not all of them. Rape is a big trigger for me, the word itself I find triggering. Rape jokes cause me to dissociate, and give me flashbacks. Domestic violence is another big trigger. It could be brought up in conversation, or I might have come across it on social media, it doesn’t matter. It will trigger flashbacks and nightmares, and panic attacks. It sends me right back to where I was during the sexual abuse in my teens and abusive relationship in my twenties. Usually my PTSD will trigger a bipolar episode, mainly depressive. I never knew how to deal with my trauma, I always just shoved it back to the recesses of my brain and pretend it never happened. But that only worked for so many years, then I started having flashbacks and recurring nightmares. It wasn’t until I told my psychiatrist about them that I was diagnosed with PTSD, and that was just over three years ago. I’ve come a long way since then, I did a lot of research and bought some self help books. I like to think I’m in recovery, and I’m doing well. I have PTSD episodes once in a while but only when I’m triggered.

I fight through my episodes and flare ups, I have to in order to keep my sanity. I can’t give in to the intrusive negative thoughts, it’s too easy to fall into that trap. I keep reminding myself that this too shall pass; I won’t feel this way forever. I will feel better soon. Better days are coming. I remind myself of everything I am grateful for, I keep a gratefulness journal and read through it often for motivation and strength. I distract myself with various activities, depending on my fibro and arthritis and how they affect me. If my hands aren’t hurting I crochet, paint, colour, bake, play World of Warcraft, and type on my laptop. If my hands are useless, I tend to read and watch TV. My children and husband help cheer me up, just by being themselves. My husband is my main support, I would be totally lost without him. He is extremely understanding and sympathetic, and compassionate. He’s there for me through it all whether it’s to hold me through my panic attacks and flashbacks, dress me and feed me when I can’t do it myself, or keep me in check when I’m spending too much. He’s been there for the good, the bad, and the ugly, and still loves me for who I am. He is my hero. My husband is an amazing partner and father to our children. My two oldest children know and understand that sometimes Momma has bad pain days and bad brain days. They will help with the housework (on top of the chores they already do daily) during bad pain/brain days, without argument. They know that I have medical conditions that are debilitating at times, they know what bipolar disorder and fibromyalgia are, as well as ADHD and autism. They also have ADHD and autism, both of them. We’re all high functioning. They are aware that they have those conditions as well. I think it’s important for them to be aware of medical conditions and how they affect people. I believe that their knowledge about my conditions and their own has helped them, in matters of empathy and compassion. My family is close knit, and when one of us is hurting it affects all of us. We all work together, as a unit. My family gives me strength to keep going every day.

Living with multiple illnesses is rough but manageable. I don’t sit and dwell on why I have all of these conditions, I don’t much see a point in doing so. The fact is I have them, and they aren’t going anywhere. There are no cures for my illnesses, I have them for life. I might as well make the best of things and live positively. I can sit and ride on the pity train, stopping at the “Woe Is Me” station, but I would much rather buckle up and enjoy the ride on this roller coaster I call my life. It has its ups and downs, twists and turns, and sometimes there is a fire, but somehow I always manage to stay on track. If I ever derail, I will pick up the pieces and get myself back on track. I only have one life to live, and this is it.

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