Mood Soothing Blooms

Yesterday I was having a tough day, with respect to pain and mood. Of course, in my case, one feeds the other and sends me into a downward spiral of agony. The day had started reasonably well – even though I hadn’t slept much the night before – then an abrupt about-face came because I was angered by something someone said to me. I know that becoming angry doesn’t work in my favour – it never has –, but controlling one’s temper isn’t always the easiest thing to do.

With the hope that it might pull me out of my prickly mood, I practiced a guided iRest meditation, but my mind kept skipping out to engage with other thoughts and memories. I had, however, committed at the beginning of the meditation to accept whatever might show up during my practice so I didn’t stop before the end of the recording. When it finished I was grateful that I worked through it because, as I usually do, I felt sleepy. I was able to fall off to sleep for about an hour until my slumber was interrupted; first by a phone call from my pharmacy and then immediately after hanging up, by a heavy knock at my door.

My annoyance was elevated again because the short sleep hadn’t helped to reduce my pain, so walking to my front door was more than uncomfortable. I was further annoyed when the person hammering my door refused to identify himself until I opened it. When I did open the door, he asked me my name from behind what appeared to be a box overflowing with shocking pink and white tissue paper that he handed to me. Because I was still somewhat foggy with sleep, I almost lost my balance when the weight of the box shifted to my hands. When I shut the door, I was a bit confused by what had just happened because I wasn’t expecting any deliveries.

Mood Soothing Blooms

The overstuffed box of tissue paper turned out to be a beautiful bouquet of a dozen assorted roses. The timing of their arrival couldn’t have been planned more accurately. I knew who sent them as soon as I ripped off the paper and saw each beautiful bright bloom and I was so grateful they arrived when they did. The flowers lifted my mood and proved to be a welcome gift of distraction from what I was feeling physically and emotionally. I know they were meant to be a Valentine’s Day gift, but they delivered a more meaningful message by arriving a day early. They remind me that even though others might engage in negative behaviours, which I sometimes allow to affect me too deeply, there are always those who love and value me for who I am.

Thank you B!

 

Blogiversary: 2 Years & 200 Posts

I received two unexpected notifications this week from the WordPress staff. I’ve been writing in this space for two years and I’ve written 200 posts. When I started this blog, I did it with the aim of unburdening myself of all the stress and emotional and psychological pain my illness causes me. I needed a space separate from the judgement and input of my family and friends. A space where I could be completely honest about what I am living with, while hoping to connect with other people who could empathize and truly understand what I’m living with. I’ve gotten that and so much more from this small corner of the interwebs that I’ve turned into my own.

This past year I started sharing my writing with some of my friends and family. I did that because they still have a hard time wrapping their heads around what is happening to me and how I cope with this illness every day. I hadn’t shared my writings about my illness with them before because I was anxious about exposing myself and the raw truth of my experiences and emotions; and I worried that I might have to become less candid with what I write. However, the feedback I received from some of them made me realize that I had no reason to fear what they might think.

In fact, my anxiety was unwarranted. The friends and family, with whom I shared my writing, were all incredibly compassionate. Some expressed disbelief that I’ve managed to hold myself together all this time while living with the level of pain I do daily. They couldn’t understand how I manage to maintain such an upbeat outlook even with the many failed procedures and pain medications that often don’t manage my pain as they should. Others just enjoyed reading my writing and were surprised with the level of detail I retain about my experiences and how vividly I convey what is happening to me.

This made me feel closer to them, which was completely unexpected. I never thought it could be possible to appreciate and love them more – let alone feel closer to them. Because of this, when I sit down to write I don’t worry anymore. I don’t feel the need to consider that I might express something that may be upsetting to them because they have made it clear that the support they extend to me and the love they hold for me is not conditional on what I might need to vent. They see this space as an opportunity to tap into the truth I might not fully share otherwise.

Two years into writing this blog and almost four years into living with my illness, I continue to learn about the people in my life and myself. Obviously, I don’t know what to expect in the coming year. My hope is to continue with the same determination to cope with my illness and to share what I’m living through with others who might connect with something I post. Writing has always been an important part of my life and even though I started this blog on a whim, it’s become an invaluable tool to help me – and now people I’m close to – cope with and better understand my life.

Blogiversary Bouquet

 

To Date (Or Not) With Chronic Pain

Some months ago, a friend I’ve known since junior high school had a very pointed conversation with me about dating and intimate relationships. He caught me off guard with his questions about my romantic life or lack of one. He was curious to know why, since becoming ill just over three years ago, I haven’t dated at all. His concern was that I am allowing my illness to define me and overtake my entire life. He pointed out that I am more than my illness and pain and that people with more severe disabilities and/or debilitating health conditions still manage to engage in fulfilling intimate relationships.

In our conversation, I told him I couldn’t get into a relationship because I was focusing on my health and all I need to do to restore it. In return, he asked how long I planned to focus on my health alone since almost three years had already passed. Would five years be enough or maybe ten? What would happen if I let all those years pass without any improvement to my health and never taking the time to explore the possibilities of sharing my life, even with an illness, with someone?

Interestingly, he didn’t talk about what I might gain from dating or being in a long-term relationship. He talked instead about what I have to offer. It was embarrassing to hear him describe me so positively, especially at a time when I don’t usually feel attractive, engaging, and bright – the brightness of my intellect is often dulled by pain and pain medications – nor do I feel particularly sexy. Feeling sexy is hard when pajamas and sweats have become my standard wardrobe staples.

Nonetheless, I promised him I would think about all he had said to me. And think I did. The first thing I thought about was the person I had started dating a couple of weeks before becoming ill and how uncomfortable I was being so vulnerable with someone I’d known for barely two weeks. As he called the ambulance, stayed with me in the emergency room, and visited me practically every day for the first week of my hospital stay, I was grateful for his support and kindness. However, having someone I hardly knew see me that way was overwhelming in the context of so much unknown. It didn’t feel right to move forward with a relationship. It felt unfair to burden him with that level of responsibility when we didn’t even know each other’s favourite colour or foods.

Thinking about that conversation with my friend led me to deciding I would give online dating a chance. I set up a profile detailing my interests and what I look for in a partner, I posted recent pictures of myself where I look happy and healthy, and then I waited for interested prospects to contact me. I wait instead of initiating contact with anyone who piques my interest because I’m still uncertain about how to explain my current life circumstances. The thought of telling a potential partner about my daily struggle with pain still causes me great anxiety. Although my hope is that those feelings will soon change.

However, being online and exchanging written messages about my interests and who I am, as a lead up to deciding whether to meet in person, has been helpful. It gives me a chance to sort through and figure out who, of all those I communicate with, might be the type of person who would not be phased by what is happening in my life now. It’s also a chance to rediscover the part of myself I’ve neglected because of my pain and better understand how I’ve changed in recent years. Being online also provides a way for me to manage the pace of the process, while making sure I don’t feel too overwhelmed.

I have to admit that, with my friend’s urging, I am opening myself up to the possibilities of what my life could be like, even if I’m never pain-free. I know that not everyone I meet will be as compassionate and open to my situation as the friend I’ve known since I was a child, but now I’m hopeful for the chance to meet someone who is.

Red (Maybe) Tulips Sketch