[Journal] 10 things I wish able-bodied people WOULD assume about my health.

I’ve been keeping mostly to myself over the last few months to make health issues much more bearable. Lying in bed last night while waiting for my painkillers to kick in, something occured to me; people make a LOT of assumptions when you’re sick and most of them are awful. How many of you have heard the old nut of “But you don’t look sick!”?

So, if I had to deal with people assuming stuff about me, what would the best case scenario be? In a perfect world, what would I want them to me thinking?

1. “They’re young and have a disability parking permit. Their illness must be pretty serious.” 

I really wish this was the first thing that went through people’s heads rather than “fuck you, you’re faking and I need to let you know how disgruntled this makes me, even though it doesn’t affect me directly”. I’ve been accosted multiple times from both parents and elderly who should know better, and even had my car vandilised because I’m a twenty-something female with an invisible illness and everyone suddenly takes up the social justice sword the moment disabled parking is involved. If people were half as quick to assume there might be a reason you use the parking spaces as they are to condemn you for doing so, we wouldn’t have half the stigma against shit like this and I wouldn’t feel ashamed to need it on my really bad days.

2. “I can’t see any physical signs of an illness in them. I don’t doubt them in the slightest since invisible illnesses are a thing. In fact, they carry themselves incredibly well to pass as healthy.

No symptoms = not sick. I mean, come on. Everybody knows that. After all, there are clear and visible signs of Diabetes, cancer, Lupus, Fibromyalgia, mental health and immune disorders. 90% of the chronic pain kitties I know have gotten so good at ‘passing’ as healthy because it makes life easier. No questions, no judgemental stares and no people acting stupid trying to do what they think is the right thing without actually asking you.

3. “I haven’t heard from my chronically sick friend in a while. Rather than avoiding me, they must be really unwell or taking important time to themselves. I should send them a message and ask if they are okay.

Being sick is hard work. It drains you in ways you can’t even imagine until you’re living it, and it often leaves you with almost no energy for socialising or outings. Sometimes people take it personally and don’t have the experience to understand that it’s an incredibly complicated situation where nobody ultimately wins, rather than you expending energy to avoid them or cut off contact.

4. “They’ve cancelled our plans at the last minute AGAIN. I can’t imagine how frustrating it is for them to want to go out, but to have their body decide otherwise.”

This is a big one. If I had a dollar for every time I’ve had to can plans because I can’t move, it would make me more sick or I simply need to pace myself, I woukd be able to get my painkillers gold-plated. We WANT to be out there with you. We want the normalcy of going out on a whim or looking forward to plans. When we have to call it off, we don’t gain anything from it, trust me. Please remember the person behind the illness and that we have the same social needs as you.

5. “My friend has a chronic illness but the rest of our group of friends doesn’t know. It’s not my place to ‘out’ them since they may not want everyone to know, and there’s a lot of information I don’t have.

There have been many times in my life where ‘coming out’ about my illnesses was necessary, but also many where I have been more comfortable to simly slip under the radar and pass as a regular able-bodied person. The reasons for this vary, but it should always be my choice whether or not that status is disclosed, and there have been occasions where that choice has been taken away from me by well-intentioned people trying to simply do the right thing. I ended up feeling exposed and uncomfortable, having to explain things that were sensitive to me at the time to people that may not have been the most receptive to the information – all because I didn’t get the choice.

In more extreme situations, this can cost people jobs and future employment, friendship and relationships and ultimately end in excusion, bullying and other generally shitty scenarios.

6. “We’re going out with a friend who has mobility issues tonight. We should ask them how much they can move tonight, try to find a place close by for food and also try to keep pace with them when we walk so they feel a part of the group.

This is such a simple thing, but there have been so many times where it’s gone neglected. Not due to malice, but simply because, unless you have prior experience, most able-bodied people don’t even consider that it might be an issue. Going out with someone who has mobility issues DOES change the dynamic of an evening out, despite our best efforts. Let us dictate our mobility level, help us fit in by either finding places that are only a short distance nearby, or be willing to compromise, and please include them in the group. You would be genuinely surprised how much a little gesture like keeping pace with them means – suddenly we go from feeling like a killjoy and a burden, to feeling valued, included and able to participate in conversations.

7. “I know my friend is displaying signs of being tired and in pain. Rather than telling them what I think they’re feeling, I should ask them to describe it in their words so that they have the opportunity to tell me exactly how they feel.

This one has cropped up because I had an encounter the other day with my mother. She meant well, but when I stumbled out of my room, she remarked “you’re tired”. Now, living with ME/CFS, the only time I’m not tired is when I’m exhausted. She wasn’t wrong, but by the same token, I felt like not giving me the opportunity to tell her how I was feeling in my body, she was effectively writing off the way I felt. I know it wasn’t the intention, but there are so many times when people with invisible illnesses don’t have a voice and that we have to dumb down our experiences so that we’re not called whingers or attention seekers. If you want to know how we’re feeling, just ask. Don’t assume you know what we’re experiencing. Give us that voice.

8. “This person looks to have physical issues. Rather than me deciding what they’re capable of, I’m going to let them set their own limit. After all, they know their body best.

A lot of the time we’re at an impasse – stuck between asking for help and wanting to keep some of our independence. Losing the ability to do things on our own is part of us losing our sense of self, so to keep this short, let us dictate our capacity for each occasion rather than just assuming we can’t.

There is absolutely no harm in asking if we need help, but the problem arises when you assume that we can’t do it and take away the opportunity for us to be involved.

9. “That person is walking/looking/moving a little funny or using mobility gear. It makes them stand out. It doesn’t matter if this is normal or abnormal for them, I need to respect them as a person, understand they may be feeling alienated and treat them exactly the same as I would anyone else unless asked otherwise.”

Sometimes chronic illness can manifest in different ways. I can only really speak for myself here, but I hate using my mobility gear like my cane, scooter and wheelchair since it really makes me stand out like a sore thumb. I feel awkward, I feel a bit like a freak and I hate the looks people give me where you can simply tell they’re silently judging you.

I have no issue with kids looking at me since they’re blissfully unaware of these things and mostly innocent, but when mummy or grandpa put down their coffee to gawk open-mouthed as I roll past, I feel like keeping a small stash of rabbit poo in my pocket so I can flick it at them. A lot of the time we don’t have a choice in these things – it comes down to either staying at home while out of milk and sugar (which spells disaster for a good cup of tea) or going out while using our gear.

Just remember that, behind all of that stuff, behind the limp and the sling and the walker, scooter or chair, we are just like you. We have feelings and are just as aware of the looks as you would be if you farted in the cheese isle in the shopping centre.

10. “There’s something I don’t know about their illness. You know what? I should just ask them about it rather than making assumptions. If I’m their friend, it’s good for me to know about their issues in case they need help in the future.

I really want to emphasise this one – so long as you’re respectful of us as people, we don’t bite. We actually appreciate you taking the time to learn about the issues and conditions affecting us. Just don’t come up and as “yo, cripple, why the limp?”.

This list is by no means definitive, but instead a collection of thoughts from both myself and others on the matter. Do you have something you really want added to the list? Comment below and let me know!

 

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[Journal] Tonight is a bad night

There’s simply nothing to make one feel more alone in the world than knowing that if you publicly ask for help, all the wrong people are going to answer.

Tonight isn’t a good night for me. It’s now almost 3am and that means I’ve been sitting on the very cusp of a full-blown anxiety attack for almost 9 hours. Despite taking all my medication and two beta-blockers (which are supposed to help with the fight/flight response), I’ve not been able to calm down. I’m on the edge of tears over nothing at all. I literally cried because I watched an episode of My Little Pony. I don’t know, really.

I’m in both physical and emotional pain, the latter being the worse of the two tonight. I’ve tried everything that normally helps. Everything. Hell, I’ve tried to go out and do a thing, have a social life and expand my brain a bit. Just shrug off the fear that some kind of horrible doom is impending or that life as I know it will crumble before me. I had a thumping heart and adrenaline rush the whole way there, the whole time I was there and the whole way home. I’m somewhere between proud of myself for achieving what I have so far, and filled with crippling doubt and emotional exhaustion.

Tonight is one of those nights where I wanted desperately to reach out to a friend, but because of the time and the day, nobody I want to talk to about something like this was around. I don’t hold it against any of them. I spoke to manthing, but sometimes you just want to talk to someone who hasn’t heard it all before, and I feel like the ones that were available would hear me, but wouldn’t actually listen.

I’m hesitant to write about personal issues and things involving friends on my blog these days, namely because I know that a few follow it through one way or another. A major fear of mine is that, in revealing how I really feel about things, I’ll face repercussions for it in person. It’s one of the reasons that I’ve deliberately kept this blog entirely anonymous. On that note, I will expect any individual that knows me in person to show me the respect I deserve here and not confront me over my views and feelings. If you respect me as a person and, indeed, as a friend, you will understand that sometimes one simply can’t be upfront and honest in the way we intent. We don’t want to hurt feelings or upset people, but to deny our own reactions and emotions is exactly what put me in this shitty place tonight to begin with.

I have some bad people in my life right now, and it really comes to the fore on a night like tonight when there’s a stark realisation that all my mental health support network no longer exists. Once upon a time, I had a ‘family’, I had close friends, I had people I called brother and sister and I felt safe. I felt like, even though I might come across monsters in the dark, I would always have those people behind me. In the last year, everything changed. People I trusted abused my emotions in the worst possible ways. In unforgivable, selfish, twisted ways when I begged for help and respite. My needs were shunted aside when I needed people most, while they marched up and dumped their life on my doorstep and looked at me expectantly. People I trusted beyond what I probably should have. People that I respected and gave a little bit of myself to. “Keep it safe, please”. Instead, they used it as a front door to my emotions and time. They played on my emotions and my intrinsic need to have people in my life when it was obvious to everyone but me that this was doing more harm than good.

So tonight, when I need someone to turn to, someone to tell me that “you know what, it’s going to be okay. I know you’re afraid now, you’re allowed to be afraid, but it’ll get better and you won’t need the fear tomorrow, so leave it here”, I have a crushing sense of loneliness. Even when manthing is one room over. I need these people in my life again. The friends, the lovers, the family, and I have only empty spaces where my impression of people once stood; their figures having wandered somewhere far from here, leaving only disappointment and child-like pain in their shadows. I find myself on a night like tonight struggling with demons that often feel lager than myself, and instead of people that listen, I have people who hear what they want and talk about themselves. I have people that tell me they understand and, on nights like tonight, I find that more of an insult than a comfort, because they don’t. They can’t feel my heart beating into a cavity the child in me has carved out with scratching nails and wild eyes. They can’t see the way it’s filled with terror from everything – named and nameless – and they don’t understand that the one thing I need tonight is someone who will truly listen and simply say “I am here for you. Please talk to me. Let me listen”.

Instead, I have people that ignore my outright plea for help to substitute it for something else that they find more fitting. Instead of understanding that, ultimately, I need to walk through this on my own, but want someone to wait for me at the other side, they walk next to me and tell me about all the woes and troubles they’re facing and do nothing but load the wagon I’m dragging down an already rocky road. I know if the wheels fall off, they won’t stop to help. They will take my stopping as a queue to simply heap more baggage on. I say this with experience.
Any other night I take that on willingly. Any other night, I grit my teeth as a simple greeting becomes a segue for them spewing their grief on me and expecting me to be a therapist. I’m not, and I likely never will be, by choice. I find my friendships abused time and time again by people mistaking my concern for their welfare for an open invitation to dump their life story on me and then demand I fix it for them. But not tonight.

Tonight I have been afraid of making it known that I need help, because the people that will answer are the ones with an agenda – they’re the ones time and time again that will see my unhappiness and take that as an excuse to ride the misery wagon in what they seem to think is tandem. The problem is that they don’t help me pull, they sit and expect me to do the work, and I’m finding that time and time again, that hurts more than all the fear and heartache in the world – knowing that this person holds their own issues in higher regard than yours but wraps them up in paper and presents them to you as a gift, and expects you to say thank you.

I have some beautiful, wonderful people in my life. I have the people that tell me that I’ve always got someone on my side, I have the ones that DO understand because I know they’ve walked that road before. I have people that respect my boundaries and, while we can commiserate together, they know that everyone has limits, including themselves. Right now, however, is one of those rare times when I feel that none of these people are around. They very well might be, but in one of those silly moments where I want to show them the same consideration they’ve shown me as a friend, I find myself very hesitant to message someone at 3am just to talk. I suppose this is somewhat of a self-dug hole where I find myself placing the needs of others before my own, but friendships are about give and take, not clinging to a drowning man and expecting him to take you back to shore.

Tonight, I am unwell. I have a sickness, a malaise of the mind and heart that is just as real as any other kind of injury or disease. Tonight I am going to crawl into bed, curl up close to manthing and do the same thing I would do for any cold or flu – sleep it off and hope I feel a little better tomorrow.

Selective exposure and when helping isn’t really helping

This is an issue I’ve wanted to write about for a while now, but due to circumstances on my end I’ve been unable to either find the time to do it, been in no headspace to write about it or haven’t physically been capable of doing it. I’m hoping that taking the time out tonight to sit down and get this out of my head will mean my brain will stop charging through at a million miles an hour.

Over the last few weeks, I’ve been party to a handful of events that got me thinking. Some were good and some were bad, but they all ended up at the same two destinations in my head – the idea of selective exposure, and when helping isn’t really helping.

Most of the time when people see me, it’s usually within certain parameters. Somewhere between the “I’m feeling great” end of the scale and “I’m not feeling awesome” end. Anything beyond that and I usually rule out any form of social contact for a number of reasons. Have you ever tried to sit through a conversation and remain polite and chatty while someone’s trying to rip your toenail off? How about trying to have genuine interest in what someone says while you’re exhausted enough to actually fall over out of your chair? There’s only so far I can fulfill my social obligations on a day when I’m in above-average pain, my fatigue is playing up, or any other number of fuckery my body likes to pull.

What this basically means is that when YOU see me having a bad day, that may not necessarily be the same as MY bad day. That’s not to invalidate anything I’m feeling at the time, but my sliding scale for social activity stops at “Fucking ow”, but my whole scale goes all the way past that up to “Oh God Why?”

The bit that really frustrates me about this issue is that so many people seemed to assume that what I felt stopped at what they saw. Like, when they didn’t see me using the cane or with a visible limp, clearly I was in no pain at all, and when I did have the cane, I was still obviously okay because I was still up and talking.

I’ve had to explain to several people, some friends, some family and some other random people on the street that, when you see me out and about, when we come over for games or when I go out to get lunch, it’s a very controlled thing. I MUST be within point X and Y in order to function as a semi-competent human being and any deviation from that usually means I’m suck at home and in bed, in a world of pain. What you see is NOT what you get with me, but that doesn’t seem to stop some people thinking I’m leading them on or I’m some kind of liar.

That’s the problem with these invisible illnesses. They’re kind of just that. You don’t see them. You see reactions from them. You see the implications of them running amok in people’s bodies, but it’s not like we turn purple or grow horns. You basically have to take our word for it and actually believe us when we say we’re not well.

And now on to my next point. When helping isn’t really helping.

One of the things I’ve been struggling with over the last few months – longer, in fact. Just about as long as I’ve been sick, to be honest – is the idea of wanting to help. For the most part I try to be gracious about the whole thing and thank people where I can for stepping in. However, there are other times when people overstep boundaries in eagerness to help the cripple or, assist the female or even lend a hand to the friend.

First and foremost, there are two different kinds of help I want to identify, and there aren’t always defined boundaries between the two.

The first is helping because they need help. This is usually the case easiest identified by the audible “Can I have some help, please”. All sarcasm aside, it’s fairly easy to see when someone’s struggling with something and you want to step in and lend a hand. It could be a case of them needing help getting up the stairs, or opening a jar, or changing a light globe, remembering a birthday or even recalling what they walked into the kitchen for. There’s usually some kind of body language on the part of the helpee and an acknowledgement of some kind on the part of the helper.

The second kind is a little different. This involves helping because you THINK they need help. This one can be done for different reasons. Sometimes because the helper wants some kind of feeling of gratification for “doing what is right”, sometimes it’s because they think that the person they’re helping is a lot less capable than they really are and sometimes it’s genuinely out of desire to assist another human being.

Now, the problem with the second kind of help is that it’s not always called for. I had an incident with a friend the other day (which we talked through and we’re back to normal again) but it made me think about the other times where I’ve had similar situations and what all my experiences combined have taught me. People have assumed I have needed help and have gone out of their way to do this, without actually asking me if I needed the help first.

Unfortunately this division can be really hard to navigate for some people and toes end up getting stepped on.

One of the issues I find most frustrating is that we’re taught straight off the bat to assist those less able than us. In my situation I can be either more or less able in a lot of areas on any given day, so I’ve found people wanting to go out of their way to make life ‘easy’ for me without taking into account my choice on the matter, while other people that obviously require some help are left to fend for themselves. One thing that a lot of people seem to forget, though, is that (for all my cripple-ness) I’m a highly independent individual and take fierce pride in my ability to self-manage. The beautiful humour in that being that, on my bad days, I need help to dress, shower, use the bathroom, etc.

What this means, however, is that I usually don’t want help until I directly ask for it. I’m no stranger to asking for help, even if I can be a little sheepish about it at times, but when you’re stuck in body that takes a toss at a dart board to decide what you can and can’t do on any given day, you treasure those things that you can still do on your own, without help of any kind. You’re fierce about those things. You don’t want help pushed upon you because someone else thinks you need to be helped. You want to do it yourself because you’ll be damned if you can’t wash your own hair, or dress yourself today, or even go for a walk.

When someone comes along and helps you out with things they think you need help with, it crosses a line where they start robbing you of that independence. Suddenly, you’re no longer strong and capable in that area because someone else has just come along and done it for you. You’ve had the rug pulled out from underneath you and yet we’re still taught that we should say thank you because this other person only had our best in mind.

The problem is that when you live a life where independence is such a flippant and fleeting thing, rather than being preemptive help, sometimes you’re robbing that person of part of their identity. Part of who they are. That last part of the strong, capable person they were before they got sick, and that’s where things go wrong. That’s where frustrations break and feelings get hurt and it’s incredibly hard to explain a concept like this to someone who’s never known dependence on another individual. It’s hard to explain how something so well-meaning can have such a vastly opposite effect on an individual’s life. Sometimes helping really isn’t helping at all.

Far be it from me to discourage assistance when required, perhaps first ask if your person would like help with what they’re doing. If it’s not a routine you’re used to or they haven’t asked themselves, perhaps ask them if they want assistance before you jump ahead, and don’t be offended if they say no. It’s not said to reject the support you offer at all, but instead is perhaps their way of maintaining some form of normalcy over an otherwise abnormal life. Furthermore, it’s always far easier to ask first than to have a negative reaction to your good deed.

[Journal] Friends and chronic illness

To start, I’d like to clarify that this isn’t me seeking attention or looking for sympathy. This is me trying to make sense out of a series of situations I’ve been in recently and to work out where I stand in it all. This also isn’t directed at any one specific person, but is a collection of memories from past and present friendships, written at a very emotional point tonight.

I’ve written in the past about how maintaining friendships is a challenge when one is chronically ill. Regardless of what you’ve been afflicted with, it makes an impact on your life that few people can understand. I’ve written about how a careless word here or there can really bring someone’s world down around them. I’ve also written about how lonely it can get when one is cooped up at home all day, every day.

This post is more than that. To me, this is an attempt to make sense of everything I’ve been through with past and present friends to date.

Right now it’s almost 11pm. I’m sitting in bed with my laptop and I’ve just had a good 20 minute sob to Manthing about how unfair it is that people just don’t ‘get it’. I’ve had 7 days of above-average pain. It’s worn me down in places I’m not usually aware of. I’m beyond exhausted. Because of how run down I am, I’m in more pain than the last few days, anyway. I won’t lie. This is hard. This is really, really hard.

I used to tell people that I was very lucky because my support network for hard times like these were a select few friends I could call upon, whenever. Some online, some a few suburbs away. In fact, before myself and Manthing were a ‘thing’, there was one night when I had hit my first 9 on the pain scale. It was 3am and he had work the next day, but I could still ring him up and he talked to me on the phone for about an hour until my painkillers had kicked in and I could sleep.

In the last few years, this has changed. I find myself here on a night like tonight with almost no support network whatsoever. People have gone their own ways, life has changed, things have come up. One friend decided it was okay to treat his friends like shit. Another got a girlfriend and suddenly didn’t have time anymore. Another couldn’t understand that being sick wasn’t like being in bed with the flu. Another still decided to tell me that my illness was THEIR problem. One by one, all the people I felt I could approach at that 3am mark drifted away and left me here on my own little island of Fuck, where I find myself tonight.

I guess this entry is a bit of lamenting the fact that I feel so alone right now. Once upon a time, if a friend caught wind that I wasn’t doing so well, I’d have an SMS within minutes. I’d get a check-in every now and then. “Just thinking of you. Hope you’re okay.” I’d get a message online or they’d even just show up out of the blue. Once, I had someone even deliver a care package because I had spent the week in bed. You know who you are, and you should know I genuinely cried, even through I didn’t say anything out of pride when it happened. It’s the little things that turn a fucking awful situation into a not so bad one. It’s knowing that someone has your back that can sometimes give you the strength to get through the day. Right now, thanks to the pain and the depression, I feel like I could vanish for a month at a time and nobody would even know I was gone.

For what it’s worth, I always did what I could. I like to see myself as ‘that friend’. The one that would always check in. If you were having a shitty day, I’d send you an awful joke or a picture. If you were stuck in bed, I made digital get well cards. Driving an hour out of my way to help a friend out even though I wasn’t in the best state wasn’t something I thought twice about. I just did it because they needed me there. I’m the one that left the messages. “If you ever need an ear or someone to talk to, I’m here.” Maybe I wasn’t that person to everyone. Maybe I wasn’t that person to anyone. But god help me, I tried. I genuinely tried to be the best friend I could be.

As I got more and more sick, sometimes I’d miss a beat. Sometimes there’d be a week where I was stuck in bed and didn’t know you were upset. I tried to catch up and still check in. I really did. With more than a few people, I tried to organise times when I was well enough to meet up, but they were always busy. Things don’t often work the way we plan, but that doesn’t mean I didn’t genuinely put an effort in.

Right now, I feel empty. I feel like, for everything that I’ve been through, I only have Manthing with me. I feel so alienated from other people that it physically aches in my chest. People I used to be really close to. I think at one point I had half a dozen people and I felt so very special because of it. I think about all the 3am nights we used to spend out getting slushies and I cry. Things aren’t that way anymore. I think about the skype calls we had where we’d see who could burp the loudest and it hurts.  You got a girlfriend and I vanished off the face of the earth to you.  I remember the times we used to make running jokes and confuse everyone else in the room. You don’t even answer my messages now.

I think about how, once, I felt like I had people who were involved in my life enough that, when I needed someone to vent to, they understood I wasn’t looking for attention. I just needed someone that understood what I was going through. I know I’m not the easiest person to be friends with. I really do understand that. I’m a lot of work. I ask things of people, I can’t always go out or catch up and sometimes I hurt people because of it. But seriously, do you think that it hurts any less for me? I’m the token cripple friends. I’m the one people make allowances for. I’m the one that forgets and needs assistance during games. I’m the one that makes the group walk slower. But I’m still human.

Yes, I do still have friends, and people I talk to occasionally, but it’s not easy. Imagine how it feels to not be able to talk about some things because they just don’t understand – or, in same cases, just don’t give a shit. Imagine someone walking away mid-conversation when you’re trying to explain why you were so sick yesterday. I’m the one that has to make the allowances for other people. I have to watch my words so other people aren’t accidentally offended because they can’t deal with their own stresses. I have to curb my own humour because, god forbid, someone might be offended by a joke I make about myself. I have to constantly remind people that, for me to go out somewhere requires some planning. I can’t just get an invite half an hour before X starts. I often don’t have money with over $200 of medication per month. I am a difficult person to be friends with, but I’d like to think that I’m no less worthy of friendship for it.

I’m genuinely afraid of making new friends, even thought I’ve tried. Try to imagine what it feels like to be immediately judged as being ‘too hard’ or ‘too much work’ the moment you mention chronic illness. On top of dealing with all my other physical issues, I then have this exhausting charade of social interaction, and it wears me out.

I won’t lie. I have very little patience for those that can’t accept me as I am, but I’m desperate. I want friends and I’ll take what I can get.

I do still have people that genuinely give a shit about me, and I them. People that don’t care if I’m in my pijamas when they show up. People that are happy to change plans to a night in when I can’t move. People that don’t hate me for something I have no control over. I hope that, one day, they read this part and understand. But those are far and few between, and with some, we barely even talk anymore.

I don’t even know if I’ve made much sense with this post. Manthing actually pushed me to blog about it and, in it’s own way, it’s been a bit cathartic. That little voice of anxiety in my head warns me that I might offend or upset a past or present friend reading this, but then the little logical Abi in the front of my head says “Let them be.” I guess if someone’s offended by this, it’s because they feel that there’s an ounce of truth in my writing. Let them fix it. If someone feels a prickle with one of the things I wrote, it’ll be because they relate to something in there. It’s never my intention to offend with these things, but people are stupid. If there’s an issue, do something about it.

After a solid half hour of writing, I’m thoroughly exhausted and no less miserable, but I’ll leave it here for tonight.

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[Comic] How to be friends with someone who has a chronic illness

[Comic] How to be friends with someone who has a chronic illness

This has been something that’s been on my mind lately. Quite often, because my illness is something that’s been around quite some time, more often than not I tend to feel that people overlook it and the effect it has on my life. Sometimes it’s big things, other times it’s little things, but I decided to make a comic about a few of the more important subjects that crossed my mind