Fed up with fear

October 24, 2017

I remember the “old” me like it’s someone else. Someone else who took risks. Someone else who moved all the way across the country to try something new. Someone else who traveled overseas alone. Someone else who went scuba diving with sting rays despite her fear of open water (and yes, I was terrified of the open water! I was happy with the sting rays. Go figure.) Someone else who simply did things.

Grand Cayman Underwater 24

My hand, petting a sting ray’s nose. It was softer than I expected.

But no, it was me. Me before I felt this sick and tired and in pain all the time. Except not really. My nausea was much worse back then. The pain was just as bad (or worse), simply in fewer parts of my body. But the fatigue wasn’t the same. The food limitations weren’t so strict. The knowledge of how sick I was hadn’t reached me yet. I figured I was ok, just with pain and nausea, and so I did things.

And now I don’t.

I haven’t been on an airplane in almost 7 years. I miss travel, but I don’t do it. What’s the worst that could happen? I hate to think about it. But would it really be all that bad?

Why don’t I try new things that are fun and exciting? Sure, I do new things, but they’re boring things. I’m writing a book. I tried a new group through Meetup. I have started dog sitting. I might enjoy the things, but they don’t open me to exciting new experiences. They don’t expand my view of the world. They aren’t like scuba diving with sting rays.

For a long time I have been frustrated by feeling like I couldn’t do things. Now I question if maybe I could do those things, but my fear is what’s holding me back. I get different opinions from my doctors. No one tells me sure, it’s no problem if I want to fly to England to visit a friend there. But they also don’t tell me it’s a horrible idea and I shouldn’t consider it. I get a lot of, “you could probably do it if….”

And then I wonder if my fear is rational. I’m worried about having a lousy trip because I feel horrible the entire time. It seems like a waste to spend a lot of time, effort, and money on a trip that I won’t even enjoy. But I could risk that. It’s not what’s ultimately holding me back. No, what’s holding me back is a fear of setting back my health.

If you have been following this blog, you know that 6 years ago, I was struggling, but getting by. I worked a full time job and sometimes went out after work. I liked a fairly “normal” life. Then things got so bad that I was on bed rest 3-5 days a week. Now I am doing much better than I was a few years ago, but no where near well enough to work a full time job. I can’t even manage a part time job. Still, things have been slowly improving. Doing something big and exciting could set me back. And a backslide could take years to recover from. I’m scared to risk that!

And let’s be clear, I’m not only talking about travel. I would love to go ziplining locally, but what if I injure myself, or my adrenals can’t handle the excitement? I want to go to a party and stay out late and have fun, but whenever I try I feel horrible for days afterwards, sometimes weeks, so now I’m scared to do it anymore. I want to try a new type of food that’s free of gluten, corn, and the other foods I can’t eat, but what if it makes me sick? I could go on and on.

Some of these are reasonable and I should avoid them. But others….. am I letting fear hold me back too much?

Fear has it’s place. It protects us from doing things that will hurt us. But right now, I wonder if it’s stopping me from experiencing great things that I will love. Things that will make me happy. Because what’s the point of life if I’m not experiencing it? Then again, what’s the point of life if I’m always making myself miserable?

I don’t have an answer to these questions, but at least I have gotten to the point of questioning my own fears and whether or not they are valid. I’m frustrated that I don’t have answers, but I am glad to be asking the questions.

Maybe one day I will be able to answer: are these fears reasonable?

If you have dealt with similar fears, how have you handled them? Do you take the risks, or avoid them?

8 Comments | Decisions, Expectations, Fatigue, Frustration, Gastrointestinal, Limitations, Pain, Rants, Symptoms, Unpredictable | Permalink
Posted by chronicrants

The power of a hug

October 14, 2017

Somehow, I did it. Despite the crappy weather that makes me feel horrible, I managed to not only survive the short weekend with my friends, but to enjoy it!

Ok, it wasn’t all great. I did feel like shit part of the time. But having friends there made it easier to handle in some ways.

Of course, having friends there also made it harder to handle. They went on walks when I couldn’t, and while someone was always hanging out at the house with me, I know they limited themselves to do it. I wanted to be carefree and have fun, but life isn’t always that way.

Not that the others were carefree. One was frustrated with a spouse, another had job worries, etc. You know, life. It’s easy to forget about that stuff when you live alone and can’t work, but health does not guarantee an easy, stress-free life.

So there we were on Saturday night, having a lovely dinner, when it hit me. Symptoms. Fuck.

I went to lay down on the couch. It was an open space. No one could see me because the back of the couch blocked their view from the dining room table, but they knew I was there, and I would sometimes speak up to join in the conversation as they cleared the dishes and put away food. I was nauseated and in pain, not that they knew what my symptoms were. They just went about their evening, because they know that’s what I prefer. No fuss.

And then it got worse. Resting on the couch wasn’t enough. I found myself breathing hard, face pressed to a pillow, willing myself to feel better. I wanted to have fun with my friends. I didn’t want them to know what was going on.

It’s lousy that we have this stigma in our society. These are my closest friends, but I didn’t want to tell them what was going on because I didn’t want to sound whiny, or like I was trying to make a big deal out of nothing.

How ridiculous. How common. How sadly natural.

And then suddenly, as if she knew, one friend came over, leaned over the back of the couch, and asked earnestly if she could do anything for me. I said no, while at the same time, wishing I could ask for a hug. She’s not the huggy type, and I felt ridiculous. Still, her asking was like a hug in a way, and it suddenly brought tears to my eyes.

I never cry when I feel bad like this. It wasn’t that bad, on my own scale of suckitude, after all. But having someone care to ask made me emotional. I’m not used to that. Usually when I feel horrible like I did that night, I’m at home. Alone. With no one around to even be aware that something is wrong, much less to offer help.

Then another friend came over and simply gave me a hug. And when I let go to pull back, she held on. She kept hugging. She hugged and hugged. And it felt amazing.

The next day I pulled her aside to tell her how much that hug helped. But in the moment, I just felt it and enjoyed it.

Amazingly, I started feeling better right after that. Well enough to at least get up for some more medical cannabis. That helped some more. And then, suddenly (though not really suddenly at all) I was able to get up and move around. Ok, my knee still had shooting pains, so I wasn’t walking well. I had to sit with my leg up for the rest of the night. But the nausea went away. The pain because bearable. And my heart felt happy.

Because for once, friends were there to offer help and give me hugs. And that made all the difference.

 

Leave a Comment » | Gastrointestinal, Isolation, Kindness, Limitations, Pain, Raves, Relationships: Family & Friends & Dating & Sex, Support | Permalink
Posted by chronicrants

Painful weather, like it or not

October 5, 2017

It’s October in New England, but you wouldn’t know it if you didn’t look at a calendar.

Every summer I count down until the third weekend in September. That’s when I know the weather will have finally shifted for good, and I’ll be feeling less pain, less fatigue, and less nausea. It’s truly a magical time.

But not this year.

This year we had cooler weather in August, and I was grateful for that, but I also knew it wouldn’t last. September was up and down. But surely October would be my time, right? Not so much.

When you have chronic illness, nothing is simple, and the unpredictable symptoms, flares, and other issues can make life hard to plan. Still, we do our best. For me, that means making more plans in the fall and winter, when I know I will feel better.

That’s why, even though a “simple” weekend away with my best girlfriends is incredibly hard, I felt I could do it if it was in the fall. My friends are understanding, and were perfectly happy to avoid planning anything in September, just in case. They get it. Every time we’ve had cooler, less humid weather, I get text messages and emails from friends saying, “This is your kind of weather! I hope you’re feeling up to enjoy it.” And I love that they understand.

So we planned for “safe” October. Who could have known? This isn’t our typical cool, crisp, wonderful New England autumn.

Thankfully the temperatures are cool enough, though way too warm for this time of year (upper 70s?!? Are you fucking kidding me?!?) My problem is the dew point. It’s supposed to get close to 70 this weekend! Even healthy people find that uncomfortable and for me, it will be near torture. But what can I do? The house we rented doesn’t have air conditioning – after all, none of us thought we’d need it. Higher on our list was finding a house with a working fire place. Last year we did this trip later in October and it snowed. We had a lovely time sitting by a roaring fire, and wanted to repeat that experience. If only.

I am in pain already, and it’s only beginning. Well yes, I’m always in pain, but this is worse, and I know it’s from the weather. My toes are swollen and painful. My knee is swollen and so painful that it’s hard to walk. My neck hurts. Everything is just wrong.

But I won’t stay home. I have been looking forward to this trip for a year. It is my one chance to do this. I will NOT give it up!

I will bring the medications that I can. I will be careful how I eat. And I will block out a lot of extra recovery time when I return. Still, I know this is going to be really rough. I will be in pain, nauseated, and fatigued. Thankfully, I will be surrounding by wonderful women, women I have known most of my life, the only non-relatives who knew me before any of my symptoms began, women who have always been supportive. And maybe most importantly, women who have always made me laugh, even at the worst of times.

So wish me luck. Because I want to be able to enjoy this weekend as much as possible. If only Mother Nature would cooperate.

7 Comments | Expectations, Fatigue, Frustration, Limitations, Pain, Rants, Relationships: Family & Friends & Dating & Sex, Support, Symptoms, Unpredictable | Permalink
Posted by chronicrants

How a weekend away is a 2 week ordeal

October 2, 2017

I’m going away this weekend and I’m super excited!

I used to travel all the time. 2 months at home felt like FOREVER. I could pack an overnight back without even thinking about it. I got on a plane multiple times each year and did some weeks and weekends within driving distance. A weekend away in the Berkshires, less than a 3 hour drive away, would be no big deal.

But that was then.

And this is now.

Now I have to plan. I am being super careful about washing my hands and avoiding germs. I can’t get sick now!

I need to bring food with me. I will be with friends and some food will be safe for me to eat, but I need to bring other food. So I went to the grocery store today (Monday) and carefully planned out what I will make and which days I will make it. I also promised to bake cookies to bring, and I can’t do big cooking on the same day I bake, because I won’t have enough energy for that, but I can’t make anything too far in advance because I want it all to be fresh.

The day before the trip I will do some packing, but most of my stuff (my ASV (which is like a CPAP), my medications, toiletries, and more) can’t be packed until the day of. I need to ration my energy that day. Thankfully, I only have to drive half an hour to a friends’ house that day and then she will do the rest of the driving from there. Still, even being a passenger will be tiring and painful.

I am already thinking about how to handle my food and medications on the day of the trip. I always feel like shit the first night I travel. So I am being careful to bring everything I need to take it all at the right times: I will take something to help with the pain and the nausea when we start to drive, something else for the pain when we arrive, then something else for the nausea a few hours after that. Between medical cannabis and pepto bismol, the right foods and lots of rest, I am hoping really hard that it won’t be too miserable. Thankfully, I will be with friends who will understand if I can’t hang out with them that night.

I have scheduled my medical appointments around this trip. I was able to get a physical therapy appointment just a couple days after I return, so hopefully that will help with the pain from the long car ride and sleeping in a less-than-great bed.

My calendar is empty for the first 2 days after my return. That will give me time to rest and recover. I will get a lot of sleep, watch tv and movies, crochet, and read. If I feel up to it I will do more, and if not, that’s ok too. During my recovery time, I still need to eat, and I might not be up to preparing food, so I am making sure to cook and freeze food now that I can eat when I return.

I want to travel more. I really, desperately do. But then I remember what a trip like this is like. I can manage it ok, because it is only two days. I will leave at noon on Friday and be home by 5pm on Sunday at the latest. And I won’t be flying. I know it would be much harder if I was flying, for many reasons. It would be more painful. I might feel anxious at being “trapped” on a plan. Not to mention, I wouldn’t be able to bring any cannabis with me, and I can’t imagine how I would manage my symptoms without it.

At the same time, a friend and I are trying to schedule another weekend that I can visit her. The drive is less than 2 hours, but I would be driving myself. She would provide food I could eat during the entire visit, but aside from that, everything else would be the same. Resting for days in advance, blocking out days afterwards for rest, figuring out medications and other things to help alleviate my symptoms while knowing that I will almost definitely feel like shit the night that I arrive.

Sometimes it doesn’t seem worth it. But I know it will be in the end. Even thought it won’t be easy. It won’t be like it was before. But hopefully it will still be fun.

2 Comments | Decisions, Expectations, Fatigue, Frustration, Isolation, Limitations, Pain, Rants, Relationships: Family & Friends & Dating & Sex, Symptoms | Permalink
Posted by chronicrants

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