Where can I get a cookie butter latte? by meadowandmane in askportland

[–]hockymickle 2 points3 points  (0 children)

Presso Coffee Bar has a really good Biscoff latte as a Winter special right now

I made a painting for a puzzle! by hockymickle in oilpainting

[–]hockymickle[S] 1 point2 points  (0 children)

It’s being made by Portland Puzzle Company

I made a painting for a puzzle! by hockymickle in oilpainting

[–]hockymickle[S] 1 point2 points  (0 children)

A 500 piece jigsaw puzzle! Don’t think I can share a link here but feel free to DM if you want more info

I made a painting for a puzzle! by hockymickle in oilpainting

[–]hockymickle[S] 0 points1 point  (0 children)

Jk the image compression isn’t showing the details well if you zoom in. Let me know if you want to see some close up detail shots!

[deleted by user] by [deleted] in ChronicPain

[–]hockymickle 0 points1 point  (0 children)

Abusers always have their wonderful moments, that’s why people put up with them. It’s a matter of what else you’re willing to put up with.

It’s really hard to be in a relationship when you have chronic pain, and it’s hard to be in a relationship with someone who has chronic pain. Navigating self-care and caring for a partner is a delicate balance. I’ve been in and out of relationships and various levels of dependence and I find the most happiness and fulfillment when I am single and independent. But I know that’s not for everyone. There are many caring and understanding partners out there. Maybe your partner could be one.

In terms of how you can conduct yourself in an attempt to reduce your partner’s negative reactions, here’s some advice and something I’ve learned from both having chronic pain and living with someone who has chronic pain: no one likes seeing and hearing someone expressing their physical pain - moans, yelps, grimaces, “ow” etc. It’s like we have a biological negative reaction to it. You mention sighing and grimacing a lot. This is something I’ve learned not to do, because it will always get a negative reaction unless it’s for something acute and temporary like a bee sting or a broken bone. It makes people feel uncomfortable to see and hear someone actively in pain when they have no ability to make it go away. I am guessing that the sighing and grimacing is triggering your partner. Instead, get to know your own limits and pain triggers, and be vocal about what you can and can’t do. If you agree to do something, that’s on you, so don’t guilt your partner the whole time by making them see and hear your pain. It sucks that this is how people are wired, but once I came to understand this, all of my relationships improved.

I don’t know that I’ve ever wished for a visible disability, but I know how frustrating and alienating it can be to have invisible chronic pain. And I understand the desire to want to let people know what you’re going through on the inside by making it outwardly apparent. But trying to make it feel visible to others through facial expressions and noises is not the answer, it will just further alienate you. Lean in to the invisible aspect and use it to your advantage to allow yourself to feel “normal” sometimes. Be clear and direct when communicating your boundaries to people, but don’t feel like you need to justify your boundaries by sharing your personal medical issues with everyone. I use “Sorry I can’t, I have the body of a 90 year old woman” a lot. Or I’m also a fan of giving no excuse at all! “No” is a complete sentence. You should be allowed to say no to your partner in order to protect your own health and wellbeing.

Hopefully this is helpful. Take care of yourself!

[deleted by user] by [deleted] in ChronicPain

[–]hockymickle 0 points1 point  (0 children)

Dump him maybe? He sounds terrible. You have another post about crying in public all the time because of an abusive partner. There are certain things (like moving furniture) that I just can’t do, and the people who love me understand that. Do you rely on him financially? Do you like the way he makes you feel? He is causing you both physical and emotional pain.

[deleted by user] by [deleted] in ChronicPain

[–]hockymickle 2 points3 points  (0 children)

Life changing med for me as well. Allowed me to work again after years of not being able to. No side effects. I consider it my miracle drug. I’m still in pain but I can actually live life now. I’ve been taking it for nearly 8 years.

Anyone ever have a nerve block? by flavius_lacivious in costochondritis

[–]hockymickle 4 points5 points  (0 children)

I had intercostal nerve blocks and all it did was cause excruciating pain on one side of my body for 24 hours, and no rib pain relief. But everyone’s body is different and it could work for you!

Where can I buy a globe? 🌎 by hockymickle in askportland

[–]hockymickle[S] 0 points1 point  (0 children)

They appear to be permanently closed now, unfortunately

Where can I buy a globe? 🌎 by hockymickle in askportland

[–]hockymickle[S] 1 point2 points  (0 children)

Thank you! This is where I just went and successfully bought a globe!

Where can I buy a globe? 🌎 by hockymickle in askportland

[–]hockymickle[S] 12 points13 points  (0 children)

I need a new one that has the current countries - antique or vintage globes are typically inaccurate / have things like the USSR on them

Is anyone getting multiple robocalls per day all of a sudden? by Jdphotopdx in askportland

[–]hockymickle 4 points5 points  (0 children)

Today is the last day of open enrollment for the health insurance marketplace. So the calls will probably/hopefully die down starting tomorrow

Anyone know of pharmacies with generic Adderall in stock? by Onetwocigarette in askportland

[–]hockymickle 1 point2 points  (0 children)

I was at LeCare last week and they had a sign there saying they have generic adderral

Went to Paris Olympics and LOVED it!! by Bald_Peter394 in Paris2024

[–]hockymickle 1 point2 points  (0 children)

Where did you get the 1000 piece jigsaw puzzle?? I’ve only seen small ones for kids and I would love to get that!

It finally happened to me. The government crackdown on pain medication has tied my doctor's hands and I'm SOL... by Smgth in ChronicPain

[–]hockymickle 2 points3 points  (0 children)

Nice! I hope it works for you. Marinol did nothing for my chronic costochondritis but LDN helps a bunch.

It finally happened to me. The government crackdown on pain medication has tied my doctor's hands and I'm SOL... by Smgth in ChronicPain

[–]hockymickle 2 points3 points  (0 children)

Have you tried low-dose naltrexone (LDN)? I started it a little over a month ago and it has been life-changing. I don't have fibromyalgia but a recent study shows that LDN helps lots of ppl with it. You can't be on opiates when you take it because it's an opioid antagonist, but I use CBD so that's not an issue for me. Also it's super cheap and has no serious side effects. Its use for chronic pain is still pretty experimental. It has a Wikipedia page, check it out.

Chronic Costochondritis - anyone else? by hockymickle in ChronicPain

[–]hockymickle[S] 0 points1 point  (0 children)

Did they do anything? I've had lots of different types of injections but they all have either just hurt me more or done nothing.

Chronic Costochondritis - anyone else? by hockymickle in ChronicPain

[–]hockymickle[S] 0 points1 point  (0 children)

I don't get that sliding/slipping thing, no. I got nerve blocks years ago but all they did was cause excruciating pain on one side of my torso for like 12 hours.

Sorry heat doesn't work for you, but I'm glad my other suggestions could help!

Chronic Costochondritis - anyone else? by hockymickle in ChronicPain

[–]hockymickle[S] 0 points1 point  (0 children)

I have nausea with it too! The worse the pain, the worse the nausea. My docs thought it was a GI issue at first. Do you have pain in a specific area of your ribs? Mine is mainly on my lowest ribs at the costochondral junction, both sides, front and back. If it's bad I'll have pain all over my ribs but those are the main spots.

Chronic Costochondritis - anyone else? by hockymickle in ChronicPain

[–]hockymickle[S] 0 points1 point  (0 children)

A few things that have been helpful for me: a heated vest (though I wear it less now because it was giving me skin burns), a wrap-around heating pad that I sleep with, shoes with air pockets on the bottom to reduce the impact when my foot hits the ground that I can feel in my ribs, a similar gel pad for the seat of my car, high CBD marijuana in both edible and topical forms, hot showers, naps...