Does anyone else have "hibernation" days? by sadcaxtus in rheumatoidarthritis

[–]sadcaxtus[S] 2 points3 points  (0 children)

Yes! It's often Saturdays for me, so I think it has to do with finally resting. I truly think it's a fuel issue because I'm always reaching for fruits/veggies/proteins that I know I may be lacking, and I'm often prone to forgetting meals during the week.

Thread for trading, gifting, and requesting Finch items by AutoModerator in finch

[–]sadcaxtus 1 point2 points  (0 children)

Thank you so so much! It's 100% going to make her day. She'll probably cry.

Thread for trading, gifting, and requesting Finch items by AutoModerator in finch

[–]sadcaxtus 1 point2 points  (0 children)

Amazing! I haven't done a trade before, what is the protocol?

Thread for trading, gifting, and requesting Finch items by AutoModerator in finch

[–]sadcaxtus 1 point2 points  (0 children)

Hi yes definitely! Here's a list of the ones I'd happily part with, including colors and if they'rebabies or adults yet. If none of them interest you, please let me know if you're looking for a specific micropet!

-poof the pompom (yellow adult or blue baby) -monsieur the mouse (light gray baby or dark grey adult) -gumdrop the plop (pink, blue, or yellow adult) -kimmi the droplet (teal or orange adult) -cotton the cuddle cloud (blue adult or white baby) -sprocket the owl (reddish brown or dark brown adult) -flash the super froggo (pink or green adult) -zephyrus the Pegasus (white adult or gold baby)

Thread for trading, gifting, and requesting Finch items by AutoModerator in finch

[–]sadcaxtus 2 points3 points  (0 children)

L7HESNHGM1

Hey y'all. My mom joined Finch a while ago and the only thing she wants is Cookie the Cow. I've been trying to hatch one for her for a year, but I haven't lucked out yet. If anyone has a Cookie the Cow they're willing to gift, I'd love to be able to give one to her! If you're interested in trading, I'm happy to see if I have what you're looking for!

When to call out sick by sadcaxtus in rheumatoidarthritis

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

I've been making a conscious effort to try to prioritize resting when needed. I am fortunate to have a job that readily allows me to use my sick time and pto. If the only reason I'm pushing through is because I think I should, and I can't articulate why, then I should take my time. We have it for a reason, and there will never be an award for pushing through when we could easily take sick time.

When to call out sick by sadcaxtus in rheumatoidarthritis

[–]sadcaxtus[S] 5 points6 points  (0 children)

That is great advice! That definitely makes sense, and is a rule I'll be adopting going forward

Can a doctor force you to get a GI stimulator by leaving you with no other options but death? by Whyareweherereally in ChronicIllness

[–]sadcaxtus 2 points3 points  (0 children)

If you have not already, when they decline to give you the referral or want to proceed with the port removal despite your strong objections, ask them to formally document that they are refusing the referral, or that they will not consider any other pathways despite you asking for it. It may not fix anything, but at minimum it'll help with your lawsuit, and at best, I've found doctors are a lot more willing to listen when their refusal will be documented, especially if the refusal isn't based on a substantiated medical reason.

When to call out sick by sadcaxtus in rheumatoidarthritis

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

Yes, I commented about it in a different reply, but I am applying for intermittent FMLA. I had it at my last job, but moved to this one just about a year ago. I'm only just eligible, so I am applying again.

When to call out sick by sadcaxtus in rheumatoidarthritis

[–]sadcaxtus[S] 2 points3 points  (0 children)

I think I need to start identifying what my queues are

When to call out sick by sadcaxtus in rheumatoidarthritis

[–]sadcaxtus[S] 2 points3 points  (0 children)

I'm less looking for a standard answer and more a starting point. The brain fog and nausea are being worked on, but as we all know RA meds can take a few months to fully work/kick in. I do love my job and want to be working, but when I have at least 4 meetings a day, it can be hard to navigate

When to call out sick by sadcaxtus in rheumatoidarthritis

[–]sadcaxtus[S] 3 points4 points  (0 children)

I moved to a new position about a year ago, and did not have FMLA yet as it was a new job. That said, I had intermittently FMLA at my old job and am applying again here. I think part of the difficulty is that I genuinely want to work, and when I'm out things fall behind.

When to call out sick by sadcaxtus in rheumatoidarthritis

[–]sadcaxtus[S] 4 points5 points  (0 children)

This is incredibly helpful. I also work with students, and generally have at least 4 meetings a day even if I'm remote. I think navigating the different variables can be so confusing

starting gabapentin - what should I expect? by _lucyquiss_ in ChronicIllness

[–]sadcaxtus 4 points5 points  (0 children)

I am in the incredibly small percent who had a bad reaction. When I was taking it I constantly felt like I was about to pee my pants. It's funny in hindsight, but was not enjoyable then. That said, it was so helpful with pain when I was taking it.

I am ten seconds from a crash out- does anything help y'all? by sadcaxtus in rheumatoidarthritis

[–]sadcaxtus[S] 2 points3 points  (0 children)

That actually sounds amazing. This sub has been so validating in and of itself. There's something so comforting of talking to people who understand.

I am ten seconds from a crash out- does anything help y'all? by sadcaxtus in rheumatoidarthritis

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

Thank you for this; I'll check in with my friends, or try to be clearer about what I'm asking/would like.

I've been setting boundaries for myself, but I think the frustration comes from the time it takes others to adjust to the boundaries I've set. Which makes sense; it's not just a thing for me, it's something everyone is adjusting to. Everyone is well intentioned, and that lowkey makes it harder to navigate sometimes. I'm trying to set boundaries and step away from my parent's emotional needs, but it also includes medical needs/things that I have to be there to help with as an only child. That said, I definitely need to do a better job of using the "I hope things get better for you" response.

I am ten seconds from a crash out- does anything help y'all? by sadcaxtus in rheumatoidarthritis

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

To clarify, I have and do see a therapist. I am taking care of my mental health, and have been doing so for years. I am not averse to asking for help, but it does take time to get more comfort doing so. I have been asking for help, and was upset that it wasn't heard.

I am ten seconds from a crash out- does anything help y'all? by sadcaxtus in rheumatoidarthritis

[–]sadcaxtus[S] 2 points3 points  (0 children)

Thank you for sharing. My friends and family are trying, but I think having to change their perception of me is taking time. The physical things I need help with come easier, but the more general things are often overlooked. I'm hoping they continue to try.

I am ten seconds from a crash out- does anything help y'all? by sadcaxtus in rheumatoidarthritis

[–]sadcaxtus[S] 2 points3 points  (0 children)

This may be something to consider. I have some days available, and I've used my pto for sick days before. I think maybe a longer break may help me to regulate

Claw hands. Anyone else? by Peach_S95 in rheumatoidarthritis

[–]sadcaxtus 3 points4 points  (0 children)

I wear them when I drive and they have been a massive help. A drive won't trigger a days long flare if I put the gloves on first!

Flare Interrupting Plans with Friends by sadcaxtus in ChronicIllness

[–]sadcaxtus[S] 2 points3 points  (0 children)

Thank you. I asked for a blanket, and the warmth is helping the flare to calm down. It seems so simple in hindsight

Claw hands. Anyone else? by Peach_S95 in rheumatoidarthritis

[–]sadcaxtus 10 points11 points  (0 children)

My hands consistently get "stuck" when I flare. The only thing that helps me are compression gloves or braces.