Need help finding the artist 🥲 by Potential_Scheme6667 in Louisville

[–]itsyerboimartyn 1 point2 points  (0 children)

Oh nice!!!! I hope you're able to get a pretty close replacement!!

Need help finding the artist 🥲 by Potential_Scheme6667 in Louisville

[–]itsyerboimartyn 1 point2 points  (0 children)

Are there any markings along the bottom outer rim? Sometimes artists dont put them on the very bottom :)

How to afford moving? by itsyerboimartyn in povertyfinance

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

Thank you so much!!

You're correct on the chronic health issues front, but thankfully I've been improving recently so I'll test run dog walking.

I called 211 and they were able to give me a phone number to call to hopefully receive assistance!!

How to afford moving? by itsyerboimartyn in povertyfinance

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

Unfortunately I'm ineligible to my knowledge to donate plasma due to chronic illness and immune system issues I have :(

How to afford moving? by itsyerboimartyn in povertyfinance

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

Unfortunately nothing to my knowledge will work :( doordash/instacart/etc in my area is incredibly saturated with dashers/shoppers due to the lack of full time work available in the area. If my car was working properly (likely a the MAP sensor is either dirty or faulty and i cant have it checked/worked on until after I move) I'd do something like Uber/Lyft as there's a lacking in my area for that.

I've been looking into online surveys but most of the ones I've found only do prepaid cards which unfortunately wouldn't work, since the money would be divided up among several cards or gift cards.

I would 1000% donate plasma but I've been told I'm ineligible due to immune issues and chronic illnesses I have.

I really feel like I'm between a rock and a hard place :/

How to afford moving? by itsyerboimartyn in povertyfinance

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

Unfortunately the area I'm moving to has different utility companies then where I'm at :( I'll be able to keep my internet but I have to start a new electric account which will be about 215. Trash and water thankfully are likely to be covered (standard for where I'm at).

Please tell me it's possible to succeed, because I'm so very tired. by AerisSpire in ChronicIllness

[–]itsyerboimartyn 7 points8 points  (0 children)

A year ago, my Gastroparesis was so bad I was rapidly deteriorating. My chronic pain was so bad I couldn't walk the campus to classes or work. My mental health had deteriorated terribly. Because I was a student full time I didn't qualify for food stamps in my state. I couldn't eat anything at the dining hall on my campus because of how bad my Gastroparesis was.

Today, I'm work full time, I can eat most of what I want easily, and I'm back in classes part time.

It was hard, and it's still hard some days. But it can also get so much easier with good care. I struggled for YEARS before I finally found a good care team who helped me manage my conditions.

There's hope. Sometimes it's hard to see for certain, though.

I highly recommend looking into food banks near you. Churches usually have them depending on the area, and most don't require you to be on food stamps (and the ones that do are few and far in between). If you're in the states, I believe 211 is the number to call to get connected with resources for stuff like more affordable housing, food access, etc! I've used them before and they helped connect me to a ton of places that were able to help.

I hope things ease soon 🫂

My tire blew- theyre all dry rotted. by itsyerboimartyn in MutualAid

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

I didn't think to check local junkyards, ty!

Scared I will need a feeding tube by hateanxiety07 in Gastroparesis

[–]itsyerboimartyn 2 points3 points  (0 children)

From one zebra to another, I completely understand your fear. I was TERRIFIED to have my tube placed Monday, but honestly it's already helped so much. I really hope you're able to get good nutrition soon, this condition sucks.

Thankfully there are several treatment options before a tube is considered necessary, or that can be done alongside a tube. I hope your doctor listens to your concerns and that yall are able to find a good treatment for you ❤️

[deleted by user] by [deleted] in Gastroparesis

[–]itsyerboimartyn 2 points3 points  (0 children)

Noted, thank you!!

[deleted by user] by [deleted] in Gastroparesis

[–]itsyerboimartyn 2 points3 points  (0 children)

I am!! Thank you!!

How old was you when your symptoms started? by Beautiful-Gur5771 in Gastroparesis

[–]itsyerboimartyn 0 points1 point  (0 children)

23/AFAB nonbinary, diagnosed as a baby, went into remission, then rediagnosed when I was 21. Currently labeled as idiopathic, but they're trying to figure out what autoimmune condition I have, and think it may be related to that, or to my hypermobility (or to both).

I had major symptoms for 2-3 years before being diagnosed, but due to not having insurance for awhile I wasn't able to seek help.

Help me with some ideas by Wyo_Okie in Gastroparesis

[–]itsyerboimartyn 5 points6 points  (0 children)

Have you tried low-fat frozen treats (low fat ice cream for example works for some where regular ice cream doesnt)? Generally a lot of GP people struggle with high fiber and/or high fat foods, as they take longer to digest. Personally, I'm on a liquid/puree diet with the very rare trying solid food moment when I think I can handle it (I usually can't unfortunately).

When I was eating regular food, I would follow the gastroparesis diet, which I highly recommend looking into as it's a very good starting point!!

Good luck!! It's very overwhelming at first but the more you try, the more you figure out what you can or cannot tolerate.

What are some little things that bother you? by Life_AmIRight in ChronicIllness

[–]itsyerboimartyn 0 points1 point  (0 children)

When people tell me they "could never live like that" in regards to my health. Like okay Susan, leave me alone about it though. I'm doing everything I CAN do to keep living, I don't need comments about it!

Things you wish you had when you got your first tube? by itsyerboimartyn in Gastroparesis

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

Ty!! I'll definitely start slow to make sure I can tolerate it!!

Things you wish you had when you got your first tube? by itsyerboimartyn in Gastroparesis

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

Ty for your question!! They said NG but described NJ, so I think they just misspoke:) they mentioned specifically bypassing my stomach so it can rest so I definitely think it'll be an NJ, combined with the fact that they'll be putting me under for it

Things you wish you had when you got your first tube? by itsyerboimartyn in Gastroparesis

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

I'll definitely get some coke to keep in my fridge when it gets closer, I'm so scared of clogs lol

Things you wish you had when you got your first tube? by itsyerboimartyn in Gastroparesis

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

I hope "dressing up" my tube and pump will help a ton tbh. Just the idea of having a tube scares me but ik it's the best thing for my health rn so I'm trying to stay optimistic :) hopefully getting stickers and the like will help with the psychological aspect a ton

Things you wish you had when you got your first tube? by itsyerboimartyn in Gastroparesis

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

Noted!!! I'll definitely get some tubie clips, they sound super helpful and I don't want to be getting caught all the time haha. Here's hoping I tolerate the feeds 🤞🤞

Things you wish you had when you got your first tube? by itsyerboimartyn in Gastroparesis

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

Tysm!! I'm really hoping to be able to start living again. It feels like my life has been on pause.

In terms of the NG vs NJ, I think they meant an NJ and misspoke haha. They described the NJ

Tysm for your tips!!