u/WoofJess

I traded with somebody named BobbyMcJoe177 > Epic: PieGuy177.

Said he’ll give Galaxy King for Gummy Dream. I give him the dream and I think I’m getting the King. It is Galaxy coloured. Back to lobby. It’s not there. He brought in an earth or something of the Galaxy variant.

I really don’t understand why people are like this. Have some shame. Literally.

If so, what papers and information did you supply that helped?

I also have endometriosis as well as undiagnosed Autism and PMDD that impacts my physical and mental.

I’m just unsure as to whether it’s worth applying or not.

TIA

So the job I applied for shortlisted me and informed me the job will be Mon-Friday 10-1 at a 29.93 rate. This equates to maybe $40ish over my jobseeker payment. So with that, I’ll eventually lose my concession card; the ability to get cheaper medications (that I do require; without concession I’ll be spending $50-70 on them), vet care, public transport fares etc, and also flare my chronic illnesses and speed up the death of my car by the back and forth driving it’ll need to do now. And if you check Carsales you can’t even get a bomb or old car for a decent price.

How’s this better than being on benefits? I’m failing to see any pros that would outweigh the cons. Should there not be some good pros?

Because GP’s I’ve spoken to kind of brush it off and move onto another topic or say that’s more a topic for psychologists or gynaecologists. I had a gynaecologist and he didn’t want to hear about it (primarily cause I was there to get a laparoscopy for endo). Right now, im self diagnosed but I need a proper diagnosis so I can push to put it on medical exemptions and other important documents.

I’ve been experimenting ever since he’s been diagnosed and he’s very sick of the prescription wet food. Then people say to not do homemade but it’s like what else is left when he won’t touch the cans?
He will eat around food he doesn’t like and eat only pieces of chicken or SPD boar (ok in moderation for renal diets). Very picky with puree’ veggies, pumpkin, and egg whites. That’s essentially all he can eat. I’m stressed.

Edit- I’ve done all 3 available in my country/ hills, royal canin and purina. He’ll eat a few and then get sick of it. All the same. Not tried dry… but I don’t think it’s worth seeing as he needs a lot of water and will probably also be even pickier with the dry. I’m not in a position to waste food and money so I’d prefer recommendations that really work and are suitable for mid stage kidney disease.

I’m losing my mind over this. I’ve tried every renal can. I don’t particularly want to do dry renal because it’s better if he’s always getting some water (he’s not on fluids at this stage and needs to go back for bloods)

My whole question is based on the fact that I’m having a very very difficult time getting him to love and eat his food. And I’m pretty sure I’ve figured out its fussiness over deterioration.

I don’t work or have a partner so I’m trying to work with options that won’t break my budget but still provide adequate nutrition.
So I do 1 tin of renal wet and then mix in white rice, puree’d veggie (carrot, zucchini, pumpkin) and some boar to make it more appealing and to make up for not using 2 cans a day because they’re expensive, and he actually won’t eat them on its own — With omega 3 oil and urinary/kidney support powder. Optional toppers, egg whites, sardine/tuna (water), or bone broth.

I’m at a loss of what to do at this point. Any suggestions would be appreciated.

And between the physical and mental symptoms from the PMDD/severe hormone sensitivity, adjustment to the pill (dienogest) for endometriosis treatment, and overlapping chronic health issues..

I can’t take it anymore. No one cares and nobody is helping me find any solutions to be able to function on a day to day basis. I feel like this phase is so prolonged now because I won’t bleed (because the pill is messing with it) I feel like a complete shell of myself. My health has deteriorated so badly that I think I’d have more peace if I was just dead.

I keep telling them how am I expected to hold a job or attend interviews if 3 weeks out of 4 every of every month I’m rage fuelled, have chest weirdness, shortness of breath, poor sleep, very bad brain fog and stupidness, headaches, mood swings, severe fatigue,
inflammation, worsening anxiety etc etc. 24.7. No breaks. Maybe what feels like 4 good days a month. If I don’t have SI, I genuinely just feel like I’m physically dying.

I have an interview they’ve found me on Tuesday and my initial thought was,
I’m sick of having to mask and prove my suffering. I can’t lie and say I’d be able to even do this role because my health is so unpredictable, in terms of the severity, not duration.

This world sucks. I don’t know what to do tbh. I just want to not be bothered by anyone or anything.

I’m looking at dumb phones or a smart phone that’s not made by anyone who’s in kahootz with 🧃s.

There’s some theories that there’s actually bombs in iPhones. Apparently Chinese made smartphones aren’t safe either cause some companies work with each other. And overall I just want to go back to a time where it didn’t control my life… and the plans/bills didn’t keep climbing in price. It’s getting ridiculous.

Anywho, I think it needs 4G VoLTE to make text and calls.

I don’t know if anyone is the same but my self control, discipline and impulse control are at an all time low, especially during this phase.

Edit: I’ve asked this question more so to combat the symptoms of PMDD because apparently eating the bad food makes things a lot worse.

I don’t even know how to explain it away 😬 and I’m not sure I want to.

THIS IS SO BAD.

THIS IS LITERALLY THE WORST DISORDER.

Because, I’m me, I’m aware but I can’t stop myself from being a rage fueled bison during this time omg

Plus they’re guys. So they would literally not even comprehend the complexity of it.

And it’s also strange because I found out at 30 I had this. But if I think back to when I was a teenager, I had similar things happen all time. And now I’m mournful and about to sob over it all.

So I had my lap 23/ Jan where they found stage 3 endo and a cyst they removed. I personally figured maybe this was the cause of the extra symptoms I experience, such as the inflammation/puffiness, waking up at 2-3am, bloating, severe fatigue, excessive eating/cravings, headaches, nausea, aches etc
But I’m still experiencing it all on dienogest.

I’ve been on it for almost 5 weeks I believe.
I asked for it because their solution was the Mirena IUD or full hormone pill. And I didn’t want that because my theory was that I had excess estrogen (if I was getting endo and fibrocystic breasts + fibroadenomas)

But now my concern is that during ovulation and Luteal I have too much progesterone or something because the pill has intensified some things.

What it’s done is change my bleeding, and maybe is working at keep endo tissue from coming back quicker; pain is also a lot more mild when I did have blood - but everything else I went in to the doctor crying about is still happening.

Just wanting to know if anyone has any ideas, suggestions or has been on a similar path.

Gut feeling is this tablet is too unnatural and incorrect.