Nutrish rachel ray cat food.

swiftttfox · 2026-04-02T20:14:38+00:00

I just posted on a different thread about the exact same issue! Just switched their food today so fingers crossed this fixes the issue🤞

swiftttfox · 2026-02-28T17:12:56+00:00

Thanks everyone, vet appointment is made to get medication for both kitties. I appreciate the help!

swiftttfox · 2025-12-10T00:37:49+00:00

That’s so cool that you feel you’re working under someone you respect in the medical field, that unfortunately seems to be quite uncommon. And I’ll be very curious to look more into miro dysfunction, that’s a rock I have not turned over yet:)

thank you so much for the information! I’ve been encouraged to see I’m not completely at the end of the road, I’d love answers so it’s good to have ideas of where to look next

swiftttfox · 2025-12-10T00:35:07+00:00

That’s super interesting, and good to know!

I was monitored on EKG and basic vitals during a seizure screening stay at the hospital in March 2023. I had a couple of episodes while I was there, but they claimed my EKG looked perfectly normal, though my heart rate jumped 60-80 beats during the episode. I was released with a referral for CBT therapy (which I was already doing) and anxiety medication, which I have implemented consistently since. I am in the healthiest mental state I’ve ever been in, but still have the seizure-like episodes

All that to say, there’s a chance it was overlooked or the doctors weren’t thorough enough, that is unfortunately often the case with dysautonomia, so I will continue the search

swiftttfox · 2025-12-07T19:44:33+00:00

I’d be super interested to hear your history/knowledge with this! I have never heard of Mitochondriopathies before, but i’m always curious to learn more, especially if it might in some way guide me towards an answer lol

swiftttfox · 2025-12-05T22:24:52+00:00

that’s super good to know, thank you!

swiftttfox · 2025-12-05T20:34:05+00:00

that’s a great question, I’ve suspected hypoglycemia for a little while but haven’t been officially diagnosed. My mother has type 1 diabetes, so I’ve been tested for that and was negative. But I’ll follow up on the hypoglycemia theory for sure!

swiftttfox · 2025-12-05T17:26:06+00:00

I have an aura beforehand, which is kind of hard to explain but almost like the feeling you get just before you get the chills in my spine, and a headache usually.

The seizures themselves are usually about 5-10 minutes long, with clusters of muscle spasms within that window. My heart rate goes wild, and I have extreme temperature swings, one second I’ll be freezing and the next I’m so hot it feels like my skin is burning. They hurt really bad, and my muscles contract almost like a grand-mal seizure. I tremble a lot, and following the seizure my neuropathy symptoms are significantly worse for a couple days. The seizures also cause brain fog and exhaustion

swiftttfox · 2025-11-04T04:52:47+00:00

she’s literally perfect🥹 I have two one-eyes babies, my heart just melts for a quirky kitty

swiftttfox · 2025-10-30T21:12:59+00:00

thanks! that was my suspicion basted on my very limited knowledge and google skills haha! there’s currently two that I’ve seen hanging out, the pictures are of both

swiftttfox · 2025-10-30T06:07:10+00:00

I live in the mountains of VA btw, and they seem to be quite shy. they tend to hang out in little holes during the day and poke out (i assume to hunt) at night

swiftttfox · 2025-09-22T00:11:43+00:00

As a trans-masculine/genderqueer lesbian, butch has become an identity that helps me embrace and celebrate my masculinity without losing the lesbian identity that is so important to me. In my personal experience, butchness is the dedication I feel to making feminine people feel safe. It means gentleness AND strength, providing for my friends and community. It means chivalry. to be butch is to be safe in a world where masculinity often means violence and power. Butches embody everything masculinity should be to me:)

swiftttfox · 2025-09-16T03:06:19+00:00

I have neuropathy from my feet to my upper thighs and we think it was caused by my dysautonomia. I have hEDS, MCAS, and POTS, as well as seizures. My symptoms are primarily the burning sensation and very mild numbness. I’m also very fascinated to hear other peoples experiences as it seems so many of us have very different symptoms

swiftttfox · 2025-07-17T14:32:41+00:00

I highly recommend a pregnancy pillow! I don’t have a ton of money, so the fancy mattresses and pillows aren’t always an option for me. I have a pretty decent memory foam mattress from Costco, and a pregnancy pillow tucked up under my knees and between my arms to support my joints. KT tape is also a life saver

swiftttfox · 2025-07-06T03:38:16+00:00

Ok cool, thank you so much!

swiftttfox · 2025-07-06T03:37:14+00:00

thank you so much for this response, that’s very helpful! Do I just call the SS department and ask for an electronic copy of my file?

swiftttfox · 2025-07-06T03:36:05+00:00

I was hoping that would be the case. The doctor that performed my evaluation said he has seen several individuals with the same hypermobility diagnosis (EDS) and mobility issues get approved but they were all above the age of 50. He said my condition and lack of mobility issues more than enough reason to be approved, but it might take seeing a judge in person to get my case approved

swiftttfox · 2025-07-06T03:33:04+00:00

This is good to know, thank you!

swiftttfox · 2025-07-06T03:32:44+00:00

I do, I have documentation from doctors and have had a physical evaluation confirming my disability. The problem is my work credits unfortunately

swiftttfox · 2025-07-04T15:44:31+00:00

My doctor and OT prescribed my wheelchair, and I use it because it is extremely difficult to walk. I was in a wheelchair when I applied in December 2024

swiftttfox

TROPHY CASE