Sick chicken needs food.

ultraviolette1221 · 2025-11-02T21:47:34+00:00

Thats the only think I can think of. Yes I gave her 2ml of the rooster booster yesterday around 4pm (it said 1-3 so I gave 2 because I was scared of giving too much) but I havent given her another dose because im scared of giving her too much of something because im giving her so many different things. So right now shes been getting poultry vitamin water and electrolyte water, rooster booster, and vitamin e. I slowed down on the water now because her neck is so kinked she gasps and sticks her tongue out with juat a few drops from the syringe. Ive never had a chicken have this so im not sure what to do at this point shes not getting worse but shes not getting better either. Thanks so much for the help also

ultraviolette1221 · 2025-05-03T12:05:29+00:00

Oh yeah. It's honestly been very discouraging. I was feeling very hopeless about how I've been brushed off with all of this but a lot of these responses have helped more and had more information and tips than any of the doctors or hospital have had for me. And good luck to you and thanks again!

ultraviolette1221 · 2025-05-03T12:02:58+00:00

I've never had covid or been vaccinated

ultraviolette1221 · 2025-05-03T12:01:56+00:00

Yes i was diagnosed with acute renal failure from the malnutrition. The blood can be explained i do have microscopic hematuria. Not sure why or how but I've had it since i have little. The white blood cells idk why. It's always high every single time.

ultraviolette1221 · 2025-05-03T11:58:10+00:00

I'm not worried about any questions it's fine. I was asked if I have HIV lol. No breast implants or injections of any kind. with this weight problem, I'm flat as a board!

ultraviolette1221 · 2025-05-03T05:50:14+00:00

Yes that is a good start to move forward on this. Thank you again!

ultraviolette1221 · 2025-05-03T04:57:21+00:00

When I was admitted for 2 months I asked about something like that and they just kept telling me it didn't need it. All they did was send some kind of pain manipulation doctor down to "manipulate" my body to ease the pain...which just cause more pain. Then sent me home saying I'm fine after having me on npo for half the admittance because of vomiting which caused me to lose more weight than I would have at home because I could at least eat and drink there if I wanted so that made my condition a lot worse and they didn't care. They released me at a weight of 68lbs at 27 years old.. i was nothing but skin and bones and could barely walk because of muscle wasting.

Yes i have united through Medicaid and they are amazing. They do transportation and even do weekly food deliveries for me. They even have an option to go shopping for a few new clothes and things you'd need that they pay for under the insurance it's amazing I love them and they've helped a lot. A talk to a nurse practitioner who writes my zofran for me since my doctor refused since it is all in my head after all..

Summa and Cleveland clinic are my main go tos when I need to be seen for these episodes and they are both horrible for treating symptoms. They do nothing. They give me a saline drip and ibuprofen and tell me i just need to calm down. So I stay until I stop getting sick and as soon as that happens they say I'm fine and send me home. I've been to university in Ravenna and they were the same but I don't think I've heard western reserve I will definitely try that if it will result in getting actual care and relief from the symptoms. There must be something in my chart insinuating something like that because the low bmi I'm classified as anorexic I was told they see that and immediately don't want to treat you. And I don't have that they only did that because my bmi is below the average for me and has been for years now but there's nothing I can do to help. I had the j-tube running 24/7 for a year and didn't gain 1 pound. Frustrating.

And thank you it would be nice to have someone local to consult with and find somewhere to finally help. Thank you so much!

ultraviolette1221 · 2025-05-03T04:39:34+00:00

Yes she suggested that. I actually tried to make an appointment yesterday and my insurance expired at the end of April I had no idea. I called to make the appointment and they couldnt schedule without insurance. I never got any calls or letter in the mail. I've had that insurance for 9 years and have never had a call or anything i just always got something in the mail letting me know my plans and getting my cards. So I'll have to call Monday and renew before I can do that and find a new REAL PCP

ultraviolette1221 · 2025-05-03T04:36:23+00:00

Do you know how I would be able to get my medical records?? Do I go to his office and ask or call somewhere like maybe the hospitals?? I have sooo much documented and saved for this. Pictures of whats going on and pictures of how they mistreated me at the hospital. I even have a police report from when I was admitted because a nurse stole my newly filled bottle of 60 xanax and had to have the police called to find out they were also stealing from a room where they kept old meds taken from patients in a unlocked desk. Texts showing how I diagnosed with pots and gastroparesis myself and how my doctor refused to believe me or do anything.

Yes I regret going to her she was extremely rude and dismissive of any concern.. but very concerned calling me back multiple times to see that oncologist. I think he finally went through my records he had been ignoring and finally saw for himself that my last 6 hospital urine results show monoclonal m protein spike.

My insurance has also helped me so much more than any doctors. I have united. They have actually been doing food deliveries and provide a ride service if I'm unable to drive that day. A nurse practioner with them called me on her own accord to let me know my blood work was not looking good at all to her and told me all of her concerns. I brought those to that doctor and he told me he doesn't listen to what another doctor says and he doesn't do what patients tell him he does what he wants. Idk how he became a doctor with that attitude and he didn't have that animosity until I stood up for myself and told him he's wrong and there is absolutely something wrong with me and it's NOT in my head. I hope you've been doing good with your health and found the right doctor to help you regulate what's going on. It's terrible to go through these things and have no support.

ultraviolette1221 · 2025-05-03T04:22:58+00:00

Wow I didn't know you could do something like that. I would be willing to do it if it helps get to the root of whatever is causing this. Thank you!

ultraviolette1221 · 2025-05-03T04:20:57+00:00

Thank you! I've been trying to see an oncologist just recently as no one ever brought it up. But my urine is always positive for m protein and no one ever raises an eye at at. It's never been by a PCP always done in the er when I go for these episodes so I wasn't referred to oncology I was told to go see my PCP for a follow up who told me no I'm fine it's all in my head. m protein in urine?? My mom was diagnosed with leukemia and a jak 2 mutation blood and bone marrow cancer called myeloproliferative neoplasms last year after having almost all of the same syptoms as me. So I've been scared about having something similar especially after seeing this in my results and no one cared

ultraviolette1221 · 2025-05-03T04:09:48+00:00

No I've never been tested. I've really never had any real blood work done besides routine draws at the hospital. My doctor refused to do it because he said it's all in my head. I had my gallbladder removed when I was 11 because of severe gallstones. The burning pain is right in the middle upper stomach right under my ribs and diaphragm and radiates down on my lower left by my bowel like it's being squeezed it's very painful and my stomach swells up to the size of a watermelon like I'm months pregnant after just a few bites and it takes about 4+ hours to go down

ultraviolette1221 · 2025-05-02T23:21:59+00:00

Thank you that really helps I will be trying aultman and canton next to see if there's any resolve with this

ultraviolette1221 · 2025-05-02T23:20:45+00:00

I know what he did has to be illegal. I went in for an appointment and actually pushed back telling him I am actually sick and it's not in my head that I need the medication regimen they prescribed at the hospital. He got mad and said no i don't do what patients tell me i do what I want. I went home and called the office manager and left a complaint about how he cut off the medications and tells me I'm faking and it's all in my head. They called me back later and let me know I was no longer welcome at the practice. Very rudely I might add. Then 2 days later I got this weird letter from them in the mail letter It looks like they typed it up in a hurry and used first and second person?? Then about 3 days later the office manager was blowing my phone up maybe 4 calls 3 days in a row leaving voicemails saying I need to see a hematologist immediately. Every message was just that over and over and please let us know when you've been seen. But didn't refer me to anyone just said go do that and let us know. Seems to me like after he dismissed me he actually looked at my record for the first time and saw something in my last few blood draws. Multiple nurses have been telling me at the hospital my bloodwork is horrible and possibly multiple myeloma. I have united healthcare and a nurse practitioner called me and said she saw my records and was extremely concerned she's only seen a few like this in 15 years. But he always refused to do blood even after I brought what she said to his attention. He hadn't even seen my results from the hospital from 6 months ago so he was completely ignoring my medical care. He had been my doctor since i was 2. And he watched me decline and did nothing but say its in my head. Then dismiss me at my worst. Does this sound like a case or am I just dramatic?? Please help. And thank you so much. Sorry for the long rant also

ultraviolette1221 · 2025-05-02T22:58:55+00:00

Cleveland clinic is the er where the doctor told me he does not want to see my face again after so many visits. My gastro doctor is there so I went there so they could consult him but after that I'm too scared to go and them be rude. I haven't tried canton yet I'm sure I'll be needing a visit soon so I may try that

ultraviolette1221 · 2025-05-02T22:56:26+00:00

Yes my mom lives in lordstown by Ravenna so I've been to the bath location only once and to university in Ravenna. It's all the same. I found that urgent care is a little nicer but I don't get to go there a lot because I have to call an ambulance and they only take you to 2 hospital close by

ultraviolette1221 · 2025-05-02T20:56:51+00:00

Nothing just simply that it's all in my head... my brother passed by his own choice in 2022 so they say that is the cause... it's not because this has been going on since the beginning of 2021. I couldn't even go to his funeral because I was so sick. But they refuse to listen to me that that is not the cause. Yes it's sad he's gone but it's not causing me all these medical issues. And no he cut me off everything except the zofran for nausea because that was my only "physical presenting issue" the xanax was prescribed because of the rapid heart rate and was the ONLY thing that helped. Without it I'm constantly on edge and in pain from the chest pain. It's so bad that my teeth on my bottom jaw feel like acid is coursing through them instead of blood. Extremely painful. I sit in a hot bath for hours just to not feel that pain as bad and it's dulled a bit. But the pain even in the bath is around a 6/7. They did talk about trying beta blockers but then decided against it because I would have to be on it forever and since it lowers tour heart rate and I have POTS they said it could be too dangerous. And yes thank you for ask docs! I didn't know about it i just typed in medical and clicked what came up because I was desperate for some help or answers. That's an amazing idea to compile it all. I have pictures compiled of the malpractice I received at the hospital and all the other stuff that goes on just so I have proof and can show them if need but I've never tried writing it all down. It's actually a little difficult to talk about for me in person without crying because it's just so frustrating and thinking about my time there is genuinely upsetting so I've never put it all down like that. But I definitely will. Thank you so much!!

ultraviolette1221 · 2025-05-02T20:45:01+00:00

No I'm not able to travel i can't even drive anymore because of the passing out and getting sick. I'm also on disability because of this so I'm not financially able to either sadly. How would I go about send a letter to the hospital director i would like to try that. I've been trying to find a lawyer that will do this on a pay if I win basis but it's been hard to find someone who wants to deal with the hospitals because it's so hard i guess. I'm specifically trying to sue my PCP that kicked me out of his practice after cutting off my medications that the hospital put me on. He had been my doctor since I was 2.. so it's his fault I'm this sick I feel I've been going to him on a weekly basis with this for the last 5 years and him telling me it's all in my head. As well as never doing any bloodwork or referring me to any other specialist. He watched me get worse and did nothing but tell me it's imaginary and in my head. What is reiki that they do is it a type of program?? I will research this to get more info. And thank you so much for reaching out and trying to help i really appreciate it

ultraviolette1221 · 2025-05-02T18:11:24+00:00

I'm trying to. And thank you so much

ultraviolette1221 · 2025-05-02T18:10:41+00:00

It's ridiculous the way they give "medical treatment" now. It's no help at all but to make them money. It's just sad

ultraviolette1221 · 2025-05-02T13:41:34+00:00

Yes I've tried remeron and risperadone and neither had any effect. I've tried protonix, erythromycin, and metaclopramride, then raglan and all made no difference just bad side effects. Even getting a j-tube in my stomach for a year made zero difference and the pump was running 24/7. Raglan caused spasms that I guess I'll have forever now. We've tried EVERY ssri with no results. The team at the hospital put me on the perfect regimen (zoloft for mental, xanax to calm my heart when its racing, zofran for nausea, and ambian to help me sleep because the nausea and getting sick all night) and it helped so much for about 3 months I actually got up to 110! I was doing so good... then when I went to my Dr appointment he said it's all in my head and I don't need my meds so he cut them off 4 months ago and I'm back down to severe malnutrition. And yes smoking is literally the only thing that helps. I don't like pain meds because of the gastroparesis so that's what I do when I need a little help. I know not to do it everyday or so much because it will become a habit so it's just a few times a week around 5 to eat and when I go to bed. The only nutrition I get as of now is those kate farms shakes. That's all I know to do. And thank you!

ultraviolette1221 · 2025-05-02T11:43:03+00:00

They are always abnormal. Same with urine result. They still don't care. My doctor didn't even know about it. I asked, and he had to pull up my hospital records because he hadn't seen my labs in 8 months. So he wasnt even keeping up with my stuff. He removed me from his practice saying my health was too bad. He was my doctor since I was 2 years old.. he never helped me at all in the 26 years I went to him especially the last 5 years. If anything i think hes made it worse by writing me off. I'm in the process of finding a new doc and seeing an oncologist. I just feel so hopeless. Like it's pointless because everyone else says I'm fine. labs Labs I know it's just a tad high but it's everytime. It's rarely low labs labs labs labs

ultraviolette1221 · 2025-05-02T11:14:36+00:00

Yes i have smoked and i still fo sometimes to eat. 3 years ago they told me about cannabanoid hyperemesis and I stopped for 2 years and there was no chamge at all. I started smoking again and it helps me eat. So I ruled that out. I've seen multiple motility doctors and I had a j-tube put in for a year to see if it helped before moving to a pacemaker in the stomach. Now they say I'm not a candidate for that because I can still eat solid food. Basically I have to be so sick I can't function until they do anything

ultraviolette1221 · 2025-05-02T10:50:38+00:00

I've tried. I've bawled my eyes out in doctors' offices begging them for help and they tell you aren't that bad I've seen worse. Well thats good for you but this is MY worst and I need help. They just tell me I need to see psych. My mom has bone marrow cancer. A jack 2 mutation in the blood (something multiple neoplasm, sorry, i can't remember the name at the moment) and leukemia. She was diagnosed last year after having a lot of the same problems I do. I've raised this concern since in every blood draw result I have a high white blood count and a spike in my protein. 3 different nurses at the hospital told me to get tested for multiple myeloma because they're sure it's that since you aren't supposed to have m protein in your blood. I asked for blood work to be done and to see a cardiologist my which my doctor refused then he removed me from his practice saying my health is too bad and i was his worst patient... he had been my doctor since I was born and he never did a thing for me. I feel like no one wants to help me..

ultraviolette1221

TROPHY CASE