Claudia A. Merandi
Region: US
Tuesday 04 November 2025 16:21:33 GMT
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joshua613o :
They are more scared of the DEA. But not scared to harm us. Something is wrong here
2025-11-04 16:37:34
171
Ms. Jan McGrew :
This is just crazy to me. Not once have I ever been refused pain medication when I've truly needed it. Especially in the E.R.
2025-11-08 04:38:44
1
Chachacha :
They should be sued 💯
2025-11-07 02:51:44
1
Kaye H :
A good friend that we grew up with is a Kennedy. He’s actually the 2nd cousin of wRFK jr. I’m going to see if he will put a bug in his ear about our issue with no help. 😬👏👏
2025-11-05 08:08:33
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Green Lantern MD :
No one EVER seems “to have a plan in place” for anything - recurrent asthma, exacerbations of COPD, allergic reactions, UTIs, migraines, vaginitis, or kidney stones, much less musculoskeletal pain. “What’s your plan?” was how I was taught FP and considered common/good practice in the 80s, not that everyone did it. Since then it’s increasingly been, “Go to the ER.” Why? It’s hardly ever necessary for chronic problems if you have a plan. I’ve seen patients with migraines who were never even given anti-emetics or later a triptan, much less a reasonable amount of pain meds to have on hand for rescue.
2025-11-07 00:53:49
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darleenberger2 :
Also, I have also mentioned to 3 different drs that my daughter, granddaughter, AND great granddaughter have been diagnosed with Ehler Danlos Syndrome and all 3 drs waived off any suggestion that I be tested for it. Many of the other symptoms I have could be related..
2025-11-06 14:05:05
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Earl-the-Squirrel 🐿️ :
I listened to a woman scream in pain with sickle cell … begging for help in a ER. I actually overheard staff say she probably is a “seeker” this is really bad folks . I’m scared .
2025-11-05 01:29:01
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Rhongepooh :
Same with patients with kidney stones.
2025-11-04 17:58:32
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rkloos :
I went to the ER because I was really sick , thought I had COVID, 103 fever and wouldn’t go down ( no I don’t run to the ER everytime im sick ) turns out I had strep throat, the doctor ask me if I needed pain medication for my throat, I didn’t but I took in case I needed it for something else and couldn’t get it prescribed
2025-11-09 23:13:40
0
Dan Greg445 :
I just had surgery, they wouldn't even give me a Tylenol.
2025-11-04 19:31:12
34
alliecat :
Inpatient now and I actually was talking with the DR about my fears around these meds and my need for them. He told me the hospital tracks it very strenuously. He also said that he is limited on the amount he can prescribe. If you need more than that you have to hope someone from pain management will see you and prescribe for you.
2025-11-04 17:07:15
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Anastacia :
im a palliative care patient a hospitalist on Saturday came into my room told me I was not in pain even though I was admitted for pain told me I did not have the diseases. I had then went into my record, changed it to “not taking prescriptions as prescribed“ which is falsifying records because he is not my prescribing doctor and I was not self administering my medication’s in the hospital nor did I have my prescriptions on except for one EpiPen and two inhalers.
2025-11-04 21:17:25
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Love ❤️ :
they are doing it with me for water pills told me they don't give them out call your doctor Monday! yes that's right Sadly 😥
2025-11-05 00:55:02
2
Chronic Pain Patient :
There being paid to hold pain medication. Its all about money and greed.
2025-11-05 01:17:41
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Laney Marie :
It's so sad to hear them cry out in pain. And most of the time the doctors and nurses are rude and some even call security or the cops to kick them out. Sickle cell is a very painful thing. It's so unprofessional and inhumane!
2025-11-05 10:43:42
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Rita Hall21 :
I love your idea of having a plan in place for the Sickle Cell patients It’s like many disorders where people have a flare/crisis
2025-11-04 17:21:47
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Katie :
The d prescription is only what helped me as well as a f patch. I have CRPS and TN multiple chronic illnesses and
2025-11-04 23:08:49
3
missysunshine :
it's sad when you have to decide what hospital to go to of you want decent care for pain. my local hospital is amazing for anything other than pain med. you have to go 2.5 hours away to be able to get the help you need with pain. I am lucky to have an amazing pain management doctor and I get the meds I need but when I'm so sick and in a flare my local hospital won't give me those meds because they don't think I need them! so I have to go hours away just to be able to get the meds I need while being in the ER or inpatient. it's like when we chronic patients have scars all over our bodies, do they really think we are drug seeking? we are looking for just an ounce of relief.
2025-11-06 03:09:37
3
molly_guitar73 :
Brittany Hightower ❤
2025-11-04 20:14:14
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❌🧚a fairy🧚❌ :
I didn’t know that disorder caused pain. (I’m not a doctor or nurse.)
2025-11-04 18:29:32
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Hollypopper :
Cruelty is the new norm in medicine
2025-11-05 01:38:58
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VantasticOdyssey.com :
I had a Dr show me a Directive that a policy change has been made. Doctors seem to be hired hands. Basically turned into to a business like McDonald's
2025-11-04 17:25:29
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OlRowdyRooster :
My wife hates the ER but goes in desperation because of Pancreatic Neuroendocrine cancer (PNET) a couple times a year at least. I’ve asked the same question but have no answers. They think because she has a pain pump it’s not as serious. Well dang it!! Why didn’t we think of using the Bolus…. We’ve had to get our oncologist to call before they do anything.
2025-11-04 17:21:22
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Laura D. :
The biggest fear i have is dying in agony with my family around me.The very last image of a loved one dying in agony would haunt my loved ones for life
2025-11-04 17:21:25
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Dale⛱️ :
In NY, there used to be migraine protocol. It's created by your Neurologist & ER. It was fantastic. Unfortunately, the ER refused to continue treating pain with opiods because they claimed that opiods don't work for migraines. I agree that there needs to be protocols for sicle cell too.
2025-11-04 19:43:08
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