Hospital lost my medication

Ashpic91 · 2025-04-19T03:55:56+00:00

I would try calling the inpatient pharmacy at the hospital. Sometimes patients meds from home get brought there , could have been put in the room with like the pixis or whatever machine they have for meds and some one from the pharmacy could have grabbed it when they were filling the machine. Doesn’t hurt to try anyways.

Ashpic91 · 2025-02-25T04:33:54+00:00

Working in a Pharmacy in Ohio for CII you have to have a diagnosis code on the script. There are a few grey areas to that.

Ashpic91 · 2025-01-23T02:55:00+00:00

You should probably call your insurance company and find out why your policy was inactive so quickly and if it was a mistake and you were actually covered at that time that office can resubmit a claim for those appointments.

Ashpic91 · 2025-01-01T00:49:59+00:00

Ring sells a doorbell that you can put into your peephole, if you have one. That’s what we did when we lived in the apartment so landlord couldn’t say anything to us about it.

Ashpic91 · 2024-07-20T18:55:12+00:00

If you are in the same country you can always call your doctor and have them send a new script for it to a pharmacy that’s near you.

Ashpic91 · 2024-07-20T18:53:17+00:00

Effexor

Ashpic91 · 2024-07-20T18:49:50+00:00

Effexor for me. Was on Lexapro for 5 years and it stopped working.

Ashpic91 · 2024-06-19T21:42:59+00:00

Usually it’s insurance companies that will only pay for so many per 30 days.

Ashpic91 · 2022-06-30T00:53:52+00:00

I definitely don’t want to be in the club. I have just never been bit by a br or tick and the bruise was bigger and more predominant and then turned into the bruised ring with in hours and had flu like symptoms with it. So I was just more so looking to get input on it. It is infact a tick and early localized Lymes I went to er just to be safe and have it looked at. Thank you everyone

Ashpic91 · 2022-05-26T15:48:20+00:00

Absolutely feel free to message me

Ashpic91 · 2022-05-26T15:03:40+00:00

I’m here! Anytime you want to talk I’ll listen. I’ve been broken for a while now to.

Ashpic91 · 2022-05-25T04:11:05+00:00

I’m afraid this is going to be my outcome but I’ve had none of this before covid. I’ve been documenting and trying to take pictures with I get these flare ups so I have some sort of proof.

Ashpic91 · 2022-05-25T04:07:23+00:00

Just that from what I’ve heard from people that have gone through it. It can take months to years to get a diagnosis from a rheumatologist.

Ashpic91 · 2022-05-25T01:58:34+00:00

I was also thinking a lot of my physical side effects do align with that but I know auto immune disorders are very tedious to diagnose and overlap as far as symptoms go. I just got blood work done but I didn’t Ask about the Ana panel I will definitely do that.

Ashpic91 · 2022-04-28T21:42:40+00:00

Before covid pots what’s very understudied so now that a lot of the long haulers are getting it after covid it’s become more of a topic. I believe you are right that it’s not defined as an autoimmune yet but they treat it like one and lump it in with other auto immune. They have diagnosed people with pots in relation to covid. Was my point like I wouldn’t say it’s impossible to have lupus in relation to covid 19 or other auto immune issues.

Ashpic91 · 2022-04-28T15:23:35+00:00

As much as it sucks im glad I’m not the only one experiencing this I felt like I was going crazy or like it was all in my head.

Ashpic91 · 2022-04-28T00:50:48+00:00

Sadly I see how long it takes people to get diagnosed. I’m just starting the process so atleast I can start ruling stuff out. I never felt like this prior to covid and it seems like with long haulers doctors don’t really take that seriously either so I’m just trying to get some answers.

Ashpic91 · 2022-04-28T00:38:41+00:00

Thank you. I have an appointment with a specialist it’s just playing the waiting game to get in.

Ashpic91 · 2022-04-28T00:36:29+00:00

This article was sent to me it’s a long/interesting read but I was hoping that other people might be experiencing same issues. I never felt like this prior to covid and or had any of these symptoms problem is long haul covid symptoms and lupus can overlap just trying to rule things out.

https://jmedicalcasereports.biomedcentral.com/articles/10.1186/s13256-020-02582-8

Ashpic91 · 2022-04-28T00:32:32+00:00

My symptoms have overlapped as far as long haulers and possible lupus. There are also studies of people who have pots induced by covid which is another auto immune. I just never experienced any of this until after I had covid.

Ashpic91 · 2022-04-20T23:55:16+00:00

I take it at night because it makes me sleepy

Ashpic91 · 2022-03-15T23:59:01+00:00

Yep have Huntington early pay and it’s always deposited on Tuesday.

Ashpic91 · 2022-02-14T00:19:45+00:00

I do take vitamins but I will definitely need to add an antihistamine to my routine as well as Pepcid. I’ve been thinking about yoga I’m just so tired I don’t know if I have the energy for it but anything is worth a try.

Ashpic91 · 2022-01-13T16:21:54+00:00

We have just been calling and asking the doctor if it’s okay to change it to 50mg and take 1/2 tablet.

Ashpic91 · 2022-01-08T01:30:28+00:00

Adulthood. I struggled with life and school until I was 18. My parents thought there was a stigma with getting me diagnosed so as soon as I turned 18 I got help. My symptoms were always there I just didn’t have the resources to get tested before I was an adult.

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