Wednesday, January 11, 2017

Chronic Pain Patients and the "absurd" information on abuse and New Medication for pain with Abuse Deterrent in it

https://www.madinamerica.com/…/stop-the-war-on-chronic-pai…/



 I found this article interesting and more to the point when "chronic pain patients" are attacked for something they are NOT causing. I great example (I was not attacked but) since I had to have surgery yesterday, of course I had to be "NPO" thus I could have have ANYTHING to eat, drink and even my meds were taken away after midnight... all of which is necessary, BUT my surgery was NOT until 1PM the next day!
So, like MOST told me and I know myself, I could have been given my critical meds, such as my muscle relaxer, pain med, & my anxiety med...but I was made to wait UNTIL AFTER 3:30PM or longer, rather than just stopping it at 8 hours...


IF the surgery would have been early morning such as 6 or 7 AM etc then it would make sense.. anyway, same with this... "true and legitimate patients are being "punished" or horrified, because with all of the "crap" out there in the news we fear being without our meds.... yesterday, I was in horrid pain by the time I got to the hospital after waiting so long, then checking in, getting prepped for surgery, & then going under (which I was thrilled to go under anesthesia, knowing then I would be free of pain, plus I would FINALLY get some pain meds for relief.... 
  

It is a nightmare if you live in terrible pain daily, or almost daily, and then are terrified all of a sudden your meds could be jerked away... so those that don't understand, should be "educated" on just how chronic pain invades and takes over your life... and quality of life goes null and void, for the patient, family and way of life...

And from the Pain News Network....

https://www.painnewsnetwork.org/stories/2017/1/9/fda-approves-new-long-acting-painkiller


FDA Approves New Long Acting Painkiller  

 

Just came out a couple of days ago!





Saturday, January 7, 2017

As Usual NOTHING is simple when it comes to MYSELF and MANY others with COMPLICATED AUTOIMMUNE ILLNESSES!


                            DO COMPLICATIONS EVER END????

Once again, my autoimmune illnesses play a difficult part when it comes to my health, my life, and after something like a major surgery.

Many of you know I had taken a hard fall on my hardwood floor on December 13th - which led to 2 fractures n my right hip. I had staples in it, due to two incisions, but I had a rod and screws put in and did not have a complete hip replacement, which we hoped meant I would be home sooner. SO MUCH for that thought! I should know better by now to :"assume" anything I have done will be "simple".

The surgery, the rod and screws, which I got to see on an X-ray yesterday January 6th, are healing well. I had a complication with my foot, thinking it was fractured, but I found out I have a torn ligament, which probably began when I twisted my ankle back in June so severely, then the fall, in which also involved my foot being "hung up" and caused the fall, then probably tore that ligament the rest of the way, thus now my right foot is in terrible pain, when I am standing or trying to rehab the hip. I've had to learn to work past the pain in my foot, thus the rehab portion on my hip is going very well.

Even my orthopedic surgeon said yesterday, that in spite of my complicated health problems, I am doing extremely well, and past schedule in a good way, compared to what he thought I might be. He was telling his nurse, that due to my attitude and willingness to work with therapy, I am doing very well. Yet, between the anemia, the liver enzymes being high, and now this "hematoma" that developed on top of the main incision after the hip was repaired, I face another surgery this coming Tuesday.

He has to go in and drain the "grape jelly" as he called it, the blood that has accumulated like a huge blood blister under the skin, and put a drain in it, so we can get rid of the huge "mass" right on my thigh, that makes me look "deformed". He said in his report, it is big as a softball. WOW! I knew it was large but "softball size"? So, rather than GOING HOME EARLY NEXT WEEK, I face yet another SURGERY! So, that delays me getting on home and back to my life, as I wanted to.

It certainly takes the idea of my neck surgery that I need so badly, completely out of the picture, and makes me want to "run" if I could somewhere that not a soul could touch me, and just be totally alone, perhaps with my puppy, Peanut, and the new puppy that awaits me once I get home.

Here are a couple of pics of my new little boy


who awaits me: He is apart of what keeps me on focus to hurry up get well and GO HOME!!!! along of course with Peanut also a Fox terrier....

Friday, January 6, 2017

Fearing...Home...Falling Again...Loss..Bad Blood work...Grieving, and more.... So Many Questions - Looking for Answers

I can't "fuss" too much about the care I've received in both the hospital and now the Rehab Hospital. Thank Goodness, it is NOT anything like a nursing home!

Although they have "long term" patients, there are 4 "Halls" of which each serves a different type of patient. So, those that like myself, are trying to "rehab" so they can go home and be able to care for themselves, we are all in one hall.

The others are for Dementia/Alzheimer's patients, and those that are probably here for the rest of their days.

I really have not encountered much that I would say was "wrong".... I usually get my meds when I ask within a reasonable amount of time, even though there are times, they have patients coming to to be admitted, or things get crazy, and I may have to wait a bit, or remind them. Most of the time, the nurses are apologizing to me, because they were not "prompt" in getting me my pain, muscle relaxers and my diazepam in a timely manner.

I've been able to shower by myself the past two times, and I am getting around MUCH better this past 4 or 5 days. Enough so, I am READY TO GO THE HELL HOME, I am SO BORED WITH IT ALL NOW!

But, complications, like a huge hematoma, at the repair site on my hip, has caused a delay in getting the staples out, my liver functions are all high, and my anemia really was a very huge concern. So far, it appears after the 3 units of blood at the hospital were given to me, my red blood cell counts have gotten better, but I look for them to bottom out again, once I am not here and on the supplements, besides I still feel that I have pernicious anemia, which is an autoimmune illness, plus even the liver issues, probably have to do with Lupus and the RA, causing the issues with my red blood cells being so low.... etc....

I realize I face yet another surgery my neck surgery,if I can recover from the hip fractures (or actually WHEN I recover enough to go and have it done...plus my lower back has to be fixed also....my lower back and neck both were already needing surgery, then between trying to take care of Mom, and now the "jolt" from the fall, both are worse than ever.

ALL OF YOU, PLEASE stay with me!!!! I am certainly NOT giving up on my blog, my advocacy, writing and my other things I participate in so I can HELP OTHERS understand they are NOT alone.....

I am trying to find ways to increase my readers here on my blog, but I know I really need to make sure I have interesting and valuable information here for everyone, or all of you will get bored with it.

IF YOU have any ideas of what you may like to read, hear about, or have me talk about, PLEASE let me know. You can always email me at: ravishingrhia@gmail.com

Thursday, January 5, 2017

#WHATTHEHEALTHCARE - Your "pet peeves" or worse with Doctors and the Medical System

#whatthehealthcare

HOW MANY OF us have dealt with wrong diagnosis, doctors with NO bedside manner,having tests we did not need, dealing with labs done but you don't get results until weeks and weeks later, doctors who make you wait 4 or 5 hours or more when you had a scheduled appt, not getting things billed properly to insurance...

... having a doctor make you wait, then the nurse comes in and says there was "an emergency" and you have to reschedule. go to:

http://whatthehealthcare.info/?spMailingID=16126899&spUserID=MTQwOTExNTk2OAS2&spJobID=921335017&spReportId=OTIxMzM1MDE3S0


WE KNOW HEALTH CARE CAN BE FUNNY AND EVEN FRUSTRATING AT TIMES…

LET’S HASH THROUGH IT!

 

 

Wednesday, January 4, 2017

Talking about "enduring" ALL of the "complications" & Nightmares of being in the hospital after breaking my hip, surgery, Rehab and "conflicts" of other illnesses #WhatTheHealthcare


 #WhatTheHealthcare

To understand this, I fell and broke my right hip n 2 place the Tuesday before Christmas. I am STILL in the Rehab Hospital and everyday there is some kind of "kink" or some complication, and guess who suffers for it???? ME, the PATIENT!!! Here is the latest example.... besides being Anemic and having 3 UNITS of blood before, during and after surgery.... I've had a ROUGH 24 HOURS AGAIN!

They decided to do that liver sonogram and I didn't know I could not eat, drink or even have meds (which I was told they would come somewhere around 3AM or so do to the scan. Well, 3 passed by, then 5AM passed by, then 6AM and nothing to eat, drink, no medications, and by 6:30AM I was about a basket case... well over time for pain meds, my Valium, my muscle relaxers and so on. So, everyone was checking to find out why the scan was not done sometimes in the early morning.

He FINALLY SHOWS UP about 11:00AM.... now this is like 20 HOURS SINCE I've had anything.... the sonogram did not take long, and I was "buzzing" for ALL OF MY MEDS, and some orange juice as soon as he got through. So, thank goodness I got lunch, and of course my stomach is so "small" that I can't hold a great deal of food or drink at a time.

But, I got my meds, and drank the juice, then ate some of my lunch, and now I am just worn out from lack of sleep, and lack of meds on time.... so it's been a heck of a day and night before.... I gather he did the sonogram of my spleen, liver, kidney's etc...so if anything is causing the blood work to be "off" hopefully they will find out.