Me & my speech.

Posts tagged ‘problems’

#10- A PAIN & Injury Diary MAY Change Inaccurate Doctoral ASSESSMENTS

Continuing from the previous post- #09- Detailing Diaries Could Limit Inaccurate PAIN Assessments–  The bone injury assessments aren’t as easy for the doctors to see after time continues to pass. BUT let me demonstrate how the detailing could add value to visual assessments by medical professionals..

8-10-2000 Original Injury Sketch

This was from a car accident! The original accident was with the weight bearing bone of my left arm. According to medical information, “Often a fracture of the mid shaft of the ulna is not associated with an injury at the elbow or the wrist, [TRUE WITH ME]. It can be treated with a long arm cast, or with surgery. Plates and screws or intramedullary pins are both effective treatments.” With my car accident the picture is my memory of the injury.

Bone fracture repair is used when a broken bone does not or would not heal properly with casting or splinting alone. Improper healing that requires ORIF surgery can occur in cases when the bone is sticking through the skin (compound fractures)…” This is consistent with the injury that I had.

The orthopedic specialist that did the surgery told me that the lack of inflammation and coloring was very abnormal. He also told me that my bone density was super high, a very good reason to expect that the screws would need to be taken away at a later time. The experimental straight plate material that was put in my arm & the external padded brace was wrapped around the bandage holding the staples and 4.5 inch scar in place.

Of course I can only share with you my visual memories, but the pain assessments can’t be accurate because I was drugged with the emergency ambulatory care.  The visual memory is from being awoken by the doctor so that the hospital could get my desire for treatment.

In that situation my pinky toe on my left foot which was dislocated hurt worse than my arm, it distracted me from really feeling any problem with my arm.  The localized pain killer had not been applied for surgery.

2000 Injury Scar & 2005 Scar after Screws were Removed

The information shared with the section about My Pain Tolerance is HIGH (A Self Assessment describes how the work in my arm resulted in minimal injury.  As stated previously the INACCURATE ASSESSMENT of the PAIN & the CT results by the other hospital could have caused other major body problems, but I knew my body better and worked to get the proper care.  The specialist did NOT base his estimates on my pain statements, BECAUSE before seeing me he had taken the time to do a proper visual survey of the evidence because I had made sure that he got the visuals so that the inaccurate technical reports of the other hospital weren’t his only evidence about the situation.

The day of the surgery after the screws were removed the surgeon who took care of the problem said that, “the screws holding the plate on my arm were removed with my fingers, they were barely in the bone.” This was after I asked why the scar bandage was so small in comparison to the whole plate scar that I had, it was less than 2 inches long while the original plate scar is over 4.5 inches long.

A visual reminder for you of my scar of 2005:

In general with a full plate removal, according to another medical document, from the Malaysian Orthopaedic Journal 2009 Vol 3 No 1 “…Refracture is the most common complication following removal of implant… The forearm should also be protected from heavy loads by splinting for [2] to [4] weeks…”

BUT FOR ME IN 2005, my screws were removed by hand & as more evidence that the PLATE WAS NOT removed I was told by the professional surgeon, “you can return to work like normal tomorrow, there are no restrictions.”  So on my return to work, 4 days after the surgery, the next week because of the extra days I’d previously taken was abnormal for a plate removal.

The plate in my arm has aggravated the present pain situation and proper doctoral assessments, even though the doctors have not heard me because they have been misled by INACCURATE reports based on other inaccurate reports & BAD PAIN Assessments.

This visual addition along with my information from #03. Inaccurate PAIN Assessments with A HIGH PAIN Tolerance and other posts can assist others to see in some ways why the Summer 2014 injury care action taken by me did not result in the better care results from doctor’s.

Detailing Information Visually

Maybe the pain & injury diary can grow value in pain assessments as well as more accurate treatments. Like

  • what if the doctors had a visual flip-book relating the pain as well as the injury progressing as I have suffered?
  • what if the medical community had made assessments accurately for me instead of basing things on their own personal ratings of my pain estimates?…

Associated Posts

Please forgive me, but you’ll likely want to right click and open in a new tab, because the click link MAY NOT WORK.

#01. Inaccurate PAIN Assessments CAN CAUSE MORE BODY DAMAGE

#02- PAIN Assessments Corresponding with UTI’s

#03. Inaccurate PAIN Assessments with A HIGH PAIN Tolerance

#04- Inaccurate PAIN Assessments with JUST Rate Pain from 0 to 10

#05- Inaccurate Doctoral PAIN Assessments based on Guesses

#06- Inaccurate PAIN Assessments because of no Patient Pain Understanding

#07- Inaccurate PAIN Ratings with NO Applicable Associations

#08- Inaccurate PAIN Assessments MADE a BIT Better

#09- Detailing Diaries Could Limit Inaccurate PAIN Assessments

#10- A PAIN & Injury Diary MAY Change Inaccurate Doctoral ASSESSMENTS

Rhapsodie’s Visual PAIN Diary- From September 2013 into April 2017

 Rhapsodie’s ideas to improve Medical ASSESSMENTS by doctors

PAIN Variables

 

#09- Detailing Diaries Could Limit Inaccurate PAIN Assessments

Continued from #08- Inaccurate PAIN Assessments MADE a BIT Better– Because of my pain WHICH HAS NEVER BEEN CHRONIC, shifting and changing based on actions and bone shifting having different time ratings to add the colors to the pictures is useful.  But there is more like the detailing that for me is necessary because there is no reference when doctors only see you every 6 months or when there is a specific problem THAT THEY HAVE RECOGNIZED.

WE AS PATIENTS, who have NOT received proper injury treatment, NEED TO KEEP Visual DIARIES, so that doctors can view the progression of pain at least with coloring in pain variables and area changes.

Like for me which pain has never been consistent, it always comes from actions that have increased problems and actions that have effected previous areas where pain was in the past but had been gone for a long while.  That is a reason that detailing visuals can really assist others, like doctors OR other healthcare OR physical therapy people, realize what issues you, a patient, is trying to share with them.

Detailing Visuals

Visual descriptions may be generified, but people with problems may also need more details.  If I had taken photos or sketches of my arm, with the problems showing, even only the pain charted I could have drawn or colored in the pain variables over time as well as the location shifts so that the doctor’s assessments could be more accurate.

The medical society could do this work also, but in my experience they haven’t done so yet.

Rhapsodie’s Visually Detailing Pain & Variations

My left forearm pain has grown with problems over time, just with using enlarged clips of the pictures from the National Institute Of Pain with added detailing as remembered over time more details of understanding could be seen.

Let me show you my recent work with detailing some of the advancing stages of arm problems based only on my memories from 2014 up to now with the newer problems that grow on my left forearm.

As previously mentioned, the injury to my lower left arm was originally fractured in a car accident. This sketch was pieced with the picture shared by the book and my information added.

AND during the summer of 2014 after taking a twisting fall in 2013 where my weak arm suffered some.  THEN there was another fall around Father’s Day 2014 that dramatically increased my problmes.  This was demonstrated later, in July of 2014 as I was carrying some envelopes of mail up from the mailbox and a piece of bone popped up out of the bone on my left arm.  Instead of taking a picture with my camera, I stood in the yard and pushed the bone down away from the skin.

NO VISUAL EVIDENCE was left for the doctors that they took time to examine or see, AND no one has even gathered accurate assessments of that arm because  the 2005 screw removal surgery report was falsified.

BUT maybe if I had previously added the visuals into a timeline of events incorporating any personal pain feelings the doctors’ would accord more serious attention to the injury now. I have not done things that way because of my ignorance of how the doctors misdiagnose based on limited information.  Previously my diabetes was appropriately diagnosed when I was 5, because the Hemoglobin A1C taken from my blood placed my blood sugar levels as being way outside normal, and my parents were witnesses to how sick I was and the amount of time I lived sickly.

The bone injury assessments aren’t as easy for the doctors to see after time continues to pass. BUT let me demonstrate how the detailing could add value to visual assessments by medical professionals…

Associated Posts

Please forgive me, but you’ll likely want to right click and open in a new tab, because the click link MAY NOT WORK.

#01. Inaccurate PAIN Assessments CAN CAUSE MORE BODY DAMAGE

#02- PAIN Assessments Corresponding with UTI’s

#03. Inaccurate PAIN Assessments with A HIGH PAIN Tolerance

#04- Inaccurate PAIN Assessments with JUST Rate Pain from 0 to 10

#05- Inaccurate Doctoral PAIN Assessments based on Guesses

#06- Inaccurate PAIN Assessments because of no Patient Pain Understanding

#07- Inaccurate PAIN Ratings with NO Applicable Associations

#08- Inaccurate PAIN Assessments MADE a BIT Better

#09- Detailing Diaries Could Limit Inaccurate PAIN Assessments

#10- A PAIN & Injury Diary MAY Change Inaccurate Doctoral ASSESSMENTS

Rhapsodie’s Visual PAIN Diary- From September 2013 into April 2017

 Rhapsodie’s ideas to improve Medical ASSESSMENTS by doctors

PAIN Variables

 

#08- Inaccurate PAIN Assessments MADE a BIT Better

As ended the previous post #07- Inaccurate PAIN Ratings with NO Applicable Associations- Notice how I varied that doctor’s statement.  It was done, in my estimate, because my doctors have taken it upon themselves to offer assessments based on their inaccurate work & because I had not read through this article with articulation for the types of pain to share previously.  This means there is a need for doctors to supply for patient’s corresponding information that can be related to by the doctor & other medical people too so we as patient’s aren’t inaccurately mislabeled or inaccurately cared for.

Rhapsodie’s ways to share more accurately pain feelings with doctors

The pain specialist information from WebMD can be used, but without having corresponding visuals doctors are likely to make inaccurate assessments.  The National Institute on Pain Control (NIPC) has a great way of assessing pain given for FREE to patients and doctors, but none of my medical practitioners have used it.  Getting this printed AND filled in for your doctors COULD greatly assist them in evaluating you and me also.

Detailing the reinjury to my lower left arm, as was never done till now, during the summer of 2014 after taking a twisting fall in 2013 then again around Father’s Day 2014 causing further problems.  Added to me by the self care for my bone popping as I was carrying some envelopes of mail up from the mailbox was NOT detailed by anyone.

Instead of taking a picture with my camera, I stood in the yard and pushed the bone down away from the skin.

  • But what if I had done more?
  • What if I had taken photos, instead of working myself out of the pain by moving the bone?
  • What if I had done a running visual report for the doctors to look at?

I don’t think they would have found anything with images, because my dense bones and the plate disguised the reinjury, but at least I could have visuals to share. But it hurt and for me, the way to minimize the hurt was to realign the bone more properly, then and there as I was walking into the house with the mail.

The medical reports as followed were only based on the wonderful ‘rate your pain from 0 to 10, and the doctors added me to a chronic pain complainer with NO ACCURATE TREATMENT ALSO.

Basic Visuals to Share

As NO VISUAL EVIDENCE was there for the doctors to view AND no one has even taken accurate visual assessments of that arm even though there are reports made with no visual evidence because it was falsified.  An ultrasound of that arm is unlikely to cause a lot of pain, is safe, and is non-invasive.  It also is cheaper than an MRI or a CT scan, but it has not been done.

But presently on top of wanting accurate treatment, I really wish the doctor’s did more than read inaccurate assessments done by the same hospital that couldn’t even discern that screws were coming out of that arm back in 2005.  My desire for that also includes having them relate to my pain properly.

Look at how the assessment is done in split assessments with both visual AND by descriptions, partially detailed from the work shared by the National Institute on Pain Control (NIPC):

They are asking you the patient in pain to make mark or color in the pain so that doctors can see it.  Also there is a packet of information that includes questions relating to the pain and the feel of it.  The question below is 20 out of 20; showing that there is way more investigative than most doctoral assessments.

This can assist in getting more accurate assessments if the doctors saw how variables shifted and changed with time and situations if they made any assessment beyond the simplified give us an estimate of your pain, rate it from 0 to 10.

Just having charted this information, maybe with multiple copies of this pain chart can add to the doctor’s knowledge if the patient is using the reports to show how the pain varies with the incidences and the work done that causes the pain to result.

Because of my pain WHICH HAS NEVER BEEN CHRONIC, shifting and changing based on actions and bone shifting having different time ratings to add the colors to the pictures is useful.  But there is more like the detailing that for me is necessary because there is no reference when doctors only see you every 6 months or when there is a specific problem, THAT THEY HAVE RECOGNIZED…

Associated Posts

Please forgive me, but you’ll likely want to right click and open in a new tab, because the click link MAY NOT WORK.

#01. Inaccurate PAIN Assessments CAN CAUSE MORE BODY DAMAGE

#02- PAIN Assessments Corresponding with UTI’s

#03. Inaccurate PAIN Assessments with A HIGH PAIN Tolerance

#04- Inaccurate PAIN Assessments with JUST Rate Pain from 0 to 10

#05- Inaccurate Doctoral PAIN Assessments based on Guesses

#06- Inaccurate PAIN Assessments because of no Patient Pain Understanding

#07- Inaccurate PAIN Ratings with NO Applicable Associations

#08- Inaccurate PAIN Assessments MADE a BIT Better

#09- Detailing Diaries Could Limit Inaccurate PAIN Assessments

#10- A PAIN & Injury Diary MAY Change Inaccurate Doctoral ASSESSMENTS

Rhapsodie’s Visual PAIN Diary- From September 2013 into April 2017

 Rhapsodie’s ideas to improve Medical ASSESSMENTS by doctors

PAIN Variables

 

#04- Inaccurate PAIN Assessments with JUST Rate Pain from 0 to 10

From previous post- #03. Inaccurate PAIN Assessments with A HIGH PAIN Tolerance– In the last 2 years I’ve suffered a lot more because doctors have failed to accurately assess situations based both on recorded lies in my files and the incomplete pain assessments.

Pain Assessments

The reasons for the relational corresponding pain chart are because of the repeated assessments done inaccurately, in my personal assessments, with me.  Please forgive me for only sharing a part of the situation, there are many areas that still have not been taken care of properly, but the pain assessments that lead investigations into injuries can cause a lot of problems if done wrong.

When a doctor asks you how much pain you are in do they do the correct work or could they do more? 

I can guarantee from the services for me that THEY CAN DEFINITELY DO MORE.

Inaccurate General Pain Assessments

At times more assessment is taken, but often not by the doctors.  In fact prescriptions for physical therapy, pain killers, and/or other drugs could result because the tests done are not accurately assessed based on the pain response by the patient to the “Rate your pain level from 0 to 10,”  which is too singular to make an accurate assessment.  Any person with a higher OR lower pain tolerance can hugely vary based on their personal rating of their pain as well as their body tolerances with pain.

With HIGH pain tolerance a person is less likely to be reacting like they are in horrid pain, but their pain problems could be tremendously worse than a person with a much lower pain tolerance while being uncared for because of the inaccurate way that doctors’ have assessed the situations. This was displayed for me because I had to assume how other people would be feeling with the injury of my LEFT Arm Rotator Cuff to fake in a number to get attention.  The MRI proved my reasoning and actions were correct, and my other personal experiences are some evidence of this.  The sample of experiences showed earlier are only some samples if there was a relational corresponding pain chart that more accurately fit information better treatment could result.

Another aspect of the problems comes with the assessment by doctors of Chronic Pain, when a patient like me hear that say, “My pain is not always there, it is not the same in the exact same area after a week of suffering it.  The pain I have at times totally disappears, so how can they make the assessment that the pain is ‘Chronic.’ In fact my perception of the word Chronic is, ‘It never ends and it never changes and it never goes away.’  My one experience with a pain that felt Chronic was a migraine that just grew for over 5 hours.  Nothing else I have had has felt like that.

The least thing that could be done is for doctors to have correspondence about other life situations and our pain assessments of those. Would you please relate any previous experiences so I can understand your rating now? Like a migraine or an infection or another injury.  Someone like me could say, ‘I fractured my lower left calf in gym at school, walked home, took some aspirin, wrapped my leg in ice, then went to the bedroom and put the bone in place, I passed out once, the pain was about a 6.  But it wasn’t bad enough to make me throw up.’

How Pain Assessments Generally Begin

Wouldn’t it be more relational for them when I’m telling them now that I felt like passing out with pain from some recent physical therapy with my lower left leg?  At least sharing the information that after passing out for over 30 minutes and standing up with an injury to my right calf, my pain was about at 7, but I walked out of it would give them some correspondence in understanding my meaning.  In general with no relational corresponding pain chart or more details for pain assessments there is more space for inaccuracies when doctors ONLY ask, ‘How much pain are you in? Rate your levels from 0 to 10.’  With just that question how do the doctor’s really assess my pain?

  • Based on their previous patients?
  • Based on their own personal experiences?
  • Based on what they think the problem really is?

How do any these assessments accurately assess MY PAIN?

In fact THEY DO NOT, it’s all a guess for them!

Associated Posts

Please forgive me, but you’ll likely want to right click and open in a new tab, because the click link MAY NOT WORK.

#01. Inaccurate PAIN Assessments CAN CAUSE MORE BODY DAMAGE

#02- PAIN Assessments Corresponding with UTI’s

#03. Inaccurate PAIN Assessments with A HIGH PAIN Tolerance

#04- Inaccurate PAIN Assessments with JUST Rate Pain from 0 to 10

#05- Inaccurate Doctoral PAIN Assessments based on Guesses

#06- Inaccurate PAIN Assessments because of no Patient Pain Understanding

#07- Inaccurate PAIN Ratings with NO Applicable Associations

#08- Inaccurate PAIN Assessments MADE a BIT Better

#09- Detailing Diaries Could Limit Inaccurate PAIN Assessments

#10- A PAIN & Injury Diary MAY Change Inaccurate Doctoral ASSESSMENTS

Rhapsodie’s Visual PAIN Diary- From September 2013 into April 2017

 Rhapsodie’s ideas to improve Medical ASSESSMENTS by doctors

PAIN Variables

 

#03. Inaccurate PAIN Assessments with A HIGH PAIN Tolerance

Copied from Previous Post- #02- PAIN Assessments Corresponding with UTI’sThere have been many occasions on doctor’s visits in the last 3 years that they have asked me to rate my pain in a level from 0 to 10, but I can only rate as I feel.  But the doctors cannot make accurate assessments just based on those numbers.  They need to have a real level to vary my level of and they need to have a way to keep the people who are really suffering accurately cared for or they will stupidly make inaccurate judgements as they have with me for over 2 years now.

My Pain Tolerance is HIGH (A Self Assessment)

The UTI infection years ago is evidential of my pain tolerance, but so are the results from care done for an arm that was in pain at a later time.  Years ago I had a plate put in my left arm after a car accident in 2000; back in 2005 the screws through the plate started bothering me.  I ended up at the ‘local hospital’ many months after the bother began, the hospital did a CT Scan and their report was, “There are no problems found.”  It’s a really good thing that I had an appointment with the original surgeon the next week, and it was wonderful that I had the CT Scan Pictures shared with his office.

You know why?

On the day of the appointment with the specialist who had placed the plate in my arm.  He said I needed to stay for surgery. Because of having driven to the office that day, the next day I went in for surgery to remove the screws that had been coming out of my arm for over 8 months.  I felt almost no pain, but the arm was not right.  The specialist had taken the time to really see the results of the CT Scan before I went to see him, and the screws were removed the following day after the first follow up visit to him in 5 years, which is common enough.

But the INACCURATE ASSESSMENT of the PAIN & the CT results by the other hospital could have caused other major body problems, but I knew my body better and worked to get the proper care.  The specialist did not base his estimates on my pain statements, he had made the time to do a proper visual survey of the evidence BEFORE he even saw me because I made sure that he got the visuals and not only the inaccurate technical reports of the other hospital.

The day of the surgery after the screws were removed the surgeon who took care of the problem said that, “the screws holding the plate on my arm were removed with my fingers, they were barely in the bone,” after I asked why the scar bandage was so small in comparison to the whole plate scar, it was less than 2 inches while the original plate scar is over 4.5 inches long.

In general with a full plate removal, according to a medical document, “…Refracture is the most common complication following removal of implant… The forearm should also be protected from heavy loads by splinting for [2] to [4] weeks…” (Malaysian Orthopaedic Journal 2009 Vol 3 No 1)  This is another evidence that in 2005, my screws as removed by hand, that the PLATE WAS NOT removed, I was told by the professional surgeon, “you can return to work like normal tomorrow, there are no restrictions.”  As I had taken an extended weekend, my return to work the next week was abnormal for a plate removal. The picture, here, displays the screw removal scar.  The plate in my arm has aggravated the present pain situation and proper doctoral assessments, even though the doctors have not heard me because they have been mislead by a lying report. AO Foundation Surgery Reference #1.

Connecting Screws are used in full fractures as is displayed with this clip of information from the AO Foundation Surgery Reference #2 pages.

Plate in surgery

My original injury was not in the formation of the picture above, it was a sliver of the Ulna punching up through the skin from the doorway pressure fracturing the arm bone.

In the last 2 years I’ve suffered a lot more because doctors have failed to accurately assess situations based both on recorded lies in my files and the incomplete pain assessments…

Associated Posts

Please forgive me, but you’ll likely want to right click and open in a new tab, because the click link MAY NOT WORK.

#01. Inaccurate PAIN Assessments CAN CAUSE MORE BODY DAMAGE

#02- PAIN Assessments Corresponding with UTI’s

#03. Inaccurate PAIN Assessments with A HIGH PAIN Tolerance

#04- Inaccurate PAIN Assessments with JUST Rate Pain from 0 to 10

#05- Inaccurate Doctoral PAIN Assessments based on Guesses

#06- Inaccurate PAIN Assessments because of no Patient Pain Understanding

#07- Inaccurate PAIN Ratings with NO Applicable Associations

#08- Inaccurate PAIN Assessments MADE a BIT Better

#09- Detailing Diaries Could Limit Inaccurate PAIN Assessments

#10- A PAIN & Injury Diary MAY Change Inaccurate Doctoral ASSESSMENTS

Rhapsodie’s Visual PAIN Diary- From September 2013 into April 2017

 Rhapsodie’s ideas to improve Medical ASSESSMENTS by doctors

PAIN Variables

 

#01. Inaccurate PAIN Assessments CAN CAUSE MORE BODY DAMAGE

For the last years my doctors have been asking me to rate my pain AND recently I also had a therapist ask that question.  But the majority of the time they are basing my 0 to 10 ratings on their previous experience and the LIES in my medical files that have grown with people that really don’t care about me.  Rate your pain from 0 to 10, how often have you heard that question?

The question of pain assessments by doctor’s and the veracity of their conclusions has given place to many articles.  Like the one found at Web MD [b]y R. Morgan Griffin stating some of the problems I have suffered from

“…’Pain is always personal,’ says F. Michael Ferrante, MD, director of the UCLA Pain Management Center in Los Angeles. “It’s invisible to other people looking at you — and that can lead to a lot mistrust and difficulties in relationships.”

Whether you have low back pain, or migraines, or nerve pain, people might not understand or believe what you’re going through. That suspicion might not only be shared by your in-laws or your boss, but even your doctor — and that can have serious repercussions, preventing you from getting the pain treatment you need…”

The least thing that could be done is for doctors to have correspondence about other life situations and our pain assessments of those.

Would you please relate any previous experiences so I can understand your rating now? Like a migraine or an infection or another injury.

Someone like me could say, ‘I fractured my lower left calf in gym at school, walked home, took some aspirin, wrapped my leg in ice, then went to the bedroom and put the bone in place, I passed out once, the pain was about a 6.  But it wasn’t bad enough to make me throw up.’  I mean wouldn’t that be more relational for them when I’m telling them now that I feel with pain from physical therapy with my lower left leg?  After passing out for over 30 minutes and standing up with an injury to my right calf, my pain was about at 7, but I walked out of it.

Recently variable accidents have caused me to seek out care by doctors, because the original incidents were not so physically dehibilitatingly painful to me that I took an ambulance to the hospital and the time between the original injury and the first seeking of care was very broad.  This has caused the results of NO CARE partly because there have been no equivalency results of my statements of pain on a good generalized scale,  Just OVER A WEEK AGO, even sharing my pain ratings in comparison with the Bloody urinary tract infection had the exercise therapist rejecting my comment, because it wasn’t in relation to the injury he was working to care for.  But the fact that my LEFT Rotator Cuff was ‘a legitimate injury’, he was willing to hear me to some degree in response to my tolerance level variances.

There hasn’t been any doctor who has taken the time to read the complete record of statements from me, like the fact that the best pain treatment has been ANTIBIOTICS that in addition to MY SUPER HIGH PAIN TOLERANCE as was shown with a urinary tract infection (UTI) some years ago has led me to suffering more and more with time and NO TREATMENT to care for the real problems…

Associated Posts

Please forgive me, but you’ll likely want to right click and open in a new tab, because the click link MAY NOT WORK.

#01. Inaccurate PAIN Assessments CAN CAUSE MORE BODY DAMAGE

#02- PAIN Assessments Corresponding with UTI’s

#03. Inaccurate PAIN Assessments with A HIGH PAIN Tolerance

#04- Inaccurate PAIN Assessments with JUST Rate Pain from 0 to 10

#05- Inaccurate Doctoral PAIN Assessments based on Guesses

#06- Inaccurate PAIN Assessments because of no Patient Pain Understanding

#07- Inaccurate PAIN Ratings with NO Applicable Associations

#08- Inaccurate PAIN Assessments MADE a BIT Better

#09- Detailing Diaries Could Limit Inaccurate PAIN Assessments

#10- A PAIN & Injury Diary MAY Change Inaccurate Doctoral ASSESSMENTS

Rhapsodie’s Visual PAIN Diary- From September 2013 into April 2017

 Rhapsodie’s ideas to improve Medical ASSESSMENTS by doctors

PAIN Variables

 

WHOOPS DISEASE-3. Males

Whoops disease symptoms for males and females are different, An Arrow-b here’s one link to find out the details I’ve lived with. Animals can get this from humans also. My cat Mystin has displayed some of the human male symptoms.  Human’s can die because our society is majorily ignorant about the existence of this disease.  And because our health system has less doctors than it needs to work properly with full government health care.  I’ve been sick for the last 10 years, first from May or was it July 2008, but so are the males in my life.mixed 065

But their symptoms are somewhat different than the female symptoms.

MALE CAUSE & SYMPTOMS:

  1. Inhaling someone else’s sneeze juice OR drinking the fuzzy pead on water in the TROPICS or in another container that’s not purified OR cleaned correctly.
  2. Feeling ‘not right’ within a couple of hours or days. Generally noticed within days or weeks ‘something is not right’.
  3. SLIGHT congestion in the lungs, generally begins at the start progressing into colds within the first 1 to 6 months after contracting the disease, but this graduates in time to sneezing BUT less than the females.
  4. SNEEZES- from the 1st year to a continuous month then more on and off.
    • SNEEZES that start and grow and grow calm down and repeatedly for some years passing on more disease for others even the animals in your life.
      • The sneezes get harder and louder the longer they are had. AND
      • they hurt also.
    • Evening & night sneezes increase and hurt more as time goes on, the first one of the night is usually the most painful, but the damage to the lungs can mean less sneezes BUT it may not be that way for everyone.
  5. Itchy skin that both males and females get from dry skin is very common. When the skin feels itchy DO NOT SCRATCH IT WITH YOUR NAILS or ANY OTHER SHARP OBJECT. Instead find a roughly textured cloth or use your fingers to rub away the itch.  This also works with bug bites, because it releases the area inflammation that generally adds to itchiness, but it doesn’t raise up more blood that will increase the inflammation in the healing processes.
    • There is an additional itch to worry about also with this disease.
      • Initially, about year 2 to 4, the bug feet on the skin itchies, with NO bugs were light and I rubbed those areas, but in 3 areas I scratched- the end of my nose and on my upper arms, until I rethought and stopped.
      • About the 7th or 8th year this has returned with a mass of rash on the body and in the places that did the scratching with the slightly itchy skin. These were in the exact same spots, but my life wasn’t tremendously worsened, because I avoided ripping my skin and digging for the itchies earlier.
        • I still feel little bug feet crawling on my body, but there’s nothing there so I rub the area &/OR leave it and they stop.
        • Presently, starting in 2017 into 2018, the men in my life are suffering what they think are fleas, ripping open their itchies because of not knowing that their earlier itching’s caused this exacerbated itchy feeling.
  6. Sores on the left thigh that seem nasty for 7 to 14 days, doctors MISDIAGNOSE THIS also at about 3 to 4 years.
  7. Age differences in disease for men, I may not have all the facts for all the ages, so please comment on details I’m missing:
    • This is for the men between 30 and ….
      • Gut Rash on the body, similar to Shingles but NOT for 30 to 60 days in a 5 to 7 year time period.
    • For men between 14 and 30?
      • A hunch back that comes about for some months, and then disappears leaving a normal body shape that’s still sick.
  8. Higher sugars, that range in the range closer to real diabetes, but they vary with normal sugars, so it’s not Diabetes-
  1. Also there are mood changes.
    • One month of severe deathly depression,
    • At least 4 to 6 weeks of one nice week one mean week.
    • And other depression mood swings that last for about 2 to 4 years.
  2. Additionally there are the days and weeks of memory loss,
    • “I didn’t say that.”
      • When they said it so nicely and meaningfully earlier, you may want to take vocal recordings because this has happened at least 3 times and it may be different with your men.
  3. Males also lose their hearing for volume control, from their mouths, so
    • They talk LOUDLY instead of speak for a 3 to 12 month time period, generally biweekly Saturdays are their loudest.
    • They do not think they are being loud but their voices expand and fill the whole space, so if you’re having waxy ears and listening, the sound is amplified more and hurts.
    • Additionally they want things turned up louder, because it’s harder for them to hear.
      • This may be because of the mass of wax in the ears, mentioned below.
  4. Heavy wax build up in the ears causes a sort of ‘deafness’ that comes in the 4 to 10 year.
    • The wax buildup starts as heavy liquid coming from the ears that feels very watery when a person is sleeping.
      • Initially normally wax colors get very dark and
      • While previously the EARS WAXES WERE WATERY.
    • Now they are really yellow and heavier. Unless they are brown or black from bloody discharge also. So
      • Using the mix of rubbing alcohol and aloe juice heats and allows the waxy build up to run out.
        1. I mix up the aloe juice and rubbing alcohol in small container,
        2. Then put a towel on my pillow for each ear,
        3. Then using an eye-dropper fill the ear that’s up, and let it stay in the ear for 3 to 5 minutes, THEN
        4. I tip my head down and do the same with the other ear,
      • This may be repeated if I still feel the need for the release.
  5. Males also have water weight gain, but it’s mostly all belly & chest gain not real body weight gain.
    • Appetite shifts increase, so that people retain weight and even gain it with fluids, but they are not eating properly towards the ends of the disease.
    • It’s sad that the less a person eats the more ‘weight’ they gain in this disease. SO the Scales are always lying.
      1. AND men as well as women that are trying to lose weight, need to take care with this disease infecting them.
      2. They should be making sure they are getting the correct nutrition to stay alive, because this disease decreases the appetite for food while enhancing the fluid needs of the body.
  6. And there is hair and skin loss, that grows as time progresses and
    • The more showers a person takes the more hair and skin they lose.
  7. There are also the Planters Warts that come, but aren’t really planter’s warts because they do not infect others. BUT they do disappear with treatment of the real ‘wart’ disease.
  8. There are also sleep situations that are not normal, that seem to happen in the 6th & 7th year of symptoms.  The can’t sleep episodes with a pattern of
    • 8 hours 1 night
    • 5 hours 1 night,
    • 3 hours 1 night,
    • 5 hours 1 night,
    • 8 hours 1 night
    • After these patterns end they get weeks of sleeplessness that grows worse and worse, especially if they already have sleep apnea because this makes it worse.
  9. Also there are the muscle cramping’s, of
    • The left leg, year 2 to 4
    • The left foot, year 5 to 6 and
    • The upper left shoulder, year 7 to 8.
  10. Then there are the groin rashes.
    • Starting first with raised dots that are in the upper leg V’s.
    • Spreading to a rash through all the upper groin hair.
      • A treatment that seems to work well is Bag Balm which can be purchased in many pharmacies & pet supply stores.
        • It’s a mix of an antiseptic, lanolin, and petroleum jelly, Wikipedia mentions how the ingredients of the past were likely to have been varied because the present ingredients are as listed above.
  11. There are also blood pressure problems, so the doctors are treating the symptoms resulting from the Whoops Disease problems and their assumptions about a patient’s weight Body Mass type.
  12. About year 10, the men also get a ringworm looking patch on the front of their right legs, this includes red dots that stick out, are dry, and stick away from their legs AND it comes again on their rear right shoulder being super, super itchy.  Using Bag Balm OR the Petro-Carbo Salve can assist them in fighting this drying itchy bumpy rash, for about 24 hours.

And I’ve not remembered everything, because I’ve only seen the events of the men in my life. But it’s somewhat odd that the symptoms run the same parallel by sex and lung size in humans even if they are genetically from different bloodlines for millennia of time.

Other Connecting Posts

WHOOPS DISEASE-1. Animals

WHOOPS DISEASE-2. Females

WHOOPS DISEASE- 2b. Water Weight Chart Comparisons

WHOOPS DISEASE-3. Males

WHOOPS DISEASE- 4. More!

WHOOPS DISEASE-5. Nano Mites?

WHOOPS DISEASE-6. Treatment Ideas & Facts

WHOOPS DISEASE-7a. Updates on Continuous & New Symptoms & Some Treatment Issues

WHOOPS DISEASE- 7b1. Problems with Diabetes

WHOOPS DISEASE- 7b2. Problems with Diabetes & MAY Details

WHOOPS DISEASE- 7b3. Problems with Diabetes & JUNE Details

WHOOPS DISEASE- 7b4. Problems with Diabetes & JULY Details

WHOOPS DISEASE- 7b5. Problems with Diabetes & INFO updates

WHOOPS DISEASE-7c. Cure for Diabetes

WHOOPS DISEASE- 8. Treatment Issues & Action Options

 

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