Me & my speech.

Posts tagged ‘United States’

WHOOPS DISEASE- 7b1. Problems with Diabetes

Many of the issues with diabetes aren’t being discussed here, just how WHOOPS DISEASE really impacts diabetics, people possibilities to get diabetes from WHOOPS DISEASE, and people with WHOOPS DISEASE have greater hassles with their diabetes if they have it. Some aspects of these pages will be shifted into new pages, but not at the moment, sorry for the massive size of this document which still needs fixing for readers.

New Diabetics…

with issues of previous diabetics also.

Some people get diabetes with WHOOPS DISEASE, eventual ‘cure’ treatment for WHOOPS DISEASE should take away the ‘new diabetes’ AND possibly the ‘previous diabetes’ also.  The diabetic issues of Rhapsodie are probable with the new diabetics also, BUT the possibility of returning to normal after WHOOPS DISEASE is ‘cured’ means that the diabetes problems will go away also with those people. This is different for people who have had diabetes.

Previous Diabetics

Rhapsodie has been type 1 diabetic since she was 5, so she reads these symptoms versus her diabetic normality’s.

Sugar & Insulin Use Records

Rhapsodie has, recently, formed a spreadsheet to keep track of the super frequent insulin changes and how these relate with her sugar levels. BUT it takes hours each day to add the numbers and interpret the information beyond normal patterns & cycles. While the spreadsheet can help doctors, for Rhapsodie, she also needs to be watching the Minimed 670G Insulin Pump graph patterns. It’s not the easiest thing in the world and it’s continuous work.

As is mentioned below the coloring added to these charts could be done hourly, but it’s not at present for Rhapsodie the best way to do that. The basal change colors are based on basal (underlying base uses of insulin for life without food as a factor) insulin amount changes. Using the comparisons from the previous days makes it easier to determine how to color versus doing it as the basals are being changed. Other insulin pump systems and sugar checkers could make this easier if the graphs are accurate enough to utilize AND if they are keeping basal rates in record with the other information.

Some insulin pump options & sugar checker options, like the CGM systems which may OR may not be insulin pump integrated, also have graphing which may allow memory systems to keep records of the basal patterns corresponding to living with diabetes also.

CGM Information

You can find information using the search engines you prefer to find

  • CGM’s; OR Continuous Glucose Monitors involve poking into the sking so they aren’t loved OR really even liked by me causing more holes in my body every time they are used.
    • The NO Prick Sugar Checkers, I’ve located in research are really not ‘approved’ by the United States FDA maybe comments can cause them to do more approving. They haven’t approved the 3 I like the most yet, but with checking my sugar up to 23 times a day recently, then poking in the sensor device, then poking in the insulin needles regularly my body is more scarred than not from needle pricks. The ones I like may OR may not be able to be linked to insulin pumps, they may OR may not be able to share that information gotten with computer systems but some of them have that available with NO PRICKING AT ALL! More No Prick Links below!

AND

But here are some links to options I’ve heard about and have observed on occasion.

Some Insulin Pump & CGM Connected Options

Other Pricking CGM options without insulin systems connected

No Prick Glucose Monitors which may work as well with CGM &/OR insulin pumps

  • GlucoTrack– Clips on ear for readings AND may be approved already with the FDA
    • Clips on ear, reads the numbers within one minute, uses a combination of Ultrasonic, Electromagnetic, and Heat capacity. (thermal) for reading the sugars and allows USB connection to cell phone, tablets, computers for charting the information, and will allow numbers to be added manually to the pump. Problem only reads when used, but that’s fine for the use with the sensor & the ear clip may hurt in repeated uses over weeks, months & years of time.
  • CNOGA– BG meter is NOT approved by FDA for blood glucose monitoring. BUT their other machines offer that as an option with the devices, but the programming needs to be loaded for this option to be active-
    • VSM- Vital Signs Monitor
      • VSM intended to suit the customers specific needs and includes 3 versions according to customers’ requirements. The basic VSM measures 3 bio-parameters includes Pulse, Blood pressure and Oxygen saturation (SpO2). Additional parameters such as Blood gases or Hematology parameters can be added to the device [BUT you need to ask, to get those, the U.S. FDA has not approved this for sugar checking.] VSM approved for marketing in more than 37 countries (Certifications: CE, CFDA , Anvisa).Cnoga Medical is the only company in the world approved by the U.S FDA for cuff less monitoring of blood pressure & Pulse
        • Pulse
        • Oxygen saturation (SpO2)
        • Continuous, Non-invasive Cuff-free Blood Pressure
        • [BUT NOT for sugar checking yet!]
    • COG- Combo Glucometer (CoG) [Not U.S. FDA approved, stupid]Place your finger, close the lid and measurement start automatically …within 1 minute.
      • Non-invasive Glucometer
      • No pricking, No pain
      • Personal Device
      • For Adult Diabetics (age>18)
      • Suitable for Type1 and Type2
      • Small and Lightweight – ˜100g
      • Compact and Easy-to-use
      • Unlimited usage life
      • 500 Measurement memory
    • MTX- Matrix Monitor- approved in U.S. but super complicated for simple glucose measures because of the multiples tested at one time
      • Continuous, Non-invasive and Cuff-free Blood Pressure
      • Non-invasive Hemoglobin,
        • Hematocrit, and
        • RBC
      • Non-invasive Blood Gases (Ph, PCO2, PO2, O2&CO2 Content)
      • Non invasive Cardiac Output , Stroke Volume, MAP
      • Less than 60 seconds test
      • Four LED lights shine wavelengths from visual light to infrared light through the fingertip.
      • As the light wave pass through the fingertip, some of it is absorbed and the light signal is changed.
      • Next, a camera sensor detects the changed light signal in real time.
      • Using patented algorithms and a vast amount of data MTX analyze the correlation between the signal and bio parameters
  • Gluco-wise– In development
    • can be used on ear OR with hands using radio waves and totally non-invasive, but still in testing, can allow the numbers to be manually added to the pump. Problem only reads when used, but that’s fine with the sensor for pump in use also.
  • GlucoTrack– Clips on ear for readings AND may be approved already with the FDA
    • Clips on ear, reads the numbers within one minute, uses a combination of Ultrasonic, Electromagnetic, and Heat capacity. (thermal) for reading the sugars and allows USB connection to cell phone, tablets, computers for charting the information, and will allow numbers to be added manually to the pump. Problem only reads when used, but that’s fine for the use with the sensor & the ear clip may hurt in repeated uses over weeks, months & years of time.
  • Diabetesnet.com- Lightouch non-invasive glucose monitoring device
  • More No-Prick Options Info

Rhapsodie’s Insulin Changes & Sugar Hassles with WHOOPS DISEASE

For Rhapsodie’s life with WHOOPS DISEASE and insulin changes having records of Blood Glucose (BG) tests for accurate uses she has built an Excel Spreadsheet chart . For her it’s generally a follow up used to double check her basal & sugar record patterns, BUT it could help others to set up their patterns if they are aware of things before they get hit with them.  A technologist reviewing Rhapsodie’s problems with the ‘auto-mode’ option of the 670G told her, “ I am not a doctor, but these numbers show me that your body is responding a lot faster than this pump is programmed to work with the automode in action.” This has meant my actions NOT using automode have kept me healthier.

Finger Pricking Hassles

I don’t like other features of automode also, but Minimed does take comments and put them on record, so some of my suggestions have worked, my sugar reports through their systems now include more of my finger prick measures.

  • I’m pricking my fingers about 11 times a day, that’s a big problem with the sugar hassles, because my skin is dryer and scarring is greater.
    • I try to remember to change my fingers regularly, but this sugar checker is a problem for using my lower ears, BUT you might find pricking your lower ear lobes works well with less finger pricking needed. The pain sensors at the lower ear lobes are less than on the fingers. The edges of the ears beneath an earring hole are better locations than higher, because pain sensitivity goes up the higher up the ear, the closer to ear stiffness you get.

Other WHOOPS DISEASE Sugar Oddities & Hassles

I’m sorry everyone, I’ve only been handling the diabetes by Minimed Insulin Pumps for over 20 years. That has meant, with more recent machines, my sugar checker in communicating with the pump have allowed my doctors some records to use. BUT I haven’t taken the time with WHOOPS DISEASE to chart the information too accurately until just recently. And (more…)

#17- Rhapsodie’s Visual PAIN Diary- April 2017

More here continuing from #16- Visual PAIN Diary- Winter into Spring 2017- Worse & Better At the present time, my LEFT Forearm, LEFT Calf, RIGHT Calf, RIGHT Forearm, LEFT Rotator Cuff, RIGHT Shoulder, 2nd to smallest toe on my Left foot, are my only real PAIN ISSUES that shift and vary with bone strain in movements. 

Presently

I generally get upmost days without any pain, but my movements during the day can and sometimes do cause PAIN.  A wrong step or a wrong lift can give me lightning pain followed by swelling and an ache that diminishes without more stress if I do not repeat that motion within the next week.

Sleeping is made way more difficult, because my left calf feels like it splits when I rest on my right side for 15 minutes or any more.  The exercises for my lower left ankle/calf assigned with physical therapy have increased and advanced the fever of my right calf. It only aches like a bruise presently.

Walking with my left calf wrapped causes pain like shoving micro spears into my bones near the last place a spike of pain happened if I’m on uneven ground and barefoot.  Walking with shoes and bracing causes me to ache whenever I take a step wrong at the store, like from pushing a shopping cart.  My right calf ONLY hurts when rubbed by hand to remove the swelling that centers over the fracture, that is as yet untreated, and when the fever in the calf gets bad my body temperature rises also.

ANTIBIOTICS CONTINUE TO REMAIN THE ONLY PAIN TREATMENT that removes pain.  But doctors’ have continued to ignore this sign of infections in the body. Prescribed treatments only fiddlefarden by brain to disguise from it the reality of pain.

  • Steroid– I was allergic so only 2 doses out of 7 were taken, a week of no pain, but I really injured areas that weren’t felt as being in pain.  Over 3 months of working to recover to the point I was previous to taking a single dose.
  • Acetaminophen/Cod 3o mg & Turmeric Cur-cumin– 24 hours of sleep with 36 hours of fuzzed brain, fluffing away the pain in disguising the problems from nerve central.
  • Aspirin/Ibuprofen– 5 to 12 hours of sleep
  • NSAID Cream– Anti-Inflammatory, I’ve only used one dose so far.

The fever in my right calf has been regrowing, today April 15th my temperature was over a degree above normal. The area of swelling on my right calf is not associated with ‘bone injury,’ but surgery was mentioned to me this last week.  My left arm though is the problem we’ve discussed through this set of blog posts, with the Visual PAIN Diary- From September 2013 into April 2017,

this is the last post for that section of this PAIN Care blog. Because I believe the plate for my LEFT arm has been moving around.  And thus the movement of the plate means that the areas of pressure from grip have shifted when pressing in areas also.

My sleep is again being problematic.  Because of so much lack of care, lack of physically moving properly regularly I’m almost incapable of walking presently.  The present medical system is set up to make sure anywhere there is a problem on your body you have to go in for a separate visit.

The Left shoulder injury could probably have been avoided if there had been care for my lower arm, but there hasn’t been, and I’m still having problems with my left lower arm & the recovery exercises for the shoulder exacerbate the problems with swelling of my Left Forearm.

But beyond them is how the patient will continue to suffer into the future and the cost settlements for injuries that are as yet uncared for as well as uncalculated into the lack of care … The lack of care results have led to a weak left arm, added to taking my ability to do the enjoyable tasks I still love as shared in the beginning of the document.

NEEDING LEFT ARM BRACING FOR ALL NORMAL TASKS,

many of which are avoided because of the work stress spiking pains:

  • Holding a bowl of soup, a small notebook, anything at all really with my lower left arm results in spiking and shifting pain with a single move.
    •  It’s really hard to eat a bowl of cereal.
  • Taking out trash, on the kitchen 15 gallon can has not been done, by me in over 2 years, my previous work at McDonalds involved lifting larger trash bags regularly.
  • Sorting through my storage of season clothes exchange took over 2 weeks, pain hindered me as did my arm not being powerful enough to brace a suit on a hanger single handedly with my left hand.
    • I have not washed a sink full of dishes since the week of the Steroid NO PAIN;
  • SWOLLEN NUMB FINGERS, specifically the 2 middle ones of my left hand, started feeling pinched about the summer of 2015 after the Steroid week & this reoccured in September & October of 2016.
  • SWOLLEN HAND, if my Left Arm is not angled up to sleep, I awake with it totally numb.
More ARM Work PROBLEMS,
  • Watering my plants is uncomfortable with my 1 quart watering container. 2 hands work best.
  • Adding water to the humidifier is done with the smallest cooking pot in the house, the 2 to 3.5 cup one. That’s between 16 and 28 ounces, a gallon of milk has to be lifted with 2 hands.
  • Lifting my drink mug with my left hand aches.
  • I do not comb my hair or brush my teeth with my left hand anymore either.
  • Washing Dishes, 1 piece at a time,
  • After doing anything normally easy for over 1 hour,
    • except for using the typing keyboard, it’s okay with resting my arm on the brace pad on my tucked down bear.
  • I haven’t sewn, sketched, crafted, read a book that weighs more than a Harlequin in over 6 months because my left arm can’t support the weight or the use angle stresses presently.

Just earlier this week a metal L door handle touched the upper edge of the YELLOW ORANGE bruise pain on the picture, the pressure felt like having a hand slap onto a bloody purple bruise beneath the skin. That area has never caused me any pain in the past; I would rate that at somewhere near ONE but less than that.  It’s the persistent re-ache that is most annoying.

Because months have passed since my last entry I’m adding details from the present situation and the pain shifting.  A situation which the doctors have listed as chronic pain, they’re stupid about that, but then they only read what others share with them before making a diagnosis. The February 2018 post demonstrates how the so called ‘chronic pain’ isn’t, it’s in fact circumstantial driven by life AND lack of proper treatment.

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

 

#16- Visual PAIN Diary- Winter into Spring 2017- Worse & Better

The pain splitting AND swelling that resulted from the shoulder bracing demonstrated to me that also the injuries of my left calf were splintering as I feel towards my knee and towards my ankle.  With use my left arm is splintering towards my wrist.  This is not normal but maybe people with dense bones are more likely to have this happen because of the greater bone resistance to splitting breaks which separate bone parts completely.

Winter & Spring 2017 Swelling & Splitting Pain Tied Together

At present my Lower LEFT Arm suffers swelling and more, pictures from February to April of 2017 are demonstrative visuals. As you can see with the pictures, the swelling green section is over the lower forearm bone, it has not reached the wrist bones, but it is very close.

Osteoclasts were not allowed to work the separated bone into the freshened injury after the Father’s Day Fall of 2014.  After pushing a part of the bone down behind the plate as it was in my arm then did not realign on the injury properly, thus it did not heal onto the base bone properly.

This is only part of Rhapsodie’s issues, but having bones improperly cared for can weaken the overall body of any person.

  • How do multiple repeated spreading fractures weaken a person?
  • How does the lack of correct bone care hurt and add problems beyond pain?

There are definite answers to these questions, but in consideration of my left arm, more and more physical weakness hinders my physical activity and the muscle mass decrease has allowed my injured bone areas to sprawl with greater touchable ease and the lack of use has caused more body problems as well as fear that Osteoarthritis & Rheumatoid Arthritis will be suffered more than it ever should have because of NO DOCTORAL CARE & self patient education.

A person should work to retain body balances, if they do not work towards this through their life they could suffer more and more as we see repeatedly.  Originally the PAIN problems I had were just rated by me as accidents in which I would heal from with time.  But the years of growing issues, evidenced on these pages demonstrates how initial pain problems diagnosed incorrectly can expand and become worse problems for both patients and their serving medical people.  Especially when medical people don’t take the time to investigate more than ‘tell us how you would rate the pain?’  Followed by let’s prescribe a ‘drug.’

To me that’s not work to investigate or learn anything, if you reported to the local police that you saw a car off the road in an odd area with skid tracks through the snow an investigative vehicle would be sent to the location. The problem would be taken care of before the police left the area abandoned with no care for the people.

If the work to pursue diagnostics was done with a little more accurate understanding of the real pain being felt with the medical requests then there could be better care with hopefully less cost as well as time wasted for both the patient searching for care and the doctors who are working to provide care.

  • Why is it if a patient talks about pain, there is no care given?

NO wonder there are so many people suffering ‘prescription drug problems.’  For me, pain is a sign of problems, taking drugs to minimize pain weaken my body and add to problems I could get.

Presently

I generally get upmost days without any pain, but my movements during the day can and sometimes do cause Pain.  A wrong step or a wrong lift can give me lightning pain followed by swelling and an ache that diminishes without more stress.  Sleeping is made way more difficult, because my left calf feels like it splits when I rest on my right side for 15 minutes or any more

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

 

#14- Visual PAIN Diary- August 2014 to Summer 2016 INACCURATE Records SUFFERED

So ended the previous post- #13- Visual PAIN Diary- July 2014- Painful Pokey Boney Walk The amount on a pain scale was about a 6 with my arm down, but with the arm up against my chest it was only depleted with shoving the Pokey Boney back into place behind the plate.  It didn’t go back onto the bone, but at least it wasn’t sticking out any more.

August & Fall 2014- Frictional Discomfort

There were months while I rubbed at a very tiny protuberance that  shifted and rubbed behind the plate that hid the bone from my fingers.  Sometimes a boney section pecked out from between my solid bone area and the plate that remained as a fracture support.  My arm continued to suffer shifting and rubbing feelings of pain, until I finally pressed it down to a more comfortable location multiple months later.

But the bruising on my arm was continually being felt.  In fact to this day I can touch the exact locations I rubbed and shifted against for months, seeking comfort with my Left Forearm, as are pictured here:

But multiple inaccurate reports used by doctors & medical technologists have caused them to fake in the estimates while not doing proper examining.

The ONLY accepted official report about my 2005 surgery was the false one stuffed in my files.  The X-rays of that arm show glass or gravel, like the plate was to be seen as, but NO CARE HAS BEEN GIVEN, because it has been the patient’s word against the doctor’s inaccurate testimony.

How can we as patient’s continue to accept these inaccuracies AND live by them when we have the exact opposite actually happening to us.  Well we human’s do like to be dumb and ignorant when it is too much work to fight for truth and right.  Isn’t that why Hitler was so successful with the persecution camps?

The Infrequent & continual rubbing of my lower arm resulted in getting the bruised deepening area feeling on the bone,  but there was ALWAYS another item keeping my fingers separated from the bone.

  • Wouldn’t a removed plate on my left arm have allowed me to feel the touch of my fingers against the bone?
    • For many years there have areas of my lower left arm that do not feel the pressure of my fingers, since 2000, and it still continues.

Presently I feel body areas under my right hand and fingers on my left arm, but my left arm does not feel the same fingers any deeper than the skin, no matter how deep I push against the painful areas of my Left Lower arm.  The pressure push feels like pushing into a deep raw bruise.


Since Then

There were many interstitial circumstances, at least from my living time, varying things between September 2014 and the Summer of 2016, but most were minor enough to not be specifically remembered.

But during the Winter and Spring of 2016 I had

  • trouble with my right shoulder, causing me to use my LEFT Forearm a lot more than over the previous 2 years.
  • My left shoulder was definitely weakened because of not being exercised properly because a leaning function in our narrow hall, 23 inches wide OR less with sliding door only partially open, in
  • July 2016, caused me to dislocate my Left Shoulder ROTATOR CUFF in more than 3 areas.

This was proven after it was brought back into position August 28th, the MRI results done in October 2016 showed there was more than one area of injury which I’m still getting care for.  The only way I was taken seriously by the doctor was my lie about the so called level of pain I was feeling, since it was disruptive AND no care for deeper injuries was ever received.

This wasn’t nice, but it was easier than suffering more shitty assessments, but the original shoulder brace shifted something else in my lower left arm…

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

 

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

 

#11- About Government & Regulation vs. LOVE & Freedom

The “U.S. Constitution has been shared in some slight degree with the recent posts here, but so have contentions about the government and how it’s regulations diverge from the “Constitution”.  Because of this please remember that the theme of that document defines the purpose of the regulations in that document:

We the people of the United States, in order to form a more perfect union, establish justice, insure domestic tranquility, provide for the common defense, promote [get behind, boost, not make] the general welfare, and secure [fortify, preserve, assure, (Webster’s New World Thesaurus, 1990)]] the blessings of liberty [the rights supposedly natural to man- freedom; independence; power of choice, (Webster’s New World Thesaurus, 1990)] to ourselves and our posterity [our children’s future, our descendant’s future, (Webster’s New World Thesaurus, 1990)], do ordain and establish this Constitution for the United States of America.”

A document prepared by men of faith, that to a degree professed a belief in God’s hand in this government and who worked, in Rhapsodie’s opinion towards LOVE.  There are multiple comments shared with the statements of previous posts, but it’s always important to remember and connect the theme of the “U. S. Constitution to the articles & sections of the “U.S. Constitution” with interpretations of it.

Take for example how the Commerce Clause interpretation, from the Constitutional definition, has affected freedom and LOVE while increasing the power of the dollar and the government.  The clause is constitutionalized under stare decisis because the Supreme Court made this judgement in interpretation, in 1832 the federal government is now empowered to control all commerce in the United States, unless they determine that there is an unsubstantial effect to interstate commerce with a business.

Rhapsodie has read multiple legal cases that cause her to see this as bad, not good for the free people in the United States. “In 1942, for example, the Supreme Court held that wheat production by an individual farmer intended wholly for consumption on his own farm was subject to federal regulation.” (Clarkson, 2012) How would an individual’s consumption of wheat raised on his own land, in his own state for eating by his own family cause ANY problem with interstate trade? Oh, maybe it would mean he wouldn’t buy wheat from another state, but he could buy wheat from his own state anyway, so this interpretation has led to federal regulation, not freedom for the people.

While the commerce clause interpretation could have legitimate value and purpose, the 175, size 6 font, double column, text book sized, pages of the U.C.C. (Uniform Commercial Code) is just a section of the law used to control people by business in the United States and this controlling effects the Native American peoples also. It’s not based on freedom and lLOVE it’s based on control and maximization of money in controlling. The blessings of liberty are actually minimized with these laws; the general welfare of the public is diminished by capturing souls in the cost of life with national healthcare and its minimization of the people’s control of their own lives.

This short dissertation shows how the actions that don’t demonstrate LOVE can fail, and since “LOVE never fails” there’s a need to make sure all regulations and control systems are done with a base of LOVE instead of Selfish Pride. The theme for the whole “United States Constitution shows that these shared aspects of control are unconstitutional and ungodly, at least in accord with Rhapsodie’s interpretations. But her sharing here is only based on a limited examination of the history of the United States and the definitions of this country. There is more for you to see, so read even if you decide to disagree.

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