Me & my speech.

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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…)

WHOOPS DISEASE- 8 Treatment Issues & Action Options

I’m adding another apology because I do not have the clinical name for Whoops Disease yet, it’s changed so much over the years name and most of them I’ve dealt with treat me for the ‘effects’ of the disease not for the disease.  Because since I’ve learned about it, so only the ‘professionals’ with the treatment have the clinical Whoops Disease, as named by Rhapsodie is easy to remember AND because many of us get it whoopsily it makes sense for us. But the clinical treatment impacts the body and systems also, this is what I’ve heard of, but more can be added after treatment shows the effects.

Please take care, no correct treatment leads to death because the parasites (microscopic organisms) overwhelm air systems and take away any ability to breathe. The wake up chokes that happen twice are only a couple of the effects with this action by the nano organisms. Asthma symptoms, with no asthma, is another effect. Having hard times fighting colds, getting bronchitis & pneumonia are other issues from this disease while it’s working. Additionally your HIV blood tests may show HIV that’s not AIDS, but it’s an immune virus impacted by the wastes of the organisms filling your body and weakening your ability to live.

Post Treatment Things

I am not treated, this is just what I have heard that there are repetition cycles beginning right after treatment. These patterns of repetition are heaviest closest to the treatment, the cycles are the same except for the new thing(s) every 3 days, I think. Additional effects may be nice OR not, but I’m not sure what the other treatment values are for sufferers of Whoops Disease.

Water Release

With Whoops Disease being a water borne microscopic organism, as described in many of the previous posts, the water is a necessity for that organism to survive. For individuals living with that disease water in take increases a lot more than normal, as is described with life in many of the previous posts also, links below. This means after disease treatment there will be a great release of water that the organism’s have stored for expansion in the body. In nature water is where it lives at warmer OR like ‘human body temperature’ or there abouts (or around). That’s why with the human body, the water intake has increased so that the organisms have a supply to use while the body still functions ‘normally’ enough.

This should mean that after treatment the water release comes out of the human body in any way that we expel water. This means with the skin through sweat secretions, the urinary tract, from around the eyes with the tear ducts, and possibly the mouth. I’m assuming that the skin water release is in the initial 24 hours the most, while the urinary tract because of processing through the system it could vary and extend a lot longer.

With the extensive amount of water expelling through the body, it’s likely that the bathroom is going to be the best friend of anyone during the early day. BUT that’s not normal even if a person falls asleep in the bath tub. If you have nature space, like outside, it could be that summer warmth will allow you to be outdoors letting go of water, that’s not going to harm the environment. But anyone in the hospital, because of other injuries that were hidden with the water in the body refracting light from image machines hiding images of the reality of injuries under the skin.

This means the water run off of the body, will likely need a flow off bed (table) prepared. Something like is used in surgery that allows the released body fluids to flow away from the body on the operating table.  Slosh there are materials that allow garments to remain sweat free, so I’m sure there could be ‘fabric’ on beds/ mattresses/ tables that allow the water to flow away from the body of the patient on bed. This is only outside the body, what happens with the body.

What happens with the body?

With the water flowing out of the body, I’m assuming that the pores of the skin will allow the releases but will expand with the water outflow. While the urinary systems will work normally BUT at a higher potential, so it may be modified water expelling systems can be prepared. Like with underwear fitted with a water flow bag, like an old hot water bottle that allows the screw thread top to be connected to a hose to a bucket OR something else. BUT what about the pores, they are expelling massive amounts ABNORMALLY.

If the pores are expelling massive amounts abnormally, then they are expanded abnormally for extended lengths of time. So a rubbing OR vibrating rubbing could allow them to shrink back to normal a lot faster. Using a lubricating solution, like pregnancy rub OR sexual lubricant, can assist the friction from the rubbing to be reduced for the skin areas and the rubbing hands OR tools OR both. If the machinery tools are prepared so they can work like a vibrating mattress, pad, or other it means that they can possibly be rubbing tools that are used for other functions also.

These are just my ideas, they may OR may not be good, they are just ideas because of my thinking without having lived this section of the disease, treatment, yet. BUT I have also heard of the repetition cycles of things, that will impact life at the same time that water flows are happening.

Repetition Patterns

This is part of the proof that this disease is nano, not normal. There are repetition cycles, of movements & speech, that go from the first day of treatment to 7, 10, 13, or even 20 days. The first day is the most with the heaviest amounts of repetition. I’m not sure if this is repetition of the day before, OR from months before. I’m not sure what it comes from, but I think it comes from hearing a pattern of sound while the memories of what is spoken OR done OR read are captured for the repetition cycles. Each individual will repeat based on what they have done.

The heaviest sharing with the repetitions is the first day/days after treatment. The cycling pattern reduces away from treatment.  For everyone away from the repeater, things will not be as loud as they are for the speaker. It may be that in some ways, like with eating OR chewing gum OR sucking on something there won’t be as much vocal repetition hassle, but I’m not sure at present, time will tell after treatments begin.

I’m not sure of the patterns OR the time cycles with that. The reduction in repetitions and the actions with those can be prepared for. The patterns will bother everyone over time, BUT THE PERSONS WITH THE REPETITIONS WILL HAVE THINGS THE WORST. It’s possible that treatments done while the individual was sleeping will be easier for doctors, BUT it could be that there will be no moves OR speaking if the ‘patient’ OR ‘released patient’ is sleeping I’m not sure yet.

This means preparing for the repetitions. (I’ve made my own copy of an Excel Spreadsheet and this bit is only ‘some’ of it, so that it can be filled in.

Sample of Whoops Disease Treatment Repetition Page

But you may want to create your own form, with a series, please note that doctors can use pages with the same pattern easier than different patterns. So preparing pages for uses will vary with treatment, and the fewer changes can mean less pertinent pages, but easier to use. Plus with movements & VIDEO RECORDS it can be that some repetition pattern problems can be less stressful for individuals & carers and this can possibly also assist recoveries to be less of a problem.

  • The record of when, what is done, and what is said made the first day will assist the other repetition day records to be prepared to be crossed out as time goes on and things STOP repeating.
    • With a spreadsheet form prepared with Time & Moves &  Speech by volume & span of cycle can allow carer’s and individual’s living with the events to prepare to live through the events. AND with the new ‘event’ OR ‘words’ that are likely once OR ???… I’m not sure to be added onto the cycle pages also.
      • This can be placed into print form OR left on computer, using the video records will allow the time records to be captured and stored correctly on the pages/ computer.
        • For individuals kept in the hospital through the treatment, it can be good that the repetition records are:
          • Kept in the doctors pages,
          • Placed in the Nurses records,
          • Added outside the door for other ‘carer’s to reference’, that is if the patient agrees to that,
          • Placed inside the room for the patient’s family and others as an easier reference,
          • Then there is the connection surface, pad, computer, page, or whatever is used, like a clipboard OR a computer that can be a go between for all the other records pages/ systems.
      • Using video records will allow the verbal and physical actions to be ‘seen & heard’, plus time captured for the cycle pattern records. BUT please remember all the video is viewer capture of the actions, which means anyone seeing this who is living with it is getting the capture perspective.
        • If you have a sports camera on your glasses/ chest/ hat/ head rim/ or arm things will be seen as you do them from the location of the camera, but if you have an exterior camera looking at you that will see things from that angle, which may mean multiple  exterior captures UNLESS one can be placed umbrella like over you where you go with what you do.
    • The physical and verbal repetition patterns in record  can help everyone treated, their families, the doctors/ healthcare givers, and it should mean that the repeater hassles can be minimized also.
      • For instance if you’re treated with ‘going to the bathroom’ as part of the repetition, how was your body held, what future actions in repetition can you pass over OR will you do exactly the same again. So what treatment repetition patterns do you plan?
        • Like for guys that use the urinal, could you have a waist wrap that ‘hides your repetition actions’ OR for a woman that squats on a low toilet is there a … OR maybe you just determine to try and use the bathroom with the repetition, so the hassles aren’t a ‘bother’.
    • It’s likely that the verbal exclamations and actions can be more annoying, especially if you’re having repetitions while at work OR if you’re being treated by doctors.
      • For any getting treated and walking out, it could be that at ‘home’ for the weekend OR  a long weekend’ could be best for recording & making pattern action guides for things that get less and less over the 7 to 10 days of repetition.
      • For in hospital people, having an ‘on the door record’; ‘in the room record’, and ‘in between record’ that allows the other records to be kept accurate is good. It can also be great if the doctors & nurses have a copy of the repetition cycle records.
    • Your plans and actions will impact everything,
      • So making sure to have a record of the repetitions will enable you to work through and with things. For instance if you drive to work, maybe before treatment you get someone(s) you can prepare travel plans with, so you don’t have driving issues in repetition actions that could cause accidents.
        • Maybe you have meetings planned, so you prepare the meeting times with the repetition schedules in mind, maybe even coffee breaks, that allow you to ‘go repeat’ in the bathroom or however is better with you for live around the repetition with the meeting situation.
      • Doctors may be learning this disease, but I’m sure they may be able to provide a ‘doctor’s note(s)’ about the repetitions, so bosses won’t be able to fire you for disease treatment actions that you don’t have control over during treatment repetition days.
  • Family & Work mates & job people might be able to work with you also, your boss can hopefully have plans to work with you through  these times.Just like they will need to with treatment

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

 

#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

 

#15- Visual PAIN Diary- July through December 2016- NO PROFESSIONAL CARE More Problems

Rhapsodie’s PAIN Diary continues from beyond the last post- #14- Visual PAIN Diary- August 2014 to Summer 2016 INACCURATE Records SUFFEREDThis 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. Some may find that their PAIN Diary progression may just have the pain minimizing and totally dropping away as injuries heal progressively.  This is what is normally anticipated with healing, and I’ve had multiple switch change pain placements that demonstrate this has been happening with me also.

BUT my lower left arm has NEVER been cared for appropriately by doctors.

July to August 2016

Problems from the lack of care, INACCURATE PAIN ASSESSMENT CORRESPONDENCE, incomplete and falsified records have extended to other body parts as well as my dignity, work ability, my family care with me and other doctor’s care of me. My left rotator cuff was knocked out of place in July 2016.  The drop in my shoulder was suffered with for months until August 28th when it was shifted back into position at home.

Then after my demand to go to emergency my need for proper shoulder care had me making my pain estimates what I assumed other people would say in the same situation.

September through December 2016

And my request at emergency got me a shoulder & lower arm brace that was used for 3 days at the start of September 2016, until I determined a more comfortable method because my lower Left arm suffered from wearing the cuff.

The MRI did display 3 injuries on that shoulder, but my high pain tolerance had me living for over 1.5 months with my shoulder dropped 1 to 2 inches below its natural location in the shoulder socket.  The accidental blanket re-shifting of my shoulder back into normal placement that happened on August 28th, 2016 was followed by:

  • August 28th visit to the Emergency Room.
  • 1 visit on September 3rd to a specialist- that prescribed a visit to get an MRI & a visit to a Rotator Cuff surgeon/specialist.
  • October 14, 2016 MRI.
  • Visit to another specialist was never handled by the office of the September 3rd visit; I set up my own, with another specialist visit on March 8th, 2017.
  • Followed by a, March 16th, visit to another surgeon/specialist for examination of my Rotator Cuff MRI.
  • This has been followed by his prescription to go for physical therapy at 8 visits, one of which cost $300. AND
  • Another visit scheduled with that specialist to review how progressive the physical therapy has been later this month.

This means I would have done better totally avoiding the doctors and doing an online search for rotator cuff care & rotator cuff exercises.

It definitely would have been cheaper AND much more progressively beneficial.  This has also been proven with the shoulder bracing. This shoulder brace, provided to me at the emergency room assisted in holding the shoulder in place, but it didn’t feel healthy.

There are multiple problems I associate with the lack of use of muscles of the arm, but the shoulder still needed to be braced because it had spent over 6 weeks out of position.  Above my wrist but below my scar some lighting bites of pain happen more and more progressively with the use of the hospital brace.

My 1st visit to a specialist confirmed that there was real injury to my shoulder.  And his prescription for another brace that was more comfortable was given to me.

My husband took me to a local pharmacy that had multiple brace types in stock.  With examining the package as well as other braces on the internet the cost of the internet brace was significantly less.  My husband purchased one of the online braces for me, BUT use of it also caused problems with my lower arm. The pressure of the brace along my arm felt like my bone was soft not stiff in the arm brace.

Another item had been used by me while waiting for the brace that I found good.

My Rotator Cuff Stuffy as shown in the picture here, held by my shoulder, allowed the rest of my body more comfort and freedom, but still braced my shoulder as you can see in comparing the pictures.

Many types of braces are available, the medical industry may not like this, but My Rotator Cuff Stuffy is not tactically bad other than the fact it was created as a stuffed animal and thus I restuffed it about a month ago for better comfort.  Its shape & size allows my underarm to be braced up and locked in place while the rear spread feet keep and raised head allow my body to hold it in place.   I have worn it under a coat, over flannel shirts, bathrobes, and against bare skin and t-shirts.

While my lower left arm has been protected there is more rawness, and I’ve felt the placement of the plate vary.  Now instead of along the scar where there was bone numbness when I touch the outside of my arm, it’s now below my arm and more towards my hand than my elbow.

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…

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

 

#13- Visual PAIN Diary- July 2014- Painful Pokey Boney Walk

As was shared with the previous post- #12- Visual PAIN Diary- June 2014- Father’s Day Weekend after the work to repair my leg you would think that if there were other injuries with my arm, I could also work them into repair.  But there is a great factor hindering me, it is the plate that still exists in my arm.  If that plate was gone, I could have put the bone fully back in position just as I originally did with my lower left leg.

From the visuals a person who is trying to understand the pain another is feeling can also relate better with the situations that led to actions based on feelings that may not necessarily be understandable without the visual connections. I’m not talking about pain alone, but how different aspects of nature can vary the actions of the person who took actions that are not understood fully by others.

Please remember that I have to make visualizations because there were no photos taken previous to suffering the many problems that resulting from real injuries AND multiple doctoral inaccurate assessments that are causing pain.  At times PAIN that has been severe enough to cause me to get nauseous or weak AND to become more and more incapacitated with doctor’s not making assessments properly because of their inaccurate basis of PAIN assessments.

The July 2014 Pokey Boney Walk

On an excursion to from the mailbox in July of 2014, the extent of the Father’s Day Weekend Fall of JUNE 2014 was demonstrated. Pulling the mail out of the box with my right hand was done, and it was passed into my left, but something popped.  It wasn’t too bad that instant, but the joggling mail envelops made things worse.

(A) Natural Walking Arm Angle

I felt like a raw scab was being ripped inside my left arm, and with a single inaccurate step I almost passed out.

The PAIN was on the lower side of my arm. The pressure on the skin shifted as I moved my arm, eventually though clumsily my right hand located a slight protuberance poking away from my left arm.  For all who have never scraped themselves and crawled on the injury, the pressure pain, from the arm with the protruding bone resting against the skin below, felt like having a raw scrape that was cared for land repeatedly on gravel against the exact same location.

(B) Raised View of LEFT Forearm

Raising my arm, caused the ache to intensify against the skin, but it minimized the scraping scratching raw pain of shifting bone weight. My right hand couldn’t really find the problem after my arm was lifted at a certain angle, but there was an angle of touch that was sickening.  The closest place was over 100 yards away from where I was standing, I HAD TO DO SOMETHING!

Shifting the mail, and trying to rub the pain away, was not helping things were getting worse.  I needed to see the problem, so capturing the mail against my chest with my partially raised LEFT arm allowed me to work on getting rid of more pain.  Working to view the situation took some effort.

My view of the painful area was not easy to see from my natural viewpoint as shown in this mirror image here. The red mark on the sketch is approximately the location of where Pokey Boney was located on my Left Forearm.

(C ) Pokey Boney Injury Sketch

With my arm across my lower breast there was nothing to see, I had to shift my wrist down while raising my shoulder up to get the bone to act like it did with my arm down.

OUCH!

Finally I saw the issue, though I felt a lot in the meantime. I do not have an accurate view to share with you, so this picture has been sketched with an oversized  Pokey Boney addition.

Please remember that the bone was trying to poke out of my skin, I was alone in the yard, the house was so far away, I had to do something.  Shaking my head to keep me from  stumbling into the darkening or collapsing from pain, I shoved my Pokey Boney down away from the skin, but NOT back into place.

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…

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

 

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