Me & my speech.

Posts tagged ‘care’

#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

 

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

From previous post- #05- Inaccurate Doctoral PAIN Assessments based on Guesses– As stated previously ‘with no relational corresponding pain chart there is more space for inaccuracies.’ There is also more likelihood of not doing more work based on the inaccurate assessments already made and reported on by doctors.  This in turn enhances the likelihood that a basic to care for problem is made worse, like I am having.

More Than the Basic Details For Pain Assessments- Dr. Savage

There are also the depth details of pain assessments done that do not necessarily have corresponding values for all people.

One article for assessing chronic pain states, “For a doctor to get a good sense of your chronic pain, just pointing to a single face or number isn’t enough. Your doctor will need some context, says Seddon R. Savage, MD, incoming president of the American Pain Society and an adjunct associate professor of anesthesiology at Dartmouth Medical School in Hanover, N.H. “I ask people to remember the worst pain they’ve ever experienced in their lives,’ Savage tells WebMD. ‘It might be a kidney stone or childbirth. That level of pain becomes the benchmark to which we compare the current pain.’”  I never was pregnant, and I have never had a kidney stone, so my estimate doesn’t even relate to others that way if it was ever requested.

For Patients- Describing Your Chronic Pain

As we have already seen with the information of this document, the assessments by doctors are based on the searches they have done, but “Your doctor needs to know not just how much the pain hurts, but how the pain hurts, says Savage[ in the article from WebMD entitled Using the Pain Scale: How to Talk About Pain.

The kind of pain you’re feeling can say a lot about the cause, experts say. Cohen says that pain that’s caused by tissue injury — like arthritis or a back injured while shoveling snow — tends to be like a dull ache.

But nerve pain, which could be caused by many conditions, such as diabetes and carpal tunnel syndrome, typically causes a more distinctive shooting pain. Others describe it as burning, buzzing, or electrical pain. Nerve pain is also associated with other sensations that aren’t painful in themselves, like tingling or numbness, Cohen says.

Savage says that it’s also important to discuss any variations in your pain. How does it change during the day? What makes it hurt more? What makes it hurt less?

When you see a pain expert, go in prepared. Be ready to describe your chronic pain, as specifically as you can, along with details about when the pain started. The more information you have, the easier it will be for your doctor to help treat your pain…”

The stink of this is that doctors assess a person as having chronic pain, without ever even referring the patient to a PAIN EXPERT.  In fact there may be legitimate pain issues that are totally ignored, like the fact that a broken bone happened, but there are multiple bones in the area and the assessments of
X-rays, CT scans, and MRI tests were not ever examined by a person who looked at the correct placement of the pain.

An estimated doctoral assessment of chronic pain does not mean that the pain is constant or consistently the same or in the exact same location, but without an accurate way of making assessments, doctors are likely to do what is easy instead of what is needed.  The WebMD article continues with more information of great value for people seeking to get treatment that is accurate.  But all of the wonderful advice of the article  will only work if the patient persists in working at getting accurate assessments.

How Does Your Chronic Pain Affect You?

Beyond the severity and the type of chronic pain, there’s a third factor you need to discuss. “It’s really important to talk to your doctor about how your pain affects your life,” says Savage. It’s a crucial and often overlooked detail… Savage says that you should think about the specific ways your chronic pain is affecting you.

  • Does pain wake you up at night?
  • Has chronic pain made you change your habits?
  • Do you no longer go on walks because the pain is too severe?
  • Has it affected your performance on the job — maybe even putting your ability to work in jeopardy?

Giving specifics about how your chronic pain is impinging on your life and changing your behavior is key, Savage says. ‘It helps your doctor understand how much you’re suffering and appreciate the pain as [only part of the] problem that needs treatment,’ she tells WebMD.”

Notice how I varied that doctor’s statement.  It was done because my doctors have taken it upon themselves to offer assessments based on their inaccurate work and 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…

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

 

#05- Inaccurate Doctoral PAIN Assessments based on Guesses

Started from previous post- #04- Inaccurate PAIN Assessments with JUST Rate Pain from 0 to 10– ‘How much pain are you in? Rate your levels from 0 to 10.’  With just that question how do the doctor’s really assess my pain? 

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

How do any these assessments accurately assess MY PAIN? 

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

The work of the doctors could improve if they did all the estimating steps, mentioned IN DIFFERENT PAIN ASSESSMENT METHODS LIKE THE SOCRATES pain assessment, but in general a patient may get 10 minutes with a doctor or less because a 20 minute visit involves, weighing, nurse recording information, and this is all part of the 20 minutes allowed for the patient.  My personal experience has shown that most doctors in the medical field do not even do the whole amount of work with asking all of the questions with the SOCRATES (pain assessment)[s] method, maybe because it just takes time OR maybe because of all the insecurities legal hassles have added to the doctors work.

The SOCRATES pain assessment AND Dr. Savages methods at least get more details than a basic rating to detail pain.  Rhapsodie’s method for improving the assessing can also be good, but it requires a lot of work through a society of medical people and patients.  So even though it will be shared later the relational corresponding pain chart is not necessarily a good thing because it has less personalization in corresponding factors than the work of Dr. Savage does.

SOCRATES (pain assessment) Information

This information is taken from Wikipedia.com, there may be more details in other places, but please my assessment of my personal care corresponding to the assessment first please.  My results are placed in [square brackets] next to the corresponding questions:

SOCRATES is a mnemonic acronym used by emergency medical services, doctors, nurses and other health professionals to evaluate the nature of pain that a patient is experiencing.

Meaning of the [SOCRATES] acronym

The acronym is used to gain an insight into the patient‘s condition, and to allow the Health Care Provider to develop a plan for dealing with it.[1][2]

  • Site – Where is the pain? Or the maximal site of the pain. [PARTIALLY ASKED]
  • Onset – When did the pain start, and was it sudden or gradual? Include also whether if it is progressive or regressive. [PARTIALLY ASKED]
  • Character – What is the pain like? An ache? Stabbing? [NEVER ASKED]
  • Radiation – Does the pain radiate anywhere? (See also Radiation.) [NEVER ASKED]
  • Associations – Any other signs or symptoms associated with the pain? [NEVER ASKED]
  • Time course – Does the pain follow any pattern? [NEVER ASKED]
  • Exacerbating/Relieving factors – Does anything change the pain? [What drugs do you use to care for the pain? The best pain treatment for me has come with the use of prescribed ANTIBIOTICS!]
  • Severity – How bad is the pain? [RATE your pain FROM 0 to 10]

This was from Wikipedia.com at this page https://en.wikipedia.org/wiki/SOCRATES_(pain_assessment)

But there is a lot more information needed, especially when the information gathered does not get enough detail to make an accurate assessment or if an individual is not exactly the norm.  It’s a lot easier for a busy person to say, “this person is suffering …” when they do not do the work, then when they take the energy, time and effort to make an accurate assessment.  In fact a person like me can be diagnosed as being a drug abuser or suffering chronic pain because the doctors have no true idea of what they are hearing from me.

As stated previously ‘with no relational corresponding pain chart there is more space for inaccuracies.’ There is also more likelihood of not doing more work based on the inaccurate assessments already made and reported on by doctors.  This in turn enhances the likelihood that a basic to care for problem is made worse, like I am having…

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

 

#1- RECEIVING & SHARING (R&S)- PLEASE SHARE IF IT’S GOOD FOR YOU

RECEIVING & SHARING- Was previously shared as RECEIVING at fawnsfall.wordpress.com. Here the information shared there will be divided into smaller sections.

#1- RECEIVING & SHARING- PLEASE SHARE IF IT’S GOOD FOR YOU

Some may suffer a feeling of not receiving,  I hope that the following information can give you useful valuable help, while the hearts above help those with small devices to see what my black shadowed picture hides from people with small devices too.  That’s at least until I have my 3 computers that are fiddlenfarten fixed…

b-rhapsodies-spring-flowers-trademarked

HAVE YOU EVER MISSED WHAT ANOTHER WORKED TO GIVE YOU, BUT YOU DIDN’T APPRECIATE ENOUGH TO RECEIVE?

I know I have, and I hurt others it’s hoped my apologies here are found by them.  And it’s hoped others will find that receiving isn’t as often physical as it is useful.  DO YOU FEEL like no one ever gives to you?  Do you feel like no one has ever cared enough to try and give to you?  Narrowing down the reasons for feeling like you’ve not received when you have, comes down to who you are.  Is it because what you’ve received isn’t necessarily physical or considered valuable to you when it was received.

Sometimes memory is a factor, at other times value is a factor, and there may even be other factors that you can share.

MEMORY

How often have your family forgiven you for a mistake or damage you’ve caused to them or their stuff? How many times were you given a suggestion that in life was so beneficial for you to have, like “I always count money back to people in reverse, smallest amount first.” (A great person, trying to give to this blog author.

VALUES FOUND & BEING SHARED as a CASHIER

Why was this so good for any cashier?

Because with a very busy day, lots of people, and lots of money is being cared for, counting back to a customer shares respect for them and your work, on top of giving you more ability to handle cash responsibly. A person with a $123.43 bill who hands a cashier $150.00 should receive $26.57 in change.  If, you count money, while talking through the altered amounts, back in reverse, smallest amount first, a person handling money is more likely to be accurate and will be caring for their customers.

Please remember, for any cashier, counting the coins back can also be good. Especially with small kids or individuals that don’t know our U.S. money, but remember others can appreciate that also.  PLEASE try to care for your customer’s time, so that when you’re so busy the customers that could be angry with every second they wait are reassured they won’t wait worthlessly, this means speaking at a speed that doesn’t delay the transaction, it is often useful to practice.

So how does Rhapsodie’s customer get their $26.57 back?  Her other conversation with them pauses for a bit, as she works returning change and she says, as suggested to her, and using our example from above, based on what the facts are, [SITUATION REMINDERA person with a $123.43 bill who hands a cashier $150.00 should receive $26.57 in change.]:

-Rhapsodie’s 1st, less preferred, cashiering count back option-

“Your change is $26.57, out of $150.00″. Then with handing the customer all of the change, of two pennies & one nickle (or 7 pennies) and two quarters (or 5 dimes) saying the partial exchange total ”  57  “, followed by handing them the $1.00 bill, and adding ” one 57  “, (this is implying dollars and cents, but American cashiers normally don’t say that because cash is in hand, like with this example detailing with a count back  ‘one dollar 57 cents’ in the midst of a count back is normally silly, but some people do because of their jobs or reasons) then adding a $5.00 bill saying, ”  six 57 is your change…” continuing to interchange with customer as is good.

Or for more detailing there’s . . .

 

WHOOPS DISEASE-2. Females

WHOOPS DISEASE, what is it?  Well it’s what I’ve named what is as yet a disease listed as unknown by the majority of medical society.  Nobody is looking for the symptoms and I got sick from being sneezed on.

Do you know how easy a sneeze crosses the air?

Ive affected my kitty? By sneezing on him and making his life horrid. And he shows the male signs, that’s for the following post because Whoops disease symptoms for males and females are different, An Arrow-b here’s a couple of links to find out the details I’ve lived with.

Me again 2015

ME- 2015

I’ve been sick for the last 10 years, first from May or was it July 2008 and of course I’m aging too, we all are, but nothing is so abnormal as to seem wrong for anyone but me.

FEMALE CAUSE & SYMPTOMS:

  1. Inhaling someone else’s sneeze juice OR drinking the fuzzy pead on water in the TROPICS.
  2. Feeling not right within a couple of hours. Generally noticed within days or weeks.
  3. Congestion in the lungs, which generally begins at the start progressing into colds within the first 3 to 6 months that continue can, and for me Rhapsodie McClintick did turn into bronchitis or pneumonia symptoms within the first 1 TO 2 years and it continues… so it’s viewed as an allergy by doctors after the bronchial and pneumatic treatments failthen later they progress to treating you with asthma inhalers which only increase lung space for the parasites to gain fluid from blood out of,
    • the lung coughs come out crystal clear and dry to white flaky crud.
    • The only cold treatment that works is
      • GINGER for the INFLAMMATION
        • Cider vinegar & honey help it taste good, and the Cider vinegar and honey is GREAT for the ACID REFLUX.
      • CHAMOMILE TEA- DAILY for the SINUS CONGESTION
      • This does lead to Asthma diagnosis’ by doctors that don’t do full scale proper tests with proper equipment. Within the first 2 to 3 years.
      • BECAUSE IT IS NOT ASTHMA! THE DRUGS DO NOT WORK for more than making more lung space for the microscopic organisms that have invaded your lungs.
    • 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 early sneezes result in crystallizing looks on the fluids that are expelled and dry on darker materials also, like with coughs in the earlier stages.
  4. Acid Re-flux begins, if you don’t already have it, about 2 to 3 years into the disease and it remains throughout. It will eat away your vocal system also. The acid re-flux is because your lungs absorb moisture while you sleep as well as while you’re awake. During sleep the ‘acid re-flux’ happens because your lungs are breathing in moisture from the stomach area, thus causing acid re-flux, so the treatment with a daily dose before bed of:
    • 2 tsp. CIDER VINEGAR &
    • 5 tsp. of real HONEY, and
    • 1cup hot water
      • These combined are a great ‘cheap’ and healthier help against acid re-flux.
      • My sore throats, resulting from untreated acid re-flux, because I didn’t recognize the symptoms of stinky mouth, sore throat, and other things.
      • Additionally the AND mouth dryness is not assisted by water, but by milk, so more liquid is drunk that’s not calorie free.
      • BADLY
        • The over the counter medications, are only for use for a limited time. AND
        • The ‘medicine’ treatment above enhances the potassium absorption in your system, SO
      • it’s better for you if you’re in danger of kidney disease OR want a continual treatment to avoid the ‘acid-re-flux drugs’ when you can use natural treatment right before when you brush your teeth.
        • This is done to keep the acid of the cider vinegar, less with the unpasteurized from eating at your teeth, because the brushing and rinsing of your mouth with water should minimize the effects of the acid, and doing it right before bed is the best for sleep time acid-re-flux problems.
  5. Bunions Begin around the same time after the acid re-flux starts.
    • My family doesn’t have bunions, and I do now, this may be true for everyone, but it really helps to avoid having surgery to remove the bunions when after the disease is treated properly they disappear.
    • b. bunions on both feet
  6. Higher sugars above 120 but below 130 have been found from Whoops disease:
    • Just recently the doctors have rearranged their diagnosis for Type 1 diabetes, but I still believe that anything, consistently, over 130 is unhealthy,
    • anything above 120 is slightly uncomfortable, it gets more so the higher the sugar is.
  7. 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.
  8. The 2nd year of the Disease has 1 outrageously loud and angry yelling episode, this only happens once.
    • But the sneezing does not begin until after the singular yelling episode.
      • The sneezing gets harder as time progresses the deeper and more painful the more time the sneezes continue for.
    • The frequency of the sneezing increases, so that with some of us, it’s like we’re in a smoky room with no ventilation.
      • Sneeze sets that repeat frequently AND
      • are infectious to anyone breathing in any of our sneeze smear.
  9. My hands, fingernails & toe nails have altered
    • from how smooth they used to be, to being wrinkled rougher on top in a finger length type of wrinkle that runs down the nail from the cuticle to the tip of the finger nails.
    • My hands have aged weirdly they look older than my aunt’s who is 11 years older than I am.
    • Additionally there has been cuticle growth on my finger and toe nails that is larger and tougher than normal, sense since youth I’ve shoved my cuticles back I’ve continued to do so. Recently the cuticle stains remain on my fingers, …
    • P1700371- 3 fingers
    • .Recently, in 2018, year 10 for me there has been staining of the cuticle remains. I used a nail brush to scrub it clean tonight.
    • AND my pinky toes are losing the top layer of skin, it turns flaky white and I can scrape it off with my finger nails, I try to avoid it a lot. AND use of foot cream that’s a mix of a hydrating cream, glycerin, and aloe seems to help keep things from getting too tough on my legs.
    • Hangnails that rip down have come and gone, with treatment the superglue works really well.
    • The ripping & cracking fingernails,
      • The ripped nail edges are being treated with a nail file, because one is carried with me all of the time, my left hand nails are rip cracking the opposite of my right hand on the exact same fingers.
      • BUT my nails are acting super dry like my hair is, so having them break at the tips seems quite normal for how dry I’ve been.
    • b. ripping finger nails
    • Flat topped thumb nails and the one on my left hand has seemed to start cracking on my right hand the small ditch on my flat topped thumbnail seems to be getting worse here are some pictures from my thumbs today.
    • b. flat topped thumbnails w-possible cracks
  10. The 3rd year began occasions where the body sweats like you’re swimming in water, for hours on end,

      • for one 24 hour period to a week I was so sweaty a dry cotton wash cloth sitting on my bare leg absorbed more than a squeezable amount of water.
      • There were multiple times since 2013 when I awoke with the bed soaked from my sweat, the mattress soaked so much that it was still damp the next day. AND
      • it happened just a couple of days ago, ‘death sweats’ I named them, because my lungs are so bad now I can barely breathe in the tub OR in trying to sleep.
  1. Thirst dramatically increases in the 6th year and the thirst continues to increase so that about a gallon or more is drank each day, but the water adds to the body weight without draining away properly.
    • My sore throat, mentioned above is not assisted by water, but by milk, so more liquid is drunk that’s not calorie free.
    • Severe thirst so that the mouth needs liquid every 10 to 15 minutes has happened from beginning about the 7 to 8 year period, at least for Rhapsodie. Things may be varied with people with different size lungs, I have large lungs for my frame.
      • The thirst gets so great that the mouth and throat dries out and hurts without a drink every 10 to 15 minutes.
      • The drinking need has dramatically increased AS HAS THE peeing amount. As of January 2018
        • I’m up to drinking over 1.25- 2 gallons per day, this is a combination of-
          1. Water,
          2. Tea water,
          3. Milk,
          4. Sparkling water,
          5. Tea with water, AND
          6. Nutrition Plus to keep my calories at a good spot.
        • Going to the bathroom,
          1. Every 1 to 2 hours, during waking times AND
          2. 2 to 3 times during sleep.
          3. Approximately 1.20 gallons about 80% or more of what is drank.
        • There is also how comfortable the shower or bath feels, which means more time is spent with water because the body is super dehydrated unless more than a gallon is drunk per day.
  1. There is also water weight gain that is noticed in the legs and ankles, on the face, thighs, belly, breasts, upper arms, chin, and other areas. AND this is the same with men.
    • There were also blood pressure problems, so the doctors tried to add blood pressure medicine, when there is not a real problem ‘blood pressure problem’ because they aren’t treating the disease, that clogs the lungs and poisons the body, only the symptoms resulting from the disease.
      • But it’s not a problem now.
    • There are cholesterol problems because I’m eating so little, that I’ve tried to enhance the caloric intake with less food, meaning higher fat food. Lower fat high calorie food is super expensive and very costly for a no income person.
      • So I’m using Red Yeast Rice & Lysine, from the vitamin areas, when I remember to do so, which should be done as dose needs daily.
    • 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.
      • For the 4 to 10 year range the appetite diminishes and this continues to increase as time goes on.
        • BUT for my mother who’s mature, they has been an increase in appetite.
      • Taking supplementary nutrient drinks and drinking whole milk has assisted me in improving my calories from the 2013 amount of 1400 calories per day on average up to the 1603 calories a day on average in 2018.
        • With the diminished appetite the body weight has increased while, food calories are less than healthy. AND
        • Doctors treat you as if you’re fat, when you’re not really eating enough to be healthy.
          1. What was it, in the German concentration camps a 1,200 calorie per day diet ‘was okay’. AND the world saw images of people that were given 900 to 1,200 calories a day, after the Allies got to the camps, and to this day we judder in horror.
        • In fact I’ve charted my calories since 2013 and the numbers show:

calorie snip for wordpress Whoops disease b

        • I’m doing great eating 1600 on average each day per month for 4 months, up and down some, but that’s good because I feel less weak and wobbly. Additionally, my bones are less likely to break more than they were when I wasn’t eating enough to stay healthy, even with doing no physical labor.
        • I’ve been as low as 1200 per month on average for four months more than once, previous to making a good account of my eating, for almost a year I was eating less than 900 calories a day, while my doctors were believing the scale, as an accurate body mass index, instead of the truth in my records.
          • You can see in the 2015 image how it looks like I’m growing a double chin, that’s also a part of whoops disease.
Me again 2015

2015 Rhapsodie

 

b. Rhapsodie w-photo picture- P1680061

2018 Rhapsodie

 

  • Additionally you can see how in the 2018 image that I look fat. BUT
    • my right hand the one that’s used all of the time looks like bones with skin.
  • My feet have shrunk in shoe size, my hands were smaller, but
    • now they are the correct size for when I was at my prime weight.

10. Additionally there are the hemorrhoids that grow from bowel movement increases and variations that increase the more fluid you take in.

  • About my 5th year with the disease, 2013 I’d poop what looked like quarts of shit at a time.
  • About my 6th year with Whoops, I had one nasty it felt like a baseball of poop, hard round and dry like a mud ball that sat out for days.
    • Sorry, I had to use my fingers or die of the pain, and I used the scrub brush and soap as soon as the relief was gotten.
    • In 2016 I had another nasty spell with golf balls of poop that were dry little chunks clogging me up until pulled out.
      • The hemorrhoids grew from baseball season, 6th year, and now I use the Bag Balm [search engine web page] OR petroleum jelly almost every time I’m on the pot.
  • Recently softer diarrhea poops are more common because of all the milk I’m drinking without a lot of fiber, I think.

11. Also there are mood changes that are most dramatic in the 6th to 10th years, but made worse by the ignorance of so called ‘doctors’ and the money they want you to spend for visiting specialists with no results:

  • About the 6.5 month stage for me, there was
    • One month of severe I DON’T CARE attitude.
    • About 2 to 5 months later there are moods of severe calm than there are weeks of calm days followed by angry days.
  • Recently, the 10th year, I’ve suffered the I DON’T CARE attitude for months, with extreme mood swings and upsets.
    • Partially because of ignorant doctors and more…

12. 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.
  • Then they were white and heavier.
  • NOW they are golden yellow & very dry from how my temperature has been out of wack.
    • If people around you are LOUD and if you’re having waxy ears and listening, the sound is amplified more and hurts.
  • Most of my headaches recently have resulted from noise, and I know my ears get clogged. 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 and 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.

13. And there has been & are odd swellings and itchiness for the last 5 years progressively getting worse with time.

ME- Eye swelling 3- 2015

Oddly Swollen & Hollow Eye Space

                                One example is shared with the next picture at my eye above.

  • There have also been
    • odd throat swellings,
    • odd groin swellings,
    • an odd behind the ear lump,
    • under arm swellings and itchiness’s,
      • the under arm itchies have continued to the present day as have the nose itchies and I treat them the same with Bag Balm, that you can buy in a ‘farm care’ OR pet place.
        • Walmart used to sell that in the pet department where I used to work, that’s I how got acquainted with it. It’s some sort of antiseptic, with lanolin and petroleum jelly. AND the rashes ‘go away’ until another week OR day of treatment depending on the location of the itch. And
        • odd right & left hand swellings that I do not associate with other injuries.

14. Additional rash locations have come about, for me the oddest has been my belly button, BUT I’ve treated that the same way as the underarm rash itchies and the itchiness on the nose mentioned right above.

  • For me treating the underarm rash itchy with Bag Balm can assist them in fighting this drying itchy bumpy rash, initially for over a week, but then later in the disease once a day before bed or after my shower or bath before bed.

15. Over the last years I’ve suffered water blisters that feel like pencil stub bubbles on the end of my fingers.

  • It’s kind of odd because they came about 3 months apart, the one on my thumb I’ve lasted for almost exactly 3 weeks. So there wasn’t popping I use a sugar picker and poke a hole and bleed out the excess water in that blister, I’ve done that every other day for the last 7.
  • Also I’ve gotten white heads, pimple blisters, on my face and when they are popped they result with an oil layer over water that seeps out for as long as it’s allowed to. It’s 8 to 12 times more water than oil smear or pus. I can reduce them by squeezing any skin area, but the water expulsion is ABNORMAL.
    • Additionally boil like lumps have appeared on my face, groin, chest, and they do not reduce they sit their for months until they start to hurt and can be reduced.

16. Eye balls feel super dry, like they are un-lubricated,

  • In 2013 the optical doctors informed me that my eyes were dry, but
    • expensive eye solution is wasteful for helping my eyes when SALINE SOLUTION &/OR the protein heavy equate brand MULTI PURPOSE SOLUTION, which is also used for contacts are the great for hydrating & stopping my eyes from itching.
      • Presently I’m using a tablespoon of MULTI PURPOSE SOLUTION on my eyes weekly. Versus using the same amount of saline solution daily.

17. LUNGS- The whoops disease lives in the lungs, it causes all the other body problems because the lungs are an air and blood filtering system for the whole body. And the shit of the ‘microscopic organisms’ pollutes the body. Additionally the lack of clean air the body takes in adds poisoning to the blood. For me, my lungs:

  • Start burning, really low, in the 2nd year,
  • by the 4th year the lower lungs are a lot heavier and burn a lot, and breathing diminishes more,
  • in the 6th year the middle of the lungs feel a block, and
  • after that the upper lungs gain heaviness and in the 7th year they start burning,
  • by the 8th year the upper lungs progressively get more burning periods and more of the throat hurts too, also breathing is A LOT WORSE.
  • For the last 24 months, 2017 to 2019, my lungs are burning daily in the upper zones.
    • For the summer with no AC the lungs feel heavy, and the breathing is a lot harder.
      • AC does dehumidify the air, but it causes my throat to burn also, while the hot dry wood heat air also dries the air, my lungs don’t while my throat does when I’m not drinking milk.
    • For Winter
      • the wood stove dry air, it’s so dry that using a humidifier greatly helps, but I’m thinking that if it’s the microscopic waterborne organism’s then the dry air is keeping me alive as well as enhancing my thirst.

18. And there is hair and skin loss, much greater in amounts and frequency than normal, in general the more baths & showers a person takes the more hair & skin they lose.

  • SKIN LOSS, seems to come with being so dry.
    • Each shower I take causes me to lose at least 1 teaspoon, or more, of skin that’s what remains in the fine screened drain grate clogging it unusably.
      • The skin loss amounts continue to increase so that if I take a bath the tub has skin floating in a layer on the water when I’m done in the tub.
      • My face, hands, legs, and arms are peeling visibly daily, the same as the tub is my sink after washing my face in the morning or scrubbing my feet at night.
    • I’ve never had dandruff, I do all the time now, but my mom recommended the baby shampoo and it works to decrease dandruff itching at a smaller cost than dandruff shampoos.
      • BUT the dry skin on the scalp continues, and the remains are not dusting’s of dandruff, the skin flakes off in larger ‘between’ hair pieces. You can see the skin sections floating down through the air like snow.
  • HAIR LOSS, I still have my own hair, at least some of it AND I do not regularly dye or perm my hair, I don’t use a hair dryer OR hair curler, but
    • I’m losing about 4 times the amount of hair I ever used to.
      • 8 years ago my comb collected less hair per month than it now collects daily.
      • My hair has always collected in the drain, but now I can fill a collection screen cup with each of my shampooing rinses.
    • I’m not 50 and I’ve had bald spots on my head because of the dramatic amount of hair loss that isn’t continuing now, even though I’m eating healthier with the Equate Nutritional drinks from Walmart.
      • Other than the previous comments that were true, about a year ago my hair started growing in at about 3 times the normal rate.

19. There are also sleep situations that are not normal. Around the 5th year and continuing to the present my sleep has been odd.

  • Super tiredness that increased so that 10 to 14 hours a day were normal sleep happened this last year for months.
    • One day I slept straight through except one bathroom break for 24 hours.
  • Then there were months where every time I went to sleep I was awakened and
    • This was weird because it was a cycle of 3 days odd up to one day normal for over 1 month.
    • And during this time there were odd dreams.
  • I’m still having weird and odd sleep cycles, that are exacerbated when I do consume enough nutrition in the previous days.

20. Additionally taking the Ibuprofen is like taking a sleeping pill, I think, drugging me for over 24 hours with a foggy head and no ability to do more than stay awake.

  • Previously if I took A COMBINATION OF ACETAMINOPHEN’S &/OR IBUPROFEN they cause 1 to 3 hours of vibrating abnormal shakiness. And that has happened for over 5 months, but IT’S GOING AWAY NOW.
    • The shakiness has diminished tremendously with my nutritional value increases.
  • So if you’re suffering whoops disease, I’d suggest not taking any acetaminophen OR ibuprofen until after you’re ready for bed. If you were driving with it, ….

21. Over the last 8 months I’ve been having dizzy spells, starting on Saturdays, that are increasing in amount and effect.

  • My mother has been suffering these for a long time now, but
    • the disease has a normal lung female with 6 to 9 months, 3 days and 3 hours getting worse and worse as time progresses. So
  • for me with the larger lungs my dizziness may extend longer.
    • I’ve been having the Saturday dizziness from about last November starting at 9 weeks, then increasing to 6 weeks, then 3 weeks, and
    • now once a week and this last week has been going on since Friday.
    • So it may be my last week of dizziness or it may mean worse weeks are ahead.

22. I have all the ‘medically mentioned’ signs for, 

  • these tropical waterborne parasites/ organisms, yes I’ve lost the ‘medical PDF’ record and the disease name has changed frequently, but I have all the signs of Whoops disease so you may also.
  • And be prepared your doctors will try to treat you for asthma, blood pressure, cholesterol, diabetes, heart disease, lung disease, and anything else they can prescribe a drug for to get you out of their hair AND they will not be treating the problem that’s killing you.
  • For testing, a waterborne parasite a urine test is used, and the test needs to be done within 24 hours after the sample is collected. IF the place you go for tests ships in amounts to a hospital lab, it’s likely a bad place to use for this type of test. Because from peeing in the cup until the test needs to be less than 24 hours, or the results will be inaccurate.

Please remember these are notes for the disease with me, my mother who got it from me is suffering ahead of me now because her lungs are a lot smaller than mine. Originally her symptoms followed mine, now they are ahead of mine. BUT because of her age, past menopause, her symptoms are different in some ways and degrees. There are some similar male and female symptoms mentioned but the timelines and the depths of problems vary to a great degree by the size of the lungs and the sex of the person.

Because my cat suffers the male symptoms in my timeline, I’m wondering if there’s a chemical animal human disease correspondence.  Eventually that may be discussed more in the WHOOPS DISEASE-5. Nano Mites? post.  The following post is organized to discuss what male humans in my life are suffering, because my sneezes carried to them.

WHOOPS DISEASE-1. Animals

WHOOPS DISEASE-2. Females

WHOOPS DISEASE-3. Males

WHOOPS DISEASE- 4. More!

WHOOPS DISEASE-5. Nano Mites?

WHOOPS DISEASE-6. Treatment Ideas & Facts

 

WHOOPS DISEASE-1. Animals

Do you love your animals?

Some of us love them & make them as sick as we are!

Whoops I just sneezed at you, did you get my disease, I sure hope not!

Whoops did you swallow my sneeze, uh oh, I don’t know it’s real name, so I hope you didn’t get Whoops Disease.

Whoops is a disease that is some sort of waterborne microscopic organism with so many normal symptoms that your ignorant doctors make misdiagnosis repeatedly for other diseases.

The symptoms are listed in the following pages, they effect humans and animals.  Do you love your animals?

I love mine, and made him as sick as me! But his vet has the treatment, that saline was added to, for the general treatment of parasites.  Because sneezing on him has made his health as horrid as mine, well maybe my 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 Mystin displays the male symptoms, and he’s still alive, maybe because he got one ‘weak parasite treatment correctly at the veterinary office, but he needs the concentrate multiplied by 10.

Mystin 2008

A clear sign for animals is the single long cut on both of the front canines, that begins AFTER SNEEZES, THE TEETH which WILL HEAL FINE if the long cuts are cleaned 3 to 6 times before they start healing, with the pet toothpaste & infant brush, AND allowed to fully heal with no touching, if the skin is broken by finger nail or toothbrush after they start healing, then the poor animal has a yucky canine. If the tooth is not brushed the teeth can starve the critter or they can heal with yuck in them.

THE SNEEZES which can KILL when the animal has them repetitiously and cannot sleep, THE SYMPTOMS LIVE A TIMELINE OF EVENTS OVER YEARS OF TIME. But there is also the food problems from the acid re-flux that swell the throat and make it hard to swallow anything not fluid. Being unable to eat and the sneezes are death dealing, I’ve helped my baby with soft kitty food AND chicken fatty water, because that’s what he prefers. He’ll drink tuna juice, but he does not tuna in olive oil. Beef  & lamb & turkey juice and other fish juices might be nice.

The itchy problems, from dry skin, are more advanced with the animals because the critters like cats and dogs with fur covered skin have hair that means only claws dig through to itch their skin.  Thus the scabs from the itching grow with the itchiness, and I hope my animal gets correct treatment before a painfully raw scratch causes and infection that leads to death through an attack or another disease. Additionally, there are weeks where he’s been blind. I think if he gets the proper parasitic treatment while he’s not blind he’ll be able to see fine for the rest of his life.

The amount of liquid intake increases the peeing need, and it also causes the body to suffer diarrhea, my poor little kitty keeps going potty about 3 to 5 times more than normal. He’s so sick right now with the diarrhea he smells stinky and he has been sleeping outside on the porch for running to the yard.

THE HUMAN SYMPTOMS ARE , in some ways, THE ANIMALS SYMPTOMS, but the animals can die from poor teeth possibly, acid re-flux, and from lack of sleep with sneezing because they have trouble sneezing laying down.  And there are side effects that alter the body compositionally and because of multiple thoughts on this disease I now am assuming that this is a technologically advancing disease.

WHOOPS DISEASE-1. Animals

WHOOPS DISEASE-2. Females

WHOOPS DISEASE-3. Males

WHOOPS DISEASE- 4. More!

WHOOPS DISEASE-5. Nano Mites?

WHOOPS DISEASE-6. Treatment Ideas & Facts

 

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