What about the people that are very sick and have insurance but you don't take insurance? That's the only way or means they have to pay for anything. They've done enough research to know what kind of tests are available and how to take them. They have done enough research to know what their symptoms could be a result of. Because they don't have a lot of money and are considered poor they don't have access to these services. How are they ever going to get better? The answer is simple they are most likely not going to get better . They're going to spend the rest of their life fighting to try and survive . Is this a concern of anybody in this industry.? I honestly am not really sure anymore. I think we should give up on the fact that any sort of health professional has our best interest at heart and wants us to get better. There's a difference between somebody who is busting their butt trying to figure stuff out then somebody who isn't but yet help is never offered. This is the reason why people struggle with doctors and this is the reason why people get frustrated with the system. It's messed up and doesn't work and a lot of people are suffering because of this. It's very disappointing.
Why is it that all these labs are not done in a medical clinic's lab? You would think that there are two bodies. One for the allopaths and one for the homeopaths! Surely there are some crossover labs that are done in both laboratories. I am a raving lunatic to the ER doctors in my town because all my labs are normal even though i am having extreem neurological symptoms. I have no spare money and am on medicare. Surely there is help for me somewhere! I litterally feel i am near death most nights and my concentrated electrolyte sports drink is all that is keeping me from entering the world of metabolic acidosis with no compensation! I feel that the electrolyte shifts in my body may not show up on labs but i feel every bit of it as if the labs are critical! The ER doctors do not wants to deal with me even though i can barely walk now. I am waking up in the night with twitching feet, uncontrolable deep breaths that do not stop until the feet are still only if i drink my sports drink. I have diarrhea and polyuria at night. Every night hokds an emergency that i am getting more unable to cope with. But i wake up so confused and i am unable to comprehend what is wrong! My O2 levels are dropping now at night and i have no lung disease. But i am concluding that i have pulmonary hypertension. I also have very shallow breathing even during the day. My resting sats are now 95-96%. At night i have captured a sat of 86%. But i don't feel distress. On one ER visit complaining of dehydration, my respirations dropped to 6-7 a minute and my sats were 94%. I felt no distress but as a nurse i knew this was serious but no one in the ER bothered tbemselves with me. I lay there, unable to speak, just counting my respirations for the next 3 hours praying that they do not go lower! During the 3rd hour my respirations fluctuated between 7-10 and then stabilized at 10-12. My speach returned then. I was wondering if i was having a focal seizure. My BP is very high through the night. In the ER it has been 200/110. I am getting short of breath just by leaning over for a second to spit toothpaste in the sink! My doctors won't learn CIRS and CIRS doctors are too far away and not taking patients. WHAT HELP IS THERE FOR ME? PLEASE TELL ME WHAT I CAN DO!
What about the people that are very sick and have insurance but you don't take insurance? That's the only way or means they have to pay for anything. They've done enough research to know what kind of tests are available and how to take them. They have done enough research to know what their symptoms could be a result of. Because they don't have a lot of money and are considered poor they don't have access to these services. How are they ever going to get better? The answer is simple they are most likely not going to get better . They're going to spend the rest of their life fighting to try and survive . Is this a concern of anybody in this industry.? I honestly am not really sure anymore. I think we should give up on the fact that any sort of health professional has our best interest at heart and wants us to get better. There's a difference between somebody who is busting their butt trying to figure stuff out then somebody who isn't but yet help is never offered. This is the reason why people struggle with doctors and this is the reason why people get frustrated with the system. It's messed up and doesn't work and a lot of people are suffering because of this. It's very disappointing.
What are you doing towards combating this problem
Why is it that all these labs are not done in a medical clinic's lab? You would think that there are two bodies. One for the allopaths and one for the homeopaths! Surely there are some crossover labs that are done in both laboratories. I am a raving lunatic to the ER doctors in my town because all my labs are normal even though i am having extreem neurological symptoms. I have no spare money and am on medicare. Surely there is help for me somewhere! I litterally feel i am near death most nights and my concentrated electrolyte sports drink is all that is keeping me from entering the world of metabolic acidosis with no compensation! I feel that the electrolyte shifts in my body may not show up on labs but i feel every bit of it as if the labs are critical! The ER doctors do not wants to deal with me even though i can barely walk now. I am waking up in the night with twitching feet, uncontrolable deep breaths that do not stop until the feet are still only if i drink my sports drink. I have diarrhea and polyuria at night. Every night hokds an emergency that i am getting more unable to cope with. But i wake up so confused and i am unable to comprehend what is wrong! My O2 levels are dropping now at night and i have no lung disease. But i am concluding that i have pulmonary hypertension. I also have very shallow breathing even during the day. My resting sats are now 95-96%. At night i have captured a sat of 86%. But i don't feel distress. On one ER visit complaining of dehydration, my respirations dropped to 6-7 a minute and my sats were 94%. I felt no distress but as a nurse i knew this was serious but no one in the ER bothered tbemselves with me. I lay there, unable to speak, just counting my respirations for the next 3 hours praying that they do not go lower! During the 3rd hour my respirations fluctuated between 7-10 and then stabilized at 10-12. My speach returned then. I was wondering if i was having a focal seizure. My BP is very high through the night. In the ER it has been 200/110. I am getting short of breath just by leaning over for a second to spit toothpaste in the sink! My doctors won't learn CIRS and CIRS doctors are too far away and not taking patients. WHAT HELP IS THERE FOR ME? PLEASE TELL ME WHAT I CAN DO!