FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
|
Reflex Sympathetic Dystrophy (RSD and CRPS) Reflex Sympathetic Dystrophy (Complex Regional Pain Syndromes Type I) and Causalgia (Complex Regional Pain Syndromes Type II)(RSD and CRPS) |
Reply |
|
Thread Tools | Display Modes |
![]() |
#1 | |||
|
||||
Member
|
Nurses gave hard time crps for then no idea
I tried for so many days to find me a dr who can see me ASAP for my gallbladder stone and gallbladder removal but their nurses gave a hard time they don't consider my surgery a priority or urgent because after all they don't have an idea of what crps is so they really gave hard time by trying to schedule in April or also wait for a PA approval come on I had ppo they don't need PA but that's only the start took me. While but I found a md in the network who will see me next week check my ultrasound and see what he deside if I got luck surgery will be th following week if I don't get worst tht ins will expired soon because I had not been able to work and a year my manager had gave all kind of excuses now the latest is that she can't take a decision because after all hr never talked to her since I left last year for my first surgery the whole year after she kept telling no because she can't not accommodate me with restrictions now she said she never had tht decision so who was it then she told me many time no no no know she washes her hand saying that hr has to decide,beside tht wc sent me a letter saying that I don't longer meet the criteria for ttd and they will cut my wages I'm half so they expect me to pay medical ins,ins card,groceries rent and bills with 460 that I will get every two weeks ,I'm really angry,frustrating,disappointment and tired,I believe in people but sometimes big corporations treat you like. Trash bag,I'm right now a disposable bad that is not good any more,I once though that all the effort a made to make my work place one of the best it was not even noticed less appreciate,people can be really mean,if I don't had the opportunity to try to work how they know if I can not perform well,there is people with more than twenty five years that don't have the knowledge I gained In five years,just because I don't speak English with perfect accent doesn't mean I don't understand everything else,I'm so frustrated and sad, no friends for real,at least I have my daughter and husband he work part time he has to drive me and y daughter everywhere mostly I was the head of the house now I wonder how we going to cover our expenses and pay for university as well,I'm happy at least to have you guys I know for sure you won't stagg me on my back because you already know how painful that is,thanks for caring and listening,I wish I had a better day but seems like i won't have any good one sooner,please if you are in my situation and advise will be great,I'm felling so down and loosing my faith in people ,I'm not like this I always put and give my best but know I feel I'm useless and find not comfort at all,after all I always believe in better days but I'm still waiting for one and is not happening,thank you for caring and for understanding my bad mood,blessings to all , from jesika __________________
__________________
. Last edited by eevo61; 03-22-2014 at 06:15 AM. Reason: Missing info |
|||
![]() |
![]() |
"Thanks for this!" says: | PamelaJune (03-24-2014), RSD ME (03-22-2014) |
![]() |
#2 | ||
|
|||
Senior Member
|
I'm sorry the nurses are not see how important it is for you to get this done. I went to the ER last year and had a catscan because of the severe adbominal pain I was having andthey siad I had gallstones but because thy were small it wasn't necessary to take themout unless they were bothering me. Well, I would n't have been in the ER ifthey weren't bothering me. Ihad to go through a series of test sometime sthe same ones over and over again until I found a gastroenderoloigist who said after thrid castscan. don't wait get stones out asap. Wow, I could have told them that a year ago and I'm no dr. I went to a gallbaldder surgeon who agreed. Even if stone sare small, they can block ducts and cause severe pain and lead to more complication. and with rsd thats even worse. If I were were I would keep trying to find a dr who will listen and take care of your problem asap. Especially if you are having bad attacks frm it. I will pray for you. I know how frustrating it is, but you have to keep trying to findthe right drs. They are out there, they are just few and far between. Try to get some rest in the meantime if you can and watch what you eat.No fatty food. Im here if you need an ear. With love, Renee.
__________________
RSD ME . |
||
![]() |
![]() |
"Thanks for this!" says: | eevo61 (03-22-2014), PamelaJune (03-24-2014) |
Reply |
|
|
![]() |
||||
Thread | Forum | |||
Having a really hard time | Multiple Sclerosis | |||
CRPS - Having a hard time trying to walk again. | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
It's So Hard To Deal With Alone. #CRPS | Reflex Sympathetic Dystrophy (RSD and CRPS) | |||
Having a bit of a hard time | General Health Conditions & Rare Disorders | |||
Having a really hard time! | Reflex Sympathetic Dystrophy (RSD and CRPS) |