i feel so alone i have no one to talk this over with my symtoms all point to RA but no one will commit to it.
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i hear ya
Feels like the TinMan
Monday, August 18, 2008 at 03:37 PMre: i hear ya
Goodeggslightlycracked
Monday, August 18, 2008 at 09:08 PMTo both of you...I have not been in this very long (going on 6 months since I first saw the Rhuematologist) What I did was I kept a daily log on my computer, of where I hurt physically and how I felt, tired,very tired, I want to just lay down on the floor tired, etc...including the depression. I wrote it for about two months, then printed it out and took it to the Rhuemetologist with me. I think it is worth the hastle of switching docs if you need to. The way I look at it is; How can they treat you if they won't listen to you? And also this wont go away in the near future so find a doc who YOU have confidence in to see you through for the long haul. I hope you both get the best help available to you.
I am struggling with severe depression right now. I am on meds for it, but they can not take away the reality of this disease. It is progressing and I am exhausted most of the time. the meds that are supposed to help have wicked side affects. Only good thing is I am losing my appetite...which is ok for me because I could stand to lose lots of lbs. I am just over 50 and was really hoping to get my energy back but , IT AINT HAPPENING!
"I can put on a face to all the world ,
That I am doing well,
But facades don't work ,
When I sit alone, assessing who I am."
My job is taking care of physically and mentally disabled people. Soon my disability will prevent me from doing that...
re: re: i hear ya
jacabeans
Tuesday, August 19, 2008 at 05:08 AMHey from what i have been reading the 1st year is the worst till they get it under controll so dont give up on the energy levels yet!am dreading the med's and wonder if i could just pitter along with out them and maybe look into alternitive,am luck my daughter dose massage and she lighly monovers my sore ankles also she's been putting warm parafin wax on them (supose to be a beauty treatment)am going to ask if its ok to continue with this and also aroma therpy, if its ok you should try that to lift your spirits,am not thinking down the how long can i continue to work bit yet as am still hoping its hypocondra i have,keep smiling it makes others wonder what you have been up to
Jacabeans
x
re: i hear ya
jacabeans
Tuesday, August 19, 2008 at 04:57 AMMy name shoild be thickasmince,i went to doc's as i suffer from anemia i thought my iron was low as i was so so so tierd, i happend to metion sore ankles,yes my iron came back low honstly i was happy with that then comes the letter we need to speak about the results, wasnt my normal doc and he said i was being referd to hospital all the time am thinkin pernious anemia, even when the appoinmet came for Rheumatology am thinking strange they deal with blood counts, sitting in the hospital i started to wonder the realisation never dawned till i came home with two leaflets on medication one of which i'll go on when i go back thusday and looked them and one they had given me (lodine SR) to start right away up on the computer, things started to fall into place, the ankels normaly so thin were like ballons that day, the tierdness the flu like symtoms,doc said she had two posibiltys it could be and wasnt ruling out any till the blood tests came back, hope the second is hypocondrac,wil keep you posted am armed now with questons and my daily ailments for thusday.
Jacabeans
Diagnosis and waiting for meds to work
Goodeggslightlycracked
Tuesday, August 19, 2008 at 10:04 PMThanks for the support Jacabean! You are right I need to be patient and give the meds time to work, but I worry about being able to support myself. Talked to my boss today. she says they can custom make my job for me based on my limitations. Thank God. I was so affraid she would tell me that they need healthy people and they would need to lay me off. Sorry about the bold my computer (laptop) wont cooperate with me.
Hope you get definitive answers at the doctors thurs. As to the potassium level being high and that relating to RA, well I can't answer that question. But when it comes to the Iodine...are you having problems with your thyroid or parathyroid glands? Because I think they sometimes prescribe that for thyroid problems. If you are having thyroid problems I think alot of the symtoms of that can be similar to RA. Keep me posted ok? And hang in there as we all do... Mel
re: Diagnosis and waiting for meds to work
jacabeans
Wednesday, August 20, 2008 at 07:23 AMDose that not make you feel great ? you must be a valuble memeber of staff and fantstic at your job if your boss is willing to adapt things for you to continue WELL DONE!maybe with that off your mind things will start to turn the corner for you as a carer your boss maybe better informed about the ilness and more understanding,( all you need now is your hubby to jump on bord) i dont do ilness never been illl i get realy tierd and have my iron checked it gets a little low and i have some iron for a few months and am fine, blood tests for thyirod came back clear the lodine SR says its for RA and other related athritis?i dont thnk its doing anything, i woke up last night with pains in my left fingers thats a first,my neck and bottom of my back are achey to but it couldnt rain any harder here maybe an going to be like the old wifies and be able to tell the weather with what ever i have,keep smiling Jac x
re: Diagnosis and waiting for meds to work
Feels like the TinMan
Thursday, August 28, 2008 at 06:09 PMhey mel,
amazing that your employer took that into consideration. my boss is type A (i'm sure you know what that means) personality. he knows what i have, although i don't think he fully understands. once i find out what meds i'm gonna be on, i'll have to face the music with him. i figure if i put it on the table right up front, and what i'm up against, then he can decide if he needs to hire someone else to do this job, of if he's gonna support my needs. i hate to sound like a whiner, but i gotta take this seriously, and so does this he. tomorrow will tell. my appt is 8:45am. i'm getting anxious.
re: Diagnosis and waiting for meds to work
Feels like the TinMan
Thursday, August 28, 2008 at 06:09 PMhey mel,
amazing that your employer took that into consideration. my boss is type A (i'm sure you know what that means) personality. he knows what i have, although i don't think he fully understands. once i find out what meds i'm gonna be on, i'll have to face the music with him. i figure if i put it on the table right up front, and what i'm up against, then he can decide if he needs to hire someone else to do this job, of if he's gonna support my needs. i hate to sound like a whiner, but i gotta take this seriously, and so does this he. tomorrow will tell. my appt is 8:45am. i'm getting anxious.
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dear jacabeans feeling alone
utah71
Tuesday, November 18, 2008 at 04:23 PMit sures feels like that when you have RA mine started with flu like symtoms achey all over joint stiffness.and omg depression.
ra can be passed down from family genes mine was from my mom.
your first step would see a genral doc and explain to them your sistuation and ask for a cbc complete blood count to test it for a ra factor .theat will determine if you have ra or not ,somre times ppl get mis diagnosed some things run side by side systoms
like lupas chrones gout so ask your dr to test you hope this helps hun
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RA, what else??
melanie
Friday, December 12, 2008 at 01:50 AMhey girl, don't ever feel alone. see all the people that have responded to you?? i myself deal with pain everyday, i've been dealing with 6 yrs of guessing. my doctor is really good to be honest and say, sometimes no one knows what to do or what will work best, it's a game of trial and error. i've taken every RA drug there is. i also have spondylosis in my hips. i have a fusion in my neck and am going to have the ulnar nerve worked on pretty soon. my test, everyone of them so far for 6 yrs have come back positive. i have everything done at least every 2 months. i had to have an EMG before my neck surgery and the neurologist said (my rheumatologist also) that 25% of people that test negative forever have RA - mine is dx due to + family history and symptoms - and don't have the horrible crippling effects, but have to deal with the pain. my family doctor blew me off forever when i was telling him my tailbone was killing me and my hips and i was so tired i was sleeping through entire weekends and couldn't finish a whole days work. well, anyway, my rheumatologist has been really good to give me what he thinks is the best thing to try next. now i take 12 medications, that including hormones and restasis for my eyes. i've taken humira for a year now and just started methotrexate a month ago with excellent results. i've been terrified of taking it, but i know know i was wrong about being so scared. anyway, if you need to talk to anyone about RA problems, you are in the right place. we're all standing in your shoes!! write us all again soon, melanie
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hi... i presume you've been to a rheumotologist? i'm in limbo too. my PCP said i had a 50-50 chance of having RA, and when i got into a rheumotologist, he said he "wasn't convinced" because i just happened to be having a good day that day. of course, 2 hrs after the exam i was in excruciating pain and just wanted to die. i go back to him on 29th, but he did prescribe relefen which takes most of the edge off. i can tell when my next dose is due because i get twinges everywhere. as the 29th gets closer and closer, i'm very scared that the rheumy is gonna tell me (that i'm crazy) that i don't have RA and it's gonna be something else. i've read on these blogs and compared everyone else's notes, aches and pains and i'm exactly the same. a friend of mine who's had RA for 20+ yrs said that you have to be proactive. she said that being aggressive about your DX, trmt, and meds will get things clicking faster. i'm already dreading going back to this rheumy because his bedside manner sucks, but i'm afraid he'll kick me to the curb and i'll have to start all over. the relefen only has one refill so i'm in panic mode because it takes forever to find and get into a rheumotologist. best bet, arm yourself with as much about RA as you, the symptoms, the trmts available, and other stuff and show the rheumy that YOU need help. good luck, and i'll be watching your posts.