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thanksView Thread
Thank you!View Thread
my mom has osteoarthritis & she does not do anything but sit on her behind on the computer (I clean up, cook, basically everything around the house but mow the yard & take out the trash). my mom will not even get a cup of coffee for herself. I take care of 2 elderly ladies which is my job at this time. so I take care of an 82 yr old, a 89 yr old, a 62 yr old (my mom), my autistic daughter, & a 62 yr old man (my dad that works & takes care of himself but cooking laundry & cleaning of any type that I do). my dad is a great help w my daughter at times when I am really down. also we have an online business that I have been trying to get my mom to help w since there are days that I can not type since the pain in my hands is so bad but she wants nothing to do w it since it is not playing games or on fb or buying stuff off of ebay. I have tried get her to let me show her what to do but she says that she doesn't want to know learn. that is another area where I get the lazy name since I can not type & get things done for the online business.
my dad thinks that having surgery will cure all of my probs. lol! how this will help I have no idea. my mom that has the osteoarthritis also acts like there is nothing wrong w me. she acts like she is dying when she has to cook (or what ever) unless it has to do w the internet.
what can I do to get my family to understand what is going on w me? I am having my dad go into see the docs w me when I see the new docs so that mayb he can get the big pict.View Thread
I loved it, hate giving myself shots but the benefits way over weighted the negatives in my book. Now in the last month my Enbrel is not doing as it should. I never thought of it stopping, why would I, I felt great could do just about anything I wanted to for all most 20 years.
Now what am I to do? I have an appt with my RA doc who I think the world of in a few days. We will see I guess. Right now the pain is overwhelming, it is literally in every joint, this flare.
I am having to go back to the way it was when I was first diagnosed and I sincerely hate going backwards. Hot water soaks, hot wax therapy for hands and feet. BIOFREEZE for knees, elbows, shoulders and where else I can reach. Right now it sucks being me, and the people I work with in the 991 center haven't a clue, just how much pain I'm in. I'm ready to cry and nearly took myself to the ER today. Not that they would know what to do. Prayer is wonderful and I know he will never give me more then I can handle, I'm much stronger then lot's of folks. I have to work, some don't so now I start earlier then usual so I can manage my pain. You do what you have to do. The LORD helps those that helps themselves so all I can say is keep at it. My other RA doc gave me 18 months art diagnosis to be in a wheel chair that was 21 years ago. I'm still walking on my own two feet , know that you can too!View Thread
I would like to change doctors but unfortunately my supplemental medical insurance provider combined with Medicare coverage doesn;\'t leave much room for changes.
I know part of my problem is I am so darned stubborn and have trouble admitting that I do need help in some matters and also I need to accept the idea of medication(s).
I am also in the position of not being able to keep my home maintained the way it should be and not being able to always afford to pay someone to do things that need to be done.
Sorry, there I go again, whining. Venting actually, because I do remind myself that things could be worse and maybe they will be in the future. But, I am going to try not to worry about that. Thanks again to all of you who took the time to "listen" and respond.
Blessings to all!
NikkiView Thread
If you would like to know more about the study, please contact me via e-mail. I will give you more information.
Jeanne@mondoresearch.com
Thank You.View Thread
Now that I have lived (if you can call it that) with the pain and aggravaton for six years or so I just can't see any reason to keep on keeping on.
I realize I am really, really tired and depressed which makes everything seem worse. But, I am tired of hurting, of having to make adjustments for every little thing, like not being able to garden or take walks without being exhausted.
My doctor tells me to learn to deal with it but he doesn't say how to do that. I don't want to be medicated to the max. I don't want people (and a lot do )telling me to "just do it", as if it were that simple. I want to be "normal" again. What's the point in continuing to live if I am going to get worse as my the last prognosis indicated?
I know thousands of other people suffer much worse afflictions than I. That's why I am truly sorry to sound so self pitying. But being unable to use my hands, walk, do normal things without pain or even talk in a normal voice seems like too much to bear sometimes.View Thread

If you have any type of deformity in your hands please look up silver ring splints; they have many many options to help with lots of issues.
Also, if you are ordering silver ring splints, have the person that sizes you give you a copy of the order form (including cust number) and a quote of the prices they will charge you. Then go home and price the splints on the silver ring splint website. I got mine straight from the website for over $100 cheaper than my therapist would have charged, per splint. And you can submit it to your insurance after.View Thread
I gave in again to the pain and tried it injecting it myself, the stomach pains not as severe, but feel like crap about 1.5-2 days after I take the shot, tired , nauseas for 2 days, did I say tired...yeah realllllly fatigued, like i could sleep all day. it scares the hell out of me taking it, as i had cancer about 7 yrs ago, i am not finding great relief, and dont want to live my life feeling sick 3 days out of every week. Anybody have any other ideas re: other alternative therapies?? Been hearing lots about gluten and dairy, sugars etc... thoughts? oh yeah I have been taking zofran with the methotrexate about 1-2 days after it kicks in to help with nausea... that has helped a bit, but overall not a great drug for me anywaysView Thread
thanks
MJView Thread
Seeing these initial symptoms, Doctor (A general physician, he is not a Rheumatoid specialist) suspected to RA and made my wife undergo series of blood tests (details and results below). And then seeing the result the other Doctor (An Ortho, he is not Rheumatoid specialist either) said this is definitely not RA and gave us couple of tablets. He said this is due to viral infection due the fever that she has contracted in Mid December. And he mentioned as "IMP: Post viral soft tissue phenomenon".
I came here to WebMD for an opinion. Kindly review the Lab results below and let us know if we need to visit a different doctor or this Ortho Dr is correct that my wife don't have RA. Thanks in Advance for this great help!
Lab results:
Anti Nuclear Antibody/Factor (ANA/ANF) — 8.63 Units
Anti CCP (Cyclic Citrulinated Peptides) — 0.70 U/ml
ANTI-ds DNA Antibody, Serum — 5.57 IU/mL
Total Cell Count — 8000 /µL
Neutrophils — 57%
Lymphocytes — 40%
Eosinophils — 00%
Monocytes — 3%
Basophils — 00%
Hemoglobin — 12.0g/dl
PCV — 36%
RBC Count — 4.4 x10^6/ µL
Platelet Count — 3,05,000 /µL
MCM (Mean Corpuscular Volume) 83 fL
MCH — 27 pg
MCHC - 32 %
RDW - 15.15 %
ESR (1 Hour) — 10 mm
Glucose (Random) — 95.7 mg/dl
Urea — 22.8 mg/dl
Creatinine — 0.86 mg/dl
CRP 5 mg/L
Medication Prescribed (For around 2 weeks):
HIFENAC P TAB
PENTOCLAS
CHYMORAL FORTE
MEDROL 4 MG TABView Thread
on my elbow she found high red blood cells in the fluid that was tested .What does this means?View Thread
on my elbow she found high red blood cells in the fluid that was tested .What does this means?View Thread
Does RA ever spread this quickly? We are waiting to see a Rheumatologist, but there is a long waiting list. If anyone has any insight to these symptoms we would be very appreciative. thank you.View Thread
Later after the results came, I was then sent to a Rheumatologist. She told me that the results came back and although the Rheumatoid Arthritis Factor came out negative, my bone is severely chewed at. She said I have RA. She prescribed for me to go on MTX (5 tablets once a week). Maybe I'm just in denial, but I just don't know. I don't have any other joint pain besides the wrist. Unless it's only just beginning?
So my question is: has anyone else been diagnosed with RA with small amount of joint pain and without the RA factor?
View Thread
http://rheumawarenessuk.myshopify.com/
For more information, visit my website, www.rheumatoidawareness.co.ukView Thread
any opinions or suggestions are welcome.View Thread
I do not know what to do from here since I can not take on anymore work since it is entirely to much on the pain aspect. also my doc wants me to reduce manual labor hours & that is mainly what my job is ( I take care of 2 elderly ladies). what to do? I can not get a different job at this time since the economy is causing layoffs in my area, not hiring. I do qualify to go to the university clinics about 200 miles away under a program, but that is the last resort since I do not drive & I have to arrange a ride for the day & it will take the entire day.
any advice will be appreciated thanksView Thread
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