Analgesic medications are among the most-used drugs for many forms of arthritis. Unlike nonsteroidal anti-inflammatory drugs (NSAIDs), which target both, pain and inflammation, analgesics are designed purely for pain relief. For that reason, they may be safe for people who are unable to take NSAIDs due to allergies or stomach problems, for example. They’re also an appropriate, and possibly safer, choice for people whose arthritis causes pain but not inflammation.
The most commonly used analgesic, acetaminophen, is also the most widely available. Because of its low cost, effectiveness and safety, rheumatologists recommend acetaminophen as a first-line option against osteoarthritis (OA) pain. Some people use acetaminophen in addition to an NSAID for added pain relief (but always speak to your doctor before combining any medications, even those available without a prescription).
For severe pain that isn’t eased by acetaminophen, doctors sometimes prescribe analgesics containing an opioid, such as codeine or hydrocodone. Sometimes these products also contain acetaminophen, such as oxycodone with acetaminophen (Percocet) or propoxyphene with acetaminophen (Darvocet – so if your doctor prescribes one for you, make sure you don't get a double dose of acetaminophen, which can be toxic. Longer-acting opioid analgesics are available, too. Some of these come in pill forms, such as oxycodone (OxyContin); another option is transdermal fentanyl (Duragesic), a patch that delivers opioid medication through the skin.
Drug Guide: Analgesics
Robie C 11 Nov 2009, 12:03 |
| Hi...I'm new here....Just found this site....I suffer from OA and have for several yrs. now...I am 54 almost 55....I can't seem to get any dr. to do anything for me...I recently went to a Bone and Joint Dr. and he gave me a cortizone shot in each knee which does help somewhat....My fingers and toes hurt all the time...At this time I take Meloxicam...Works somewhat....He told me on a scale of 1-10 I am at 7....And in time I will have to have knee replacement in both knees...I also have arthritis in my lower back to which prevents me from doing alot of things....Like sweeping and mopping the floors....I don't work...Thank goodness....Don't think I could make it everyday...It is hard enough on me now and I get no help from anyone.....I am glad to have found this site....I think I finally found a place I can go to and talk to people that understand what I am going through.... |
Abby 08 Nov 2009, 08:57 |
| I can relate to most of all your comments I am dealing with the same thing back and leg pain., I have been to my primary doctor over and over and each time he has told me try this take over the counter pain meds but they dont work. I feel sometime I dont have the engery to do my job or play with my 4yr daugther I do know that dr alan brown in Bellevue is a bone and joint doctor and he works really hard to get the help you need without making you feel like you have a problem just in yur head I just would like any help on how to deal with this pain in my back and leags and sometimes i get types of headaches that last 3 days or more I live in the Renton Wa area If anyone can help please email |
Barb G 05 Nov 2009, 05:04 |
| Wow I just read a few of these comments and my heart goes out to all of you. I was diagnosed with RA in 1998. The Rheumatoligist put me on 6 methtrexate 2.5 mg a week plus Daypro anti-inflamatory 600mg 2 a day plus folic acid, not to be taken the day of or the day after I take methatrex. So I take the 6 methtrex on mon with Daypro only one a day sometimes Tylenol if I hurt more. Ideally I would like to have methtrex by a shot but I have no health insurance. I am 64 yrs old Still rolling. I WILL NOT TAKE NARCOTICS I AM A RECOVERING ALCOHLIC 23 YRS SOBER. I BELIEVE I SWITCHED THIS BABY ON BACK IN 98 WITH THE DEATH OF MY MOM, BROKEN RELATIONSHIP AND BANKRUPTCY. YOU CAN'T UNBREAK A LEG. I TREAT IT PHYSICALLY AS WELL AS SPIRITUALLY I HONOR ME AND I PACE MYSELF I REFUSE TO TREAT MYSELF AS AN INVALID OR I WILL BECOME ONE. WE ARE SPIRITUAL BEINGS IN A HUMAN EXPERIENCE. CARRY ON. love to all. Barb |
Cheryl 04 Nov 2009, 15:16 |
| I am new here, and to arthritis in general. I've had pain problems for what seems like forever. I'm 40 years old, and have had Migraines and just bad headaches since I was 7, and have been on every pain medicine just about known to man. I'v been treated like a druggie over and over, and it just gets old. I have developed a high tolerence and nobody seems to understand that. Now, I find out after having jaw surgery for TMJ in 97, I now have arthritis and joint issues again. Which just makes my headaches THAT much worse! My face hurts all the time, and I don't know what to do. I was only diagnosed like 2 weeks ago, and so I use moist heat/cold and Motrin, don't u know that helps?! My headache doc gives me the smallest lortabs and I just want to scream!! I hurt all the time!!! Anyone with any advice?? I just moved to Florida, and they are really tough on people getting narcotics. Which I wish I didn't need them, because honestly I have issues with taking too many. But, I also hurt all the time. What's a person to do?? |
Tammy G 29 Oct 2009, 10:48 |
| This is in ref: to Patricia Graci- Patricia my name is Tammy G. and I too was diagnosed with Psoriatic Arthritis 1 year after my Hysterectomy...I alway's wondered if it had something to do with the amount of blood I lost during the surgery- I was given alot of donor blood and back in 1993 it was not screened for certain things.I asked my Rheumatologist and she said she didn't think that was the reason."I still do" she said it was because of all the trauma my body went through. When was your surgery ? Did you recieve in donor blood ? Did you ever ask your Doctor why or if it was because of what your body went through because of the hysterectomy ? Just wondering and I have never talked to anyone that had a hysterectomy and then diagnosed with arthritis before. I'm just curious- I felt like I was alone ! Look forward to hearing from you ! |
algranny 20 Oct 2009, 13:28 |
| this is to mary sue.you were talking about the pain management clinic they do think you are an addict i belive that why drs.send us there not to manage pain but manage the drugs we take.it's crazy to me.hope you find a good dr. that don't believe in pain clinic.have a blessed day mary sue |
Patricia Graci 20 Oct 2009, 12:57 |
| I was first diagnosed with RA 2 years ago after i had a hysterctomy.It was
terrible i had just returned to work and atthe time i was a bank
teller.Every time i felt pain in my hands i thought it was carbel
tunnel.Well that day my body was not right everything was hurting me about
4:00 when the bank closed i couldnt take the pain and i was swelling in my
ankle hands and knee..They rushed me to the Hosiptal where i was given
morphine for the pain and stood on for 4 days for tests.I was then told i
had RA.Depressed and not understanding where and why i got this disease i
saw a great doctor . Today after trying enbrel which didnt help me i am on Orcenca infusion once a month Methotrexate 8 pills ix week,mobic and folic acid,percocet for pain.I take antidepressitants and i know its not getting better its just in remission but know 2 yrs later i am a branch manager of a bank and still fighting this illness.I will continue on striving to fight this with all my meds and yes you need your pain meds to help you through the day.I do know someone that is getting full disability from social security for her illness but i like to get up and go to work.Even if it tkes alittle mor time i do it for my sanity |
brooke 10 Oct 2009, 16:03 |
| wow!im 32 with rheumatoid! iv'e had had it 4 about 5 yrs now. yeah ican so relate u guys i started out on ultram & lortab. moved up 2 percocet & the fentenyl patch.but u know what i am addicted 2 my pain meds and always will be. thats the price im paying for taking these strong narcotics.what happens is your body builds up a tolerance to the strenghth & amount u take it's inevitable.it's not our faults as chronic pain patients, it's a medical fact. i know iv'e been battling this demon with my R.A. as well !! so these idiot drs that put us on these strong ass drugs in the 1st place dont inform us that maybe just maybe we will build a slight tolererance& they might have to start to do some med adjusting, so we dont look like dr shoppers!!!!! i had 1 of the best R.A. DOCS IN MEMPHIS T.N.& BECEAUSE of her nurse had a problem with my lortab refill, i lost my doc. i had an awsome pain dr for 3yrs. until 1day he fired me because he thought i may b addicted 2 my meds!! anyway my new pain doc well im not goin there he's got me on some kind of new contrlled released morphine pill. i do take enbrel shots 1nce week & metho. i also have a tens unit helps 2! HOPE U GUYS GET A GOOD DOC!!!!!! & GOODLUCK |
Danielle 22 Sep 2009, 08:35 |
| I am 37 and have suffered from a genetic form of OA since my early teens. I also have fibromyalgia. I take Cymbalta for the fibromyalgia which actually does help. I take piroxicam for the OA, which is systemic, so it has attacked several different areas. The most severe is in my right knee. I recently got an unloader brace which also helps and will prolong the need for a knee replacement (hopefully). I tried the Hyalgan injections, but they did not work for me. Currently I get a cortisone shot every three months. Has anyone heard of the inflammation diet? It is supposed to work well. |
Tammy G. 09 Sep 2009, 15:27 |
| Spinal nerve stimulator- it really work's !It really work's to take the pain away - it's better than pain meds- it takes away the pain without many of the side effect's caused by pain meds. |
Faith in Chicago Dr! 04 Sep 2009, 00:04 |
| TO: HELPLESS MOM ABOUT TO LOOSE IT: I do know a Dr in the Chicago area that is AMAZING. He is a rheumotologist by the name of Dr. Robert Hozman. He works in Buffalo Grove, IL, Lake Forest Hospital and Skokie, IL in the building across from Rush Northshore Hospital. You can look him up on google.com. He is the best dr that i have ever seen. I have Ankylosing Spondylitis which is extremely rare and difficult to treat but he has been amazingly helpful and he is not afraid to Rx pain meds. I am 26 yrs old and he DOES believe in the pain that I have and will listen and cares. He takes all insurance except Humara Select this includes medicare and medicaid. I wish you the best of luck. |
LUCY HERRING 01 Sep 2009, 10:08 |
| I just awhole page and it disappeared. |
Lucy Herring 01 Sep 2009, 10:05 |
| I'm 75 years old. I've had RA. since age 10, also have the
osteoarthriris. In 96 i had my right thumb joint re-built in Walter Reed,
in 97 had the left thumb joint re-built...in Walter Reed. I don't have
a strong pinch grip.......but the intense..screaming pain is gone!!!!!! I have spinal stenosis..entire spine...and have sclerosis in my right hip..and have a bulge n my cervical spine area. I take epidural shots there and in my lower back q 4 months.....also use Lidoderm pain patches, take Flexeril for muscle spasms,....800mg. motrin 2x daily. I work out at our ymca....walk the treadmill, use the recumbebt bike, go into the sauna and bak for 10--14 minutes these ALL HELP. IHAVE SOME WONDERFULLY GOOD DAYS...THEN SOME BAD ONES. CAN STILL DRIVE...DON'T USE A WALKER OR CANE. i TALK TO OTHER PEOPLE WHO ARE DISEASED..BUT SOCIALIZING IS GOOD MED...CAUSE YOU CAN MAKE EACH OTHER LAUGH...AND WE CELEBRATE BIRTHDAYS AS A GROUP. |
peter v 25 Aug 2009, 03:54 |
| To Mary Sue04 Aug 2009; I am also 62 and was hit with severe OA 3 years ago. I had to try 3 different pain mgt specialists but I did find one that believes in NO PAIN - they go to any length to help you get there. Find another one. Mine are 5 Neurologists/Anesthelogists who specialize in chronic pain management. It's not a complete solution; but their motto and attitude sure do help. p |
Barb 23 Aug 2009, 19:17 |
| I have learned that to prevent crippling effect of RA the drugs to use are
metheltrexate and Humera. Would anyone know what drugs will do the same for OA? |
johnny v 19 Aug 2009, 14:21 |
| i have r.a. and im 45 yrs. had it for two yrs now. my rheum prescribs me leflunomide,placnil, prednisome,celebrex and percocets for pain. my problem is that im always tired & have chronic pain syndrome.got laid off in feb. and im using unemployment to get by. they keep telling me that getting disability is going to be impossible.to tell the truth, i really want to keep working but im so tired in the mornings and days. any ideas to help me out? here in Az. i feel for the rest of the people in the u.s. that cant get proper pain management from the doctors who are too scared to issue them..... |
Dorothy 18 Aug 2009, 19:38 |
| I was diagnosed with severe RA 2 years ago and with fibro.....about 3 months ago. I take weekly shots of enbrel, mobic every day, 8 pills of methotrexate 1 day a week, 5 mgs of predisone daily for maintenance. I take percoset for pain and also take methadone (10 mgs three times a day). People think that methadone is just for drug addicts and is very misconceived. It is not a get high drug and works for me as a long lasting pain medication. If it was not for the methadone, I would not be able to even get out of bed some days. Look it up on the internet under Methadone and an article written by James Babicky. I also take Cymbalta for my fiber....and it helps. These combination of drugs work for me and I hope it helps all that is lestening....Thanks |
shirley ditmars 04 Aug 2009, 22:03 |
| Ihave mixed arthritis and gout.. in 2005 i had complete knee replacwement (both knees at the same time) and i am happy that i did.. pain one time is enough.. i went to rehab 7 days the surgeon ordered the machine for both legs , so i was moving my legs all night , and god bless him- i think that helped my recovery so much. went home had therapy 1 week and my ins co. ordered the machines for me at home so my legs were moving all nightand i was walking fine, no walker , no cane and i'm doing fine.. but now i have arthritis in my spine and am seeing a pain treatment specialist and have had 2 shots in my spine going in tomorrow for the 3rd one..i still have pain inlower back if i am busy all day long... i take arthritic75 1 tab bid and take one arthritic tylenol, if i still have alot of pain.. i will not take alot of medicines.i take allopurinol for gout 1 tab bid ..i take glucosamine sulfate with chondrotin?? but wonder if i should take that with the articles that i have read about lately about the med..i can not take a lot of different pain med .. and don't want to if i can do without them.my mom had arthritis too., i had rotar cuff operation few yrs agoand should have in the other shoulder but trying to get along without it.. i can not lift heavy objects or raise my arms up high anymore or pick up things that are heavy and lift above my head.. its very aggravating ...i turn on music and try to think positive and i think i could be a lot worse off so deal with it... |
Mary Sue 04 Aug 2009, 18:43 |
| I am 62, have chronic pain daily. My doctor sent me to pain management clinic. They are treating my pain as neurological associated and giving me meds that can cause seizures. I cannot function on these meds. They want to do a Lidocaine Drip, which I have researched and it scares me. They prescribed a Tens machine without results. The clinic say's thats all they can do for me. I know what your're talking about when you say they don't want to hear that you have PAIN. I have never taken pain pills. They treat you like you're some king of addict and thats what you're there for. If that was true I would continue on what they're prescribing and be a walking zombie waiting for seizures to happen. If only they could walk a mile in my shoes. |
mary Falls 01 Aug 2009, 19:23 |
| I have dig disc disease and getting worse, I've taken Vicodin, percoset,
meloxicam, flector patch opana morphine, gapbatin and nothhing gives
relief, trying volataren gel maybe 10 percent relief,Pain spec may try
something else, being in water is relaxing, but when you get out same pain
go to the gym, do my walking, try some exercise , nothing works, and no one really wants to hear it hurts, Pray for something. |
cindy shackleton 01 Aug 2009, 01:46 |
| I have chronic migrains daily, and I have RA, and neuropathy in my feet and
in my hands. I have been seeing my Dr. for about 3 1/2 yrs and ahve hd all
the same problems. My Dr. has tried all of the older and the newer meds and
they didn't seem to work so she put me on oxycodine 5 mg immediate release
tablets every 6 hrs. that helped a little and so she sent me to a pain
clinic her in oregon and they put me on methadone for my chronic pain and I
am still in pain but it does a good job most of the time. I still have my
rough days but I am doing better than I was b4 I started these meds. oregon |
wayne 30 Jul 2009, 15:46 |
| how do u get doctors to understand ur not druggie just in pain heck my doctor doent even talk to me back mirs or xrays just says talk to pain spec? where r we in health care its worse than ever before sometimes death seems to be answer where is our help none here for sure and if no ins? you will be lost =( |
brenda 21 Jul 2009, 20:35 |
| I was diagnosed in 2002 , I tried Enbrel and it affected my lungs, I was put on methotrexate and put my liver count up, then I had a spell with my heart. I am now on plaquenal 200 mg, prednisone now only 2mg.,vitamin D 1000mg., fosamax weekly. and for the pain I take morphine, at night I take time released pills and for the day I take regular morphine. My Doctor is great. It was my heart doctor that got the ball rolling for me to go on a disability pension , I worked at a hospital in the cleaning for 27 years.I'm now on Canada Disability, hospital pension and a top of insurance. Everyday is a challenge, between depression, fatique stiffness and the pain . There is no support system around here but now I can read about other ones who share my illness and I can relate to them. It's a terrible disease, and one that not many people understand. People don't understand what they can't see. and if you look fine then you can't be in pain or sick.It helps to know I'm not alone . |
Helpless Mom about to lose it!! 16 Jul 2009, 22:54 |
| I am really starting to lose faith in doctors. I have been diagnosed with RA. I am on constant pain. Some days it's mild. . and I can deal somewhat ( still on edge all day) . Other days it is excruciating .. and you know what my doctor told me? Take 4000mg of tylenol a day plus aleve twice a day. It do this, as she suggests, and I am still in pain. . even on the easier days. I feel like the Aleve makes it even worse. Is this possible?? I have pain but do not have inflammation, so I dont know why she told me TAKE IT IN THE FIRST PLACE. I am 23 and a mom of 2, and work 8-12 hours a day. . and have a 1 hour commute. I cry just trying to press the gas pedal. I cry every day on my way home. Why wont a doctor help me??? I got better medicine when I had an infected tooth. . but now that I have CHRONIC PAIN . .that NEVER EVER goes away. . they tell me to take tylenol?? I cry just thinking about it. . if I was an opiate addict, i would just go buy some heroin. It is right down the street and it's cheap. But I am NOT a drug addict. . I just dont understand why they will not help me. If anyone knows a good doc around Chicago, that will listen to me, and help me, please let me know. All this tylenol is doing is damaging my liver .. but does not help with pain. at all |
Angel 16 Jul 2009, 12:09 |
| Right on, Linda! We have a chronic illness that causes chronic pain yet its
hard to get prescription pain medication. The whole damn medical community
is afraid to pass them out due to FDA laws and regulations. It disgusts me!
I have RA, Fibromyalgia, and bursitis in my hips! I have real pain.... Addicts are going to continue to get their drugs off the streets like they always have. I believe if you are dx with a "chronic illness that causes pain" you should have a choice of getting prescription meds for pain. I BELIEVE ANOTHER REASON WE ARE NOT GIVING THE OLDER MEDS IS BECAUSE THE DR'S RECEIVE "NO" KICKBACKS OR BENEFITS FOR PRESCRIBING THEM. HAVE YOU EVER SEEN A PEN, CLOCK OR NOTEPAD THAT HAS HYDROCODEIN WRITTEN ON IT IN YOUR DR'S OFFICE? I SURE HAVE SEEN PLENTY OF LYRICA BANNERS AT MY RHEUMY'S OFFICE...AND IT SEEMS HE IS MORE THAN WILLING TO PRESCRIBE THAT TO EVERYONE!!! HMMMM???? WE HAVE TO STAND UP PEOPLE...THE GOVT AND DRUG COMPANY'S ARE SLOWLY TAKING AWAY MEDS THEY DONT WANT US TO HAVE AND GIVING US NEW ONES WITHOUT KNOWING THE LONG-TERM AFFECTS!! TAKE TIME TO WRITE THE FDA AND YOUR LOCAL GOVT BEFORE ITS TOO LATE! |
judy s 13 Jul 2009, 02:08 |
| Vivica: Is Methotrexate the only med you are using? I have been on Metho for several months, very low dose (5mg once per week) which was increased about 3 weeks ago to 7.5mg per week. It doesn't seem to be helping. In fact it seems as if my pain actually increases after taking the Methotrexate. I am also on Plaquenil, 200mg twice a day with a daily Prednisone 5mg. For pain I have an gel called Voltaren as needed. My question is; how long have you been on Methotrexate? When you take the Metho, do you notice any increase in pain for the next few days? Are you on anything else in addition to the Metho? Does your Doctor also have you on Leucovorin Calcium the day after taking the Metho to combat hair loss? How long since you have been diagnosed with RA? I was diagnosed last Sept. Right now I am rather discouraged. Seems like it is escalating even though I am taking more drugs and higher doses. I hope this isn't to many questions. This is my first time I have used a chat board. Comments from anyone are welcome. |
Judy 08 Jul 2009, 23:57 |
| Sabrina, You need to check with the rhemys in your area for some that are working with drug companies testing new bionics that are not out on the market yet. It's free. I take hydrocodone (not codeine so no allergy)for pain '75s' for $5 for 60 pills which is a month supply for me, 1 am and 1 pm. That's cheaper and easier on the stomach than ibuprofen. Gary mentions taking Ultramm for pain. Ultramm you take one a day but it is expensive. My dr gave me Trammadol which cost much less than Ultramm but you take 3 a day. When the pain is bad and the hydrocodone doesn't stop it, he has me stack the Trammadol on the top. I hope this helps you a little. |
Margaret 07 Jul 2009, 18:10 |
| Jodi...It is NOBODY'S BUSINESS that you are on medication for pain. Believe
me, if they had to struggle with pain like you do, they'd be first in line
for help!! I always say "I'm doing great" when anyone asks (and you'd be
surprised that hardly anyone asks, even when I've had to "unfold" myself to
stand up. Marlene...as for the Lyrica, I've never heard of it being used as an antidepressant. You were on it for quite a long while, so your response must have been just your system responding to the sudden loss. It's a great med (the doc prescribed it when I had the shingles...really stopped the pain) Hope you are doing ok now. |
vivica lanier 07 Jul 2009, 11:39 |
| i am on methetrexate and it doesn't seem to be working i also take ibuforpen 800mg it seems like nothing helps with the pain |
Tammy G. 06 Jul 2009, 18:33 |
| Tim go back to your Doctor and talk with him or her and get on some form of treatment!Exercise always makes me feel worse even swimming but my arthritis is so progressed nothing seems to releave the pain anymore-sorry to say but this disease takes alot out of a person, and changes ones life forever! |
tim 26 Jun 2009, 22:53 |
| yah,I hear you all..This is first time on this site ..about a month ago my hips and back are killing me..sometimes i cant get out of bed..havent been to a doc..but once a long ago he put me on celebrx..but the heart scare keeps me away from that even though that helped..ive tried riding bikes but when i get done i ache all over..so so much for some peoples advice to excercise..i need advice thanks |
Gregory Clem 16 Jun 2009, 19:49 |
| I found that the best medicine that help me with my Chronic Pain is Medical
Marijuana. I thought I understand what my friends where going through with their pain till I was in pain myself. Till you walk a mile in someones shoes that are in Pain YOU do NOT know what they are going through. |
Tammy G 12 Jun 2009, 02:16 |
| Thank-you Jodi, it's so nice to be able to talk with each other, so many people do not realize what we go through each day just to get by.Thanks again for you insight it is calming... |
Jodi 11 Jun 2009, 11:00 |
| This is for Tammy G I started Rituxan 6 months ago. I have been on methotrexate for several years and tried Remicade for 1.5 years without success. I received my first Rotuxin infusion and the process is a little different than what I experienced with the Remicade. They give you Tylenol and Benadryl by mouth before the infusion and prednisone IV then start the Rotuxin IV. They do everything they can to prevent a reaction prior to the infusion even starting. The only side effect I had was in the middle of the first infusion, I started to itch a little. They gave me more Benadryl and I was fine. You get another one 2 weeks later and I had no problems with that. I am going for the second round the end of this month. I don't read side effects any more and I'm a nurse! I found that it works better for me to trust my doctor, I know she's good so I just try what she thinks is best and go from there. I haven't had any side effects from it at all. I look at it this way, the diseases themselves ( I have RA, OA and fibromyalgia) are so bad that the side effects can't be much worse. I also look at the fact that in clinical trials, if one person in a million gets something while on the medication, they have to report it as a side effect, even if the person may have gotten it anyway without the medication. That's another reason I don't look at side effects too seriously. I've been on a lot of meds and never had a life threatening reaction to any of them. Just the way I look at things but I wanted to let you know I've had no problems with it. I think it helped a little but it takes awhile to know for sure. I hope this helps you. Good luck with your decision and I hope whatever you decide will work well for you. |
Tammy G 10 Jun 2009, 08:43 |
| I have Psoriatic Arthritis and i have been on all the medications for Arthritis so far nothing has helped! My doctor now wants me to try "RITUXAN" i'm scared it has soooo many side effects, has or is anyone using this medication-doe's it work - i know that each person is dfferent but what about the side effects, please help ease my mind if possible! |
Cheryl 02 Jun 2009, 17:11 |
| For some reason, the thing I find that works the best for me, for the arthritis in my knees, wrist and back of the neck is Excederin for migrains. Works quite well and I can tell you, I live in pain, just like the rest of you. |
Kim 02 Jun 2009, 14:05 |
| This email is for Glenn. Psoriatic arthritis is associated with Psoriasis. My husband is a dermatologist and specializes in Psoriasis and Psoriatic Arthritis. Biologics work fantastic for this disease. I have just been diagnosed myself with anklyosing spondylitis. I am in the process of finding the right medication for me. I know that Enbrel works very well for Psoriatic Arthritis and the AS that I have. |
Gary 02 Jun 2009, 09:20 |
| I have been taking Ultramm for severe arthritus in my hips for about 3 months now. It seems to be working well as I can tolerate the pain much better than before. |
Sabrina 30 May 2009, 20:31 |
| I can't get any relief because I have no helath insurance. All I can get is
800 mg ibufrofen for my RA. I have been walking with crutches since Jan. 09, I need help. I am unemployed and I cannot arrive at an interview with crutches. South Carolina is no place to be sick. |
Mlee 21 May 2009, 22:02 |
| Just blow out me left knee this week. Have had foot pain for two years and now back pain and hand pain. I am a mess. My md's suck and have done nothing. UNtil today I got told I have RA,OA and fibromyalgia. Good God I can barely walk some days. Spen crazy money on Doctors, diets, shoes to get me though. Nothing helped. When I blwo out my knee I lost it to my doctor. She tried to tell me it was in my head. I got smart and get a second adn third opion and now got her back to do her job... I am scared and upset. I get wipped out fast, have stress in my job, Type A person. I know I have to chill out more now. She got me on Meds and they are helping. Boy 3 yrs of pain some medical system this county has for people like us. The Pain is Real and we hurt.. thanks for letting me shout out. M in VA |
Connie 21 May 2009, 14:06 |
| I have rheumatoid and osteoarthritis and am in constant pain. I was on Darvocet but read an article where they are trying to ban it as it can cause heart problems. I am allergic to Codeine and Demerol. The nurse at my doctor's office acts as if I am bothering her when I call. I have been in bed for over a week after stopping the Darvocet. Does anyone know of a pain medication that does not contain Codeine or Demerol? |
teresa beard 19 May 2009, 13:25 |
| I was going too a doctor up north from where i live here in washinton state
and she gave me pain med's well then i came too where i am living now and
they are all against the pain med's they took me straight off and didnt
give me no more i hurt so bad i had too lay down on the curb for my friend
too come and pick me up... I went back too him and told him how i felt when
i was feeling better... he tell's me well i cant give you what the other
doctor was giving you intil you go too a pain management which i already
did up north and they should of taken me and then continued what my other
doctor did and then lessen my dose if he needed too not just take me off
them that hurt big time.... i think he just thought i was addictied too the drug's and i was not.... so i am still tryin too find someone too take me and my insurance.... hopefully i can find someone soon i hurt all of the time and sometimes i cant do anything but lay down and put heat on it so i know what you mean they think that we are addicted but we are not i wish there were some more people too complain about that |
Linda 19 May 2009, 11:00 |
| Dear Jodi, I was reading your message, and I understand where you are coming from, I to have RA and am on some pain meds. If it wasn't for them I could not get out of bed. My doctor also prescribes me pain meds, if it wasn't for that I don't know what I would do. People did not wait over a hundred years for something that can keep them from not having any pain, just the opposite. People should back off of the issue of pain meds, this is what works for us, and we are not abusing them. Just ignore them, apparently they don't understand your pain. Linda |
Jodi Schell 19 May 2009, 10:41 |
| I have RA, OA and fibromyalgia. I work a 40+ hour a week job in the medical field and my situation demands that I continue to work for as many years as I can accomplish. I have been on Lyrica, methotrexate, Rituxan infusions and pain meds for a while now. I am fortunate that I have a physician who understands the amount of pain I'm in on a daily basis and a rheumatologist that works very hard to keep me mobile. One of the things that I have a very hard time dealing with is the stigma you live under from those who don't understand that you must take pain meds to function. When is that kind of prejudice going to be addressed and stopped? I'm just trying to keep food on the table and a roof over my family's head, not get high on pain pills. I would love it if I didn't have to take them but I can't even walk if I don't. Does anyone else feel the same way? Do you get treated differently if people know you take pain meds? Because you don't "look" as though something is wrong with you? I truly don't know how to handle this and would love some input from others. Thanks. |
glenn 14 May 2009, 17:34 |
| i have psoriais is this linked to any form of arthritis |
Marlene yeager 06 May 2009, 19:31 |
| I have been on LYRICA for over a year now. My insurance company stopped it for almost a week and I went out of my mind. they say that it's not a anti-depressant. But when it was stopped I cried, I grabbed my hair on my head and said i can't think ( to my husband ) he wanted a phone number and I was looking at the address book and told him I can't think, I don't know. I hurt all over. Every step sent a shock to the bottom of my feet. Is it a anti-depressant? or does it work different ways on ddifferent people? I'm on it for nerve pain and arthritis. |
david hermary 23 Apr 2009, 19:00 |
| Hi, I have ankylosing spondylitis, I'm 42 have pain everyday.I had bin given dilaudid in the emergence room about two years ago, had to go there because the Demerol i was taken for pain didn't work. In November of 2008 my doctor lost his licence to proscribe what i needed for pain, I'm allergic to Tylenol and codeine so am limited to what i can take i cant find a doctor who can help with my pain. I'm takin 300 mg of zytram, helps some what but feel ill most of the time because of this i no the most important thing to do with my condition is to stay active its hard when your ill and in pain. apparently zytram is going to be hard to get from a doctor. So then what do i do. Right now i feel that these doctors don't want to help me because of the laws governing these drug that so many of us need. what now?. |
Cherel Michelle 22 Apr 2009, 01:27 |
| I have three types of arthritis, which includes RA and I have been on the
Duragesic Patches for about a year now and I love them, even when I have a
serious flare up I can handle it with these patches, which is only the 50
mcg/h, since I am not looking to get high. When I have breakthrough pain I
only need a mild pain pill and I can still function and enjoy the day. Only
on rare occassion do I need to rest in bed and then that isn't anymore than
30 minutes. I can drive a car now, not be afraid of road rage, my personality isn't always on edge because of the pain and I have more energy and find more enjoyment in life. Even my family likes me better. |
