Bone / Joint :: How Long Does Enbrel Take To Start Working?
Dec 3, 2013
I'm a 29 year old male. I have been diagnosed with rheumatoid arthritis in October and my doctor put me on Enbrel. He told it's a miracle drug promising me it would change my life. I took my 5th injection today and I still don't see any major difference in my body. I still have morning stiffness and pain, and I still have a couple of swollen joints. I'm waiting for the Enbrel to take effect, but I'm starting to get worried that it's not working with me. My doctor said that after few weeks I could expect significant pain relief, but I'm still in pain. I've also heard that Enbrel can take effect anywhere from a few days to couple of months and that it doesn't work for all people equally. Anyone here with the same symptoms or Enbrel experience I'd love to hear your feedback. What was your experience with Enbrel?
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I've been taking Venlafaxine (75mg twice a day) for the past 5 weeks for Generalised Anxiety Disorder.
How long does it take to start working, and can it increase your anxiety levels before it starts to work.
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If any ones knows how long is takes for steroids to start working iv just been on 2 weeks of antibiotics not done nothing, now iv been put on steroids 8 a day started yesterday still no change think I will end up in hospital again it's been a year since I was last there, hope your all not to bad .
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I had surgery on June 14, 2011 to remove a bone spur on my left clavicle and to remove arthritis near (but not in) my shoulder joint. It was the worse experience of my life. I was in constant agonizing pain for 2.5 months. Just for the record, I've had two ulnar nerve surgeries on my left AND right elbows and never even needed pain medication. This shoulder surgery apparently did not relieve any of my pain. I still have a dull aching pain through out the day starting in my neck (left side) to my shoulder, and down my bicep to my elbow. I still can not sleep at night, and through out the day while working my shoulder/arm/ neck is killing me. I continue to take an Naproxin and continue to rotate heat and ice. I did physical therapy for the first two months after surgery. My concern is that had arthroscopic surgery, and there was NO rotator damage so why is my shoulder still in pain? My shoulder pops when I do try to rotate it.. and often when I simply reach outward for something..I'm in excruciating pain. I'm a baker, so I am constantly lifting a 34-50lb metal mixing bowl and have to reach many times through out the day. There really is no way to not do my job duties and still retain my job. Any ideas why I'm still having this problem?
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I'm having TKR on September 1st and I have asked my doctor and my Rheumy when to start Enbrel after the surgery and she wasn't too sure , she responded with a vague Maybe 2 weeks after? I didn't feel too comfortable with that I will ask my OS
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despite using strong painkillers, oxycodone-both long lasting plus short acting plus amitriptyline for sleep plus topical ointment, I cannot get on top of the pain or swelling. I started Stelara in December after DMARDs, Enbrel & Humira failing. I'm also on 7.5mg Prednisone daily. I can't cope much longer, this flare started in November. I suppose I should be grateful that my skin is clear but the pain in my joints is horrendous. My knees, hands and wrists are so swollen. Mobility is crap, I'm virtually crawling to get upstairs, getting dressed is so difficult and painful. I'm seeing OT in 2 weeks plus my rheumatologist on 8th March, also I'm seeing another rheumatologist in may for 2nd opinion because I'm not convinced my current one is expert in PsA. I've been going to hydrotherapy for a few weeks and am going to continue as a paying client because it's been good for me mentally and I don't want to sit around waiting to become completely immobilised. My knees are like melons today, should I rest, elevate or what? Sorry for negativity but I've just about had enough
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Saw an orthopaedic consultant yesterday who confirmed, after an xray, that the osteoarthritis in the big toe joint is getting worse. He suggested two different types of surgery: a fusion of the bone or a replacement of the joint. I am leaning towards the latter although I don't know much about it and the consultant admitted the success rate isn't great! Has anyone had it done or know more about it?
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I have a problem and need advice! My family is known to have history of arthritis. I am 34, male and I am afraid I have this disease too. I feel tingling in my temples. Is this a symptom of arthritis?
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I had bunion surgery on my feet last year, since then i have been in more pain than before i had surgery. To be honest they weren't actually painful before the surgery, just a pain to wear shoes and they were very bent. now my left foot feels weird and my right foot is extremely painful.
what to do? i regret having the surgery i want to go back to being my normal super active self. They hurt so much!
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I have been having back pains in my upper back between the shoulder blades as if I need to pop my back but I can't. i feel like there is tension all the way up my neck and i always have headaches. When I twist my upper body, there is a loud pop coming from my chest that does not normally hurt, but sometimes the pain is a 10. I have no idea what is the cause.
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I had bunion surgery about 5 months ago. I'm 16 years old and have severe bunions on both feet. I play sports and am constantly running around and going through a lot of shifting and moving. before the surgery the pain was unbearable and felt like I had two broken toes. I went to the doctor after a few years to when the pain was just too much and he told me I needed surgery. I chose to do one foot at a time because I wouldn't be able to walk on it for about 6 weeks so I chose the one that hurt more. I had nerves being pulled on the side by the bunion and my toe was shifted to the side. Now 5 months after I am in the same about of pain as before and then some. My big toe is not only still numb( which the doctor told me was apart of the normal healing process) but the big toe also does not touch the ground. The pain is so bad when I am playing basketball that I need to stop. It's the bottom of my foot under the big toe and around where the bunion was removed that hurts it feels like pins and needles and like I'm walking on rocks. It's very tender on the area, should I be worried/get this checked out? Or should I just deal with it?
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I have been in pain off and on for about 5 years now and xrays show that i have greatly reduced and/or missing joint cartilage and bone spurs including bone cysts that seem to come and go. The Ortho surgeon said from the x rays alone, I needed a full replacement. Most days its painful to walk for too long or bend, twist etc which does interfere a lot with my life and i often find it hard to sleep or reach a deep sleep. Id love to travel but but can never tell when my hip will feel okish and when it will be agony! Every day can be different! I have been told pain like this comes and goes and is all part of the slow deterioration of the joint. As my surgery date looms in the next week i am starting to feel maybe i don't need it ( hip is feeling okish today!) or am i just getting cold feet? Im mid 50s and pretty healthy and active but this hip has certainly held me back especially in the last year. I've never had a big Op but some websites say sooner is better than later. Any ideas or thoughts?.
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For the past 18 months I have experienced joint & bone pain, predominantly in my fingers, hands, wrists and elbows but also affecting my forearms, feet, ankles, knees, hips and shoulders. I have spent months trying to ignore it and at other times have kept detailed diaries, but can find no pattern relating to the area and level of pain and what I may have been doing, eating, drinking or how well I've slept.
I am nearly always fatigued ... I do work hard but even when I have time off, I'm exhausted to the point of needing to nap or walking around like a zombie. I used to run a lot and completed marathons, but now can't face a short jog.
Whenever I go to give blood, 4 out of 5 times my blood is too low in iron. It's not considered a dangerously low level for me but it is too low for the blood service to accept. The last time I went I succeeded in giving blood but was borderline and they only just accepted me.
Diarrhea; like many women I usually have this around the first couple of days of my cycle. However in recent months this is happening more frequently. Again there is no pattern relating to what I eat, where I eat or who prepared it. When it happens I get cramps and an urgency to go, but no nausea, sickness or loss of appetite.
Finally, I've recently begun getting pins and needles in one hand / fingers in a pattern that suggests carpal tunnel syndrome. It lasts for a few days then fades.
All of these things could be related or entirely unrelated, I just don't know. Also, one or two on their own might be easier to deal with but combined they can really get be down. My doctor has recently given me blood tests for arthritis and they came back normal. Any other ideas please?
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I am getting the big"V" done tomorrow and was wondering how long I had to put aside running and let the boys heal.
If any of you guys have had one out there I would like to know how many days after did you start exercising again.
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So I'm 40+5 and when I wiped, I saw blood. It wasn't too much for me to be alarmed but how long does labor start after this?
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Today is Day 11 for me after surgery and I have been taking it relatively easy but due to boredom decided to do a little ironing today and then I went with my mother to the supermarket. I was going very slow and relying on the trolley to go round but it was a bit of a struggle. I'm now home feeling very tired even though we only got a few things and were not very long.
My question is how soon did you ladies attempt something like this? Did you find t a real struggle. I've been told I should stay active and try to walk a little every day but I couldn't wait to get back home and in bed! Also i get this funny almost numb sensation in my tummy just above my scar. When I touch my tummy I can feel every touch But it's also almost like the area is a little numb. Is this normal? Is it due to all the swelling and bruiskng inside??! I hope to god that there isn't anything wrong and it's just part of the healing process
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Can anyone please tell me how long it takes for these blocks to take effect,had them done a week ago and still in bad pain,MRI report said severe deep space narrowing at L4-5,have had 3 microdiscectomy and 12 epidurals over the past 9 years.
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for the past week I had severe joint pain and weakness, muscle weakness, bone pain in extremities ( had a blood test for lupus and RA[ no family history of either] Starting to get a bit better as long as I rest. recently sexually active with one person, now I just noticed feeling swollen like I was getting a UTI ( hurt when I urinate), but noticed it hurt in my vagina not urethra, checked and there are 4 small red bumps in my right labia minora and 1 in my left labia minora-odorless, feels inflamed and hurts now. Is this related to possible lupus or separate problem? I feel exhausted and run down.
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So I dislocated my knee in January of this year. I was given a device that isolates my knee cap and hold it in place. I wore the device off and on over the year whenever my knee would feel sort of irregular. I worked out routinely to help strengthen my knee, it helped the pain somewhat, but mostly just made me feel better about the way I looked, and kept me healthy. I haven't worked out since some time before Thanksgiving. Starting this week i've started to feel this new akward feeling behind my kneecap, sort of like the ligament behind my knee cap is tightening, sort of similar to how it felt when I dislocated my knee, but not exactly the same. I get the pain after fully bending my knee, for example when I am on my knees doing my job stocking shelves at work, when I stand to my feet I can usually feel the pain. I try doing a couple of different stretches when to make the feeling go away a bit, but it comes back, and then it eventually goes away again.
My knee "pops" (makes a loud popping noise and pressure) pretty regularly now but when I get off of work and off of my knees I experience the discomfort much less. I want to start exercising again on Monday, but I am scared I might dislocate again. I will try using the knee cap device again tomorrow, but I feel as though whenever I use the device, it makes my knee feel like jello the next day, and make me want to use the device again, even though I was advised by my doctor that I should not need to use it regularly. ....
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My vagina opening is wide enough to fit a tampon, which i've done on many occasions however, anything larger than this and it doesn't seem to stretch anymore. The actual skin can stretch fine and does but at the opening is a small ridge of bone. Once you reach past this bit of bone, inside the vagina it can stretch fine, it's just that one ridge, i can put my finger round it and hook it but I can't actually move the bone (obviously)So my problem is just that when I come to having sex, nothing will fit. I think this bone is the pubic bone which is just sunk down too far. I can also feel it right behind my clitoris and urethra opening like everything has been squashed down into one small area. It doesnt come very far up on my front 'mound' but comes too far down underneath in my vaginal area.Is this normal? Has anyone experienced this? What should I do?
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I am a 47 year old female. I had Microfracture Knee surgery on January 12, 2016 and it was not a success. My doctor said that I am still bone on bone and will need a partial knee replacement. He uses the Oxford Partial Knee and says it is the best one to go with. I was able to get a Synvisc injection on May 12, 2016. My doctor and I are both hopeful that this will give me some time to make this big decision. I have had a really hard time recovering from the microfracture surgery. I was on crutches for five weeks and my knee got stuck in a bent position. I was in therapy for three months and I still cannot walk with a straight knee. The thought of undergoing another surgery is so scary. I just want to be normal again and do all the things that I used to do before.
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