Gabapentin For Spondylolisthesis Grade 1
Jul 11, 2014
I have spondylolisthesis grade 1 and have had a discectomy and cage in my neck. I have pain in my hands, arms and lower back all the time at varying degrees. I have been taking Naproxen, tramadol, co dydramol for approx. two years and was worried about the side affects of taking these long term. I spoke to my GP and he has prescribed Gabapentin as an alternative. I am a little worried about starting, is 300mg very high does. What can I except when I start them and will it affect me working?
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I am 40 and have grade 1 l5 s1 spondylolisthesis. When I read forums, all I see is people having to be on painkillers, fusion surgeries that don't work, people who can not work, have children (pregnancy) and so on because of this condition. I am so terrified I will end up in a wheelchair or without a social life. There is so little information about the condition online. Please, please, can someone give me some hope that you can live with this condition, perhaps by doing exercises, yoga, pilates etc? Please tell me I can avoid surgery, have a pregnancy to term without complications from spondy. I feel so alone. I hope all of you are having a good day.
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I have a Grade 2 Spondylolisthesis at L4 plus two severely degenerated disks, I have suffered with it for almost 30 years. I have got used to the back pain ,but since 2010 I have been experiencing numbness at first but now a deep gnawing pain in my right leg if I stand for more than 30 minutes , or walk more than half a mile. I have been taking DHC Continus for the past 3 years , it helps a little,but a few months ago the pain started in my left leg so I had another MRI done , the scan shows severe compression of the right hand side nerve root at L3 , and compression of the left hand side nerve root at L4.....
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Degenerative discs and spondylolisthesis,had injections worked well for 5 days now all back ...
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I had an MRI scan around 4 months ago now and they found a thyroid nodule that I have had scanned and graded at a U5. I have now had 2 sets of FNA'S which was horrible.
Has anyone else had a U5 grade? I've looked it up and its graded malignant. Is this saying I have cancer but not sure what stage yet?
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I had surgery exactly three weeks ago. I developed a fever (99.9-101.8) in the hospital two or three days post op. They gave me antibacterial iv and oral meds from the surgery on. As I developed the fever, they gave me antiviral medication to treat a huge and painful fever blister I developed just two days after surgery thinking that this sore was the culprit. The fever had gone down to low grade but now i'm concerned because it does not want to go away. Im taking Norco and the tylenol in it keeps the fever below low grade but when I don't take Norco ( which i take less and less) the fever and chills/ night sweats keep returning. It is generally starting at noon or afternoon, almost always present in the evenings. Usually 99.5-100.5.
Im very worried that it can be some kind of a stubborn infection. I'm three weeks after surgery, i should not have a temp at all. Plus I'm not fever prone, i hardly ever had a fever in my life, flu or any other illness i pull thru with no temps.
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I had op 17 days ago and feel today like I can finally see the light! After suffering the agony, bleeding (continually wearing san towels) and life changing effects they bring you i finally decided to have the op. I have had a terrible 17 days 2 visits to docs and 2 to hospital. part of the prob was caused by managing pain relief, allergic to anti-inflammatories, Tramadol gave me a panic attack and made me vomit, been on 60mg codeine 4 X per day and have been more or less sleeping in the bath. Saw surgeon day 15 who told me the op had worked and delay in recovery was because i couldn't take anti-inflam. He offered me morphine for the terrible pain which I declined. Had 6 hours sleep longest since op (only been cat napping due to pain) so cut down on codeine all positive today. Then I went the loo and felt a lump come out like my old piles (only 1 use to have quite a few), now stressing that I have had a prolapse. The surgeon warned me I would have flaps of skin left but this feels more hard and shiny sorry to be graphic!! Just wondered if anyone else had experienced this and whether it would go down again, I have never been able to push them up as some people mention.
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I've been to see a consultant this afternoon and he has recommended a haemorrhoidectomy and the process to that is now in motion. Apparently my piles are Grade 3.
I have to say that the thought of this operation does not really appeal, especially after I've read various reports of just how unpleasant and painful the process is.
I've read about the HALO method which doesn't seem quite as barbaric but when I mentioned this to the consultant he seemed to dismiss it.
I have just made an appointment to chat with my GP who referred me to the consultant to see if he can offer any possible alternatives.
One thing the consultant did say was that if the piles were left untreated they could become ulcerative which obviously would then make the whole situation more serious.
While I realise the clock is now ticking down to the time when I go in for an operation in the end it's my body and I have the ultimate say on whether I go ahead with it.
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Prolapsed grade 4 ulcerated haemorrhoids
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I feel really down. Terrible sore throat & low grade fever. I am trying hot honey and I tried gargling salt water but it made me sick.
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2 and a half weeks ago I tore my calf muscle. I went to minor injury unit at local hospital. They didn't need to do a scan. They diagnosed torn calf muscle and gave me crutches and told me to rest it for two weeks. Not sure but I think it must have been a Grade 3 tear as I could not walk on it without intense pain and only now can I actually stand on it. I've walked/hobbled about five yards at a time but it is very sore and tight.
After one week I went to GP to ask about recovery. The only advice was to do some stretches and try walking on it a little. I just wondered if I could find anyone who has been through this to see what steps they took.
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I recently had outpatient gynecological surgery, following which I had frequent urination, burning, stinging when urinating and side and back pain on the right side. Went back to my doctor, and she diagnosed a UTI and put me on doxy and Cipro. Took them a few days, but the side and back pain persisted, on and off, in waves. I also became debilitated with extreme fatigue and weakness--i went back to the doctor, and couldn't even fill out a simple form in the office, simply couldn't think or have the energy to write. She sent me to the ER, saying she thought I had a kidney stone. They did a CT scan and said I have stone in my kidney, but that normally when it's in the kidney it doesn't cause pain. They couldn't explain my other symptoms (included also sweating, fairly frequent urination, low grade fever, confusion). They gave me 2 rounds of pain meds (& fluids) in the ER and I felt better for a couple hours. The next day I felt so rotten and weak I could barely sit up, i couldn't talk, check email or texts, read, move, shower, etc. over the past 3 days it has gotten slightly better. The pain has virtually subsided since the ER, but the fatigue is debilitating. Two friends described their experiences with kidney stones as similar--has anyone experienced the same? Does anything help?
I have heard water and beer help a kidney stone pass, but is that only once it's descended? I'm not really in pain, so my doctor thinks it may have shifted around in the kidney (she thinks my symptoms are something else). Anyway. I don't know if it would do any good to try to flush it out at this point or just wait and see. I simply can't go on for much longer feeling this extreme weakness and cloudy head, feeling rotten, etc. I continue to have a low grade fever, but my labs came back after the antibiotics clean. I do have similar symptoms when I get bad sinus infections, but that's clearly not the case now. Thanks!
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I think I am going insane... I have been suffering from episodes of hot flashes followed by cold chills with 99.1 to 99.7 degrees fever for about 4 years now.. I have had Blood tested for almost everything- Lupus, Thyroid.-Aids, Sed rates.. etc... and nothing comes back... The dr's can not find anything.. This last episode is lasting 31 days and counting.. I am starting to get a lot of anxiety, my body aches and I have headaches that come and go..
I am 45 years old and feel like I am90! I have been in relatively good health.. Is is possible that this is perimeno? I just started hormone replacement therapy and My obgyn has me on a very low dose of progesterone - pills and testosterone..I am hoping this helps.. I am so sad and scared, I don't know what to do.
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I have been on 1200 mil a day for 3 mos. my pain has gotten better and I an thinking about getting off of gabapentin . I am not going to stop a once. I will gradually get off. Is it any side effects I can expect from stopping the drug?
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I am now on my third rheumatologist who now tells me that the painkillers I take - oxycontin, co-codamol and oxynorm all of which are opiate painkillers are obviously not working -give the man a star - he has said that gabapentin may work has anyone used this for arthritis before.
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Dr. Just started me on Gabapentin. I'm taking it for anxiety. I'm very sensitive to meds so he started me on 100 mg 3x day. Depending on how I feel, he will up dosage in 2 wks. Will I feel anything on this low dose?
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Was on Gabapentin for a year and worked up to 3200 mgs a day. Was taking it for Osteo Arthritis in feet and knees. Didn't do much for pain so decided to get off of it. My Dr said to take 1600 mgs for 5 days the drop to 800 mgs for 5 days! This was 3 weeks ago still fighting withdrawal. It's eased up some but still have some anxiety and like pressure in my chest. Almost makes me feel short winded at times. Has anyone else had this and how long will the withdrawal last? Have heard the longer you was on it the longer it takes. Tired of it just want to feel normal again.
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Has anyone else had this experience? I started out on a low dose and had great results. Now I am up to 1,800mg/day and it doesn't seem to be having much effect. I am actually ok if I am not doing anything, but as soon as I use my foot, it gets so hot I could probably fry an egg on it!
My story: was in a car/bike accident and ended up with the car parked on my foot. Broke all my metatarsals in multiple places, but things were not that bad until...SURGERY. After finally starting weight bearing I found I couldn't really feel my foot, but it worked. Then I had oral surgery and my world exploded. Insane nerve pain in my face and jaw which then transferred to my foot. Anyone else here with CRPS?
Oh yes, and shooting pains up and down my thigh and calf whenever I stand or walk.
Thanks to anyone who responds. Especially interested in those who found the gabapentin working at first and then not and those who are suffering from CRPS.
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I'm 17 years old and have had tmj for the last 3 years. i first was given numerous night splints to see if that would work,they didn't. Next i was referred to a specialist who gave me a night splint which still didn't work. From here i had xrays and then had an mri.
Right side:
There is an anteriorly displaced but intact meniscus, which mostly overlies the articular tubercle. There is thickening of the retrodiscal lamina tissue. The intercondylar head lies within the condylar fossa with a slight deformity to the articular surface. No fluid or inflammation is present in the residual joint space but there is absolutely no anterior translation when the mouth is open. the adjacent soft tissue of the lateral pterygoid, externally auditory canal, parotid and deeper face are normal.
left side:
The left condylar head is normal in morphology. The meniscus is probably normally located although it is quite anteriorly displaced extending on to the articular tubercle with only a small portion overlying the condylar head from 10 o'clock to 12 o'clock. No fluid or inflammation is present within the joint space of note with a small amount of fluid on either side of the intact meniscus more anteriorly. No oedema or erosions are present within the condylar head. The soft tissues adjacent to the joint are unremarkable.
Conclusion:
There is complete anterior displacement of the meniscus on the right which is intact. it now sits on top of the superior boarder of the lateral pterygoid muscle and overlies the articular tubercle. No current inflammation is seen within the temporomandibular joint, erosion's or bone oedema. however on both sides there is no translation during attempted mouth opening.
From here i had an arthrocentesis where he put a cortisone injection in. This also didn't work. From here he put me on amitriptyline for 2 months but that didn't help so we stopped it. 3 months ago I had surgery on my right tmj. My specialist removed the disc, reshaped the bone, and put a fat graft where the disk should be. This also hasn't helped, I am still in constant pain, m jaw locks up, migraines nerve problems and other symptoms. Because of the pain i have only attended 36% of school this year. It's my last year but i am keeping up. Because of tmj i have to stay home next year and study through distance learning for university. My specialist has applied for permission to put me on gabapentin to see if it will keep the pain at bay.
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I've read some of you responses concerning RA & Gabapentin usage. I have been taking Gabapentin since 2000 for various pains throughout my entire body. I have recently been diagnosed with RA, but doctors will not put me on the required meds because I have COPD & Polycythemia which I am continuing to aggravate because of my smoking addiction. For the past month, I have had excruciating pain in my hip that radiates to my lower back and throughout my right buttocks. The pain is so bad, I have had to begin using a cane. I have no insurance. I have increased my dosage of gabapentin (which has been OK'd throughout the years by my DR's) to try and reach a comfort level of reduced pain. I counter the drowsiness by drinking more coffee to get through my workday. I obtain "pain-free" periods with the increased Gabapentin usage, but I also seem overly energetic or "excitable" during those pain free periods. (reminds me how I used to "feel" before the pain began so long ago . .about 15 yrs already). I'm a 55yo man, have many other health issues as well, including deep depression & PTSD. Because of insurance, I'm only purchasing the Gabapentin and have also started using Turmeric to TRY to help with all the other issues. The Turmeric seems to help, so far. Is there any problem you can see with the increased usage of Gabapentin to become "pain-free" and the mood change during those pain free periods? I cannot afford numerous DR visits w/o Insurance and have to earn a paycheck.
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I have been taking 100mg x 3 per day for nerve pain and it seems to be working but noticed i have lost appetite been on this medication for around 2 months
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