Fibromyalgia :: Creams, OTC NSAIDS, Yoga - Not Working
Jul 9, 2015
My family doctor and I have concluded (yesterday) after various tests and trials of other things over the last 1.5 years that I have fibromyalgia. The symptoms coincidentally (or not) started when menopause started for me (I'm 54). I have been on HRT for one year and it has relieved the hot flashes but not the body/muscle pain and sleep problems. Since all OTC NSAIDS and arthritis type creams don't help, he prescribed Voltaren gel and to continue with all of the alternative therapies I'm trying: Yoga, walking, monthly visit to chiropractor, acupuncture and massage and meditation. He said to try the gel for 4 weeks and if that didn't work for me he'd prescribe nortriptyline for sleep/pain. Do you agree with his assessment/plan? He didn't think diet had any impact, do you agree? I am trying to eat a more plant based diet. Any suggestions you have would be most welcome. thank you!
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Besides Creams/ Lignocaine twice a day anything else i can do ?...I've brought Prune juice, Husk to put on cereals...even the softest of BM aggravates these things. Sometimes i swear i feel it going down my leg the pain from them and into stomach. Dread what the internal ones look like, I'd think large, can they grow really big?..the pain these cause is just incredible. Least i feel i have company here, most ppl just say oh they are just Hems!....but it's not nice visiting someone and wriggling around in your seat and it consuming your every thought.
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My 6 year old daughter has had Molluscum Contagiosum spots for about 3 months now. The doctor has given Steroid Cream but it doesn't seem to be doing anything. She also has eczema and the creams are just irritating it and making it flare up.
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Phimosis is ruining my sex life. I can't fully enjoy sex because of it. I've tried some stretches, but it only helped a little.
I've heard of over the counter steroid creams. I'm thinking of buying some. If I do how long would it have to use it for? Where could I buy some?
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Does anyone have any suggestions for anti-inflammatory drops, creams, oils or ointments of any type that has helped with your MGD/blepharitis? I do all the hygiene stuff which keeps the crusts absent and eyelashes from falling out which is amazing to a certain point.
My problem is constant inflammation of varying degrees to my eyelids (or to be more precise the Meibomian glands). when they are at their worst inflamed there is literally no oil getting through to my eye which is really irritating and my eyelids become reddened around the lashes which creates a really annoying self-image paranoia + the inability to converse with anyone without being distracted by blinking a million times and feeling like I would like to close my eyes altogether or rip them out lol. I have tried drops but the lubrication effect seems to wear off after 10 minutes and I just don’t have the patients to be doing it that often.
The only thing that has seemed to work well for me so far is a tiny amount of castor oil applied to the lids at night (takes a few days to adjust to it). I have not tried steroids yet or antibiotics with anti-inflammatory properties but right now I am using chloramphenicol drops which are hopefully doing something + bead type warm compresses regularly which are helping but only slightly.
I saw an American youtube video recently about a doctor prescribing androgen gel to patients with MGD/Blepharitis and after researching why I realised that it’s because it reduces inflammation in the body, for the MGD/Blepharitis type that I am sure I have it seems to work well for patients that have tried it. That said there is plenty other things on the market that would have the same effect on the eyelids but more localised and less side effects are preferred, I don’t like the idea of roid-rage, shrinking nether regions and pancreatic cancer etc. It seems like too much of a trade-off in my situation.
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I have had knee problems off and on for about seven years. Yesterday my doctor decided that my cartilage has finally 'Gone', probably finished by getting off our local trains where not only do you have to Mind the Gap but have a good two feet to step down. He is arranging for another X-Ray prior to discussing my surgical options. Two years ago after the last X-ray I was told that my knee was in good condition for my age:-)
Meantime he reluctantly prescribed an NSAID ( Naproxen) after considering my BP and past stomach ulcer and other problems.
Reading the packet insert it tells me that Losartan and most hypertensive drugs may be affected by how NSAIDS work.
Googling Naproxen + Losartan I read, "Significant interaction possible (monitoring by your doctor required).
losartan oral , naproxen oral . Either increases toxicity of the other by Other mechanism. Combination may reduce kidney function, particularly in elderly or volume depleted individuals.
naproxen oral decreases effects of losartan oral by opposing drug effects. Combination may reduce blood pressure reducing effect"
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I take Naproxen for Rheumatoid arthritis but as I have high blood pressure I also need to take Losartan 50 mgms daily. My GP now wants me to have 6 monthly blood and urine tests. I think this is because these drugs combined can cause kidney problems. Has anyone come across this before?
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My instructions for taking Naproxen indicate that it should not be taken with aspirin. My question is; how much time should I let go by after taking a Naproxen to be able to take aspirin?
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GP has given me Naproxen as I am suffering with sciatica. I also take Citalopram and asked him whether it was ok to take these two medications together - he said it was fine.
Several sites however mention that you shouldn't take these medications together.
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I find these tablets really good for my arthritis. I have arthritis in hips, knees and at the back of my neck.
I do not have any side effects
One day this week I had a toothache and wondered whether I could have taken something for it on top of Naproxen. I wondered about Ibuprofen or co-codamol.
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I was on Naproxen for an elbow injury - torn tendons - and had to come off them due to the terrible constipation I endured while on them, despite the limited pain relief I enjoyed. I have had a medical today with my employers M.O. who is surprised to hear that Naproxen would have such a side-effect. Has anyone else experienced similar?
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I have been taking naproxen now for over a year and recently found that ,it's this tablet making me have profound hot sweats though the night ,that much ,that i have to change my bedding and nightwear, also i've found ,that when i wake in the morning ,i have a nasty foul salty taste in my mouth ,i will only have to carry on taking them for another 3 weeks as my specialist is putting me on methotrexate, I have also heard a lot about this tablet too ,risks to the liver and kidneys, and other things that are very scary.
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I developed severe blisters, toothaches tightness of the throat and mouth and tongue sores after taking this drug.
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I have various back problems I have posted about in the back section but due to this I'm on 500mg of Naprosyn 2x a day. I also take 20mg of omeprazole 2x a day at the same time as the naprosyn as it was giving me heartburn. I started on 20mg but went up to 40mg because I was still getting the heartburn which is now acid reflux bringing me close to vomiting.
I've told my doctor about this and the latest thing I'm on is peptac liquid at bed time but I'm also taking it after meals if I have to.
It doesn't seem to be improving. My doctor said if it doesn't improve soon she will have to take me off it. The only reason she hasn't done yet is I am already in so much pain and the naprosyn is one of the few things that has helped.
I also have noticed I'm beginning to have difficulty swallowing hard or dense foods. Soft ones are fine but now I'm kind of afraid of and completely avoiding anything hard or dense. Could this be to do with the acid reflux?
I am going to ask my mum to help me raise the head of my bed (as due to my back problem propping myself up on pillows just makes things worse) but is there anything else I can do?
I'm really worried about developing a peptic ulcer.. it's the last thing I read right now. Can anyone tell me what the symptoms are I need to watch out for? If this carries will I end up with permanent acid reflux as well does anyone know?
I see my doctor again on the 4th of November so will discuss it all with her again then but I just am worried in the meanwhile.
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Is it good to east before you start working out? What to eat which will give you extra energy. Share here
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So it's been 3 weeks since I started orlistat and slimming world. First week loss 8lb, second week loss 5lb, third week loss 3lb. I am not eating much fat at all and am wondering if the tablets are doing anything for me? I'm really disappointed with only 3 lb loss this week. I know the weight loss will slow down, however I am very overweight, doing slimming world AND orlistat, shouldn't the weight be falling off? I haven't cheated once in these three weeks! My body has gone from having around 3000 cals a day to just 1000 cals plus exercise!
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When did ya mom's started exercising?
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Is it okay to workout in the 1st couple months of my pregnancy?
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have horrible insomnia. Every night I wake up at least once and have trouble falling back asleep. This has been going on for years. I have tried melatonin but I still end up waking up and am always tired in the morning. Does anyone have any advice or medicines they can recommend that will help?
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I have been off work for 6 months because of physical health problems then my antidepressants stopped working. I have been referred to CBT so am waiting for an appointment.
Can you have CBT while you are working?
I am also waiting on OH for work. Would it be better to have OH first before CBT or at the same time/similar time?
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I have some questions and I think I'm in the right place. My BP has been high for quite a few years. My old GP of 20+ years tried different meds but they all made me sick.Except Diovan, which I have been on for a long time but it stopped working. I am really sensitive to all sorts of stuff. He just retired and a kid fresh out of med school took his place. On my first visit, my BP was 211/90 and he freaked out and insisted I be admitted to the hospital for a few days. I refused and said lets just try a new med (or two) before we get too drastic. He agreed but wasn't happy. He gave me Amlodipine and that was the worst thing I've ever taken. I was short of breath, heart pounding, dizzy and weak and nauseous. Could barely get around. I thought I would die. It lowered my pressure to 180/90 and that was it. I stopped it after 10 days and told him I had too many side effects and it didn't work. I brought my BP monitor in and showed him. He acted like I was crazy for stopping it. Practically said it was all in my head. I said go tell that to my husband. He had to drive me here because I am too out of it to drive. He just shook his head and said OK let's try Clonidine. I said OK but only after this has cleared my system. It took 3 weeks. I'm not kidding. So I started the Clonidine 0.1 3xday. It worked good for 3 days. Pressure went down to 158/70. pulse down to 54. It's normally around 60. I was so out of it, I slept for 4-5 hours during the day and an hour after dinner. Dizzy and headache but no nausea or diarrhea. About 6 days later it stopped working. Pressure back up to 211/90 pulse back to normal (60). Blurred vision and headache. Still falling asleep all the time. Can't read, can't drive a car. Having trouble typing this actually. I sent him a fax this morning and told him it stopped working and I need to wean off. He called me right away and told me OK.. no need to wean off it. What? All I need is a rebound and my BP will be deadly (as if it isn't already) So he told me cut back to 2xday for a week and then 1x day for a few days. Then he said you need to try a Beta blocker and said metoprolol and he wants me to see a kidney specialist. Now I'm really scared and my BP is probably sky high. I'm too afraid to check it. My kidneys didn't look all that good on my last blood work so that's probably the problem. I've heard about stents but haven't found anything on these boards. I'm also worried about taking the Metoprolol in case it lowers my pulse way down. Oh, and he said there is no need to wean off that if you have too many side effects. I'm starting to think he wants me to die. I would like to force feed him some of this stuff.
A few things about me. I'm 67, have type 2 diabetes and have been on a low carb diet for 4 years. Blood sugar totally controlled. I weigh 115 lbs. I'm a nature photographer and WAS very active. I've been practically bedridden for the past 2 months on these meds and missed the entire fall bird migration, which is very upsetting. My husband took me birding last week and I fell asleep for most of the 3 hr. trip.
I am truly nervous about taking the Metoprolol. Anyone have any ideas? Also if anyone knows about kidney issues and HBP I would appreciate it. Thank you all so much for being here!
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