Archive for June, 2009

I am a twenty-one year old, female, diagnosed with Fibromyalgia, Chronic Fatigue Syndrome, and REM sleep disorder. My Dr. is now questioning the possibility of Myofascial Pain Syndrome... In the past I have tried physical therapy, acupuncture and multiple prescribed medications both for the pain and the sleep problems... none have been quite sufficient or cost effective, in the long run... any suggestions?

My mom has Type II diabetes and is suffering from neuropathy in her feet. I have read on websites that there is treatment but was curious if any of you out there who have this have any remedies for relief...like home remedies or know of any kind of over the counter cream that helps? She also has the burning and tingling sensation at times that keep her up at night. Diabetic community....PLEASE HELP!!! Any suggestions?

I suffer from migraines as well as depression and have been on so many different drugs over the last 3 yrs I could start my own pharmacy. Nacotics trigger migraines. The anit-depressants make me more tired. I am not sleeping well and feeling like I just cannot see another damn doctor. Anyone have anything that helps??? Is there a specialist out there for this type of thing. I am seeing a primary care, a psychologist and a phychiatrist. Its getting too expensive and not helping me very much. Any suggestions would be appreciated. Thanks

I have had fibromyalgia and myofascitis for over 7 yrs. and have had every possible treatment...injections and more meds than any one person could handle...I am looking for alternative treatments that don't cost alot of money

I've been suffering with Chronic Myofascial pin in my upper back all the way across & the only thing that really stops the pain is if I lay down (I'm not going into that business). I have NOT been to a therapist that specializes in myofascial pain but I do see a LMT every 2 weeks. I take muscle relaxers & Tramadol along with other pain relievers. Help!

I; have had fibromyalgia for over 10 years, other than just taking pain meds. there has been nothing to relieve the symptoms, have tried many natural remedies as well. Is there anything new on the market, or any new treatments?

I have been taking corticoids for two months now because of a neuropathy problem. I have noticed some improvement, but i haven't completely recovered. How long will it take for the corticoids to make full effect?? I have gained a little weight and a lot of pimples, i would like to get rid of this treatment as soon as possible.

Cousin is crippled due to peripheral neuropathy. Permanent nerve damage, limited use of hands and feet, and chronic lifelong pain from intensive and aggressive chemotherapy for large, fast growing cancer. (Cancer is gone now. Treatment crippled her. She is 35.)

Anyway, she collects 780 bux social security disability check each month, and also has Medicaid. Making ends meet on this small sum is near impossible, because she can no longer qualify for food stamps. Also, because she recently qualified for Medicaid, she now has to pay a small amount towards rent on her apartment. (Rent was free last year, now it is 125 bux a month. She has to pay electricity and water.)

Her 15 year old son lives with her, and gets something like 250 bux a month. That helps.

However, all things considered, it's not enough. Needing to know, can she take a little part time job, like answering phones or something, and supplement her disability income that way, without losing the disability check?

Not MS, not Lupus, then what?

I have been seeing a neurologist due to extreme muscle and joint pain, i stumble a lot, drop things, forgetfullness. I do have fibromyalgia and have for years. I also have peripheral neuropathy ( no diabetes) I have had tests to rule out Lupus and MS (which does run in the family) Lupus is neg, not enough points or evidence for MS, ( no lesions on the brain) but does not mean i do not have it. So now he wants to do more aggressive and specific testing. What I want are some suggestions of what it might be from those who experiene this, so that i can read up on it so that I can ask questions and not look like a dope when we discuss different possible causes and treatments.

recent optic neuritiis has left her (50yo F), dx MS, basically blind (light perception) only, she is also unsteady and objects appear and disappear (bathrooms in hallways......) Thanks

Does anyone have a ?

diease call progressive motor/sensory peripheral neuropathy and what do you do for treatment to control pain?
Taking 2400 mg of neurontin daily 2 pain pills I hve had it for 8 years I got it right after a triple bypass I currently have a double nerve stimulator in one for the arms one for the legs but no help yet my surgar runs around 75 to 80 I am not diabetic, I seen a neurolgist for 3 years all the testing he called it idotpathic and said good luck he had done all he could do, pain clinic done the nerve stimulator thanks for any help seems like nothing works

Was in a car wreck in Oct. - doct. says I have peripheral neuropathy, possibility of it being crushed nerve. Have been on Lyrica(to rejuvenate nerve-not working), also was given Tramadol(for pain-not working). I'm in pool therapy 3x a week(not working). Doct. has me wearing the AFO brace(so I won't get drop foot). Need pain relieve- and want to know treatment if it is crushed. Thanks/All Have A Good Day!!!

I have been recently diagnosed by a neurologist. What kind of treatment can I expect. The pain is incredible in my feet I can't stand it. Sometimes they are numb, sensitive to cold, tingling...does this get better?
I do not have diabetes yet but it runs in the family...recent fasting glucose was 112

me but I am in MO and she is in CA, It is such a severe case I almost lost a foot because of an ulcer and i have had several IVIG treatments it would just be nice to see if someone close to my age had some suggestions or just to understand it. Mayo did accet me so I have explored multiple avenues, hopefully someone has some ideas thank you

I have a relative with Neuropathy in the foot, he has tried Alpha Lipoic Acid for several weeks, and supposedly that did not help.

I found Capsaicin (topical) Cream, Gotu Kola, and Evening Primrose Oil as possible solutions from the University of Maryland, Mayo Clinic, and University of Michigan Medical Databases.

So,which is more effective? Anyone with any experiences of these complementary alternative treatments? (Any treatment that I have overlooked?)

I know that a huge one is to stay away from Monosodium glutamate (MSG) also allowed to be called Natural Flavoring, guaifenesin, having low stress, and avoiding caffeine and alcohol.

I also know how important a good diet it and getting enough good rest is.

But sometimes all H*** breaks loose and despite all your hard work you just can't maintain the house of cards you have built to deal with this DD.

So what I am looking for is any other treatments, supplements, techniques or something to fix the damage that the last couple of days of chaos have caused.

As for the chaos, we are having two rooms in our house redone and stuff ended up blocking up my kitchen so that I ended up not cooking at all -- so where do you suppose my food came from! And all the stress of people being in my home and on and on... Now when it is done it will be so very nice but in the meantime... And I am really hurting even after two doses of guaifenesin.

Any idea would be appreciate!

I am a diabetic who is currently undergoing a lot of medical treatment. To make a long story short, I have pain and nausea (which they can't find the source to. I am undergoing a lot of tests), so they prescribed me Ultram for the pain and Compezine for the nausea. They knew that I was taking Zoloft 50 mg once a day. They knew all of my medications including Klonopin for anxiety, Geodon for my mood swings, and Lyrica for my neuropathy, and amitriptyline When I went to my behavioral health doctor, she was concerned that they gave me Ultram, because apparently they interact. Doing some research, I found that my amitriptyline also interacts with Zoloft. She warned me about them, but she didn't tell me the side effects. Are they dangerous? Has anyone taken both before? THey are both really low doses, and I won't take them at the same time. I am going to call my doctor Monday, but I really don't know if it is safe to take any Ultram over the weekend. Just so everyone knows-I WILL GO ASK A DOCTOR. I am just asking for anyone's experiences themselves. Thanks.
I am sorry I meant that she was concerned that the Zoloft would interact with the Ultram. I apologize for not being clear. And thank you for your input!

his feet hurt so bad he threatens to have them cut off. He is taking Neurontin 300mg 3 x day but its not helping. If he tries to take more it makes him sick. What else can we do? What other treatments are out there? He knows he should have taken better care of his diabetes but now he is. Also now his skin is getting sensitive especially when he first puts on his shirt, then it gradually subsides. What's causing this?

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