i have just realised that a small part of one toe is numb - start of neuropathy? I hope not. Has anyone tried using the homeopathic tablet Kali Phos for this or indeed anything else?
View 2 RepliesI've been with my boyfriend for almost a year now and we've just started getting sexually active. He has confided in me that he has penile neuropathy due to complications of diabetes.
He's been to doctors and had tests done. The result is there is no problem with blood flow, it's nerve damage, the nerves don't transmit the signal to the penis to become fully erect. I've noticed the base does become semi erect but that's about it. Just curious if anyone has any experience with this and is there anything that will help such as over the counter medications like Cialis?
I am 74 years old and I'm having diabetes type 2 for last 4 years, than i have controlled my diabetes with proper diet and exercise without using any medication. but nowadays this seems not be working any longer, as my HbA1c level is above the normal range that is 7+ ....
Has anyone found anything to help neuropathy after ALIF surgery? It has been 19 months and the pain is increasing. I cannot bear to wear anything except the loosest of clothing, I cannot walk without a cane or walker, I have new bowel and bladder function problems within the last 3 months. Is there anything that would even work temporarily to allow an airport ride? I buy even groceries online. I am in pain management with a respected doctor. I have have PT, water PT, massage, acupuncture, and narcotic medication. The fusion on L4/L5 and L5/S1 is fine; my life is not worth living.
View 3 RepliesIn May I was told I had a vitamin d deficiency. My level was 11. Right before i was told about my low d i had burning pain throughout both of my thighs. If anything touched my thighs it felt like bees were stinging me. I went to the neurologist because I was also getting numbness in my arms. He told me i had mp or another name for it is lcpn from wearing tight pants. I bought new pants and waiting six weeks. Saw him again and now he thinks it's because my d levels were so low. D is up to 50 s now so why am i still in pain. I had an emg done on my legs and it was normal. Emg on arms showed mild carpal tunnel. I was tested for hiv 5 months after any exposure results were negative. He tested me for a bunch of other stuff all was negative. Could all of this be vit d
View 2 RepliesJust going into an air conditioned room; a fan is blowing on my legs; even at home in the evenings my feet and calves get cold. Then comes that cold-to-the-bone feeling for hours. Does anyone else have this problem? If so, what do you do to prevent the misery from cold feet that are hard to warm up?
View 3 RepliesWas on 600mg Gabapentin 3 times a day for peripheral neuropathy to little effect. Was prescribed Amitriptyline, took 25mg for 3 days then 50mg for 5 days - replacing the 2 Gabapentin at night. Reduced Amitriptyline to 25mg after awful side effects. Took for 2 days with 300mg at night (in addition to the 600mg in morning and new GP said stop Amitriptyline and increase morning dose to 900 mg. Was OK for a while, but then feet and lower legs started severe pins and needles, difficult to walk. Disturbed sleep last night and feet and legs still bad. Is this withdrawal from Amitriptyline? How long will it last? GP rang and said gradually increase Gabapentin to 900 mg 3 times a day and if necessary go to 1200 mg 3 times a day.
View 7 RepliesI have heard they have this to help neuropathy. Have not thoroughly checked it out. Has anyone tried this or know anything about this?
View 1 RepliesHas anyone tried methadone for nerve pain? I've just started a low dose and wondered if you had any side effects and how long they lasted? Most important, any relief?
View 1 RepliesOver 2months ago in jan 8th, when i took generic benadryl with dextromorphan, acetomeniphen, phenyleprine,(pill. after about an hour, noticed i loss about 99 of smell which in turn made me unable to taste certain flavors. Throughout the whole day i started feeling unusually shivering and cold. and notice i started to get tingling on the left side of my body. the next day my smell hasnt returned, and i went to the ER, was afriad it was a stroke or some brain injury. Spent 5 1/2 hours trying to find out the cause, but was unable, the whole time the doctor did notice my other symptoms i was jerking twitching while on the bed, and felt very tingly, i also have tachycardia. i was eventually discharged, over the next few days, i still had sense of smell loss which went to 50% but went to 90% loss very quickly over the next few days. While i was sleeping, at night my neuro symptoms intensified, my myclonic jerks, twitching increased, and RLS developed, at the same time i realized i also pins and needle show up on the left side of my body.
After about 1 week, the pins and needle came back on my left hand and feet. Then a few weeks later i noticed i had loss all internal sensations(full or empty bowel,stomach,bladder, eye movements) Any internal movement you can think of is loss. Actually about 99% gone, because i can still have a bowel movement, pee, and stomach sensations only when its overwhelming and prolonged stimulation. i do not have loss of bowel movement, no loss of bladder control.
The pins and needle came and went and move around my hands feet above the ankles. this is over the weeks as its now.
The pins and needles eventually started to appear more frequently on the right side, but not as frequent as left.
In feb 2 i went to the pcp, for possible diagnosis, but i hit a wall, as the pcp kept insisting that my conditions were mental, or genetic in nature.
Within the week, my pins and needles progressed to cool feeling(randomly but not frequently), now im experiencing random joint pains(1-2 sec bursts, not frequently or constant). Also the twitching is more prevelant when i am still.
I have been diagnosed with vit d deficiency, i am taking 2k per day(i dont know how long i have to be on) but she wanted 4k but was scared it causes itchyness, i already have itchyness from the so-called rashes i got, she diagnosed me with atopic dermatitis, which i dispute, as some other doctor said was contact.
Due to me being on welfare(MEDI-CAL ) i am not able to see my medical tests or records online, as they do not have this technology, but the medical center i go to seems to have it integrated into thier database. I do not have to acess to it, unless i pay for copies of medical record, they dont accept cash.
Furthermore, my specialist appt is in aprl 30th, which cannot be changed to earlier, because of me being a mED-CAL patient. i did not go the pcp appt last week because its across the city from where i live, and the pcp is already losing favor, because my previous visits with her was not finding whats wrong with my present conditions, but trying to make up a diagnosis related to mental health issues, hypochondriac, and i felt like i was going to get the same answers as b4.
i was tested for b12 and cbc blood count, but i do not have access to those results. when i requested other vitamin tests, she refused, i also requested lyme(because my symptoms only fit the neuro portion, now that i have limited joint pain). The parasthesiasins and needle, spider web on arm and leg feeling, tickling,prickling, pin priks, coldness feeling,some joint issues) these are constant everyday, there were days where they subside, and when i wake up. loss of sensations prevents me from feeling (if im about throw up acid). abnormal sensations of my right hands. i do not have numbness, loss of pain or itching, but i am certain thats coming next. Any ideas its lupus.i am in college, and i had to drop a class so i can deal and try to find out what my mysterious neurological condtions is..
My pcp thinks this is also hypochondria, because i stupidly told her i had kaiser records, before turning to WELFARE.
You wouldve think that sudden loss would warrant an immediate red flag, but she/they are not taking my condition seriously i am currently taking 4000IU, (2x2000Iu) per day. and taking b12 (1000IU prophylactic, i don't have test results for this yet.
I have peripheral neuropathy with severe edema from the waist down. My doctor will not give me water pills. Is there anything I can take homeopathically?
View 7 RepliesI've suffered with chronic pain in groin area for over 2years now after a few tests and Mri exam my specialist Dr Chawla told me there's no cure for Neuropathy besides help with medication and pain clinic. None of the painkillers have worked, bad time with side effects! I recently had Acupuncture with Gp only for the pain to spread all over body.
I have had no help and as single parent to 2 children this puts a strain on my depression. I don't want this to take over my life.
I'm scared that all the sweets I crave and eat throughout the day will cause me to have GD.
but even worse, I'm wondering whether that could cause my baby to be born with type 1 diabetes? what are the effects of GD on the baby?
I suffer from sciatica and peripheral neuropathy in the feet. Have tried to address both with diet restrictions and daily walks. Yet, the arthritis like pain in the back of my calfs and legs is getting intolerable.
My girlfriend has extensive lung problems and chronic resultant pain from coughing for hours on end - in the back and thorax areas. She was prescribed Gabapentin to relieve that pain. Works for her.
So she gave me two tabs to try for my problems. It was as though a miracle had taken place. No pain whatsoever. Almost no side effects - other than a slight feeling of increased relaxation.
I have been living with neuropathy pain for about 4 to5 years now. it seem as of lately that about 5 to 10 minutes after I take my pain medication that pain get strong for about 15-20 minutes and then the meds kick in and ease the pain. is this normal?
View 3 RepliesI was suffering from almost 8 years from chronic throat clearing and cough I have tried everything acid reflux medicine and allergy medications but nothing work for me I did all kind of tests but nothing comes up all comes later negative my problem was clearing the throat after eating and sometimes even without any warning I was clearing my throat and coughing it was ruining my life and I was having like a sensation in my throat back in my throat that I know I have to clear my throat and instant all of a sudden I was coughing did everything but nothing work home remedies everything but then in the end up my doctor prescribe me amitriptyline 25mg from taking the very first day I start feeling better like 60 to 70% I want to say everyone who is suffering from my kind of problem must ask your doctor about sensory neuropathy chronic cough and throat clearing to give it a try of amitriptyline 25 mg
View 8 RepliesMy blood glucose level after 4.15 hours of eating was 123 mg/dl also, I do not have urine glucose. I had eaten at 4.45 pm and the sample was taken at around 8.15 pm. Do I have diabetes or prediabetes
View 3 RepliesI was diagnosed with PMR 6 months ago and am currently taking Prednisolone which has a big effect on my diabetes control. I am having a bit of trouble controlling my blood sugar levels and keeping them out of double figures. The levels are not consistent so counting carbs can be a problem. I test before I eat and try to tailor the insulin to the food I am eating but it seems very hit and miss and I sometimes end up with a hypo or a 20+ blood sugar result for no reason that is clear to me. I am eating a low carb diet but not cutting it out completely.
View 2 RepliesI am looking for any diabetes patients, or people who know diabetes patients, who are treating their condition with herbs. What I am after is some info for a blog post I am currently working on. I am a bit clueless on this subject - I don't know if treating diabetes with herbs is a realistic approach?
View 1 RepliesI came across this syndrome when searching the Internet about extreme pain I have when I take the first bite EVERY time I eat and sometimes drink. That this could be a symptom of this syndrome but I don't know. I do have some of the other symptoms, i.e. neuropathy, blurry vision, muscle pain, fatigue but these can also be associated with Type 1 Diabetes which I have. Also, came across parotid/salivary glands are affected which also can cause the jaw to ear pain I'm having. Has anyone heard that the Coxsackie virus can have anything to do with it? How do you know for sure if it is Sjogren's and what type of doctor do you see about it - a primary?
View 1 RepliesI'm a diabetic patient and i want to have a tattoo, is it safe for me?
View 1 Replies