Hemorrhoids Flare Up :: Chronic Pain And Itching
Feb 1, 2015
This is embarrassing but I've been experiencing haemorrhoids on and off for at least 2 years now. I think they are external. They are big and blue. When they flare up I have chronic pain and some itchiness. They don't often bleed though. I am a 20 year old female. Two Drs have told me to increase the fibre my diet. One said to drink 3L of water per day. Clearly I haven't been very successful.
My question is what do you do to relieve the pain when you have bad haemorrhoids? I have bought Retinol cream but one of the Drs told me not to use it, I'm not entirely sure why. Also, at what point do you know if you need surgery for haemorrhoids?
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I have been going through a second flare up and dermovate is not working. Now been given protopic as not responding to steroid creams. I need advise on the itching which is literally driving me mad and the lack of sleep is interfering with my work now any advise on creams, diets etc!
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I'm 16 years old and suffering from what I've been told is medullary sponge kidney disease. I have been to countless doctors, including the mayo clinic in Jacksonville, Florida, Children's hospital in St. Louis, and many local hospitals. Every doctor that I've seen has thrown around many ideas of what my disease "could" be, but none of them have ever actually diagnosed me. It started out as a kidney stone two years ago, had gotten better on and off for the past two years. I had always had at least one kidney stone every six months or so. We call my kidney stone's "flare-ups" because when I get them, it is impossible for me to control the pain without being hospitalized. Also, the doctors have said they are not entirely sure that my pain is kidney stones. The pain is a burning, stabbing pain that goes down my right backside and to my lower stomach on the right side. The stones are calcium-oxalate and are usually small. In the past six months, I have been passing a steady amount of "gravel" in my urine, which is basically small stones. Therefore, I am in pain all of the time. I have been put on countless medicines such as potassium citrate and hydrochlorothiazide. Not to mention the pain medicines, I have found that only Percocet and Norco can even touch the pain. And Phenergan helps with the nausea sometimes. I throw up from the pain almost every other day; Some days I am unable to get out of the bed, eat, walk, and keep anything down. On top of all of that, I am unable to urinate on my own. I have to use a straight catheter 4-5 times a day. I have been unable to go to school, and have been put on homebound through my school. All of this has been very frustrating and we basically have no answers. I have recently had a cystoscopy to look at my bladder and ureter. The doctor said it was completely normal, other than that my ureter tube is smaller than normal. I need some way to cope with my pain and get a better quality of life.
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I had a hemorrhoidectomy on 3/12 and I just had my follow up appointment. My doctor didn't even look to see if I was healing properly. He asked about pain and discomfort then offered to write another prescription to get me through even though I told him I stop taking the prescribed pain pills and moved to over the counter Tylenol after a BM. Let me rewind, this was my first case of external hemorrhoids which occurred during a LUPUS flare. On top of me having LUPUS, my first case of hemorrhoids were thrombus. Anyway back to the concern at hand. I still see what appears to me as two hemorrhoids, one red, and constantly bleeding and the other itching like crazy. I'm not sure what I can do for the discomfort due to one of the hemorrhoids appearing to be open, I'm afraid to put any type of medication on them due to the fear of pain returning. This surgery was my first surgery, I've never had kids, so the pain I experience during these last three weeks had me on the verge go asking God to take me now. I'm not sure if I should be concerned and schedule another appointment with the doctor and request him to take a look or if this is the normal healing process.
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I have been dealing with a small lump around my anus. It has been a year and when i first got it, i looked for it online and the articles that i read all said that the lump will heal by itself. It already been a year and im more of tired of it. It's not painful, but sometimes it does itches, when defecating, sometimes i will find blood on the poo, but all this happens really seldom. The lump does not bother much, but it's been more than a year and it is still there. Sometimes the lump will shrink but sometimes it will grow back, and i really do not know what to do. I am definitely going to see a doctor about it, but i will like to know ideas or anything about what i am dealing with.
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One day I didn’t have hemorrhoids and the next day I did……I wasn’t even sure what it was but then went to my local supermarket that same day as I was in pain and got the regular creams and suppositories for hemorrhoids and this eased the pain. However, worse was to come as although I had eased the hemorrhoids I was left with a very embarrassing and itchy bum! I wasn’t sure what to do so went to the doctor who gave me Canesten hydrocortisone cream and this did work but it said to not use it for more than a week or 10 days (something like that) as it caused thinning of the skin etc and I know this can cause itchy skin. It was like a vicious cycle. I had to get off this steroid cream fast and came across a few articles that helped so I wanted to sum it up for anyone who has had this same problem, whether the anal itching was caused by haemorrhoids or something else. This is the routine I followed…..
I iced my anal passage with a lolly pop covered in kitchen roll and then applied what I can only describe as a miracle cream that is only available in this strength in America. The cream is called ‘Desitin’ maximum strength 40% zinc oxide diaper rash cream….yes it is basically just for babies with nappy rash but it is a true godsend. As I live in the UK, I had to get it off Amazon! It was a little dearer with shipping costs etc than normal but I would have paid anything. It has to be the 40% zinc oxide to work.
Within a few days my symptoms eased and have not returned. I think the cream helped to mend the skin and ease the itching at the same time and please make sure YOU DO NOT SCRATCH.
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I am a 23 year old male.
I've been having periodic rectal bleeding for some time now, and I haven't gone to a doctor because I can't muster the courage to do so (I'm just too ashamed to present this problem to my doctor and family), and the amount of blood is small enough for me to be calm about it and my overall health is good.
So I decided to ask a question here before I go to a MD. Also, I informed myself on this issue from various sources on the Internet.
I first experienced rectal bleeding back in the summer of 2013. I was shocked initially, but then I regained my calmness, and on the next day there was no blood in my stool. Then I had another bloody stool a month after that, then it went away after 2-3 days.
So for 2 years, the rectal bleeding is periodically appearing then fading away. Each time the rectal bleeding occurs a few seconds after I pass the stool. So when I pass the stool, the feces are perfectly normal, not mixed in with blood or looking tarry. The way I understand it, that when I pass the stool, it somehow manages to hurt my anal area and causes a small wound, which explains why several drops of blood fall on the toilet several seconds after the stool passes and goes into the toilet bowl.
After doing some research online, I (in my humble opinion) suspect that I have hemorrhoids. Each time I experience rectal bleeding, it's only a small amount. 2-4 drops of blood, rarely more, unless in cases when I pass a hard stool. Sometimes I experience minor anal pain, which fades away in a few hours.
I don't match the symptoms of colon cancer, and if you leave out the rectal bleeding, my health is great. So it was something serious, I'd be in real trouble by now, right?
So right now, I have normal stools for 1-2 weeks, then I have one bloody stool for 1-2 days, then again followed by 1-2 weeks of normal stools. It's been like this for nearly one year out of the 2 years.
Also, I am an athlete, and I already eat a green vegetable with almost every meal - a cucumber, a piece of lettuce, cabbage, etc.
What can you tell me based on what I've told you? Have I took a serious risk to my health by ignoring this issue for so long?
Also, I am thinking of finally going to my doctor, but I wanted to ask online first. What should I expect of my doctors visit? What kinds of questions? What kinds of exams? Treatment options?
I understand that what I'm doing is really foolish, but the shame of going to the doctor and explaining this issue to my family greatly outweighs the fear I have of this issue. I hope you understand.
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I have been suffering from sciatic pain from last 9 months. The degenerative changes are at L5-S1. Had an MRI(attached as thumbnail) and one of the docs has asked me to go for surgery while other have told me it will heal on its own. I have been doing exercises in this period. But the thing is that it has not healed. There were periods of like weeks
where I was almost pain free but then again it would flare up out of nowhere and suffering would start. Another thing I have noticed is that some times with exercises the pain increases, and the days when i don't do the exercise i don't feel any pain. Sitting is the main culprit, but I can sit for like 2 hours and if my posture is good it would be normal.
My job requires me to sit for like 4-6 hours and then stand for 6-8 hours(i work in 12 hours shift). Had days off from the job, I thought it would go away with with rest and light exercises but that didn't happen. Now I am required to work otherwise I would lose my job.
My request to all of you is, does sciatica go away/heal on its own and if it does how long does it take, or do i have to live like this. I can't even sit as a passenger in car let alone drive, couple of road
bumps would trigger it right away(by the way is there a way out avoiding jerks to your body while travelling). ANd for the job I have to travel long distances in remote areas.
Thanks
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I was diagnosed with fibromyalgia about 18 months ago and I'm having a really bad flare up at the moment and still trying to work full time! I'm a beauty therapist so I Found I don't go in I let people down! I'm struggling to walk and my back and wrist is really swollen, I'm taking nurofen and paracetamol but they're not touching it.
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Does anyone that has back problems have sharp nerve pain in their groin private area? I have had back problems for years and sometimes would get a sharp pain up my vagina. After a bad muscle strain in my back and using the elliptical machine I've had twitching and burning all over but also in my private area. Like around my **** it will twitch or vibrate, and then I will get the sharp shooting pain up my vagina and around my butt. I notice it more if I bend over that's why I thought it might be my back. I remember when the stabbing pain started I thought it was a female problem and my OBGYN said everything looked normal with my cervix and my paps have always been normal so she didn't know. She seems clueless.
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I have had ulcerative colitis for a number of years, I recently had a bad flare up with bloody stools, lots of pain and loss of weight, I can't put weight back on again. I had a colonoscopy three weeks ago and was given pessaries to calm it down again. Has anyone else had this problem. I also diverticulitis and non cystic fibrosis bronchiectasis.
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I just started reading about this and it really sounds like I may have this but I'm not sure. I have headaches sometimes that are awful and seem to start from my neck and back of my head. I see a chiropractor once a month and my x rays showed problems in c5 and c6 in my neck. I also have notalgia paresthetica which itches me too death sometimes in my right back shoulder. We figure it's caused from the c5 and c6 in my neck. I never sleep all through the night, always tossing and turning. And I feel fatigued ALL the time no matter how much rest I get. I had a blood test and my vitamin D is low. I can find "knots" on my back, usually I can find about 5 or 6 of them, even on my sides. I work a very physical and mentally stressful job and this causes me a lot of pain. When I am working usually mid day I will get a horrible sharp pain somewhere in my back and it just stops me. It's like someone taking a hot knife and stabbing me with it. It's hard for me to straighten myself up. My pain is in my mid and upper back, rarely ever in my lower back. I do get dizzy sometimes also and feel off balanced.
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After the bowel movement it looks like very hot around anus for at least one hour. there is little bit of pain around anus, some redness and it feels like itching. Looks like the area is swollen.It looks like it is piles but while searching i found piles is something bigger
IS IT PILES OR SOMETHING ELSE?
IF PILES THEN IS IT THE INITIAL STAGE?
ANY SPECIFIC DIET TO FOLLOW?
DOES PILES IS LINKED WITH MASTURBATION ?
IS PILES A BIG PROBLEM??
DOES PILES IS LINKED WITH EATING TOO MUCH OF OILY FOOD??
it started around 20 days back earlier it was only a pimple like thing ....
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hi, i am 36 old man, 3 hours before red ant bite me at my penis skin 3 to 4 times, and it has some swelling,no pain, but itching(very little ) sometimes, so its serious or not, what should i do
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I am a 16 year old girl and i have been really getting pains from my left breast. You can see veins and it hurts when i lay on it. Also it sometimes itches on my nipple.
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Has anyone else been diagnosed with this condition? I shall explain! for 10yrs i've been told i had arthritis in my right hip and right hand giving me chronic pain, only to be seen by 5 different doctors due to a recent change in location and investigations i've now been told i have , mild osteoarthritis in my right hip and the joint between my thumb and index finger.
Not only that but all differnet 5 doctors have said it was different things. seeing my own doctor today, she said (or applied) that the pain might be in my head, then to turn round and say that she was certain that i had A chronic medical condition and what it was she was unsure of.
Is this Chronic pain syndrome another name for they havent a clue whats going on?
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I had both hips replaced in Feb and Sept 2011. Prior to this I had many years of pain and a great deal of difficulty with medical fields trying to determine what was causing my pain. Anyway once it was decided to replace both hips I was happy they had at last found a cause and what I thought was a solution. My first his replaced was my right and this seemed to go okay, it was a total different story with my left. I have been in excruciating back and leg pain since, I cannot walk any distance or stand for any more than five minutes. I need to use a wheelchair if I go out and crutches also, I am stuck at home all day while my family go out to work - I am frustrated and feel useless.
My pain is across my lower back and generates down my legs, my last three toes on my right foot go numb constantly. The pain is tingling, numbness, sharp, deep pulsating pain and electric shock type pain. The more I try to do the worse the pain gets. I spend most of my time with my legs raised as this helps, the pain never goes away but does ease when resting. I have painkillers and muscle relaxants but they do not really help. My hip surgeon like most of the forums I have read told me my hips are fine according to the MRI scan. He then referred me to the Spinal consultant, after nearly a year of seeing the spinal people they have now turned round and said the pain is not coming from my back and there is nothing they can do to help. I asked them what I was supposed to do and they said they had no answers!! I have attended all the physio appointments and even did a three week intensive course along with hydrotherapy - nothing has made a difference.
I lost my job due to all this pain and I am now registered disabled. I had more mobility (although painful) prior to my surgery than I do now. It was nice to read that other people are going through what I am experiencing (although I would not wish this on anyone) it somehow makes me feel better.
I have had numerous cortisone injections in the hips, nerve block of the L4/5 nothing has worked for me post surgery. I had cortisone injection prior to my surgery and guess what it helped - work that one out. I am now being referred to the Pain Clinic (again) and Rheumatology as it was noticed on one visit to the hospital that I had a butterfly like redness on my face and they queried Lupus (still waiting for those appointments - surprise, surprise).
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I have had five kids and i have been having pain in my rectum with sharp shooting pain that also goes to my front also like a swollen pain ill get it every once in awhile i have been having the symptoms of ibs for several yrs and i got the pain right now and it hurts like crazy what could that be i'm really ain't that sexually active since i had my kids and got a tubal.
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For the past years, I've been taking 5 tabs of Methocarbamol 750 mg. along with 600 mg.(6 caps) of Gabapentin during supper and right before going to the bed, because I have not only leg cramp and spasm but also nerve pain on my legs. Those two meds. have been alleviating my pains that mostly occur during sleep, ... specifically during early morning hours before getting up from the bed.
Prior to those two meds. I had an excruciating and unspeakable pains that waking me up in the middle of the nights lasted about 10 minutes or so. Furthermore, the pains made all over my body sweat like taking hot bath, because of excruciating and unspeakable pain. Those nights, I self-exercised stomping, and often back and forth legs on hard floor in trying to subside the pains.
However, despite maximum doses of two pain meds., I still have been experiencing 'stiffness' along with 'pain' on my legs, some mornings before getting up from the bed.
Is there any good meds. for me more to manage and first of all control muscle spasms and cramps on my both legs?
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I live in the U.S. so the drug names may be different. I have been taking hydrocodone (norco) 2 x 7.5 a day for over 2 years. I had neck surgery in 2012 and within 6 mos the pain in my neck and left arm returned, along with the nerve pain in my arm. After ruining my digestive system with ibuprofen ( I was taking at least 8 to 12, 200 mg each, a day) I gave up and went to pain management for help. I had successful injections for low back pain a year or so before that, so I thought that is what they would want to do for this. But the doctor said that it would not help, probably because of my surgery, I'm not sure now because its a distant foggy memory. Anyway, the result was pills. At first it was only 5 mg 2x a day. Then he upped it within 2 mos to 7.5 mg. 2x a day. Since then I have read a lot about opiates and know that it is very addictive. I take it as prescribed but that means that I am just addicted to the prescribed dose. I had surgery in September for my digestive problem that all started with the ibuprofen. After the surgery they gave me Oxycodone. Within 3 doses I started sweating and having a headache soon before my next dose was due. I recognised this right away as a symptom of withdrawal. I immediately stopped taking that and just suffered through the surgery pain with my "usual' med, hydrocodone. Within a month, I started to realize that I have the same symptoms to a lesser degree with this med. This can only mean that I am addicted to it. When I went to my doctor for my usual appointment and med refill, I asked if there were any alternatives to Opiates. I said I was uncomfortable taking this and wanted to find something else. He said "Tylenol?, that's your only choice." I was floored. Well, I know tylenol can ruin your liver, so that wasn't even an option. He then said, "the holidays are coming up, why don't WE wait until after that and rethink this". Wow. I was truly speechless. So I took my scripts and left. I did NOT make another appointment. All that to ask this question. Does anyone know if there is ANY option to opiates for chronic pain and permanent nerve pain? If I do not take the med, my pain comes back, but the Nerve pain is the one that drives me back to take the pills. Now it's in both arms and when the med starts to wear off they start to ache, then burning and tingling. I have tried reducing the dose by taking half a pill, but all that does is make me count the hours to the next half pill. ugh. I want off this stuff and I know it can be done! I have read several success stories right here. Other symptoms I have are anxiety, depression, anger, constant waking up at night with the sweats. I need support, answers, and a way to do this without losing my job,all my friends and my mind!!
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I have had CP for almost 3 years. I can't remember life without it or being able to sit down in real comfort. I have had all the hospital tests and regularly have a well-man check every autumn. I still try to keep fit and go walking and having recently retired so I am determined not to let it spoil my life. You always continue to worry that it will not turn into something else. I probably don't take as many pain-killers anti anti-inflammatory drugs as I should because you feel that can't be good for you as well. I dream of the day it will go but I fear it will be around for a long time yet, if not for ever.
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