Hemorrhoids :: Botox And Laser THD Didn't Work
Sep 24, 2015
Basically in april 2015 i went to consultant for pile treatment, he advised me to have them treated by injection, i went ahead with this procedure, for a week i was fine then i noticed the itching and pile/pain had returned went back to my consultant he told me he thinks it was a fissure and to take creams and come back to him in 3 weeks time for further consultation.
alas 2 weeks later i was in severe pain and discomfort and phoned the consultants office that i was in bad pain and was told the consultant was on holidays and would not be back for a further week!
at this stage i was told by my doctor to attend hospital a+e for emergency
treatment ,this i did and was told to present myself at the hospital fasting from night before to see a new consultant---Phew it gets worse!
arrived at the hospital new consultant in fairness said he would put me under a full GA and see what is going on there
the following morning he told me yes indeed the piles were back there was one internal and one external and that i was better off going for the laser treatment called THD, which i booked in for the following week this was at this stage mid may had the procedure and for 2 weeks felt great
however on the third week i was in severe pain in the anal area and knew something was wrong (bearing in mind i was told the THD procedure has a 90%success rate..presented myself back to the consultant in hospital had to go under a full ga again he told me afterwards that the procedure had not worked for me for fu..s sake i was one of the 10% that it did not work for so i was booked in for the following week to have the piles which i was now told one of them was thrombosed removed by surgery so have had this done in mid june and have been in terrible pain since, especially after bm to the point where all i could do is sit/lie in the house all day taking pain killers stool softeners and baths every day. every time i phoned the consultant i was told it takes time to heal so after 7 weeks of severe pain id had enough, i went to my doctor got a letter of him to see the consultant urgently as i was in severe pain meet with the consultant am now booked in again for early next week this is what he said the wound is healing however it is a time thing, he will have a further look at me to see if there is something else causing this awful pain he said there is no fissure but wants to give me a botox injection in the anal area to help with the healing, can anyone please advise with this as i do not want to get any worse pain than i am in presently sorry for the long rant but this is actually what happened to me it has changed my life whereby in the last 6 months being in terrible pain and discomfort and am now wary about this botox injection
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I've had worms since last September which is almost 7 months. The worms are white and small. I've take ovex about 10-15 times in the past 6 months. I've taken pripsen about 4 times. Neither have worked.
My nose has been itching and really bad itching anus which is depressing me. Could this be anything other than threadworms(which I've sent a stool sample and sticky tape test off and all come back negative).
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I am healthy non smoking 65 year old, very active physically and overall healthy. I had the urolift procedure done May 23 2015 at which time the surgeon installed 5 clips. Prior to surgery I was on 8 mg of flomax which made it possible for me to urinate.I did wear a catheter bag for awhile then. After surgery I was on 4mg of flomax for approx. 1 month. I was able to urinate adequately for about 8 weeks. Never but once what you would consider a flow. At about the 9th week I started slowing down again until it got to the point (about 11 weeks) where it took me 8 minutes to start peeing and then it took two more times in the next half hour to finally eliminate somewhat completely. Now in the 14th week of post op I'm on 8mg of flomax right back where I was before surgery.I am now considering what options are available to me now.
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I'm 17 years old I've played volleyball basketball and track my whole high school career and I've always had problems with my knees and ankles but I've been going to the doctor for my knees for like 2 years now and I've had like 3 MRIs they never tell me anything I've tried braces but they don't work. My left knee is way worse than my right but they both hurt. It started out feeling like I just had to crack my knee like if you straighten your elbow and it cracks but then it progressed and know it hurts extremely bad when I start running and I can't stand up after sitting like straightening them hurts horribly bad. Sometimes while I'm sitting they ache and I feel like it's on the inner side of my knee and on my left knee it's on the left side inside and if I go on my tip toe it hurts really bad like a shooting pain kind of it's like a line kinda. And it's also worse when they're cold like I have to drive with the heat on them even when it's 80 degrees outside.
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Degenerative discs and spondylolisthesis,had injections worked well for 5 days now all back ...
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After meeting someone on a dating site (getting along very well) a month later I started to itch and little lumps with a white centre started to appear. I thought I had been bitten by mosquitoes and treated them as such. Another few weeks past and they were getting worse not better. That's when I realised what they were. I told the person who I had met and they would do nothing about it so I discontinued the relationship. However I was left with this mess. So far i have used 20 tubes of lyclear and a bottle of tea tree oil. All to no avail. I am at my wits end now especially after reading a lot of the stories. This is horrific. I desperately need help in getting rid of this curse.
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I am 25 female and have been suffering with hemorrhoids for years, 8 I think now, they resulted in a nasty skin tag and when I thought it couldn't get worse, I have now had a fissure for over a year.
Anyway, after many GP visits etc, and fainting from pain, I finally got put on the NHS waiting list for botox and skin tag removal. I thought to myself this is great to get this done and will solve all my problems, as I can't continue life as it is now, right? I got a date sent to me last week for the surgery, meant to be today, much quicker than I thought (Surely they would have wanted to review before, the Surgeon hasn't seen me in over 6 months?!) but after reading so many horrible posts about Botox I postponed it, so they will be sending a new date. But before I go ahead I really hope lots of you can advise me on your experience and give me information.
It is painful for me every day, I almost faint sometimes from the pain. And for some reason for the past 2 weeks, I have lots of blood during EVERY SINGLE BM - why now?? And is this something I should be worried about if it is every single time?
I am tip top about diet and exercise, I only weigh 54kg, I am healthy and active all the time!
The advice that I really want from you all - should I do this botox? Or should I accept life as it is now?? [sad] could things get a lot worse if I go for Botox?
Also I don't know if I get 'spasms', what are spasms? I am in pain for a long while after a BM is that what they are?
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Is there any natural medicine to cure fibroids?
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I opened a heavy window at work in April this year 2014 (twice in a matter of a few days) I've had 11 sessions of physio to which this didn't respond to. I've had horrendous pain over the months and now had a scan to show a prolapse disk. On Thurs 27 November I had an epidural injection which doesn't seem to have made any difference and I am currently off work this is my 5th week off. Prior to this had four weeks off intermittently. I am due to see the Neurosurgeon again on 17 Dec to discuss surgery that he said he can offer me. I keep as active as possible but to walk sometimes if really painful and I can't work with this. This has gone on for so long, any advice on how to treat this? Should this have gone off for this long? The L5 S1 disk is prolapsed.
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I was diagnosed with SVT from an early age, and spent most of my childhood going to and from appointments at the children's hospital. Eventually, after many many episodes (and of increasing length!) I was suitable for an ablation. I had the ablation at aged 17, however, unfortunately it did not work and I had an episode 6 weeks later - frustrating! However, it has somewhat modified it and my episodes are less frequent and the length of episodes has decreased substantially from 3 hours to just 5 minutes! So I would definitely recommend the ablation surgery, although it didn't quite have the desired effect for me it has improved the condition and the effect on my life. I now control my episodes through the various maneuvers suggested (and with success thankfully.
My question is, how do people with SVT get on with exercise? I have always been keen to compete in sports, especially during school - however the severity and frequency of my episodes before the operation meant that this tailed off a little. I am now 22 and I am keen to get back into running, moreover, running distances for charity etc.! I am just a bit apprehensive about overexertion and effects on my heart! I would thoroughly appreciate any help/advice about how much exercise people tend to do! especially those who have been diagnosed with SVT from birth or a young age.
I am due to run the race for life in a few weeks, and have been running a little in preparation for that. But I am keen to get back into running longer distances with a view to doing half-marathons/marathons. Has anyone run these kind of distances with SVT?
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I'm not sure if anyone else experiences this? I tend to find something will work for me down there, then it does not. For example: coconut oil has been quite soothing in the past, lately it just irritates me no end.
I tried Olive Oil but it wasn't that great. The Doctor prescribed Sylk vaginal moisturizer and that can either be Okay or not.
Has anyone else got other 'comforters' for LS? Mine gets sore and stingy as opposed to itchy.
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I have got lichen planus on arms very bad, legs, vulva, oral and now starting on my chest. I have used cetraben, dermovate, dermal, doublebase cream, hydrocortisone, calamine lotion, aqueous cream..my GP been excellent.
Also Tramalgin, betnovate for below and am now tearing my hair out with sleepless nights with itching.
I go to work like a zombie and it's so embarrassing having to scratch, they say the monkeys here as a joke.
This has gone on for 6months nearly...am waiting to see the dermatologist. I had a vulvar flare 4 years ago and was ok up until early this year.
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I have diagnosed with IBS for nearly 2 years now and have tried a number of medicines (including Fybogel Mebeverine, Colpermin, Wind Eze, Buscopan hyoscine butylbromide, and VSL#3). This has been complimented by cutting out gluten and following the Fodmap diet. Nothing has changed and I’m an in constant discomfort i.e. every day, with peaks of pain (stomach pains, wind, need for toilet etc.) and troughs of just simple discomfort in the stomach. I have lost count of the amount of times I have gone to the doctors and I’m now being broadly told: “you have IBS, deal with it”. Does anyone have any similar experience of this and has anyone got any suggestions as to what I can try next? I feel that I am stuck.
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they were banned last summer but it has not worked and even though I eat more fibre and drink water they are painful. I have three that protrude, don't know what treatment to ask for now banding has not worked.
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i had hemorrhoids for about 6 years now and it pains like hell...just feel like that u r going to die .. i have external hemorrhoids. i sit in a warm water with salt in it...and i use ice packs as well...but it does not seem to help...i am also using a cream to get pain relief.
is anyone can suggest a better cure for hemorrhoids...i don't wanna operate it. i want to use herbal product...as i am also scared that i don't have any kids yet...what if i can't conceive and if i conceive will it get more worse...
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I have had this condition for almost ten years and although not painful it has altered my life by reducing my confidence.
i recently enquirer when at one of my Botox appointments if there were any new treatments and was told that surgery was now more successful.I have been offered an operation on the N.H.S. And am going through the decision .As I am quite a fit 66 year old I really don't want to be having Botox for possibly another 20 years!
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My wife has been diagnosed with SOD and has been offered botox injections for it. Has anyone had experience of this or got an information on it.
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I have suffered from migraines since I was 9. These are the drugs I have tried:
-Metoprolol which did nothing just lowered my already low blood pressure
-Topamax, it worked amazingly until my hair started falling out
-Amitriptyline which worked but all I wanted to do was sleep and eat
-Nortriptyline which gave me a headache
-Wellbutrin, worked until I had a Steven-Johnson reaction and am still waiting 4 weeks later for my taste buds to grow back.
-Botox, total waste of my $280, except that I had couldn't move my forehead muscles, lol.
Then my doc wanted me to try depakote, which I drew the line at! All of these toxic medications and I was back at square 1. My hubby did research and out of 300 reviews of BUTTERBUR (all natural), they were almost all positive. It did say might take a month to work also. I was having migraines daily. The first day I took it, no migraine. I was shocked and relieved. I am now on day 8 and yesterday I had the teensiest migraine ever so I also took a feverfew, which according to Dr Oz and internet research, helps with migraines. It went away. I hope this is the solution. So tired of medications with horrible side effects. Butterbur is also used as an antispasmodic/muscle relaxer and I have noticed since taking it i have had no back pain, and I sleep so sound at night (used to wake up 4-5 times a night).
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I've had a squint all my life (30 years) had two previous surgeries that did not work. My right eye turns inward.
Recently I was referred to hospital for Botox treatment. This was carried out 9 days ago.
My eye is now straight. (Yay) I am however suffering from double vision when I look to the left and what I can only describe as slight 'ghost' double images (not constant) that seems to appear randomly and when looking in any direction,
Has anyone had Botox and experienced something similar? I'm just looking for reassurance that the double vision will pass and I can continue with the Botox treatment?
The botox kicked in 3 days after it was administered so I've only had double vision for about 6 days.
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After 15 years with Achalasia and difficulty with food passing into my stomach I finally had Botox injections yesterday. During the endoscopy the dr said the valve at the bottom of my oesophagus was really tight and he's hoping the Botox will help me.
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In 2003 I had really painful headaches so bad I could hardly put my head on a pillow, pretty scary as I do not suffer from headaches. Then as I was eating bowl of cereal I kept missing my mouth and realised I couldn't feel my lips or tongue as though I had been given dentist injection. My sister took me to hospital thinking I was having a stroke, this was the first time I had heard of Bell's palsy and I was given steroids, i was very tired and it was an effort to do anything like eat, speech, it did take three months to go.
february 2014 I got a rash on my stomach which spread to my neck, to my back, to my feet, then to my scalp and then my ears, I was in agony, it was urticaria. Whilst trying to cope with this I then got Bell's palsy again, possibly due to an immune system at a low. However it has taken a lot longer to recover this time. Eighteen months later and I still have a twitchy eye and lopsided smile. I am now considering Botox, has anyone here used Botox to correct any of the nerve damage left after palsy and if so what are your thoughts?
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