Itch And Little Lumps - Lyclear And Tea Tree Oil Didn't Work
Apr 19, 2016
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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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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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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My daughter is seventeen and has Molluscum Contagiosum all over her neck. She also has some on her arms and I fear maybe getting them on her face. This is extremely distressing for a girl of her age. She has had them for about eight months. I have been trying the tea tree oil and giving her extra vitamins. They have gone red around the outside, but I wondered if that was just because I am burning them with the tee tree oil as it smells quite strong. Does anyone have any more information about this terrible condition.
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I ordered four packs of the Key E suppositories from US because they were so much cheaper ( then got walloped with £18 in import duty so no they weren't) and ordered some Tea Tree suppositories at the same time as I had read how these were soothing.
Tried one yesterday and as expected very tingly but by last night I was dry as a bone, sore and today burning up like crazy so will not be using these again. Back to the Key E and coconut oil for me
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In from my evening shift at work, and I have got to say that I spend the time before I had to go in, scrubbing my eye lash margins with a wet cotton ball and baby shampoo (the old standard) both top and bottom, then after rinsing it off, I proceeded to wipe the rest of my face with some full strength tea tree oil on a cotton ball, and let it sit for a while before I took a shower. Scrubbing the margins (insides where the oil glands are) really was a bit uncomfortable (it didn't hurt though) and it did produce some of that lovely old whitish stuff, but I cannot believe how much better my eyes felt all night long (and they look better too) after doing this. Now I am going to hit this full force and keep doing this every single morning and every single night and see what happens. (I fell by the wayside on the Wet Ones, b/c they dried out my skin in the eye area too much, sadly). But I did mention in a previous post that my skin under my eyes felt like it was "pulling" and it was VERY crinkled looking and pulling upward. After doing this, it seemed to lessen that feeling (and it looks better too). I am hoping and praying that with dedication and persistence in encouraging my m glands to produce oils again, this could be something to get excited about. I sure hope so, but wanted to share. Has anyone else had success in doing this persistently? What inspired me to really get to it was watching the video today on the BlephEx procedure. I can't afford to get that done so I thought to myself, well I can certainly deeply clean and stimulate those glands on my own at home (especially after I saw all the gunk that the lady in the vid had come out of those areas). I saw some of the same thing with my own eyes after doing this and it is giving me some hope so I thought I would share.
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I had BV a few years ago but it was very minor and managed w/ antibiotics... So my long time boyfriend and I recently got back together about 2 months ago and we were apart about 2.5 years in that time I had a few initiate relationships but never intimate enough to let them ejaculate inside me which leads me to believe my boyfriend's semen has caused the BV because it was almost instantaneous.. I am not suffering from any other symptoms other than the odor which is causing a severe problem with intimacy. We just got back together after so long and all we want to do is have sex but I feel extremely insecure. I've come to a point in my lifestyle where I would prefer to use natural methods rather than antibiotics which led me this discussion. I have purchased a number of different treatment options such as the vitamin c w/ rose hips, acidophilus, tea tree oil and folic acid. I'm not sure what to try first and how long I should wait to try another treatment if not successful. I'm ready to get my confidence back!
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I'm now 10 weeks post op and I have two lumps on my big toe and can clearly feel the pin,I'm in pain was wondering if anyone else has experienced this.
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I am now 30 years old. I did not have serious acne problem on my face until the age of 27. Since the age of 27, my face started to have acne as shown in the images as attached. They usually start with little lumps under the skin. If I apply pressure to it, luckily there will be some grease in white color coming out from the pore, but more often the grease fails to come out, and the area becomes darker and darker, water starts to diffuse out of the area. Then the area starts to become painful ....
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My pee smells like asparagus but didn't eat any, can something you eat cause this besides asparagus?
About two weeks ago, I noticed a pain in my back together with the asparagus smell, I took an antibiotic for a few days, the pain cleared within a day but the asparagus smell did not clear.
Two years ago my pee smelled like asparagus too and since I was convalescent from a physical injury and had antibiotics I took them and the smell cleared. Am a celibate person with clean health habits so it could not be an std, and I don't have any of the symptoms of a uti. Can something you eat besides asparagus cause this?
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I have been getting these lumps for a few years now every time I go to the doctors they put me on antibiotics the seem to go in a few weeks but then they come back .....
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I have a problem with easy bruising. I am 40 years old, reasonably fit and have no major health issues. For the past year I have noticed that I have been bruising very easily, and in particular the bruises are always quite hard lumps. I even had some pretty big haematomas on my legs after a few knocks playing football.
Anyway I have been to my docs, and had all the basic blood tests and everything came back normal. Then I was referred to a Haematologist for another 2 sets of tests, all of which again were normal - some of the common bruising things tested for were - Von Willebrand's, platelet functions, factor 13, all of which were fine. I think I have pretty much had all the tests that can be had for blood disorders.
So I don't really know what to do now - the specialist couldn't come up with anything really. The bruises are more annoying than dangerous, but I'd like to try and get to the bottom of the issue. I don't have any other problems with bleeding.
One thing that happened that may be connected is that just before I noticed the increase in bruising, I had a second infection of Strep throat (bacterial tonsillitis). I had to go through 3 different types of antibiotics as I was mildly allergic to 2 of them - one gave me a mild rash, the other gave me a sore back (i though it was my kidneys but the doctor checked and said it wasn't). So it may be just a coincidence by it seem to me that this has messed with my immune system and caused the bruising problems.
Currently I am taking a course of probiotics to see if that can re-dress the balance, but it does not seem to be making a difference.
I have a healthy diet, play tennis twice a week and football once a week.
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