Has Anyone Done Keratin Hair Treatment?
Jun 11, 2015
Has anyone done Keratin hair treatment? I want to know how could it is and if they have faced any side effects after that. Thanks in advance )
View 1 RepliesHas anyone done Keratin hair treatment? I want to know how could it is and if they have faced any side effects after that. Thanks in advance )
View 1 RepliesJust wondering if anyone has had any success with laser hair removal as a way of preventing this disease escalating from stage 1? I was just struck by a passing mention in a post by a doctor about antibiotics, and remembered that a few years ago, before my diagnosis, I used to have terrible problems with my upper thigh areas: I put it down to being sensitive to using razors and so invested in laser on that area. Now I don't get bumps there at all, but I do still in my groin and armpits. I would have thought that logically, if there are no hairs, that the area can't get so infected and sore. Laser hair removal is now widely available and relatively inexpensive.
View 1 RepliesI'm looking for advice. My 60 year old father (who has had HCV for more than 10 years; previously treated with Interferon but bad side effects) finished his 12 week Sofosbuvir+Daclatasvir (considered same as Harvoni) treatment a month ago. Already first tests after 2 weeks showed virus was Undetected, but yesterday he received his most recent results and he has a relapse of the virus. He is genotype 1, fibroscan result 4 (close to final stage). He is based in Poland and I'm not sure if our doctors are fully informed of the new generation medications and HCV itself.
Is anyone able to give us any advice? We are pretty desperate and my dad is just so depressed as he thought he finally got rid of the virus (he got infected while on an operation in a public hospital) and now it is back...
Are there any specialists that you are aware of I could possibly get in contact with?
A few weeks ago my bf noticed some bumps in his pubic area. He went to the dermatologist and was diagnosed with molluscum contagiosum, which is thankfully not that big of a deal! He got his treated with cryotherapy. Around this time I noticed a few bumps and because of the area they were in, went to an OBGYN for treatment so my bf and I don't keep spreading it to each other. The OB GYN agreed that they were also MC bumps and lightly scraped each one, then applied an acid treatment. That was a few days ago and while the bumps are mostly gone, the skin surrounding each one is dark and almost looks like a scab in color. Is this normal post acid treatment?
View 1 RepliesDoes anyone here relapse after harvoni treatment?
View 3 RepliesI began seeing bald patches on my head: one rather large one and 2 smaller ones. I also am losing a ton of hair each day. I have been diagnosed with a ferritin level of 8 and an iron level of 28. I am taking 325 mg of iron 3 times a day along with other vitamins. Approximately how long before I see an improvement in hair fallout and regrowth. I am also seeing a dermatologist for corticosteriod injections to help with regrowth in the completely bald spots. I am strongly considering shaving my whole head?
View 4 RepliesI suffer from the problem of hair loss before marriage at the age of 19, where he was my hair loss, which is a dense tuft and continues to now (24 years old) so my hair has become very small and too short
Use Pantene Shampoo
To know what to make .....
I want advice and guidance and your directions even know the main reason
What are the required medical tests ....
I've felt so frustrated for many years. I too was told muscular/skeletal. While experiencing short breath, extremely tired, pain that shoots like a spear on left side from upper rib cage, center of left breast through to back.
In 2012 after hours of waiting, the blood clot I guess hit me hard, I was out, woke in room with heparin drip. Then told blood clot in upper lobe of lung and pleurisy.
After doctor visit Thursday my pain got so unbearable, and cough, husband drove me to ER this past Sunday. Again sat for hours. Then x-rays, and told had pleurisy. Sent home, told to take tylenol and bed rest.
My pain is off the chart now, I can't take NSAIDS since on coumadin.
I'm feeling very spacey, lightheaded.
I can't drive myself anywhere.
I need to work around husbands very long work hours.
And, if do go, what do they do, say, "more bed rest and stay hydrated"?
I don't have money to burn, for such non-sense.
Is there not any treatment for pleurisy at all?
Just recently, me & my boyfriend were diagnosed with Chlamydia. I got treated one week before him...on a Tuesday & was told to wait 2 weeks before having sex again. I did. He got treated a week or so after me but we ended up having sex (with a condom) during the 2 week period he was taking his medication. Is it possible that he could still have the disease? Im afraid now because since then, we've had sex again (with a condom) but we also gave each other oral sex.
View 2 RepliesI'm curious if anyone has any experience using Cialis as a treatment for BPH? Any "unpleasant" side effects?
what is the best treatment for bell's palsy.
herpes zoster and bell's palsy illnesses
I'm a 25 y.o male and have been suffering with stage 2-3 hemorrhoids for two years following a long term stomach infection. For many months local GP's telling me nothing was wrong and to leave it alone. It was only after kicking up a huge fuss did they finally refer me to a surgeon who confirmed I had 3 malteaser sized hems in my rectum. They were treated by banding twice in the course of 4 months to no avail, and eventually I was offered HALO in April this year.
The HALO helped stop bleeding and reduced swelling/pain, but not enough that it no longer affects my life. And the itching - OH MY GOD THE ITCHING!! Also since the procedure I have been experiencing pinching of the nerves which cause sharp stabbing pains. About 90% of the symptoms are coming from the larger of the 3 hems on one side.
I had a follow up with the surgeon last month to discuss surgical removal as the constant itching and pain are still unbearable, but he has refused ANY further treatment on the grounds that it's too soon after my last op and also that it may cause further nerve damage.
While I trust that he is giving me his best advice, I cannot continue to live like this and was thinking about booking further treatment privately. I'm afraid to have a hemorrhoidectomy especially after what he's said, but I was considering going back to less invasive treatments such as banding or sclerotherapy now that the hemorrhoids are smaller.
I would be very grateful for any advice or personal experience you guys could pass on to me as I don't know what to do, I just know I can't "learn to live with it" as the doctors keep telling me.
I have been diagnosed as having Grade 1 hemorrhoids, and it has been suggested I may be treated by having them binded. Has anyone else had experience of this and what does it involve ? I have already had a sigmoidoscopy and am awaiting further results from that. Original diagnosis was from initial consultation.
View 5 RepliesI have been diagnosed with Hep B. I was admitted to hospital with exceptional readings (ALT >4,000, bilirubin 180, all pho 162, gamma get 417, AST >2,500). I've been given various drips and the numbers are coming down. ALT has now halved. In addition to the drips I was also put on Viread.
My physician was concerned how my immune system was attacking the liver and between all treatments, in three days the readings are coming down. My jaundice is going and my urine now looking paler (almost normal).
Given the symptoms indicate a severe acute response to infection, does this suggest my body will put up a good fight to rid itself of the virus. Also, is there a risk Viread could actually lead to my body not developing the antibodies? I've read the following study, which suggests Viread can be highly effective in treating severe acute Hep B and also assist (or at least not inhibit) the development of antibodies.
i realise people are trying to be helpful but when it is said "i promise you or i guarantee you the cramps will stop if you take xyz...." i just tune out. i have seen several specialists over the last 15-20 years without relief and last chance trying a muscle expert in the next couple of weeks. started a diary of the amounts and types of cramps experiencing to give the doc a little picture of my life. at 65 i can unhappily say i will not be here for a long time if i cannot get relief and a decent night's sleep. at the moment i am lucky if i can get an 1 1/2 at a time before i am up under the shower or using a powerful hairdryer to heat the muscles into relaxing. i am not depressed and have attempted throughout my life to put troubles behind and move forward positively. Our children are all grown up and happy with their own family. If this is my reality of life now my husband understands exactly how i feel and my desperation to find relief and peace.
View 3 Repliesmy penis was not straight why is there for any medicine.
View 1 RepliesI have just been copied in on a letter from the Consultant Urologist to my GP giving an update on the appointment I attended following an MRI.
it says:- "Mr "Sailor Sam" was reviewed today. He is a known case of prostate cancer on active surveillance. His PSA has been slowly creeping up suggesting that he is progressing on a biochemical level. In view of this , radical treatment was discussed but "Sailor Sam" is not keen on this for fear of side-effects. His preference is to continue with active surveillance and therefore he will be seen in clinic in 3 months time"
Now on the letter it says Diagnosis:- Gleason 6 adenocarcinoma of the prostate diagnosed in 2012. Latest PSA 3.3
MRI Scan shows T2 N0 - prostate cancer in 43cc prostate gland.
Staging is small volume. A small low signal foucs at the junction of peripheral and transitional zones on the left lateral aspect at the base does show restricted diffusion and is likely to represent a small focus of prostate carcinoma. It is organ defined. No further focus suspicious for prostate carinoma. The seminal vesicles show normal appearance.
The MDT 17.9.15 concensus of opinion - OFFER RADICAL TREATMENT.
So what I would like to hear is what people think about this? My Psa resutls have been May 2013 2.4
Aug 2013 1.5
Mar 2014 1.7
Aug 2014 1.7
Jul 2015 3.2
Sep 201 3.3
I know there are some very knowledgeable people on this site but am I missing something? Offering radical treatment to a 52 year old man with this history? Is that right? I am a Mental Health Nurse myself and work as part of a Multi-Disciplinary Team which is why I am having trouble coming to terms with their conclusion.
Could I ask for the MDT decision to be reviewed by a different MDT? would it make a difference?
Or are they the "experts" who arrive at this decision following a certain protocol. Not sure if there are any NICE guidelines for offering treatment for example.
I know I will need treatment and I recognise we are lucky that we live in a society that has a health service that can help us so much, but is this a case of over-treatment which I've come to hear more and more about
Since last three month I am suffering from Tinnitus – sound like pressure cooker whistling/ summer insect sound coming out constantly and loudly from my Right ear. I have no idea of actual reason of my present symptom of Tinnitus
2. Location of symptom - In right ear
3. What first started it off - May be after a cold and cough infection
4. When it's worse = in evening and night.
5. When it feels better = in day time.
6. My sleep pattern and details of any recurring dreams – Before suffering from Tinnitus I have silent sleep without any disturbance. As about dreams some time I saw flood water dream otherwise no issues.
7. What I am sensitive to – Heat, I don’t like summer temperature.
8. My state of mind – I am not an angry man, normal behavior can work in cold mind and can handle a situation by my brain without confusing (fears, anxieties, attitudes, moods, etc)
9. Any desires or aversions for particular foods, - like sweet items.
10. Details of any major diseases suffered in past – In fact I have normal body and health. I have not suffered any diseases. Oh yea, in 1994 I have small pox.
11. Details of any reactions to other medicines taken.- I have taken some homeopathic medicines of 200c power without guidance’s of a doctor, the medicines were published in a local news paper for acidity. I have a doubt that after taking those medicines without proper advice, tinnitus has attacked me. I consulted ENT specialist, took antibiotic and medicines, but no result.
I am a woman of 56 and have never been overweight and up to these eleven years ago enjoyed good health.
My first symptoms started eleven years ago whilst on holiday in France. My elbow and knee joints became difficult to move and painful, particularly when carrying shopping. A fortnight later on my return to England the pain had increased, my ankles had started to swell and I felt generally very unwell, not unlike an onset of influenza. My doctor thought it may have been an insect bite and prescribed a course of antibiotics which had no effect. He then tested me for Lyme's Disease and put me on a further two courses of antibiotics, none of which made any difference. The Lyme's Disease test was negative.
By this time, six weeks from the first symptoms I was almost bed-ridden. The joint pains were almost unbearable, I felt itchy all over and isolated little bumps that were extremely painful to touch appeared under my skin, two on my hand and one on my rib bone. After a couple of days they disappeared and I was left with bruises. Some of my knuckle and finger joints were swollen and started to become slightly deformed. I found that I was passing water about every 30 minutes and had pronounced anxieties, insomnia and depression....I had never suffered from depression before. I also started to experience heart flutters and eczema in my ears.
In desperation I began searching (pre-Google days) for clues in some home medical dictionaries. I came across gout and one of the recommendations for managing this affliction was to cut out all rich and fatty food. Although I knew I did not have gout I thought my problem may have been related, particularly with my swollen ankles which by then had turned a rather nasty brown colour. I decided to experiment and immediately cut out cheese, butter, mayonnaise, oils and fatty meats to achieve a very low fat diet.
Within two days I was feeling much better and over the course of the next month I continued with my experiment and found that within about 24 hours of starting on a higher fat diet again my symptoms would begin to return. Over the next four years and after spending a lot of money on private consultations with no diagnosis being given my doctor eventually referred me to the Royal National Hospital for Rheumatic Diseases in Bath. The consultant diagnosed Poly-Reactive Arthritis. I told him about my very low fat diet (under 20 grams a day) which I had been trying. He said if that worked for me I should keep doing it. Subsequently I developed lactose intolerance. Symptoms from this appear two hours after eating any dairy but I have not found any known connection between this and Reactive Arthritis. I also developed problems in my lower back and X-Rays confirmed that this was caused by arthritis. I am unable to lift even fairly light weights and cannot operate a vacuum cleaner without getting severe back pains for a couple of days.
The diagnosis of Reactive Arthritis was six years ago and if I keep to my very low fat diet I am able to lead an almost normal life. However, I now find that in the past year I have had an increasing amount of urological problems such as cystitis and what were though to be bladder infections, although all the urine tests proved negative. I have also been investigated for possible kidney stones but again this has been negative although on one occasion there was blood in the sample. I have found out in the past few days through Google that symptoms like this are often associated with Reactive Arthritis and called Interstitial Cystitis.
Recently I found the web site for the Arthritis Research Campaign which has a very good information booklet on Reactive Arthritis and in an answer to my questions advised me that cutting down on fat can make a difference in most types of arthritis including inflammatory arthritis, particularly saturated fats which can increase pain and inflammation in the body.
They directed me to their information booklet Diet and Arthritis on their web site at www.arc.org.uk. In this publication they recommend concentrating on oils such as olive oil, walnut oil and oil from fatty fish. I thought I would again experiment and only eat the fats they recommended even though I felt sure that too many olives and olive oil dressing would cause a reaction. Twenty four hours after crossing my 20 gram threshold my symptoms reappeared then slowly subsided after I returned to my strict diet.
In all of my research I have not come across any suggestion for treatment of Reactive Arthritis by a low fat diet. I only know that it has worked for me so far.
Having had Sepsis 18 months ago and not rid of infections, I now have Prostatitis with bacterial infections of the Prostate. Antibiotics do not seem to be working and i have been reading about Hyperbaric treatment to get at deep sourced infection and clean the blood.
View 1 RepliesMy doctor has started treatment for infertility as I have a problem of PCOS. Doctor has told to do HSG for tube test and also she started ovanac-cc and HMG 75. My query is can I go for HSG and Ovulation inducing treatment simultaneously in the same cycle.
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