This sounds super irritating, especially when at night all you want is to sleep!
My dad had severe Pruritus upon diagnosis and was prescribed Colestyramine. His itchiness has decreased massively. He still gets itchy but it’s much much lower than it was. It’s prescribed for as and when he needs it, although he has it most nights.
Ask your doctor for their advice, they might be able to prescribe this, or something similar to ease the discomfort.
I'll see the GP and ask for some. On second thoughts the local surgery is so overworked I'll get it from the hospital.
Best wishes
John
Hi readie. You could also try pure potions skin salvation intensive moisturising ointment. You need everything you use to be non purfumed.
I've had excema and itchy skin isn't pleasant. I use elecon which is a steroid ointment on prescription only and must be used sparingly. Don't know if it would be suitable for your needs but may be worth asking about while you're at the hospital ?
My son suffered massively from birth until this year aged 16 when he had his transplant. He has alagille syndrome and this is associated with terrible pruritis and as a small child he would rip himself to shreds. We kept him cool, moisturised, cool showers...pretty much all you are doing really. He did take rifampicin and cholestyramine with limited effect.
Make sure your t/p team know of the increasing issue with pruritus, I know you are already listed and a rare blood group but we were always told that diuretic resitant ascites and quality of life affected pruritus would make you a higher priority.
Hope you get your call soon and all this will become a distant memory.
I am allergic to Dove products so I use sea salt in my bath. Smother yourself in emulsifying ointment. Prescription or a couple of quid from a pharmacy. It is greasy but effective. E45 is the more expensive option! I tend to shower rather than bath and use stuff aimed at children.
The emulsifying stuff really is quite horrible and gets all over your clothes and bedding. But if you are anything like me it is constant washing because of the bleeding! I have a steroid cream too but I try not to overuse it. Mine is, strictly speaking, psoriasis but reading on here I think some of the itching is not linked to that. Certainly my liver is not a happy bunny.
Oh, I scratch till I bleed, especially at night, unless I pile cream on. The flakes are abundant here. I flake from head to toe. Seems to come and go of its own accord. Haven’t got a prognosis, or even a proper diagnosis, and failing to get an appointment with a consultant. I’m guessing no-one is too worried about me. Local hospital are normally really good. One appointment available on 22nd August when I will be abroad. Nothing else available!!
Thank you for your reply. I could get referred to another hospital but I suffer from severe anxiety so I couldn’t get there on my own. My GP is on side with getting things done but it is out of her hands. I would look a bit silly turning up at A&E because my only symptoms are the itchy, flaky skin. Some dodgy blood tests but I simply cannot justify using resources.....
I suppose I am a little too laid back but if there was a serious problem, I would have an appointment, wouldn’t I?
Unfortunately,as I have found out over the years, quiet assertion in needed or just plain old going on and on and on is needed least they overlook you.
I only use baby products now or paraben free products and goats milk soap is worth a try , it’s more an aftercare For the skin of you have been itching intensely.
The itching was getting ridiculous for me also and so I was prescribed hydroxyzine but I had to quickly point out that patients with cirrhosis must not take it. If you can see if they will prescribe you doublebase by dermal it’s relief in a bottle, they do one for the bath, shower and moisturising , it’s not the nicest stuff as you are coating yourself in a film almost but before bed on my legs is a must for me. You can get it online through chemists but it’s pricy , I only found out about it through a friend who’s son has severe MS and so gets bed sores and eczema , otherwise I doubt the doctors would even suggest it to me
Oh I hope you do find something , I was like that on the tops of my feet and hands . I think the problem is that’s everyones skin is different so whats works for another doesn’t always work for you, a lot of trial and error but stick with it!
I greatly, greatly reduced the frequency and intensity by taking Alpha Lipoic Acid and (standardized) milk thistle. It's working wonders for me- health food stores usually have it. ( Avoiding potassium seems to help, too.) When I do itch (excessively) I apply pure tea tree oil to the area(s). Gold Bond lotion with colloidal oatmeal helps a lot after a shower. Vitamin B complex, among others, is also suggested.
One of my husband's doctors recommended Alpha Lipoic Acid for itching also. The doctor suggested 600 mg and I found a store that sells it in capsules of 600mg so he only has to take one capsule which he does after supper. It seems to have helped.
We also both use cornstarch [carefully due to its fineness] in areas of creases or around the waist.
I'm trying menthol cream as it cools the skin... For a little while anyway
Best wishes
John
Hi,
With regards to the above post mentioning the use of Milk thistle, The British Liver Trust does not recommend the use of homeopathic or herbal remedies for those with any liver problems as these have to be processed by the liver and could potentially damage the liver.
More research needs to be done on the use and safety of such remedies and therapies.
If you are considering using complementary or alternative remedies &/or therapies always discuss this with your doctor.
Here is the link to our webpage on Complementary & Alternative Medicines;
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