Psoriasis Pustular

Question: Can Pustular Psoriasis be stopped from spreading? I have been seeing my primary care doc about a skin irritation for a couple of months and it finally occured to me that a family member has psoriasis. I told the doc and she got me an "emergency" appointment for next week. I have looked at a bunch of pics and if I have Psoriasis, it is definately pustular. Does this mean my hands will be covered? Right now the infected area is about the size of a 50 cent piece on the palm of my hand.

Answer: Suzanne, hello. Psoriasis is treatable and yes, it can be stopped from spreading. The problem is that there is no single remedy that would work for all. I strongly recommend that you Don't use steroidal medications doctors prescribe: side-effects are worse than the psor. itself. Check out http://www.psoriasis.org (us) or http://www.psoriasis-help.org.uk (uk) for information and support (both sites have community forums with great people). What helped me personally was the herbal cream and spray from http://www.champori.com It cleared my p. in just under 3 weeks and I haven't had a relapse in more than a year. You may want to try it as well. Best, Bernadette

Question: What percentage of the population in the US has Pustular Psoriasis? Disease with no cure.

Answer: http://emedicine.medscape.com/article/11… This site states that Pustular Psoriasis is uncommon in the US.

Question: how can you get rid of pustular psoriasis? have had for about 8 years and not even the doctors seem to be able to help so if anyone can HELP really appreciate it.

Answer: First be sure it is pustular psoriasis- that is a very very VERY rare condition- only 7 cases per million people in Japan. Next-watch out for triggers: withdrawal of steroids, infections, irritating topical medications, and sunlight may all trigger. third- make sure it isnt a fixed drug eruption. Once qa year go on holiday from all medications to see if spontaneous improvementoccurs- if it does, you may have fixed drug eruption. Next- topical- bland compresses, oatmeal baths. Next- the long listof things that dermatologists try until one works, usally in this order: retinoids, methotrexate, cyclosporine, hydroxyurea, tacrolimus, inflixamab. When you are not on a flare, PUVA will likely help. the reference lists a lot of potential an d promising new therapies.

Question: Does anyone you know have pustular psoriasis? What do they do to treat it?

Answer: I have seen a few people with it. Pus Psoriasis is not infectious type nor contagious. From my reserch, it is related to nutrition problem that causes anti-body problem, meaning your immune system attacks your own system. The nutrition most needed are essential fatty acids and phyto (means plant) hormones, especially alpha linolenic acid ALA. Falx oil has morethan 57% of ALA. Many vegetables, seeds, beans, grains and nuts come with good quantity of phyto hormones. However, you can only cook it below 130C os that you have good fat from the plants. Therefore, do not eat roasted nuts. Keep away from fried foods. If you see the infections, you also can treat it with diluted essential oils (Natural Aroma Water from www.naturalessence.ca). Cortisol stuffs will likely cover the sympton in a short time but problem will get worse. The essential oils I suggested are: lavender, sandalwood, carrot seed, but need to be diluted to be 0.01%-0.1%. If you have dry skin, add 4 drops of one of above essential oil to 120ml (4 Fl Oz) uncooked corn oil, gently apply on the skin for a few weeks.

Question: PLEASE HELP, i have pustular psoriasis on my feet dr wants me to try methotrexate or enbrel? Ive tried creams and steriods nothing seems to work. what are the risk of these drugs and side effects thanks for all your help

Answer: Alright, Methotrexate is a pretty strong drug. It's used in psoriasis as well as in cancer treatments, arthritis, etc. It's use in psoriasis is warranted only when other treatments havent' worked, so I'm assuming that you've already been on other prescription strength meds. As I mentioned, this is a very strong drug. There is a long list of the possible complications and side effects with this drug. The most common side effects are ulcerative stomatitis (mouth sores), problems with blood cells (white blood cells = used to fight infection), nausea, abdominal distress, fatigue, fever, chills, dizziness, and malaise (which means feeling "sick"). If you're taking this drug for psoriasis, then once the beneficial effects are noted, the doctor should reduce the dose to the lowest possible level with long rest periods between doses (again, b/c it's very damaging). Take this medication at bedtime with an antacid (tums, rolaids, etc.) to minimize stomach discomfort. Do NOT take OTC vitamins! Avoid ASA and alcohol (this medication is hard on the liver and ASA and alcohol can cause damage and bleeding). Also avoid contact sports (increased risk of bleeding and increased risk of infection). If you notice any mouth sores report it immediately, b/c that is one of the first signs of toxicity! Keep in mind that some people experience hair loss, but it should regrow after the medication is discontinued. Also make sure to drink at least 2-3 liters of fluid a day to prevent kidney damage. This drug can cause the acid levels in the body to rise, so your urine should be checked for the pH. Because of the increased acid, you may be at risk for developing "gouty arthritis" so if you notice problems with your joints tell your doctor. And because I mentioned earlier that it decreased the white blood cell count, you should avoid crowds and those with infections, also do NOT get any vaccinations while you're taking this medication. Etanercept (Enbrel) is commonly used in conjunction with methotrexate. Some of the more common side effects of etanercept are upper respiratory tract infection (URTI), injection site reaction (this is administered as a shot), headache, nausea, dizziness, infection, rash, abdominal pain, cough, swelling in the extremities. If you're going to be self-administering these injections, just remember to rotate your sites (you can use the thigh, stomach, or upper arm). Your doctor or nurse SHOULD explain all of this and more to you when you receive the medication. Whatever you do, make sure that you don't leave that office without a firm understanding of exactly what you're supposed to do and who to call if you start experiencing adverse effects (especially with methotrexate). These drugs are used to control psoriasis, but just be careful. Methotrexate is a strong drug and can cause serious damage if taken incorrectly. Your doctor should be following you closely while taking these meds. I wish you the best! :)

Question: I need some help; I suffer from pustular psoriasis on my hands and feet.? The doctor's say I could be on steroids but that causes other side effects, that I would rather not endure. But now I am breaking out in other areas they are bumps that are similar to ring worm in shape but it is another form of the psoriasis, it is on my neck and spreading to my stomach and back area also around the back of the neck, they itch really bad, is there something out there to stop the itch and maybe something for the psoriasis that does not cost an arm and a leg?

Answer: I wish I could help here because I suffer from Scalp and Flexural Psoriasis, I know how irritating and painful it can be. Luckily, Im under 16 and get my medication free from my doctor. I use these- go to the shop- e.g. a Supermarket in the toiletry section and look for them wash brushes that you wash your back with. [I dont know what they're called!]. I use one of these every time I have a bath or shower- but I use this with Emulsifying ointment. Go to the medical centre and get some of this. It may cost £9-10, but trust me it lasts like nearly 2 months! Psoraisis can spread on the body very easily so I would recommend trying to keep it down as much as you can. The idea that I said before helps with the breaking out and the itch too. They only cost 99p! Other option- go to the pharmacy and buy some liquid paraffin. This isnt too expensive. It helps with the dryness.

Question: pustular psoriasis!!!? my mum has pustular psoriasis on her feet which is often painful as it cracks repeatedly with walking. she applies oinment fron the g.p twice a day but in my opinion it does not seem to be doing much? i know treatment of this kind of psoriasis is different from other kinds i was just wondering if any body had any remedies or possible treatments we could ask her g.p about at our next visit. Kind regards

Answer: Well I have guttate psoriasis I have had it under control now for a few years but it has recently put an appearance on my face, as the only treatment I can have is steroid based (but that makes your skin thin) I have been using Body Shop Hemp, its been fantastic for me, Maybe you could try it!!!! You might wanna check with the Dr first, just in case, but as its totally natural I cant forsee any problem x x

Question: what do pustular psoriasis look like and what is the cure? please have pictures

Answer: Pustular Psoriasis In pustular psoriasis, fluid filled pustules appear on the red skin. The pustules collapse after a day or two and new pustules appear. If pustular psoriasis appears on a wide area of the body, it can be life threatening. In some cases, pustular psoriasis appears on palms and soles. It is called localized pustular psoriasis. Fever-like symptoms may accompany the outbreak of pustular psoriasis. It is treated with topical or oral medications. This kind of psoriasis needs total care under medical supervision.

Question: I have Generalized pustular psoriasis. I need help.? I got "Generalized pustular psoriasis " about three years ago in grade seven. It has severely affected my life and lowered my self esteem. I recently discovered the name of my condition and I realize it cannot be reversed and will stay with me through out my whole life. I've seen several doctors and they are not help at all. I searched up my condition on the internet and my mother is taking me to see a doctor very soon. This is really affecting me emotionally and I'm really, extremely sad and exhausted on trying to find a cure. What do I do... (I'm only fourteen.)

Answer: you write rather well for a fourteen year old, most of them on here cant even spell right. im sorry hun, i have bad breakouts and thats enough to make me feel like ****, so i know you have to be hurting. all i can say is good luck, and dont be sad :) it will be okay.