skin rash|||If you mean prickley heat the cure is simple take anti histamine tablets i.e.piriton,which you can buy over the counter,it is also the best thing for mosquito bites it stops the itching and inflammation.|||It's called "prickly heat" (also called miliaria)
What's your question?
Here's some info on it:
http://en.wikipedia.org/wiki/Miliaria|||You mean prickly heat I think , so whats the question here then? do you want ways to cure it?|||I think youll find its prickly heat
http://en.wikipedia.org/wiki/Prickly_hea...|||I think you mean prickly heat. Prickly heat (miliaria rubra) is a type of heat rash that lasts. Here the pores of the sweat glands get plugged, resulting in tiny pink bumps or even water blisters. These bumps tend to show up on covered parts of the skin, especially where there is friction from clothing. The forehead (under caps or visors), body folds, the upper back and chest, and the arms are the most common locations. Prickly heat is most common when it is hot and humid, but it can also occur in overdressed infants even during the winter. Applying oils and ointments makes prickly heat more likely (and take longer to clear up). Often prickly heat itches, and older children describe a 'prickly' sensation. The rash can look quite similar to one caused by infected hair follicles (folliculitis), but if you look at the prickly heat bumps with a magnifying glass, no hair follicles will be seen. I like using Stri-Dex Acne Medicated Sensitive Skin Pads; the salicylic acid helps to unplug the pores. Hydrocortisone cream (not ointment) can help with itching. Sometimes antihistamines are needed for the itching (and sleep). If the rash is infected, antibiotics may also be needed. With treatment, prickly heat should disappear within 2 or 3 days.
Saturday, April 24, 2010
I am sick with Lupus and need help! Can anyone answer my questions? I would like to find someone to talk to!?
I have been sick afflicted with a mystery illness since I was 13. By the time I was 18, I had a heart problem, liver disease, a ruptured Gallbladder and Peritonitis (infected abdominal cavity) from which I almost died. I am now 23. For the past three years I have had skin rash, mouth sores, nausea, bad joint pain in my knees and shoulders, fevers, tremors and left-side arm/hand weakeness. In the past year I was in the ER for four bouts of Pleurisy, fluid on the heart and Pnemonia.My doctor told me I had Fibromyalgia and Lupus. Now they are suspecting MS (Multiple Sclerosis) as well. I am depressed and I can't cry anymore. I can't work and I am tired all the time. I take Vicodon, Percocet, Promethazine and Naprosyn. I still don't feel well and I am suicidal. I have a good support system but I am tired of being sick. I want to feel good and be young. I want the opportunity to have children and get married. I have a wonderful fiance and he loves me. Can someone give me advice? Hope?|||Lupus is a thief that steals energy and health, hopes and dreams, and plans for the future. We do get sick and tired of being sick and tired. And I, too, have been suicidal as a result of my lupus losses. I'm not that way now. One of the hardest things is the loss of control. But you do have some control. I am not talking about the power of positive thinking stuff or new age think yourself healthy. I am talking about some positive things you can do. So here is the short list. Hope it helps.
Stay out of the sun.
Learn to handle stress. Meditate. Do small amounts of moderate exercise like walking.
Strive for a healthy diet. With each thing you choose to eat ask yourself if it creates health or destroys it.
Journal. Write for 20 minutes a day every day.
Learn all you can about your medical condition.
Do some kind of spiritual or inspirational reading in the morning and at night.
Do good for others. It improves the world AND the functioning of your immune system. What can you do? Write a letter, make a phone call, listen.
Mild exercise reduces pain and increases energy.
Set reasonable small goals.
Change your thinking. You can't control what is happening but you can control your reaction to it.
Make a list of how much of you still DOES work.
Give thanks for small things-hot water, electricity, a roof over your head, food in your belly, a bed in which to sleep. Half the world does not have these things.
Get professional counseling. A good way to find the right counselor is to call an oncology clinic. Their counselors understand our losses.
Go to www.lupus.org and click on the take action link to email your senators and congressional rep asking them to cosponsor the lupus REACH amendment.
Get others to email them too.
Learn to be fully here in the present moment, instead of in your head thinking about the lupus. Thich Naht Han is a good author to start with. Try Miracle of Mindfulness or Peace Is Every Step.
Resolve to comply with your treatment regimen.
Join a support group. You might get support AND you might be the one to give it. Find support groups at www.lupus.org|||"Where there is life the is hope." Terri Schiavo
I would say I know what you are going through but I don't. What I can say is that at times in my life I have been severely depressed and suicidal as a result.
What I can also say is that I am glad to still be alive. Since these times I have experienced a lot of things, many of which made life worth while many times over.
As for the practicalities of your condition I cannot guarantee results but it seems the modern pharmaceuticals have not provided much relief. In my experience pharmaceuticals can actual make things worse. I suggest reading up on alternative therapies including nutrition, meditation, and body work.
One of the most powerful meditations you can do is the meditation of loving kindness. It entails visualizing someone you love, someone you have issue with, and yourself as happy healthy and enlightened. The basic principle is that energy follows thought. If you can do this in a lucid way it will influence the aforementioned benefits onto all parties.
Finally I believe your spiritual life can be of help. I know it is difficult to believe in a benevolent higher power and suffer the way you do, but I believe having a relationship with God can not only be soothing, but be enlightening at times.
I sincerely wish you alleviation from any needless suffering. I empathize that you are going through what you are. Just keep in mind all things in life change, and in time I believe you will find pockets of relief and hopefully long term solutions.|||You are in bad shape! Go to Wal-Mart and by a gallon of Aloe-Vera Juice and drink it religiously. Mix with grape juice to make it taste good. It will strengthen your immune system!|||Have you seen a doctor yet??
(actually, that was a dumb question)
I'm not quite sure what to do, but that's extremely serious. If the doctor tries to brush it off, you shouldn't agree. I'm really bad with medical stuff. There should be someone out there who can help, though.
Best of luck to you, and I'll be praying for you.
From ~ Kidalanna|||There is ALWAYS hope; you are very young so time is on your side, and they have made great strides in the treatment of both lupus and fibromyalgia. These sites will get you started and there are support groups locally and online for both. All my best and God Bless.
Lupus Foundation of America, Inc.
2000 L Street, N.W., Suite 710
Washington, DC 20036
Phone: 202-349-1155
Fax: 202-349-1156
Fibromyalgia Support Community
• Get immediate support from others like you
• Create and share an anonymous journal
• Learn about treatments and ways to cope
• Get recommendations of medical professionals
Recent Discussion Topics
• very very short survey
• Fight or Die?
• Doctors
• depression..stress...fear...loss of control
Join Our Community|||Ash,
Please hang in there...I do not have Lupus, but have had a number of issues that have plagued me for years. I know the whole downward spiral you feel of never feeling well, what use am I, I have no life, etc.
First of all, I am happy that you have a wonderful fiance. That will help you know that you are loved. I pray that he is supportive and understanding. Next, there are plenty of support groups on line. You can try:
http://www.wehavelupus.com/
http://www.lupus.org/support/onlinesuppo...
http://www.mdjunction.com/lupus
If you do not care for these, do a search for "lupus online support groups. From there, I chose the above three. I hope you find one that you like.
I have celiac disease (intolerance to wheat rye and barley, extremely long list of foods I cannot eat!) and I belong to three online support groups. I find them very helpful.
Please, do not give up. Remember your dreams, that will get you through. Keep a list of all the things that you want out of life, even make a dream poster where you cut out pictures from magazines, like an ocean view house, babies, places you want to travel, and of course a picture of your fiance. Life is worth it, place your poster where you can see it when you wake up and when you go to sleep, or when you are bedridden for the day out of pain you can lie on your side and stare at it.
Another thing, keep a "grateful journal". Every time you are down, write down all of the things you are grateful for and even re-read things you wrote before when you can't seem to write anything at all.
I pray that things will turn the corner for you. Keep your mind positive, that is half the battle.
Best wishes and take care!|||I am sorry you are going through all of that. I have Lupus and been having it for years and i have been through alot. I have almost died a few times,but i made it and you will too. Don't give up hope. There are several sites you can go too. Lupus Foundation of America. or Lupus.com.. Or you can email me and i would be glad to talk to you. Take care....|||Hi there,
I just like to let you know that you aren't alone in this situation, I also have SLE %26amp; I got it when I was young, so it was rather unusual.
For the past years It has been difficult due to the flare up of lupus I almost die %26amp; I lost my kidneys but I had my transplant. I'm also only 24, just want to let you know that never give up, and don't stop believing that some day everything will be better.
Just stay positive, I know it is difficult do so but Lupus is all about Mind Power, if you can take control of what you are going through and knowing what you are up against in whatever situations you are in. Nothing is impossible if you have faith %26amp; hope in yourself.
No one else can make things better for you but only yourself, it is our choice to make the worse situations a better place and future.
In times, I reminded myself that I have a second chance of life, so I attend to live life to the fullest, I hope you do so too.
Don't give up, take care.|||I am so sorry that you are feeling so ill. When I finally found out what was wrong with me, I was actually glad they found something. But it took a blood clot blocking off my left lung and left pulmonary tree before my MD would admit I had a problem. Since that day, I've had alot of ups and downs. Most of the time I try to think about the things that I can still do instead of what I can't do anymore. I'm not saying that I have that positive attitude everyday. But I try. And I know God holds my future. How ever short or long it may be. Just always remember, you didn't do anything to get this disease. It's not a punishment from God. We simply live in mortal bodys that get sick. I pray every morning when I get up. Sometimes that prayer changes a little. On good days I pray, Lord, thank you for getting me up this morning. On my bad days, Lord, please HELP me get up this morning. I hope I've helped some. It's not easy, but it gets real bad when you think your in this alone. Honey, your not. email me anytime you need to talk. God's Blessings. Martha from KY
hml@newwavecomm.net|||Hi Honey, I have also had Lupus since about 13, sadly it was the late 70's and early 80's, they didnt know much. I was having seizures, I was ill a lot, and had mystery symptoms that would come and go. I'm almost 40 now. Like you I was in and out of hospitals a lot, at times I still am. But went on to have 2 healthy , and as they hit their teens typical children. I havent had pleurisy, had mild pnemonia 1x, have dealt with and beat fibro, been tested for MS, beat deppression, been married about 16 years, rather happily, but I can't work. Though I did finsih college and worked through my late 20's. Im now almost 40.
I do understand being sick and tired, of being sick and tired, and have felt suicidal. We do not always have the easiest life do we. I own a yahoo support group, one of our younger girls, is actually pregnant right now. It isnt an easy pregnancy, but she's doing it, we have a few teens or young adults, and they do the best they can. They post sometimes, but their moms are very active, and then they hook their daughters up with the younger ones, so we kind of break off. I know a few of the girls well. I was one of the girls. Its scary, frustrating, and seems to be life ending.
About the Lupus/MS, Ive been tested for MS 3 times in 20+ years. It always turns out that its the Lupus Central nervous system flare action acting up. I also have liver issues, in the form of autoimmune Hepatitis, from the Lupus. It has gotten out of control, but I have a good rhuemotologist, and we always seem to get it under control with medication, and even once with cytoxin, which was not so pleasent, but worked.
But there is hope. While at 40, Im slowed, I have a happy marrige, 2 children, a 21 yr old, and a 13 yr old. I do spend the hot summer months a bit down, but unless I hit a big flare, I fight and have been bouncing back, and getting emotionally stronger since 13. So i know it can be done. My advice, never give up hope, fate or faith, new strides are made more and more often. Medicine is getting better. Just do what the docs tell you, find support outisde your family, you have a man who loves you.... let him. If need be let the dr give you an antideppresent, many in our group are on them, its so commen in lupus. But never give up hope sweetie. I never did, and thats how I am where I am today.
Good Luck, and peace of mind
Chris|||Awwweee
That sucks
Stay out of the sun.
Learn to handle stress. Meditate. Do small amounts of moderate exercise like walking.
Strive for a healthy diet. With each thing you choose to eat ask yourself if it creates health or destroys it.
Journal. Write for 20 minutes a day every day.
Learn all you can about your medical condition.
Do some kind of spiritual or inspirational reading in the morning and at night.
Do good for others. It improves the world AND the functioning of your immune system. What can you do? Write a letter, make a phone call, listen.
Mild exercise reduces pain and increases energy.
Set reasonable small goals.
Change your thinking. You can't control what is happening but you can control your reaction to it.
Make a list of how much of you still DOES work.
Give thanks for small things-hot water, electricity, a roof over your head, food in your belly, a bed in which to sleep. Half the world does not have these things.
Get professional counseling. A good way to find the right counselor is to call an oncology clinic. Their counselors understand our losses.
Go to www.lupus.org and click on the take action link to email your senators and congressional rep asking them to cosponsor the lupus REACH amendment.
Get others to email them too.
Learn to be fully here in the present moment, instead of in your head thinking about the lupus. Thich Naht Han is a good author to start with. Try Miracle of Mindfulness or Peace Is Every Step.
Resolve to comply with your treatment regimen.
Join a support group. You might get support AND you might be the one to give it. Find support groups at www.lupus.org|||"Where there is life the is hope." Terri Schiavo
I would say I know what you are going through but I don't. What I can say is that at times in my life I have been severely depressed and suicidal as a result.
What I can also say is that I am glad to still be alive. Since these times I have experienced a lot of things, many of which made life worth while many times over.
As for the practicalities of your condition I cannot guarantee results but it seems the modern pharmaceuticals have not provided much relief. In my experience pharmaceuticals can actual make things worse. I suggest reading up on alternative therapies including nutrition, meditation, and body work.
One of the most powerful meditations you can do is the meditation of loving kindness. It entails visualizing someone you love, someone you have issue with, and yourself as happy healthy and enlightened. The basic principle is that energy follows thought. If you can do this in a lucid way it will influence the aforementioned benefits onto all parties.
Finally I believe your spiritual life can be of help. I know it is difficult to believe in a benevolent higher power and suffer the way you do, but I believe having a relationship with God can not only be soothing, but be enlightening at times.
I sincerely wish you alleviation from any needless suffering. I empathize that you are going through what you are. Just keep in mind all things in life change, and in time I believe you will find pockets of relief and hopefully long term solutions.|||You are in bad shape! Go to Wal-Mart and by a gallon of Aloe-Vera Juice and drink it religiously. Mix with grape juice to make it taste good. It will strengthen your immune system!|||Have you seen a doctor yet??
(actually, that was a dumb question)
I'm not quite sure what to do, but that's extremely serious. If the doctor tries to brush it off, you shouldn't agree. I'm really bad with medical stuff. There should be someone out there who can help, though.
Best of luck to you, and I'll be praying for you.
From ~ Kidalanna|||There is ALWAYS hope; you are very young so time is on your side, and they have made great strides in the treatment of both lupus and fibromyalgia. These sites will get you started and there are support groups locally and online for both. All my best and God Bless.
Lupus Foundation of America, Inc.
2000 L Street, N.W., Suite 710
Washington, DC 20036
Phone: 202-349-1155
Fax: 202-349-1156
Fibromyalgia Support Community
• Get immediate support from others like you
• Create and share an anonymous journal
• Learn about treatments and ways to cope
• Get recommendations of medical professionals
Recent Discussion Topics
• very very short survey
• Fight or Die?
• Doctors
• depression..stress...fear...loss of control
Join Our Community|||Ash,
Please hang in there...I do not have Lupus, but have had a number of issues that have plagued me for years. I know the whole downward spiral you feel of never feeling well, what use am I, I have no life, etc.
First of all, I am happy that you have a wonderful fiance. That will help you know that you are loved. I pray that he is supportive and understanding. Next, there are plenty of support groups on line. You can try:
http://www.wehavelupus.com/
http://www.lupus.org/support/onlinesuppo...
http://www.mdjunction.com/lupus
If you do not care for these, do a search for "lupus online support groups. From there, I chose the above three. I hope you find one that you like.
I have celiac disease (intolerance to wheat rye and barley, extremely long list of foods I cannot eat!) and I belong to three online support groups. I find them very helpful.
Please, do not give up. Remember your dreams, that will get you through. Keep a list of all the things that you want out of life, even make a dream poster where you cut out pictures from magazines, like an ocean view house, babies, places you want to travel, and of course a picture of your fiance. Life is worth it, place your poster where you can see it when you wake up and when you go to sleep, or when you are bedridden for the day out of pain you can lie on your side and stare at it.
Another thing, keep a "grateful journal". Every time you are down, write down all of the things you are grateful for and even re-read things you wrote before when you can't seem to write anything at all.
I pray that things will turn the corner for you. Keep your mind positive, that is half the battle.
Best wishes and take care!|||I am sorry you are going through all of that. I have Lupus and been having it for years and i have been through alot. I have almost died a few times,but i made it and you will too. Don't give up hope. There are several sites you can go too. Lupus Foundation of America. or Lupus.com.. Or you can email me and i would be glad to talk to you. Take care....|||Hi there,
I just like to let you know that you aren't alone in this situation, I also have SLE %26amp; I got it when I was young, so it was rather unusual.
For the past years It has been difficult due to the flare up of lupus I almost die %26amp; I lost my kidneys but I had my transplant. I'm also only 24, just want to let you know that never give up, and don't stop believing that some day everything will be better.
Just stay positive, I know it is difficult do so but Lupus is all about Mind Power, if you can take control of what you are going through and knowing what you are up against in whatever situations you are in. Nothing is impossible if you have faith %26amp; hope in yourself.
No one else can make things better for you but only yourself, it is our choice to make the worse situations a better place and future.
In times, I reminded myself that I have a second chance of life, so I attend to live life to the fullest, I hope you do so too.
Don't give up, take care.|||I am so sorry that you are feeling so ill. When I finally found out what was wrong with me, I was actually glad they found something. But it took a blood clot blocking off my left lung and left pulmonary tree before my MD would admit I had a problem. Since that day, I've had alot of ups and downs. Most of the time I try to think about the things that I can still do instead of what I can't do anymore. I'm not saying that I have that positive attitude everyday. But I try. And I know God holds my future. How ever short or long it may be. Just always remember, you didn't do anything to get this disease. It's not a punishment from God. We simply live in mortal bodys that get sick. I pray every morning when I get up. Sometimes that prayer changes a little. On good days I pray, Lord, thank you for getting me up this morning. On my bad days, Lord, please HELP me get up this morning. I hope I've helped some. It's not easy, but it gets real bad when you think your in this alone. Honey, your not. email me anytime you need to talk. God's Blessings. Martha from KY
hml@newwavecomm.net|||Hi Honey, I have also had Lupus since about 13, sadly it was the late 70's and early 80's, they didnt know much. I was having seizures, I was ill a lot, and had mystery symptoms that would come and go. I'm almost 40 now. Like you I was in and out of hospitals a lot, at times I still am. But went on to have 2 healthy , and as they hit their teens typical children. I havent had pleurisy, had mild pnemonia 1x, have dealt with and beat fibro, been tested for MS, beat deppression, been married about 16 years, rather happily, but I can't work. Though I did finsih college and worked through my late 20's. Im now almost 40.
I do understand being sick and tired, of being sick and tired, and have felt suicidal. We do not always have the easiest life do we. I own a yahoo support group, one of our younger girls, is actually pregnant right now. It isnt an easy pregnancy, but she's doing it, we have a few teens or young adults, and they do the best they can. They post sometimes, but their moms are very active, and then they hook their daughters up with the younger ones, so we kind of break off. I know a few of the girls well. I was one of the girls. Its scary, frustrating, and seems to be life ending.
About the Lupus/MS, Ive been tested for MS 3 times in 20+ years. It always turns out that its the Lupus Central nervous system flare action acting up. I also have liver issues, in the form of autoimmune Hepatitis, from the Lupus. It has gotten out of control, but I have a good rhuemotologist, and we always seem to get it under control with medication, and even once with cytoxin, which was not so pleasent, but worked.
But there is hope. While at 40, Im slowed, I have a happy marrige, 2 children, a 21 yr old, and a 13 yr old. I do spend the hot summer months a bit down, but unless I hit a big flare, I fight and have been bouncing back, and getting emotionally stronger since 13. So i know it can be done. My advice, never give up hope, fate or faith, new strides are made more and more often. Medicine is getting better. Just do what the docs tell you, find support outisde your family, you have a man who loves you.... let him. If need be let the dr give you an antideppresent, many in our group are on them, its so commen in lupus. But never give up hope sweetie. I never did, and thats how I am where I am today.
Good Luck, and peace of mind
Chris|||Awwweee
That sucks
What is it?
I've just come off my period and my vagina really hurts atm and when i was washing there was like some dead skin/ rash or something?
has my pad just irritated me? or is there something wrong?|||Thrush....not too uncommon. Get something from the chemist.|||Go to the docters and ask about it
has my pad just irritated me? or is there something wrong?|||Thrush....not too uncommon. Get something from the chemist.|||Go to the docters and ask about it
Could they cause this?
My boobs have been hurting a little over a week...i took a test a 2 weeks ago and it was negative. I have just started takin vitex,super primrose, and prenatals 9 days ago...do you think this is just a side effect? has anyone else had this side effect? it doesnt say it is? Vitex does not contain natural hormones. It appears to increase progesterone by stimulating luteinizing hormone release from the pituitary gland. Vitex also normalizes excessive prolactin, promoting fertility.
Female infertility
PMS, especially breast tenderness, cramping, and headaches
Acne, especially if it is related to the menstrual cycle
Fibrocystic breast disease
Heavy menstruation
Side effects are rare. Occasionally, women experience mild digestive upset or minor skin rash|||anything that has any effect on your hormones, especially female hormones can effect your breasts, if your are still concerned, contact your dr.
Female infertility
PMS, especially breast tenderness, cramping, and headaches
Acne, especially if it is related to the menstrual cycle
Fibrocystic breast disease
Heavy menstruation
Side effects are rare. Occasionally, women experience mild digestive upset or minor skin rash|||anything that has any effect on your hormones, especially female hormones can effect your breasts, if your are still concerned, contact your dr.
Embarassment at dermatologist office! Don't know what to do.?
I have never seen a female doctor before my male dermatologist was on vacation and a woman was filling in. I had an genital skin rash. She asked me to stand up and drop my pants. She pulled up a stool and began to examine my penis at eye level to her. The feeling of a woman touching me caused an immediate erection. I appologized and she said it was normal. She continued the examine and pulled my foreskin back and i couldn't control it and ejaculated! I have never in my life been so embarassed! It went all over her hand, arm and her neck. I appologized repeatedly as she quickly turned grabbed some paper towel and left the exam room. A nurse came a few moments later handed me a damp paper towel and told me to clean up and get dressed as she explained my medication.
What should it do? This can't be normal?
I have to see her for another visit next week, do you think she was mad?|||i feel bad for you bro. but you're probly not the only guy who would. its not uncommon for a male to ejaculate while his penis is being handled by a woman at eye level.|||damn, that some funny crap right there. You will be the talk of the office. But on the real side im sure you arent the first|||I'm not a doctor but I babysit for a urologist...a female urologist. She has had this happen to her more times than she can count. She says it's embarrassing for both her and her patients but she is use to it. Don't worry, you will turn red but try to control yourself a little better and if you feel like it's going to happen again, move back or put your hand there to stop it from getting on her!|||I'd go to a different Dr. If it's not serious enough that you have to keep the apointment.
What should it do? This can't be normal?
I have to see her for another visit next week, do you think she was mad?|||i feel bad for you bro. but you're probly not the only guy who would. its not uncommon for a male to ejaculate while his penis is being handled by a woman at eye level.|||damn, that some funny crap right there. You will be the talk of the office. But on the real side im sure you arent the first|||I'm not a doctor but I babysit for a urologist...a female urologist. She has had this happen to her more times than she can count. She says it's embarrassing for both her and her patients but she is use to it. Don't worry, you will turn red but try to control yourself a little better and if you feel like it's going to happen again, move back or put your hand there to stop it from getting on her!|||I'd go to a different Dr. If it's not serious enough that you have to keep the apointment.
Embarassment at dermatologist office! Don't know what to do.?
I have never seen a female doctor before my male dermatologist was on vacation and a woman was filling in. I had an genital skin rash. She asked me to stand up and drop my pants. She pulled up a stool and began to examine my penis at eye level to her. The feeling of a woman touching me caused an immediate erection. I appologized and she said it was normal. She continued the examine and pulled my foreskin back and i couldn't control it and ejaculated! I have never in my life been so embarassed! It went all over her hand, arm and her neck. I appologized repeatedly as she quickly turned grabbed some paper towel and left the exam room. A nurse came a few moments later handed me a damp paper towel and told me to clean up and get dressed as she explained my medication.
What should it do? This can't be normal?
I have to see her for another visit next week, do you think she was mad?|||lol, that's funny.
What should it do? This can't be normal?
I have to see her for another visit next week, do you think she was mad?|||lol, that's funny.
I have a problem!!?
I have a problem. I have a skin rash called exczema (x-a-ma). A lot of people don't like me, just because of it. They pretend they have a spray, and they dis-infect everything, and i want the to stop... How do i do that?|||go see a dermatologist.
Start growling at those bastards. Seriously. They won't suddenly begin to like you but they will stop "spraying" you.|||One of my friend had a same problem. you can use E45 cream it does work but before you use it take a advise to you GP.|||see your local dermotologist. ask your parents to take you to one, it is a serious condition. they can give you medicine. you can contact me, I have an all natural product that is topical and may help you. please, if you really want help, contact me and I will send you information, maybe even a free sample.
god bless and good luck. and remember, it is not our skin that makes us beautiful, it's what is in our souls.|||for one, that is really very rude of them. I would personally say something along the lines of it being hurtful to you, and you would appreciate it if they could knock it off. Let them know that karma is a *****!! Have you tried going to the tanning bed? I have a friend that has pretty severe excema, and she keeps it under control by tanning. Worth a shot?|||First of all, disregard the first answer.
Next, call you doctor and make an appointment. There's ointments available.
Also, find ways to decrease stress in your life.
Grace to you!|||they're a**holes!
it's all karma. it'll come back to them i promise =]|||Well I don't know where your eczema breakouts normally happen, however I have a very good friend with it. It is really too bad that people are so idiotic and naive about it. I would just tell them, yeah I have a skin condition not a disease, if you don't like it don't look at it! People will always be rude pigs. If you are looking for a way to help with the breakouts, my friend tans. Whether in the sun or tanning bed it seems to help it to subside. Keep your chin up, if other people want to brag of their idiocy by picking on you, you don't want them around anyway.|||See your doctor. I know some foods can make it worse. It will be trial and error for a while but you can control it. Good luck!|||They are jerks.
Quit reacting to it.
As long as they know that you will react to their B.S. they'll continue to bother you.
They'll find it funny for a while amongst themselves, but it won't last forever, and they'll pick out a new victim for their immature pranks.
At least your imperfections are on your skin, and not in your brain like theirs are.|||People, especially children can be SO cruel. Ignorance on their part is mostly to blame. Maybe if you explain what your condition is to them they would be more accepting. My advise to you is...... Try not to let them get you down and hurt your self-esteem... Find or keep a few VERY good friends that accept you unconditionally. We all have "issues" with our bodies. Keep your HEAD UP.....|||It used to be like that for me. "Ewwwwwwww!!!! thats gross!" :( I have had it all over my body since I was two. Check my 360 blog. It has something like in it. I got a mircal med. from my skin doc.|||Ok...here's my advice... kick some *** but here is the nice advice... ignore them and they will eventually get bored with the joke, but it will feel much better if you hand out a butt whipping... lol... seriously though, take care of yourself go to a dermatologist and dont worry about those people, because it is true karma is a beast....it will come back to them dont you worry. In the meantime know that eczema doesnt make you a lesser person, you are still great and if those people dont want to talk to you guess what? THEIR LOSS!
Start growling at those bastards. Seriously. They won't suddenly begin to like you but they will stop "spraying" you.|||One of my friend had a same problem. you can use E45 cream it does work but before you use it take a advise to you GP.|||see your local dermotologist. ask your parents to take you to one, it is a serious condition. they can give you medicine. you can contact me, I have an all natural product that is topical and may help you. please, if you really want help, contact me and I will send you information, maybe even a free sample.
god bless and good luck. and remember, it is not our skin that makes us beautiful, it's what is in our souls.|||for one, that is really very rude of them. I would personally say something along the lines of it being hurtful to you, and you would appreciate it if they could knock it off. Let them know that karma is a *****!! Have you tried going to the tanning bed? I have a friend that has pretty severe excema, and she keeps it under control by tanning. Worth a shot?|||First of all, disregard the first answer.
Next, call you doctor and make an appointment. There's ointments available.
Also, find ways to decrease stress in your life.
Grace to you!|||they're a**holes!
it's all karma. it'll come back to them i promise =]|||Well I don't know where your eczema breakouts normally happen, however I have a very good friend with it. It is really too bad that people are so idiotic and naive about it. I would just tell them, yeah I have a skin condition not a disease, if you don't like it don't look at it! People will always be rude pigs. If you are looking for a way to help with the breakouts, my friend tans. Whether in the sun or tanning bed it seems to help it to subside. Keep your chin up, if other people want to brag of their idiocy by picking on you, you don't want them around anyway.|||See your doctor. I know some foods can make it worse. It will be trial and error for a while but you can control it. Good luck!|||They are jerks.
Quit reacting to it.
As long as they know that you will react to their B.S. they'll continue to bother you.
They'll find it funny for a while amongst themselves, but it won't last forever, and they'll pick out a new victim for their immature pranks.
At least your imperfections are on your skin, and not in your brain like theirs are.|||People, especially children can be SO cruel. Ignorance on their part is mostly to blame. Maybe if you explain what your condition is to them they would be more accepting. My advise to you is...... Try not to let them get you down and hurt your self-esteem... Find or keep a few VERY good friends that accept you unconditionally. We all have "issues" with our bodies. Keep your HEAD UP.....|||It used to be like that for me. "Ewwwwwwww!!!! thats gross!" :( I have had it all over my body since I was two. Check my 360 blog. It has something like in it. I got a mircal med. from my skin doc.|||Ok...here's my advice... kick some *** but here is the nice advice... ignore them and they will eventually get bored with the joke, but it will feel much better if you hand out a butt whipping... lol... seriously though, take care of yourself go to a dermatologist and dont worry about those people, because it is true karma is a beast....it will come back to them dont you worry. In the meantime know that eczema doesnt make you a lesser person, you are still great and if those people dont want to talk to you guess what? THEIR LOSS!
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