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Did you get a hive where your cpap mask pressured to your face because I am and not sure if I should just start taking my prednisone daily again or what. Thanks
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Hi,
What is the wheat free diet? I am at my wits end with this pressure Urticaria, I am currently trying to loose weight but even the walking is making me swell and the pain at night is depressing me even more than the pain during the day!
One can only take so much.

Kind Regards
Kel
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I am also suffering. But it gets cured when I sweat it out. Regular exercise.. when I exercise for 5 days it gets disappeared.
Try it out nothing to loose
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Exercise .sweat it out. Believe me. I was also suffering.. my email ***this post is edited by moderator *** *** posting of private information such as name, phone number or email address is not allowed in order to protect your privacy*** Please read our Terms of Use

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Hi there are u taking oil cbd ? How is it going? Is it working?
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Does any one with dpu also have chronic sinusitis? I have only dpu whis out classic urtricarial rush. Usualy my dpu controlled by cetirizine, loratadine, bilastine, but when I get cold with hight temperature drus stop working. Does any one else experience this? My allegist told me that dpu is kind of cholinergic urtricaria.
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Hi there
Has anyone tried CBD oil with THC being an autoimmune disease and knowing CBD’s can help autoimmune I thought asking the question might be worth it!
I will try the cutting out of wheat products also
Maybe we are just all allergic to roundup
I’ve had this for 2 years now I do not take pharmaceutical of any type I just push through the pain of it and accept it
Any info on my question would be greatly appreciated
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push through the pain of it and accept it, - I whish I could be so brave, how do you do it, does your face swell?
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I suffered from awful DPU with fevers and thick painful lesions. Only prednisone helped. Then I discovered the trigger. Alcohol. Not just any alcohol. Beer and wine but not distilled alcohols. Further investigation revealed that it was yeast. Avoidance led to complete resolution. A year later I tried beer and completely relapsed. Another year without drinking and I was fine the whole time. Tried wine and it started all over again. So, I just stopped them entirely and I’m 100% healthy.
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Hi DPU Fellas, beacouse of urtricaria, I have checked my stomach whis endoscopy and there was chronic errosion found in esophagus whith out helicobacter, so I try to heal it now. Also i foud some late researches, which say that patiens hwo healed stomach errosion got urtricaria remission, independantly of helicobacter erradication. May be that information help anyone.
Also after 2 years of antigistamines I feel endless soar throat, and endless fever and cough, like my imunne system got broken, doeas anyone else experience that? My family members think I got mad, and create illnesses for myself like hypochondriac. Sorry for bad English
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I've been dealing with this issue for 12 years. It seems I have a lot in common with many here.
I've had several root canals and flu shots
I'm allergic to cats
Stress, alcohol, extreme heat or cold trigger it
Bras, belts, coughing too hard, sitting on a hard surface, holding a heavy object, kissing... Everything seems to make it worse.
If I push through the pain, I'm down for an entire day with the worst fatigue and a fever high enough to make me worry.
I have to be careful coughing... If I cough too hard, my throat will swell just enough to make me feel like I might need to grab the epipen.
Friends and family thought I was a hypochondriac and my doctor thought I was just clinically depressed, until I started taking pictures.

Hopefully one day, DPU will be well known and better treated.
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Check into autoimmune progesterone dermatitis. That is what I have and I get pressure hives and a ton of other symptoms from it.
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I also agree with the Plaqunil. After suffering with severe DPU for years, I started Plaqunil and the DPU almost immediately was gone. I weaned off the Plaqunil after several months, but now know if I have a reoccurance which drug I need.
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Hello, fellow sufferers..

I’m going on 7 years now suffering from DPU, I have had the same symptoms as all of you. And same results from doctors visits. The only thing that has ever helped me, is Prednisone, I have never taking it daily, only in the begging stages of an outbreak, or like now, I’m a fully broke out, on my feet, hands, both hips and butt, I have swollen wheels the size of basketball on my side, but I am out of pills.. It is Sunday, but tomorrow I will see my doctor for a Steroid shot, which usually keeps it away for a few weeks , up to a month. And will also get the prescription refilled for the next outbreak. usually 20 MG will knock it out within 4-6 hours. They start working after about 2 hours. I suggest this method to any of you, as a way to maintain it. It really helps, especially when you know you have work the next morning , or an event to tend to. Good luck, hopefully in the near future, the medical field will get down to the cause and solution of DPU.
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