Experiences with

Hives and angioedema

My symptoms have been allergic in nature with angioedema of the airway, hives and joint pain, burning skin, diarrhoea, urinary incontinence and shortness of breath. Fragrance seems to trigger me the most along with many other variables.

I have had terrible hives and angioedema for the past two days. I look like I've had lip injections. And my hands are both incredibly swollen. I'm itchy to the point of misery. I'm going to see my PCP this afternoon. I already take Claritin and Pepcid daily.

Hi there I'm still waiting on thyroid bloods, but just so I if anyone has ever experienced this? I have had this happen to me alot over the past 2 years as recently as yesterday.. Its starting to fade now. Some are spots like hives but mostly red itchy rash. Thanks x

feeling fed up I started with contact dermatitis on my hands about 8 weeks ago and after numerous creams it’s just still there but this morning I’ve woke up with hives on my hands and all over my legs I’m currently on 200 mg of levothyroxine could my dose need increasing or decreasing does anyone have

Hi again I still have hives. ( back to allergy clinic at end of month) Now I have developed digestive issues both stomach area and upper abdomen. Pains that come and go but seem to be on the increase. I am anxious about this but do you think hashis hives and stomach could all be related? I gave up

I have terrible urticaria at the moment. Had it for weeks and weeks. No known cause. Have seen specialist and was told to take cetirizine up to 4 times day. Now montelukast been added. I do have under active thyroid… on 75 mcg levo. Anyone else suffering with hives and been on this medication? (I

Good day to everyone. I was diagnosed thyroiditis last march this year and started on carbimazole 10mg once a day and propanalol 20mg twice a day. after 3 weeks i developed hives so my endocrinologist changed my carbimazole to PTU 100mg twice a day. I only having hives but not too much during the night

Hi Everyone! Disgusting outbreak of hives. I have been lucky - been awhile. Usually later on in the summer. any rec’s? I am on the east coast not too sunny yet OTC & calamine. chill Any suggestions? 🎱☔️ Ty

Good afternoon, I keep hitting the wall and all I do is call different doctors. It's been since 2.14 since my son ( 11 years old) has been experiencing bad hives daily. Pediatrician send us to allergy specialist, they did not find any allergies and I pushed for more blood work. TPO came back very high

last 6 days i change from lt4 to euthyrox75mg and i am geting hives on fece and arms legs sometimes its few when they go i get them in other part of my body i dont know if i am alegic to euthyrox or is because i am not on right dosage . any one had hives fromm euthyrox?

Hi Folks, I have autoimmune hyperthyroidism, awaiting diagnosis from a consultation with NHS endo but it’s likely Graves given my blood markers. GP prescribed me 20mg of Carbimazole which have been great for 3-4 weeks, only last weekend I have come out in hives. They are traveling, so one day it’s

Hi, new here. I was diagnosed with Graves disease from a thyroid scan two months ago. I've been on Carbimazole for three weeks ( didn't want to deal with side effects so delayed taking it). Yesterday I woke up with patches of hives on my legs and hips. They spread through the day until they were all

Hello all,I have had my levothyroxine increased from 75mg to 100mg approx 2 months ago. I have suddenly developed hives on my face and wondered if it could possibly be as a result of the above increase?apologies of this has already been answered. All the best T

I haven't posted for a while but I developed Hives on my scalp, few itchy spots on my upper body and itchy ears in February. Was given fexofenadine and lotion which calmed the itching down but never went away, every time I've tried to stop the antihistamine I have to start it again. I've got oral lichen

hi I’ve recently received my latest Erfa top up . Conincidentally , I’ve started itching causing raised scatch marks like hives. Do you think this relates to the Erfa or could it be something to do with the dose. I am under a consultant near Bristol so could contact them to raise this new reaction

Hi There, My mum (stage 4 NSCLC with mets to spine and ribcage, Diagnosed Jan 2024, started treatment March 2024) stopped immunotherapy as it's not working, she originally started on the usual cocktail of Pembro etc alongside it, which initially caused some shrinkage but she wasn't tolerating it

Dear fellows, I want to share my positive experience with cancer, and to encourage you to take the similar path. First of all, I thank God for the cancer, this last temptation that he gave me, in order to change myself and become a better person! I was diagnosed 11 years ago prostate cancer with bones

Here’s what they answered. It seems a reasonable answer to me. Anything you think they have missed? What are best supplements for castrate resistant prostate cancer? Sources ncbi.nlm.nih.gov favicon pmc.ncbi.nlm.nih.gov favicon cancer.gov favicon cancer.org favicon prostatecanceruk.org favicon

A short overview history of the development, use, and specific characteristics of the most common targeted radiopharmaceuticals in use today, like Pluvicto, with much content focused on PCa. Very good article with a lot of development history most of us probably unaware of. The following paragraphs are

Hi, I've been on Ibrance and anastrozole for 7 years. The Ibrance got toxic, so I had 2 recurrences. We lowered the Ibrance to 75 mg. No problem. But I was still concerned so we added Metformin. Now the Ibrance is toxic again, so I am off that. I am still in remission. Possible next steps are everolimus