Tag Archives: Appetite Loss

Appetite Loss

Seeking help…

Is there anyone located in Oregon with advice for ongoing adverse affects from Botox? I have been to every doctor I could get in to. GP, neurologist, Psychiatrist, ER .  None of which have any ideas, answers or advice.  I suffer from severe anxiety, aches in my bones, muscle atrophy, weight loss (40#), no appetitive, chest pain, and nausea. I am 6 months out from last Botox injections. Will this ever end? This is truly a nightmare. If only there were a doctor that would show an interest in figuring this out. I have called Allergan several times. Their answer, “We recommend you contact your provider for this, we have no data to support your symptoms.” Oh my gosh!  Is there any research going on? It seems there are a lot of people suffering.

Someone, please help!

3 year update

3 year update

 

Hi it has been 3 years since my injections. As I’ve mentioned before some of my major issues were the vestibular migraines meaning that I got dizzy and had head painI all along the right side of my face and head. I had eustation tube issues, loud humming in the right side of my head , anxiety swollen lymph nodes, neck pain, eye pain, pressure in my head . About a year ago I also had sudden hearing loss in my right ear .

I was put on 2400 mgs of nueronton and 100mgs of  Nortriptylin . Today most  of my symptoms are gone. I no longer have severe head pain, dizziness or blurred vision. After getting a steroid injection directly through the eardrum my hearing came back.  I no longer have anxiety or swollen lymph nodes. I do however still have tinnitus but it’s a lot lower. I still have to take the nortriptylin or my dizziness and migraine symptoms will come back. I also still have eustation issues but I hardly notice it anymore.

I believe my body reacted to the Botox by attacking itself. I notice that Botox is putting out there more and more side effects, I am glad to see that. I am like 90% back to my normal self . Thank god for the medication. I would say I felt better at the 1.5 mark maybe 2 year mark. Please hang in there it does get better with time. You may have some symptoms that don’t go away but the majority for me have cleared up.

First & Last Botox!

Hi all,  I want to share my Botox experience to warn others.

I received Botox for the first time 2 weeks ago. Having injections around my eyes, between brows and above brows for cosmetic purposes.

This is my Botox diary below..

DAY 1

Botox injections at 12 pm
Bruise to one injection site on right hand side of my temple/crows feet lines.
Black dots in front of eyes for a few moments after the Botox

went home and rested.

Hot and cold tremors and awful feelings of anxiety by 6 pm onwards
Clammy hands and feet
Couldn’t eat all day after injections
Anxiety remained and got no sleep. Dry mouth
Nauseous
Pain to right side of temple

DAY 2
Anxiety hell/Deep feeling of dread
Tremors
Nausia
Clammy hands
Foggy brain
Dry mouth
Twitching right eye
Couldn’t eat all day complete lack of appetite
Knotted stomach
Slept well tho

DAY 3

Slight Anxiety but much better
Foggy brain
Twitching left eye – black dots in front of eyes twice
Dry mouth – peeling inside of bottom lip
Was able to eat lunch & dinner with effort
Not feeling like myself & low

Day 4

Anxiety almost gone
Still have dry mouth
Still don’t feel like myself
Didn’t sleep well, woke 3 times during the night with hot sweats, bed soaked became a bit anxious after waking each time

From day 5 till now (day 14) symptons have gone, anxiety has gone but still get twitching in left eye and black dots in front of my eyes when in bright sun light.

I am hoping this was it for me, a short spell of hell, & never to return. I will never have Botox again even tho the results are good those few days of hell knocked me for six I have never experienced anything like it in my life and never wish to again!

 

 

 

 

Teeth related symptoms

I have been having some teeth related issues and want to know if anyone has any recommendations. Over the past 6 or 7 months I have noticed that my teeth have changed. There is more spacing between them and when I brush them they don’t feel the same. Also, there is a transparent look to them. I have been using a special toothpaste for enamel, but I don’t know if it is helping. I have also been taking a mineral supplement. Another support member has been having problems with teeth related sensitivity to eating cold foods and has had a tooth break off.
Thanks so much!
Wishing everyone lots of healing.
Kris

Botox used to relax my esophagus pre surgery.

I started having an issue with food and liquid going past my esophagus into my stomach about a year ago.  Food would get stuck and liquid would refuse to go down.  My body would hiccup to help move it along or it would eventually go down with quite a bit of pain.  Finally, nothing seemed to be going down and I was waking each night literally drowning in liquid and food.  My doctor sent me to get an upper GI.  The diagnosis was “Achalasia”  my esophagus was literally closed and turned up into what is known as a birds beak.   I was admitted to the hospital and had an upper endoscopy to confirm the diagnosis.  The Gastro told me that I had to make a decision right away whether I wanted to do a “Botox” treatment or surgery.  I asked if he could explain both and he said he didn’t have time.  Later that evening I was being taken to do the “Botox” treatment.  I was told that since it was Memorial day weekend that there wouldn’t be anyone available for the surgery and that the Botox would relax my esophagus until the surgery could be performed.  No explanation on how it was done exactly or any info on side effects or future care or concerns.  Within a couple of days I started to have confusion issues.   By two weeks after the injection I was having pretty serious memory and confusion issues.  I was extremely fatigued and dizziness was starting to be more frequent.  I thought these symptoms were from lack of food and possibly dehydration.  There was some food and liquid going down but not what would be considered usual.  I work with Senior Citizens and know as a fact that quite often major surgeries have been shelved for folks over 80 due to the fact that anesthesia can bring on dementia.  I personally have known quite a few over 80’s that have had anesthesia induced dementia.  So I thought that the problems I was having was from lack of nutrition, liquid and having anesthesia two times in one day for the “Achalasia” confirmation and treatment (Botox).  I scheduled my surgery, called a “Heller-Myotomy” for a little over 3 weeks from the Botox treatment.  I had an event that I was putting on that needed my attention before I could take the time off.  It ended up being the most stressful event of my entire marketing career.  I couldn’t figure out how to organize anything.  The day of the event I was so stressed, dizzy, confused, fatigued and was so filled with anxiety I didn’t think I was going to make it through the day.  After the event, which was a fundraiser, I couldn’t even add up a stack of checks that needed to be turned in before I was off for a couple of weeks to a month for my “Heller-Myotomy”.   Before I went in to the surgery the Anesthesiologist came by to see if I had any questions.  I told her that I was very concerned to go under anesthesia again due to the extreme confusion and memory issues I was experiencing since the two times three weeks earlier under anesthesia.  We decided since I couldn’t eat or drink I needed the surgery.  After the surgery I was extremely fatigued.  Slept a lot, had dizziness and still had pretty severe confusion and memory issues.  I thought they would go away as I healed.  2 weeks after surgery I was still experiencing all the above symptoms but my body was healing fine.  I was on a liquid diet for 30 days but I was getting my nutrition and calories so I didn’t think the fatigue, weakness, dizziness was still connected to the surgery.  About 3 weeks after my surgery and about 6-7 weeks after the Botox injection I started having speech difficulties.  Slurring and confusion on which words to use.  Even stuttering at times.   I feel the surgery for the “Achalasia” was a success.  The symptoms that I have discussed earlier are all over the map.  Some days I feel like I am coming out of it.  Maybe a little more clear, especially in the afternoons, not as fatigued, dizziness will lift although the memory issues don’t seem to lift much.  Then the next day I am trying to work and end up laying my head down on my arm as I try to keep my eyes open and concentrate on the task at hand.  Then the dizziness reappears, and the confusion and weakness along with the speech problems are just as bad if not worse.   I have had a CT scan,  every blood test available, even a spinal tap to try and find out what is causing these symptoms.  Nothing to be found.  My doctor thought I had an adrenal crash and after treatment from doubling my hormones we found that that wasn’t the case.   My surgeon has referred me to an Endocrinologist and I am waiting for an appt. with them.  The surgeon is convinced that I need a different general physician and wants me to meet with the Endocrine specialist.   My daughters father started looking into Botox, botulism poisoning and finally found this site.  I was experiencing such severe depression that I have never had before this wild ride that I literally thought I was losing my mind and asking for prayer from all who knew me to help me deal w/the depression and other symptoms.  When he told me he found this site, I broke down crying.  It lifted the huge dark cloud that had been hanging over my head for quite a while now.  It isn’t gone completely but I can breath just knowing this is real.  I am not crazy, imagining these symptoms.  I am going to do the 5 step detox tomorrow that is suggested from a site about the botulism poisoning.  I am willing to try it to see if I can function enough to do my job.  I may lose my job soon if I can’t find a way to be able to get behind the wheel of a car again, safely, and on the road.   I feel blessed to have found this site and I will keep all posted on my journey and will cherish all your input and wisdom.

Much Aloha for now,  Cathyann

My head is fuzzy and my nerves are tingly….

Hi All,  I am new to the post.  I had my most recent injection crows feet with Dysport on Jan 10, 2014.   What was I thinking… prior to that had Dysport on Oct., 22, 2013 and had full blown chest pains, heart palpitations, droopy eyes and blurry vision, insomnia, memory loss, tingling, dehydration, mouth sores.  I honestly thought it was the flu and my body was just reacting, I now know it was the injection.  For some crazy reason I thought I was better and went for that injection in January.  I am so STUPID!!!!! I have been using botox and Dysport for 6 years  WHAT HAVE I DONE!!

After the injection on Jan. 10 I just had a little blurry vision, which I always blame on my contacts and dry eyes.  Onset of symptoms came 10 days later with chest pains, heart palpitations, blurry vision, insomnia, memory loss, tingling, dehydration.   The worst is the Insomnia and no appetite… I am afraid to eat.    I went to doctor Blood work PERFECT!  Went to cardiologist EKG perfect…. they all said don’t do anymore botox.  I feel as if my memory loss and confusion are getting worse.  My breathing is okay just tight throat, no heart palpitations in the past few days.  My muscle tone is barely there.  My arms tingle and at times I feel itchy on my dry fingers and elbows.  Insomnia and anxiety are full blown, I am a real sleeper so this is making me confused more.

WHAT TO DO??? Please advise, I am scared I am going to die and doing this all alone.  My vision is still weird but clear… Any help for anything is greatly appreciated.   What can I eat so that this doesn’t get worse, what can I take?  Do I go to emergency room?  Will my breathing stop? I am so scared…

I am so sad and lost xo

Sadlady

 

 

 

 

 

 

 

To drug or not to drug…

I go back to the psychiatrist tomorrow morning.  I’ve tried zoloft and now paxil for my anxiety.  Both seemed to work for a short period of time, but then symptoms came back with a vengeance.  Clonazpam works well. I’ve read past posts.  I really want to get off the paxil and not try anything new.  I’d like to just take the Clonazpam when things get really bad.  Usually 1/2 of one works (not sure of the dosage, but it melts in your mouth).  The problem is that I have several family members (extended) that have anxiety.  So do I really need it, or is it just the botox?

I like the simple format, so her is what works for me.

1. acupuncture, more than probably anything else.

2. massage. Like someone else said, at times it annoys me and at times it makes me worse, but when it’s good, it is damn good.

3. Eating clean with a lot of added vitamin B12 and probiotics.  I feel like too many supplements can aggravate the toxins.

4. Talking about it with my husband.  Crying it out when I need to.  I don’t bother to tell anyone else because really, they can’t understand.

5. Wine.  But we’ve been friends for a long time =-)

What DOESN’t work

1. coffee.

2. Strenuous, new exercise.  I tried I total body conditioning class the other day and 3 days later I was full on symptoms.

3. Not sure what else.  We need to start keeping track of triggers.

Finally, I know that this has effected our nervous system.  I know the toxins are in my body.  I feel the twitches, swollen glands, hear the horse voice, am now experience skewed vision, etc.  But what is the goal?  Are we suppose to let our bodies rest or are we suppose to fight hard to get it out?

My story

 

Hi everyone im new here and was so happy when i found this site, i have had most of the symptoms listed on here. 28 year old received about 50 units of botox in forhead and frown lines. It was for preventive of having wrinkles in the future, the Dermatologist convinced me of doing. Same day extremly bad headache, followed by constipation next day and few days later vertigo, head pressure, migranes, unbearable migranes i had to force myself to sleep through it, feelings of being out of it, confused, i would loss my balance all the time couldnt walk. Heat palpitions was given beta blockers, throbbing pain on chest arms neck, back, heartburn , reflux, 3 weeks later shortness of breath, feeling of something stuck in my throath and chest, like food wasnt going down, had MRI on my brain done back in May , nothing found, Cat Scan for lungs nothing found except for enlarged lymph nodes Dr. said it was probably from a recent flu. Many blood tests all came back fine, xrays, pulomonary function tests, echo test , all normal!! Went back to the doctor who did the injections he was so cold and so like not caring and said he never heard of that, “i was probably fighting a virus” before i had the injections i never knew of the black box warnings, the only thing i knew and was the only thing the Dermatologist told me was that i could have a little headache and swelling and drooping eyelid. Time went on and daily migranes, confusion, dizzy, weak, fatigue, lossing balance, shortness of breath, ended up in the ER like 10 times, with them telling me its nothing. On one of the times i was hospitalized because i was so dizzy faint like feeling and my heart rate was now slow down to 39 and 40s and low blood pressure. Was put on a heart monitor and sent home 2 days later , nothing showed up , had upper endoscopy, all normal, this was all back in July. My main concern now is that i still have ao much muscle stiffness all over my chest back and neck and its painful, also under arms, they feel so stiff i cant even continue my singing career, i get so out of breath and faint like feelings, cant use my rib cage muscles , but its always like this not only singing but any physical activity i have diffuculty breathing, even eating, wow its horrible feels like your chocking, my burps seem so hard to come out, i have to force so much, it feels like my esophogus is weak, or stomach too, because food takes long to go down and i have so much reflux of the food and shortness of breath.,, deep breaths are hard to do the pull, muscles feel weak. Im always bloated, gasy, looks like im pregnant. I dont have the headaches and loss if balance and all that was going up on head as much anymore, those symptoms have subsided, sometimes a relapse i have noticed a relapse after using nail polish or dying my hair, im probably sensitive to chemicals now.
Does anyone have these stomach, eaophogus problems and breathing issues,?? Dont know if i should request another endoscopy etc, because from July to now it has gotten worse :-( if i could just go back in time.. My family has a well know Doctor in Brasil he is a neurologist and Cardiologist and his daughter is a Dermatologist, and he is the only doctor who has really helped me along this scary journey. He said everything im going through is because of botox. :-(

Dizzy and Head fog. How many have had these symptoms?

I see a lot of anxiety and stomach issues within this group.  Not had the stomach one yet.  Breathing problems were early on and awful!  However, the brain fog is the worst for me.  I will cry for days because there is nothing else I can do.  And today I am dizzy and feel like I am constantly about to pass out. And my kidneys hurt. How many on here have had the dizziness and brain fog, and for how long?

Thank you.

Heather

Wanted to give some helpful info

I posted on my profile page this info also but wanted to get it out there again.  I am at my 2 month and 3 week post Botox.  My symptoms started the very next day, it was every symptom on the FDA website, I found out later after I could not get help from the ER docs or my own doctor.  So, my husband helped me research reactions, because I could not use my lap top at the time.  We found hope in a woman’s post who fully recovered in only 2 1/2 months.  Who also had the full reaction.  She said no caffeine (that has helped), she said juicing is essential, (so we went out and bought a juicer, and I believe that’s how I got stronger and able eat solid food again),  Drink lots of water (that’s all I drink, except for the occasional lemon and honey water, or a Gatorade).  Now having said all that I will say I was getting so much better.  My bad days weren’t as bad and my good days were longer and very good (Normal days). Last week I had five normal days!  I am still early on so that might be why the relapse last night and today, I feel awful today and my head fog and anxiety came back.  I have no idea why.  But I focus on the fact that I am doing everything to get better and that their are people who have survived this.   I hope that helps some.  God bless and best of luck.

I’m in hell!!!! I don’t k ow what to do. I’m so embarresed.

I had Botox the 7 of may and have been miserable since. I got 28 units in my forehead and between my brows and I’ve been feeling awful. Dr said that she had never heard of my symptoms associated with cosmetic botox. Choking feeling that comes and go’s, ear pressure, stomach burning. I hate this. I wouldn’t get Botox again for ANYTHING!!! I feel like a terrible mother and wife because this has consumed me!!!

Botox is BAD

After 5 years of saying “NO” to Botox for Migraines I agreed to try it. It was a bad decision, I have regretted doing it because I had an acute adverse reaction. It shut down any normal breathing and I got so sick, attacking my respiratory system and infecting my lungs and sinuses. I felt like I have been literally burnt with chemicals. My lungs burn, my eyes burn, my insides burn, my skin burns and I am either sweating or feel chilled with a fever. The paranoia & anxiety beyond explanation, the panic attacks come on out of the blue day & night. Nightmares and frantic night sweats are very frightening. The doctors are eager to give you the Botox, but have no answers or help other than more medicine that is like adding fuel to a raging fire. After 8 months & 8 rounds of antibiotics and steroid treatment I got thrush all over my insides and under my arms I had to take diflucan to clear it and I have had a major flare up of eczema all over my face which will not clear up. Been to lots of specialist & it’s costs me a lot of $ and put me in bed for months. I have had chronic illness’ diabetes, asthma, fibromyalgia, migraines and seizures for years, but they are nothing compared to this adverse reaction to Botox. I think Botox is a BAD idea for anyone! I wish I had continued to say “NO” But sadly I am living with the remnants still in my system. I hope it will end soon, it makes me sad that it has consumed my life. I literally have been trying to recover. There are more adverse reactions to mention in one entry. I hope that relief is in the near future!

Numbness and tingling

Hello all!
I have so much tingling and numbness in my hands and arms. This started happening right after the botox. I am so concerned that this permanent. I really haven’t seen posts about this. Does anyone have any experience with this symptom? I am concerned that I have permanent nerve damage. This is scary.
Also, does anyone have experience with any helpful tips on heavy, sunken eyes?
I would so much appreciate any input.
I hope everyone is improving!
Thank you!

Help

I had cosmetic botox injections 8 days ago and have been searching for answers ever since. I went in for botox above my eyebrows and the “nurse” convinced me to get them around my eyes. I had been having some issues with my eyes and asked if the botox would effect my eye muscles. She said no. She also said that my only other option was to spend $17 thousand dollars on a facelift. So, hesitantly I had the botox injected for crows feet. I had this done by a dermatologist. The nurse is definitely a salesperson. She said that soon everyone will be asking “did you have your botox today?” This is sad. As soon as I had the injections, I felt strange. Not long after them, my head felt like a ton of bricks, dizzy and my right arm felt numb. I called and talked to someone in the office that said there is no way that the botox would cause the symptoms. She said I should just go about my day. Later that evening, I felt worse so I talked to the doctor. Once again I was told there is no way the botox would cause this and said that I should go to Urgent Care because I could be having a stroke. Over the weekend my symptoms got worse. Anxiety, horrible insomnia, no appetite and a panic attack. I have never had a panic attack before. My eyes looked half closed and sunken with bags. My whole face felt tingly including my nose. My right cheek felt numb. It was a weekend that I never want to have again. About 5 days after the injections, I was at work and my face just felt numb and tingly. It was an awful, sick feeling. I am still having symptoms. My throat has been really dry, my head still has a heavy feeling, my eyes are still sunken with bags. I still have an odd feeling in my face and the numb feeling in my arm is horrible. I just really feel out of it. Does anyone know if the botox triggered some sort of autoimmune disease or if my symptoms were caused from the botox and it will go away when the botox wears off? I am hoping for the latter. This is pure torture. Oh, I was also told it was probably allergies.

Anyone sick from a filler only without having Botox?

It seems that the majority of people here have had complications with Botox. There are a few people who mentioned that they had Botox along with fillers and were sick. I am wondering if there is anyone who suffered an injury from a filler alone.

Mornings Just Got Worse

Something sort of snapped in me about a week ago, and the mornings have become unbearable. When I wake up it’s like 90% of me is still asleep. My eyes are swollen and heavy and nothing is moving in real-time. There is strong, high-pitched ringing in my ears. This weekend, both days I slept from about midnight to 10 a.m. and had no great obligations during the day, spring weather, should be a pleasure. But getting up has been the most wretched ordeal imaginable. I splash cold water on my face, slap myself, drink tea, do anything I can think of but I’m moving in this heavy heavy mush of existence. Yesterday I made it all the way to the gym still in this state about 3 hours after waking up. The world was whizzing by me and I’m in this dense bubble. During the day I take 0.5 mg or 1.0 mg of Depas (same as equiv. doses of Ativan) and I might sort of start to come around by mid-afternoon, and by evening I’m more disoriented and dizzy than I am brain-fogged. This pattern doesn’t correlate with any of the psychiatric medications I’ve tried either. I keep a diary and I traced that route. My partner noticed it too the couple of nights I stayed with her about a week ago. Two weeks ago mornings were still crap, but I could sort of scrape myself together. This is so rough.

Please help

I cannot believe how ill I feel. I am on day 9. I had 37 units of Botox around eyes and forehead. I really wish I could turn back the clock. I am 47 years old, My daughters begged me not to do it. Day 2 buzzing in the head and ears, day 3 after the most horrific night of my life with hot and cold flashes, insomnia chest palpitations ,my head felt on fire,anxiety  I went to the emergency room who could nothing but give me  Xanax. I took the Xanax, slept friday night felt ok Saturday, took another Saturday night felt ok Sunday. Thought hmm i’m ok now so did not take one Sunday night. Monday my ears started to buzz felt unwell again, so I took one monday night, woke up the next morning, ears blocked, dizzy weak, a friend took me back to the dermatologist who said he has never had a reaction like this, he looked in my ears said they look stuffed,he wanted to give prednisone but i had it once before horrid side effects. So he said well maybe sinus infection,  he gave me a zpack and i took a double dose of that and a  sudafed. I have been up all night with full blown again like day 3…worst night of my life.full pins and needles, hot/cold flashes, anxiety.  My husband is away on business and i am so so scared. I am not sure wether to take the z pack today or take a xanax or both.I have never taken pills in my life. I have a trip booked to visit my parents in the UK tuesday, I have not been back in 3 years. I am going to have to cancel today. I am beyond devastated. My derm emailed me this morning and said there is a medication called Lyrica that is used to help with nerve pain, but it has side effects of its own. Others medications that can help with nerve pain are antidepressants and mild tranquilizers like Zolft and Xanax. Given your history of sensitivity to medications, I think a short course of Xanax taken at night might be the safest bet in getting you through this.  My Family Dr said the same take the Xanax.  My question is… is there anyone out there that only has this for a few weeks and makes a full recovery or do i have to tell myself  this is it for me, I’m done? My vanity has ruined my life and my families life for good.?

Has anyone taken Lyrica?

On the 5th Jan I stopped taking Endep – I slowly weaned myself off and my last dose was approx 6mg.  I have been incredibly sick ever since.  I am just wondering has anyone taken Endep and come off it?  Did they have any withdrawal symptoms?

I have had intense jaw/face neuralgia, anxiety only on waking in the morning, my teeth are buzzing again, return of the sore throat/mouth ulcers, my ears are feeling blocked again – they are burning and itchy also, I have the car sick/fatigue feeling and am back to crying from exhaustion/frustration on a daily basis.  The most concerning return symptom is the intense neck/shoulder pain – to an intensity that I haven’t had since approx the 12 month mark (I am now at 23 months).

I am sure this must have something to do with the stopping of the Endep?????  My Dr wants to put me on Lyrica which he says serves the same purpose as Endep but without so many side effects (when I was on the Endep I didn’t really have that many side effects from this drug though).  I read your post Soloist and I feel your pain about the relapses – I just feel defeated at 23 months and still dealing with this.  This week has seen the return of Botox thoughts consuming my everyday existence.

This sounds bizarre but for 2 weeks in December I felt so good – slight jaw pain every now and then and some twitches but really feeling good about life – this is probably what prompted me to come off the Endep.

I have seen some of the discussions about auto immune responses to the injections – do people think their symptoms are more Botulism related or auto immune related – I am just confused and worried again.  Katie you mentioned reading a book by a young girl who had an auto immune response – you didn’t say how the book ended – did she recover?

I keep hoping that fact that we haven’t really got any members past 3-4 years on here with severe issues means that eventually all of these things do resolve themselves and people get on with life…..that’s what I am going to keep thinking anyway.  Cameron has once again been my life line – the person who continues to be there no matter how low I get – I can’t even put into words how much this means to me – I only wished he didn’t have to put up with all of this :(

 

Edema/swelling around eyes after botox

Hello everyone,
I introduce you my story :
I was injected in November 2011.
The 1st week : the worse effects, I was very tired, impossible to see objetcs in 3D !! Nausea, dizziness, breathing difficulty, dry mouth, difficulty to speak
1 month: dry mouth, dizziness, nausea, eye problems…
3-6 month : head pressure, headeaches and big big suffering in my brain, insomnia, eyes problems…
1 year (NOW) neurologic problems have decreased à lot !! But I suffer now from à big edema, maybe nettle rash according to doctors, my face is swelling, I first tried Extranaza and antihistamine .. But I am very scarry because swelling does not stop. Have you heard about edema, swelling problems one year after the incident? How can I fight it? And does It disappear? And when? Please I need help.
Thank you, thank you, thank you so much