I just posted this in my comments on the post below, but decided to make it a post too for anyone that might wonder or might have more information to share.
I had allergy testing done because every year I have sinus problems (to the point I’ve asked a doctor before if they could just cut them out) – and any time I end up congested from allergies, I then end up with a sinus infection – or this last time I ended up with tonsillitis. We know it is allergies because Claritin helps keep the congestion away. I’ve had swollen glands most of the fall & winter this year and my doctor suspected it is also due to allergies. Now that we have tested me and found out what my allergies are, they will mix up a special serum just for me and I will go in once a week for injections. (I think it is once a week – maybe once every two weeks?) This will help me build up immunities to my allergies – hopefully preventing the sinus infections and tonsillitis of my past.
My family doctor just gave me Claritin constantly to fight my allergies, without ever testing to see what they were. I went to an Ear, Nose & Throat specialist for my tonsillitis though, and he is the one that recommended it (I’ve always wondered why no one did it in the past). Now that we know what we’re fighting, we can fight it better.
On a positive note, I called my doctor’s office this afternoon and she had me come in so they could check my itchy arms. They hooked me up with some special prescription ointment that made the itch go away. For now. Cannabis products from https://d8superstore.com/category/cbg may also help reduce the effects of allergies like swelling or inflammation. If stress is what triggers your allergies or any other health conditions, Dab Pens offers products that may help relieve your stress.
1,336 replies on “Itch Relief…”
OK, I think we all need to find a centrally located University Hospital and sit in protest until some doctor finds a cure. Not a temporary fix but a cure!!! This itch is driving me nuts as you can probably tell at this point. I have never protested a thing in my life but I sure would be willing to march on Washington if it would help this miserable itch. It rules my life anymore. I don’t want to go through life drugged to the hilt and still itching. I have tried to get my doctor to pull this website up and read to understand what is going on but to no avail. Just a nod and some more drugs. We are changing again today. I’ve been on klonepin, cymbalta for several months now so its time to change to something else that will have just about the same results because it is still in the same group of medications. I think the main thing they are hoping for is to find something that will make me loopy enough I won’t care if I itch or not.
I’ve been the route of dermatologist, allergist, primary care, neurologist. I have spent enough on this to have had a wonderful month or two luxury vacation. Anymore ideas form anyone else? I’m just rambling at this point. I feel defeated to the max.
JW
My arms have itched for past 20 years. When I was a student I had occasional bouts..now at 48 I have it permanently. It may get slightly worse in the sun but it is much the same all year….particularly bad at the moment..January..no sun. I take amitriptyline tablets 10-20 mg a night and use emollient creams to minimise the itching and the feeling of despair! I have tried higher doses of amtriptyline 100mg which is great for the itch but side effects- extreme fatigue and weight gain – were not good. Has anyone had any success with Chinese medicine?
Hi Sarah ( in Mexico)
I had noticed that I was the only itcher from the southern hemisphere.
I have itched daily, worse at night, from Dec 1st until 17th January. I have tried Telfast allergy tablets, cortisone cream, and am now on Endep 10 mg
for the past two weeks. Also I have been covering my arms when out doors. Now I have managed two days and nights without that terrible itch and have slept through without having to get up for ice packs. I think the Endep has helped, even with such a small dose. I do feel a bit dopey first thing in the morning – that seems to be the only side effect.
Since finding this site, I have been trying to pay more attention to my daily activities and diet to see if I can relate any specifics to the itch.
I have been doing intensive bike riding most days in training for a two-week ride coming up in March. I am wondering if the riding position is causing pressure in my neck and irritating the nerves in that area. Also being out in the sun a lot more, albeit smothered in sunscreen.
I guess I will just keep up the small dose of Endep and hope that will keep the itch at bay. As far as I can remember, it usually goes away in the cooler weather. We are in the middle of our summer in Australia right now.
This year I intend to keep a detailed record of “THE DREADED ITCH”
Jude
Hi
I’ve had this for about 7 years. It started in a small area on one arm and has progressed to both arms. My cure-keep cool!! I only wear short sleeves, with vests when it’s cold and will lean against a cool wall or anything to cool my arms down. I lived in Costa Rica when it started but now live in Washington state. It’s not climate but heat. Oh yeah, try sleeping with your arms out of the covers with a window cracked. I love to be warm but the ithching is not worth it!
Good Luck
thank you all, read most all the postings, just started this mess this fall and been puzzled. Im not one who runs to the dr. and have been putting it off but almost at my witts end. so glad to find this arena and found several good suggestions I will try. Will be glad to share results if any work for me.
what a “affliction”! good luck to all, I will keep reading for more info….I do feel better knowing its not “in my head”
I’ve been awhile writing and I just want to update you. My arms aren’t as itchy (not as intense) but it pops up mostly in the evenings and when I scratch enough a rash forms. My arms have a lot of blemishes on them now and they don’t seem to want to go away, even with moisture creams.
I use Aveeno cream because it’s the only things that doesn’t cause more itching. After reading all the posts I no longer go to doctors. I suppose I will if I’m about out of my mind. In the evenings I usually take a benedryl and after some time the itching stops. The only thing I don’t like about taking this medication is because it is also a sleep aid and acts like a sleeping pill. Fabrics and my arms getting warm, still plays a big part. I don’t use much ice at the present. I dread to see next Fall coming.
Hi, just tried the Vicks Vapor rub, it’s the first thing that’s worked, put it on last night after a stressed ‘itchy’ day of visiting both physio and dermatologist and reading posts on here, what a relief! I can still feel it slightly tingling and it does get hot, but no itch and I slept, oh my god everyone must try it, my poor partner bought it for his cold only yesterday and I’ve swiped it, and it won’t leave my side, well not while it works anyway!!
Saw dermatologist yesterday and told me my itching is not a skin ‘disease’, and they signed be off but they have prescribed Antax anti-histamine which is for the treatment of Brachialradial Pruritis, it also treats anxiety (hey at least when I’m scratching I won’t be anxious about it!!!). I also saw the physio who checked over my neck, reflexes etc., I had a neck injury 3 years ago and was treated by a physio and resulted in having a steroid injection, the itching is in the same arm/shoulder, she can find nothing wrong, but has booked me in for a 2nd opinion in a couple of weeks.
I have copied and printed lots of the posts from here and highlighted several paragraphs that particularly highlighted my problems and although I have produced them at drs, physio and dermatologists, not one of them has looked at it… what can I say, nothing new from reading other posts on here, no one seems to have a clue.
I am blonde blue eyed and fair skin, I don’t tan easily but do sunbathe but not excessively and I go on a sunbed maybe 6 times for 3 minutes each before I go abroad. I live in sunny England so obviously the hot weather is not to blame here! What does concern me however and I’m wondering if any other writers can help me here, is whether to go abroad for a holiday, we had planned to go to the Canaries or somewhere for a week at end of Feb or March time, but not sure if the heat will aggravate my condition, I don’t want to spend my time totally covered up and scratching! Any thoughts or experiences on this would be gratefully received!
Stephanie,
Hi, although I personally never had this, my cousin suffered severely this year. I researched and commented here, we recommended the vicks vapor rub… i called my chiropractor he said that 2 ingredients make it work, which are the same in another one thats prescribed and cant think of what. I still believe its nerve damage… or BP… same thing… My advice if you can tolerate it… take your trip. I wouldnt let it control my life, which may make it worse. You may have to cover up more, as heat seems to agitate… but… Also, check into a chiropractor… if you can go a few times before your trip you may find relief. This is just my personal advise. I wish there was a cure for you guys, I have seen the suffering up close, I know its hard and frustrating. Good luck!
Hi Karie, thanks so much for your advice and reply, I must admit that you may have a point with the BP, as the tablets seem to be working also, I tried using the ointment and the tablets separately and had a few problems but together… I haven’t itched for 2 days! Just some tingling and I’m wearing long sleeves today, apart from a tiny scratching on my shoulder (I put on the Vicks) that has been it!
Hi, just checking in. The site comments have definitely slowed, both here and on the Men’s Health site. For most of us it is that “itch free” part of the year. I quit taking Neurontin in December and have been doing great!
To Stephanie – Although I have itched from Aug -Nov/Dec for many years I also travel in the winter to Mexico & Hawaii, Even though I get tanned I have had no problems with itching. Sun, heat etc seem to have no ill effects until Aug – Nov/Dec. This continues to be the mystery for me.
Hope many of you are for the moment “itch free” and enjoying the new year.
Kathy
hi to all! also just checking in after several weeks away from this site. An update on my nuerontin dosage: I am now at 1800 mgs/day and am virtually itch free. Before my follow-up at the University of Alabama Birmingham dermatology clinic, I was dosing at about 4 hour intervals. Rather difficult to keep up with and complicated. The doctor told me I could just take 600 mgs 3 times per day. Much easier schedule to follow. I am not experiencing any discernable side effects and I do still have a flare-up every now and again, but seldom and only need to use ice for about 10 minutes when it does occur. I’m not especially happy thinking that I’ll be on this medication forever, but I believe it is possible some other remedy may be found in the future and am grateful for the relief now. sweet dreams!
Haven’t updated in a while, but thought I would let everyone know that here it is February and I’M STILL ITCHING!!! Maybe not as bad, but it has NOT gone away by any means. I take Neurontin and Benedryl but they don’t help. I’ve tried the Vicks Vapo-Rub, Gold Bond itch cream and anything and everything else I can find. I’m still using ice at night just to get to sleep and the Neurontin helps me to stay asleep. But I still have itch spells throughout the day and night. I’m also on Allegra and Flonase for a recent sinus infection but they haven’t helped the itching either. I have always had neck problems and will try and find a chiropractor that may be able to help, if that’s the problem. If it is Brachiroadial Pruritis, I can’t seem to find anyone in the medical profession who knows what it is or can treat it. I’m going crazy.
Hi I am a male 53 yrs old with itchy arms. Mainly my right arm in the afternoons and night. I’ve been to all sorts of medicos with no answers. I have spent years in the Australian sun, so maybe that is a cause. I am blonde but with olive skin. Ice works and I also use Vicks vapour rub which gives some relief.
Just finished reading your entire site and must say I am dumbfounded that so many of us suffer from the same symptons. Also, that the majority of Doctors consulted blame “STRESS”. I will definitely E-Mail Dr. Phil in the hopes that someone with some clout can get the medical profession to pay attention to us. Someone posted a question about the electronic itchstopper (sells for 59.95) I purchased one and it works if the itching episode is mild. However, it was no help for episodes that woke me from a sound sleep. Thank you for a very informative site. I plan to visit often in hopes of finding relief from this horrid itching.
I must get my two cents worth in also. I have been reading this site for quite some time and this is what I have to offer. I am 60 years old and have been a sun worshiper all of my life. I am very dark skinned and never really burned but let myself get to the “black” point. I have been suffering from itchy arms for approx. 5 years. It usually starts in October when the cold dry air arrives in our area. However, we go to Florida for 3 months (Dec. Jan. Feb.) and two days after we arrive the itch disappears. Ice has been my only relief but I have purchased Sarna which I understand is a new product on the market and will have lots of it on hand when we return to the cool dry air. I have not read all the threads on this site but I understand that sun causes this condition so why does it go away when I return to the beach and warm weather. I have not sought medical help as I know what they will probably tell me. STAY out of the sun!!! Is anyone on here similar to me???? This itch is unbelievalbe!!!!!!!!
To Ralph Bowler – Since you are “down under” I am curious is your itch is seasonal.
kathy
Hi all
My last post was Jan. 19th when I had just started taking Endep tablets for the itch. I have 10mg per day, and I have stopped itching completely. I can’t believe it. I am still bike riding daily but in long sleeves and suncream everywhere – it is our mid-summer in Australia.
I dare not stop taking the tablets in case the itch flares up again.
Good luck everyone. Life’s a bitch with the itch !!
Hi Kathy
Sorry I forgot to mention that my itch is seasonal. I only get it in our summer months. It’s mainly on my right arm which has probably received more sun over the years as it is the right arm which is closest to the window when you are driving down under. I suspect it could be related to sun damage although I have no sun spots or cancers.
I have read all the posts over the last month and had nothing to add so just watched and waited. I realised that only people with the itch are searching for answers – the others have somehow found a cure and got on with their lives.
1. Mine is seasonal – summer time for the past ten years but in varying degrees. I have it in three areas – both arms and centre back over an old injury.
2. It is worse if I eat bread.
3. It is relieved if my husband massages my upper spine and the knotted muscles on either side and the itch often stays away for a couple of days. Also, seven years ago, I broke my central back and the skin over the damaged vertebrae itches like crazy but it stops with very firm pressure on that part of my spine. I had a deep Thai massage in Hanoi which I thought would kill me but I had no itch anywhere for two years. The deep theraupeutic massages here in Australia only temporarily relieve it.
4. I think it is something to do with a depletion of blood supply caused by damage to the spine and the itch is the body’s attempt to get blood to the area. A couple of minutes of rotating my arms slowly and alternatively in both directions also relieves the arm itch for several hours.
5. At the moment, massage of the damaged areas are the keys for me.
Good luck to everyone.
I woke up this morning with my husbands condition on my mind and it just dawned on my that I’d never written about him. Several years ago Jerry’s arms started itching. Severely intense itching. The best I have determined over the years is that we really can’t tell that it’s seasonal condition. For that first several months we were lucky to get 3-4 hours of sleep a night. He literally had to sleep with ice packs on his arms. We went to our doctor who didn’t have a clue but who sent us to a dermatologist in our area. After our visit with him, he informed us that Jerry had Brachial Radial Pruritus – which is as he stated it, a rare nerve disease – and incurable. He tried creams, antihistamines, etc … on him but nothing worked long term. He told us that doctors have never honestly figured out what causes the disease. Part think it is strictly sunlight related and for the life of me I can’t remember what he said the second reason was. So, he sent us to Baptist Hospital in NC to see a certain doctor who he said was the worlds leading authority on this disease. We made the trip and this doctor basically told us the same thing the dermatologist did. It’s incurabe and the best you can do is help control it, so he put Jerry on Neurontin – which we all know is an anti-seizure med. He told us that that was the best they had to treat the condition. Jerry took about a weeks worth of the drug and said no more. It just zoned him out till he couldn’t even function. I called and talked to Jerry’s chiropractor who is just a sweet heart of a guy. He was very concerned and started doing his own research. He spent a lot of time studying the condition and he called Jerry in to see him. He worked on a specific place in his upper back and the itching was gone instantly. I don’t know exactly where in his back that doc does this, but I could ask if anyone is interested in knowing. The itching comes from this radial nerve that runs in the back of the neck and down the arms. From time to time Jerry’s neck itched like crazy too. Now about once a year his arm will start itching and he’ll go back to his doc and tell him his arms are itching and he will work on that spot and solve his problem.
I think it’s a shame that our medical doctors don’t see the benefits of using alternative medicine along with traditional. Some things aren’t always cured with a pill.
Hi Virginia,
That really is interesting and ties in with the massage helping. I will print out your response and go see my friendly chiropractor. Thank you. Judith
Glad to hear from Virginia about her husband’s treatment. I am going to print it out and take it to a chiropractor. Although I’ve never had a neck or spinal injury, I’ve always had problems with my neck….stiffness and discomfort. Perhaps a chiropractor could help. And even though I live in Georgia, I have NEVER been a sun-worshipper and my itching is not seasonal. It is year-round. This year however, it has creeped up above my elbow, whereas in years prior, it stayed between my wrist and elbow. Both arms are affected. Sometimes just one at a time and sometimes both at the same time. Keeping ice packs on both arms at night is not easy!! I will keep checking here in hopes that someone is finding relief.
I have had this severe arm itching for about 16-18 years. I’ve been to so many doctors, tried every cream, now when it gets unbearable I just scratch to get relief, wipe off the blood and put ice on it for a few minutes. Sometimes I double-dose Claritin. (generic is cheaper and works fine). I too have light eyes and blondish/brown hair, but it seems that so many people of all types have this problem. One year it will be on my left forearm, then it may change to the other arm. Makes no sense at all, just comes and goes as it pleases. I have to wear long sleeves at work so people don’t see the scabs on my arm from scratching. My daughter laughs at me because I’m always telling her “don’t touch my arm!!!
I have also been following an English chatline on itchy arms and a post last night is well worth reading. In summary, the chiropracter/masseur needs to work on C5-6 vertebrae, topical creams don’t help as it is not a skin problem but a new drug called “Lyrica” seems to work wonders.
The site is http://www.men‘shealth.co.uk/talk/
There are many threads and scroll down to Health, then Skin and you will see the itchy arms site. The relevant post is right down the bottom. Good luck.
I thougth I’d post a copy of the message that I posted to men’s health this afternoon. I had called and talked with Jerry’s chiro today and what I posted is from what he told me.
I called this morning and left a message and he called me back a little later. He spent about 25 minutes on the phone with me talking about BRP (Brachioradial Pruritus). He also believes that for a lot of people there has probably been some sort of trauma or such to a person that causes this condition to begin. For Jerry, he did a lot of riding mountain bikes and one day he went over his handlebars and landed hard.
Anyway, Dr. Reagan said that for Jerry’s BRP, he specifically works on levels C5, C6, and C7. He added that depending upon how easily he could gets Jerry’s back to move (or whatever you’d call it) sometimes he also works from T1 – T4, although not necessarily all of these (T’s) at the same time. He said it depended upon how much inflammation he found there as to which one specifically he deals with.
He also said he checked or worked up in the plexis – behind the collar bone.
And lastly he said he remembers having Jerry use cold packs on the side of the itching up on the base of the neck and top of the shoulders.
I totally agree with the statement that the topical creams and ointments just help calm the irritation – they don’t address the true problem which is from that radial nerve. The one lotion that Jerry found that help calm the beast was called Sarna. At our WalMart they don’t have it out on the shelves, you have to ask for it. Dr. Reagan said he spent a bit of time studying that radial nerve and it’s path. Hopefully anyone who wants to visit their chiro. will find one as concerned as ours is, who was willing to do some research and really hunt a solution.
Heartfelt thanks Virginia
Hi, all. I’m a 52 year old and it took me 5 dermatolgolists before I heard the term “brachial radial pruritis” and then I thought, “Thank God, I’m not crazy!” I have cervical dis disease (lots of arthritis and degeneration of discs plus spurs) suffered trauma in a car accident long ago, and this condition is directly related to that. My doctor prescribed a cream with steroids that works, but I need to exercise tremendous willpower to not scratch before it sinks in. Flucinonide is what it is (check that spelling, though – I’m not sure) I also highly recommend another prevention that has worked incredibly since I’ve been doing it for a month – and that is swimming 3x a week. I find that the neck movemnet if I breathe bilaterally releases some of the tension in my neck and is as therapeutic as massage. In any case, the episodes of itching have nearly disappeared – so much so that my arms have completely healed. Try it!
Hi All!! I am SO EXCITED and couldn’t WAIT to get home and write to all of you. I haven’t written in quite a while because I had nothing new to say – just still itching. But I have been reading what all of you have been writing. I FINALLY went to a chiropractor this evening. While talking to the nurse when I got there, I told her I was told 4 years ago that I have a herniated C5-6 disc. I wanted the doctor to know so he wouldn’t hurt me and this was my first time to a chiroprator. She showed me a chart of the spine that diagrams what disc affects what part of your body. Guess what??? C5-6 affects the shoulders and upper arms!!!!! For the past 4 months, the itch has been concentrated in my right shoulder, right upper arm and left upper arm!!! I am so mad at myself for not going to this doctor sooner but, like most of you, I had given up hope of having any relief. I don’t have any relief YET but I feel like I’m on the right track. I have taken every drug the dermatologists could think of to give me. All they did was provide minimal relief, if any. I go back at 7 tomorrow morning for another adjustment and can’t wait!!! I have an ice pack on my neck right now since they highly recommended I use it. I panicked at first because I don’t want ice anywhere near my itchy arms. But with this on my neck, it’s not bad at all. I’ll write more tomorrow evening with any results I may have. I’m not expecting miracles, just relief. We just may be on to something. THANK YOU VIRGINIA!!! If it wasn’t for your words of wisdom, I may not have called the doctor yesterday!!!
Hi Judith and Cathy. You both are very welcome – for whatever small part I may have had. I don’t have a clue why, but when I woke up the other morning it just stayed on my mind to get back online and see what was being said about this disease and to tell how Jerry has been helped. My heart sincerely goes out to anyone who has this. I’ve just wanted time and again to sit down and cry for Jerry.
When Jerry was first diagnosed, all I could find online was statements about the cause being sun related and that was about it. Then I chanced up on one little statement someone had made in some medical paper that was located outside of the US. They brought up the fact that they felt there was a great possibity that the disease could be brought under control/cured/helped with spinal manipulation instead of drugs. This was what I’d been digging for. I immediately called and spent a good hour on the phone with Jerry’s chiro and that got the ball rolling for us. I so hope that you guys get the same relief.
Cathy please continue use of the ice packs the doc recommended. They truly help the inflammation. Every time Jerry goes to see Doc Reagan, he immediately comes home and grabs his ice pack out of the freezer and does exactly what the doc suggested. He’s proven for himself that they are very beneficial.
Please don’t be discouraged if you don’t get immediate relief at the chiro. Encourage him to continue working in that area until he finds the place where you get relief. That isn’t to say that you can’t get immediate relief – I know Jerry did. It was miraculous to witness the change that took place in about 30 minutes.
Hi everyone just wanted to update you from the 1st of Feb, I have been taking Atarax especially for Brachioradial Pruritus, and using vicks, since then, my arm has just got better and better, I hardly need to use the Vicks only use it, if I get a ‘bit’ of itching, and am taking 4 tablets a day (could have up to 5), my arm has stopped burning and flaring up as well this past few days, so although I am not going to shout to the roof tops I’m cured, this so far is working extremely well for me, so for those in the UK who have not been prescribed this (prescribed by dermatologist) please try this.
HELLO ALL, IF ANYONE SUFFERS PRICKLING ITCHING, REDNESS AND BURNING AFTER WATER CONTACT — TRY THIS. STOP EATING SUGR AND SWEETNRS AND START A VERY VERY VERY LOW GLYCEMIC DIET IMMEDIATELY. THIS IS A FREE AND EFFECTIVE CURE, I’M LIVING PROOF OF IT. IN THE FIRST WEEK YOU SHOULD NOTICE IMPROVEMENT.HOWEVER, FOR IMMEDIATE RELIEF TAKE COOLER SHOWERS, AFTER A SHOWER STAND IN THE SUN, WASH-UP INSTEAD OF SHOWERING AND WEAR LONG CLOTHES TO STAY CLEANER LONGER. I’VE TRIED MANY REMEDIES FOR MANY YEARS AND THIS IS THE ONLY ONE THATS WORKED FOR ME, HOPEFULLY IT WILL WORK FOR YOU. TELL EVERYONE!!! barrywilllwin@yahoo.com
Well, three days after deep massage on upper spine, no itch at all except I went to the Blood bank today and they put a conscriction bandage on my left elbow. Within 20 minutes, the whole area was extremely itchy under the bandage which follows my theory about restricted blood blow causing the itching. I took the bandage off, did my rotating arm exercise forwards and back about ten times and the itch just retreated. Twelve hours later, still nothing! I really feel I am getting control of the itch.
I wonder if glucosomine and chondroitin (Shark cartilege) which is good for osteoarthritis would help repair or relieve the damage in the spine which seems to cause the BRP.
Thanks so much to everyone with information on itchy arms. With all the things that Virginia wrote, I feel much more hopeful and I think everyone is getting closer and closer to the answer. My itching had died down for awhile but it seems to have popped up again so I didn’t have much relief. It’s not too intense but it’s always there, worse in the evening and overnight. Maybe it’s the way I sit and/or sleep. I do have a sore neck most of the time and it hurts especially when I hang my head. Would arthritis contribute to this I wonder. I’m not saying I have arthritis because I don’t know. Sorry I don’t have information for you. I wish I could contribute more.
Virginia, Am so glad your husband has been helped by his chiropractor. I was advised a year ago by a friend who is a nurse, altho he didn’t know exactly what I had, that work on C5-6 might be helpful. I am going to get someone to work on me, altho I have not been bothered much by the itching lately. Since your chiro seems to be so helpful and understanding, could you please ask him if he has any explanation as to why most of us are affected by this seasonally(and NOT when the sun is strongest) That is the biggest mystery to me. And to everyone- I have found that coffee aggravates the condition. Has anyone else found this to be true?
Coffee does not seem to aggravate my itchy arms, but I do notice that desserts and sugar sometimes starts the itching. I’ve cut down on as much sugar as I can, but am still going to contact a chiro if it gets unbearable again. Mine has finally subsided a little and my arms are finally healed up. I just dread next Fall. I can’t imagine what the correlation would be to the seasons and a spinal/neck problem. This is such a mystery!
I’ve been suffering from pruritus since October, and it affects my entire body. It primarily kicks in once my body temperature rises, which really sucks because I used to work out regularly. This has affected my entire life, from my work environment (I work in an office) to my personal life. If for some reason I become agitated, it flares. If a particular room that I may be occupying is a tad bit too warm, it flares. If I perform physical activity, it flares.
The only relief I’ve found was, of course, ice. It became so intolerable that I sought the advice of my physician. She placed me on Atarax 50mg daily. This was completely ineffective. So, after a month of ineffective treatment, she referred me to a Dermatologist. He placed me on Doxepin, initially 10mg, and finally increasing it to 30mg daily. Additonally, I began using Eucerin, and some anti-itching lotion which contained menthol, and dimethicone. Although, this was soothing on my skin it was absolutely useless for the itch. After a month and a half of treatment, he finally opted to refer me to an Allergist. This was the best choice anyone has made. He placed me on 50mg of Doxepin, 50mg of Atarax, Allegra, and Kenalog cream. I realize this may appear drastic. However, I am extremely appreciative. His primary motivation was due to my vacation plans to Egypt on March 9. And, because I cannot tolerate the heat, he felt that we had to take drastic measures in order to get this under control. And, I must say that it has been very effective.
I’m planning to minimize the medications upon my return to the States. I hope this has provided some assistance to someone. If anyone intends to replicate my treatment, I would be remiss not to warn you against receiving Kenalog injections. I have read horrible things about it, so I must advise you against it. The cream is fine, but avoid the injections.
Oh, and I am an African-American male, 30 years old, fairly dark complexion (despite my Caucasian, and Native American ancestry).
It has been my experience that, when I heat up, the blood vessels constrict and I itch. High carbohydrate food will also cause it. I do have upper spine damage and I find that I can increase the blood flow to my arms without heating up by just slowly rotating my arms forward and back about ten times each arm, slowly being the operative word. The itch then retreats. Don’t know why this works but it does. I found the topical creams thin the skin, especially if they contain steroids, and this seems to make the condition overall worse. I have had this for eight years, generally in summer and this is the first year I think I understand it.
My itching started slowly about 2 years ago….it began with itching in both my arms just at the elbow…. there was no obvious allergy, and what frustrated me was that I would itch until I made little spots on my skin that would sometimes bleed….I wondered what the problem was but at age 45 put it down to being pre-menopausal…. Just a few weeks ago….I had my first bought of ‘real itch’…the itch was now moving up my arms and was not just itchy, but felt ‘prickly’ as well…..I began itching more often and began to notice that the area i was itching began to ‘generate its own heat’!! I was dumb founded by this as my arm would be cold everywhere else except the itchy part…..I would touch the itchy part and it would be hot to the touch…..and it got worse…..a week or so later it was moving up the the upper part of my arm to my shoulder…. This burning (or feeling of generating its own heat) facinated me as I could not think of anything related to the skin that would result in the generation of heat and wondered about nerve damage…..
so…here I am on this site….reading comments and thinking that I am doomed to a miserable life of itching…..:( Some of my stats are:
1) I live in the north of Australia and it is very hot (perhaps being exposed to the sun more often)
2) This year has been particularly humid (a fungus of the skin: Nah!)
3) I have put a pool in the back yard (some have said chemicals?)
4) I have had a back injury in the past that resulted in tingling across my shoulder blades for some years (this is the most likely cause of the symptoms in my opinion, ie: nerve damage, at 47 years old probably some osteoperosis, and a dash of old bones)
5) I’ve got blue eyes….go figure…lol
Anyway………will be seeking advice and help…..Pray for me please…:)
I
Thanks for your input. The itching mostly is triggered by my arms getting too warm, such as in a very warm room or wearing too many clothes. If I’m cold then the clothing doesn’t bother me. I spend most of my time bare arms when I’m indoors. So heat definitely starts the itching in my case. I’ve also noticed if my arms are constricted they start to get itchy.
Funny how they can get men on the moon but this itch is a mystery to the most intelligent of people. Thanks for listening, once again. Can’t wait for a permanent cure.
Hi everyone,
I haven’t written for months – just suffered in silence and scratched. However, I have just started my annual diet – I give up sweets and chocolates for Lent every year in order to lose half a stone (I had to start 2 weeks early this year as I have put on extra weight) and guess what – the itching is now down to almost zero!! I can only do this for 6 weeks in the year as I am a chocoholic!! I have always been a sun worshipper, so I guess that hasn’t helped either. Can’t stay in when the sun is out. Is there anything you can buy over the counter at a chemist as I don’t wish to go to the doctors?
Hi all fellow itch sufferers
It has been several months since my last entry,the itch has gotten alittle better but is still there. I am astounded at the amount of people from all over the world that are suffering from this and most doctors know nothing.
Thanks Virginia for your Chiro info, I am going to email that one and also #215 (Eva) to my Chiro today then I will make an appointment with her next week. Everytime I go see her she asks how I am doing so I know she is interested.
I stopped going to all the other drs because they weren’t doing anything to help. If you go back and read my first entry #103 which explains all that I have been thru you will understand.
The only things that I have found to be helpful is the ice (but instead of using ice packs I made myself some corn bags to freeze) they don’t seem to be as harsh as the ice packs, also the Vicks cream.
I seem to remember one of the comments was about itching on the legs, has anyone had any problems with that. My sister has leg itching but isn’t exposed to the sun that much. In the past I have itched on one are then the other, this year it was only the left arm (closest to the driving window), it started in late Aug/early Sept and slowed down about a month ago. It all seems very strange that it happens at the end of the summer season here. He have a boat and I have always been a sun goddess…..but no more….we are selling the boat too.
Let you know what happens when I see the chiro next week.
Good sleeping to all
Rosie
Hello all, First let me say I am a 49 year old male / my life’s background is in heavy roadway construction. I have worked “Many” days in the sun and have had “Many back and neck pains for years. I have worked in a office now for over 5 years.
I have had this same “Uncontrollable” burning, prickly, under the skin itch you all have been talking about for over 20 years. Not every day mind you (I would have been in a rubber room if it had), it has came and went through the years (spring, summer, fall). It has been in both arms (top forearm area, from 3-4 inches above my elbow, to a little more than halfway down my forearm, but mostly in my right arm.
Last night I read through every single post while I was close to tears from this burning itch. I have seen a few doctors years ago and neither one could come up with a cure, and both had no idea what it was, stress was mentioned most, Zanax was prescribed but it was no help for the itching. I have tried every thing there is in over the counter itch creams, none of them have worked. Years ago I would use whole tubes of cortizone cream rubbed on both arms then I would cut the toes out of my tube shocks and tape them on my arms so I wouldn’t scratch. I consider myself a pretty tough guy, but when these itching bouts come over me I am taken to my knees, I fill so sorry for my wife at these time’s because I am so irritable that I can’t even be around anybody.
The only thing there is that will cut the pain of this burning itch is……”ICE”. I have used every thing and anything cold in past years. Bags of ice, frozen water bottles rolled on my arms, ice cream containers rolled on my arms, bags of frozen vegetables, bags of frozen chick breast strips…….anything cold or icy. Last night it was frozen black eyed peas( and yes (Rosie,corn is also my favorite :-0). My wife has found me pasted out sleeping on the couch in the morning with thawed out melted bags of vegetables many times. I know this may sound funny but at the time I will do anything to get relief from the “Itch”.
After all this time in pain, this is the first I have done any researching here on the internet. I was so surprised to find so much on the subject, or at least others with the same symptoms. Thanks so much for sharing your thoughts. It really does help to know there are others.
I have to say that after all the years, the doctors, and all the reading last night and this morning I believe there is a direct link to my back / neck pain. Not always, but in some case’s they have shown them self’s at the same time. Like rite now…. For the past few weeks I have had a sharp pain on the right side, between my shoulder blades, this pain also runs up to my neck and down to my forearm with numbing of my fingers. The filling is almost what I have read about carpo-tunnel
I am going to try the doctors again both general and a Chiro, and I am going there armed with all your symptoms and cures,(Brachioradial Pruritus)will be discussed as well as the spine C5-C6 ideas.
Thank you all, and I’m real sorry for “Such” a long babbling of my “itch” history but I fill I finally mite be on to something that will cure this for good.
Please, please, please, please.
Joe
to Virginia, would you please ask the chiropractor why this is not an ongoing thing instead of seasonal? I am really curious as to why its not everyday of every month for 12 months. My itching came back in august with a vengence. I have been on lyrica 75mg and lunesta at night, prescribed by the same dr. in winston salem,n.c. I have been sleeping and not itching for a while now. I have had this for about 5 years. I went for months and months without sleeping and thought i could kill myself. I went to every kind of dr. imagineable in s.c. and n.c. I went to my allergy specialist in charlotte who sent me to wake forest baptist. I am so releaved to be sleeping and not itching, but in my heart i know its not gone. every now and then i’m reminded by a slight itching sensation. i am very interested in this situation with your husband. please see if his chiropractor has an explanation for the on and off deal. thanks for your help.
I’m finally done reading all the previous entries! Took me three seperate sittings, and now I guess I’ll add my own two cents. Firstly, before I forget, I want to mention in case some of you don’t know, there are packs filled with a gel substance that you can buy at drug stores (chemists, for you Britts) instead of actual ice. I have a couple that I alternate. They’re soft and pliable to mould around the curve of your arm and they might even fit under your sleeve. Having said that, I stopped using ice several days ago after reading above (my presentation of this site doesn’t have numbers??) that it might not be the best idea. The explanation made sense so I gave it a try. Whether it’s the reason or not, my itch has lessened. Do what you have to NOT to scratch and NOT to ice, I know it might be impossible seeming especially if you’re at the hight of your spell, but try to distract yourself and see what happens.
This is only my second year with this but I am so determined to find a solution. At first I wanted the cause but now I’ll settle for a solution. I did love some of the eager-beavers earlier who suggested a survey/questionaire be compiled. If I were more computer-literate I’d try myself. Last year it arrived in September (right, upper arm) and lasted ’till March! This fall, like clockwork it came back in September (left, upper arm) so I’m hoping I’m almost done with it again. After it’s peak, in November and December, it’s become more manageable. Perhaps that’s why I can keep from scratching or iceing.
My stats are; female, caucasian, brown hair and eyes, 45, live on the west coast of Canada where it’s temperate, sunny and very dry in the summer and cloudy and very wet in the winter, never really hot or really cold. No known alergies. My history could support either of the suggested causes. I have a notoriously bad lower back and my neck is frequently stiff and sore. I also play a lot of tennis so although I’m relatively fit I’ve had lots of rotator cuff (shoulder) problems and tennis elbow currently (but both on my right side, the itch is on the left this year). I used to be a total sun worshiper in my teens and twenties (in Toronto) but not so bad any more. I have been know to visit the tanning salon in the winter months, but not lately! That’s something I find interesting about this site…how many of us have or do use a tanning bed. Are tanning beds just that common? Or could this be more significant??? I do tend to support the sun damage theory (or something related to weather) a little more than the neck compaction theory, even though I don’t want to, I adore the sun. Here’s why. My back and neck are sore all year round so why only itch September to March? Recently our weather took a dramatic turn from record-breaking rain to steady sunshine. After two or three days of sun my itch was GONE. No itch for several sunny days, I was so happy. Then the rain came back and so did the itch! I don’t know much about atmospheric/barometric pressure and it’s effect on the human body, but perhaps there’s a connection??
Like many of you I’ve tried all kinds of things, many lotions, anti-histamines, sleeping aides, accupuncture, herbs, massage, chiropractor (not a good one I don’t think), psychologist (recommended by the chiropractor!). I’ve been for blood tests and x-rays of my neck (no problems indicated?!).
In the end, here’s what has helped me. A simple remedy for not-too-bad times is an arthritis relief gel sold in Canada as Mentholatum “Deep Cold” Gold (extra strength). It may be what Susan refered to since it has a blue label. It’s probably a lot like the Vicks some of you use (I’ve not tried Vicks). Here’s something funny, I live in an old, drafty house so I need to keep warm but not my one arm so I went to the used clothing shop and bought some cheap (but actually pretty good), soft cotton, ski-type turtle necks ($5 ea.) and cut off the left sleeve! They’re really weird and ugly but around the house they do the trick. I even sleep in one. Oh, too much information!
Finally, I did try the new drug, Lyrica (pregabalin) recently. I took 50mg twice daily for a month (mid Jan to mid Feb) and it really helped but I’d try a higher dose if/when I take it again. Another woman with BRP takes 150 mg twice/day and had better results–hers vanished! I believe I’m coming to the end of my ‘spell’ so I did not go back to my doctor for more (I hate my doctor and the drug is expensive). I do plan to get more for sure if this returns again next year. I experienced no side effects, didn’t feel like I was taking anything at all.
Thanks everyone who’s ‘listening’. I appreciate all the info. and I hope I can help someone too.
Hi again,
I woke up this morning with the same thought as Deborah, if this is BRP why would it be seasonal, I am curious to find out if Virginia’s husband’s chiro has an answer to that. I sent some of the comments to my chiro over the weekend and am going to make an appt for later this week…..we’ll see what she has to say.
Joe, So.CA, when I mentioned the frozen corn bags I wasn’t referring to vegetables per say. I buy dried corn from the pet food store and sew cotton (actually jersey) fabric bags with the corn, then put them in the freezer. They work great because they mold to your arm and the icing isn’t quite as harsh as the other frozen items you mentioned or even the gel bags. I did this because I actually freezer burned my arm so I had to find an alternate before I ended up with an additional problem.
My episodes diminshed somewhat in Jan although I still have some slight itching in my left upper arm occassionaly, almost not enough for icing. I just don’t understand the Aug to Jan (Feb) timeline.
By the way, I am not and have not been taking any medication at all for over a year and a half, it didn’t seem to help me so why bother.
I will let you know what my chiro says.
Rosie
My chiropractor said to tell you to see a “Corrective” chiropractor. Guess there’s a difference. I plan to go for a while. My itching has subsided quite a bit. I’m only using Sarna lotion at night, only because I’m so afraid it’ll start itching again. But so far, so good. I itch just a little, and close to the surface of the skin – not deep – and the intense, prickly sensation is gone. Good luck!!
I am not a sufferer (thank goodness) — but it appears that my father has just started with these symptoms [both forearms — he has poor/slumping posture, and had just switched beds/mattresses when this started; he has also had Shingles].
I do want to point out a fact that strikes me as important, based on all the accounts regarding this being a seasonal syndrome:
The sun starts leaving the northern hemisphere in June, and starts returning in January. August into December (especially) are the months of the year when we (in the north) have the LEAST exposure to sunlight, which is obviously important to our overall health. Secondary triggers of the syndrome like a lifetime overexposure to the sun that has caused nerve damage, and excessive heat triggering nerve-related symptoms, are probably unrelated to the underlying seasonal effects of diminishing sunlight on our skin, seems to me.
I also think the “parallel” factor of both arms triggering at once, etc., makes it clear that this is some sort of nerve/back-related (and under the skin) syndrome as the later posts are indicating. And maybe it’s something a certain type of person is more susceptible to than the general population (former Shingles sufferers, or constant worriers, or very stressed individuals, etc.).
Anyway the “corrective” chiropractor leads sound very much worth pursuing — I hope that turns out to be the answer for people. I wish you all blessed sleep and itch-relief soon.
I’ve suffered with itchy arms for the last ten years.It started during my first pregnancy but stopped as soon as my son was born. Throughout my next pregnancies I suffered again but this time the itch remained.It affects my upper arms and sometimes my neck. I’ve noticed it isn’t really bad during the day, but come night time just after my shower it gets really bad. I don’t get a rash at all and it feels like something crawling under your skin. I’ve been to 4 Doctors over the years and have been told I have everything from Hormonal problems, being allergic to water( itch is terrible after a bath)and also that it could be from taking iron tablets or panadol (get a lot of headaches) It is such a relief to find I’m not the only one suffering from this horrible condition.It has affected my life for such a long time and after reading some of the other entries it scares me that some of you have had this for 20 years or more.I’ve tried Cortisone creams (with minimal relief), Anti histamine tablets, Telfast, Polaramine ect. I haven’t used ice yet but I’m going to give it a try. I am so glad I found this site as it has given me peace of mind that it’s not just all in my head. Lets hope we all have a cure very soon.
Hi all….Cate from Australia here…..12:30 am and i can’t sleep…just finished the ice pack and going to have another go……some comments I’ve been thinking about are:
I don’t think my itching is related to ‘sun’ persay as I do ‘heat’….. being in the north of Aus….I spend most of my time in are conditioning….. and the itch is ok…..but if I heat up….. it starts again…..exercise (swimming in my pool) can do it….or getting into a hot car….leaving the airconditioned house or just laying on a couch made of foam rubber.
I thought it was my back injury that had caused this dreadful itching….but I’m not so sure anymore….. I’m wondering if the back injury results in damaged nerves and the nerves react to heat?……
My other idea is “I have been on anti-depressants (Ciprimal) for 5 years now….could this have injured my neurological system?….
I don’t know….I’ll have to see a Dr soon……
Thanks for your posts everyone…..:)