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Heat and itchy skin
 |
Jun 10, 2011 - 11:20 pm
For the past few months, I've developed extreme all-over itching when I get hot - hot flash, hot weater, exercise, anything that heats my skin. It's making me crazy because it's getting hot now. It goes away immediately when I get cooled down. It's like what I imagine prickly heat to be, except not rash or redness. Anyone have/had this? I see oncologist on the 23rd, and this is hardly an emergency, just makes me want to tear all my clothes off (not a pretty sight) or stand in front of an a/c. Because I've never had this before, and because I'm a cancer survivor, it's worrying me. Suzanne |
Joined: Apr 2010
Hi Suzanne, Yes! I have the
Hi Suzanne,
Yes! I have the pricky skin sensation, usually when I am over heated or when I bathe. I mentioned it to my oncologist. She said it wasn't related to BC or chemo (of course, once you're done with chemotherapy they seem to think nothing is related, don't they?) She suggested it might be dry skin. I use lotion and try to keep cool. Sorry I don't know what else to suggest.
See you the 25th!
Chickadee
Joined: Feb 2011
Yes...
I definately experience that itchy, prickly feeling when I get hot...also when taking a shower or bath. I also get hot flashes whenever I wear a hat and wigs. Once I cool down it quickly goes away. I try to keep lotion on to avoid the dry skin. Hopefully, this too when pass, when chemo is over. I still have 3 rounds of chemo to resume in July.
At one time my palms and the sole of my feet were also very itchy. The onc gave me some Aquaphor, Really helped...
Not sure what I'm going to do when I return to work in Sept, since wearing wigs also make me Real hot and ultimately itchy. Hopefully by then, I won't have the itch attacks and hot flashes. ;0(
Any Suggestions???
Thanks for the post.
Mitzi ;0)
Joined: Aug 2016
wigs, scarves, beanie hats
I cannot stand my wig. I just cant wear it. I wear scarves and knitted beanie caps. Sometimes both at same time. And when I am home alone, I take them all off, until I get cold again. Do what makes you comfortable.
Joined: Jun 2010
Heat and itchy skin
I, too, experience the all-over itching when I get hot and then it goes away when I cool down. I get itchy when I'm in the shower, too. I finished chemo October 27, 2010 and it started to appear early this year. My oncologist does not think it's related to the chemo in any way. It's starting to happen less often and it isn't quite so intense.
Joined: Apr 2011
I am so glad you asked that.
I am so glad you asked that. I've had that prickly feeling and I thought it might be in my head! And I'm like you, I haven't told anyone because it seems trivial. Thank you everyone for confirming my sanity.
Joined: Jun 2010
Couldn't possibly by from the chemo . . .
Oh, of course not! "They" won't blame anything on the chemo once it's over. We're supposed to recover completely. Well, how about it went around our bodies doing damage and some of the damage is permanent? All I know is I didn't have this B4 I had chemo (or cancer) just like I had hair before I had chemo and now have only about 40%.
I'm making a list. I see my oncologist on the 23rd and will tell her all the odd things I have now that I didn't have a year ago.
It is interesting to learn from some of you that you, too, have this not related to chemo anomaly. I would not have done anything different - the chemo was important I think. I just wish they'd own up to after effects.
Suzanne
Joined: Feb 2011
Itchy Everywhere
I finished chemo on March 31, 2011. I have had insatiably itchy skin since mid-April. I believe it is related to chemo as our skin begins to get back to normal, shedding and growing new skin and hair, and our bodies cleansing all the chemo chemicals out.
I'm 42 years old and I asked about the hot flashes, sometimes so overwhelming I need to cool down in a shower, or like today, run ice cold water over my head after being outside for a bit. I was told that chemo could very well have thrown me into early menopause which would also explain all the physiological changes.
Joined: Feb 2007
I've found the hormonal
I've found the hormonal therapy...tamoxifen, aromasin affects my skin and it becomes itchy. It's an itch that continues even if you scratch...so annoying!! Just to add to "can't be related to chemo". A favourite saying I hear when I complain about something is "you're getting old". I say, yes but it isn't suppose to be aging 20 yrs in 2!! Hope you find a solution...
hugs
jan
Joined: Oct 2016
Thank God
I thought I was going out of my mind. It took me some time to realize heat was the culprit. I had Stage 3 IDC Breast Cancer. I underwent 8 rounds of chemo, double mastectomy and full hysterectomy adn 9 weeks of radiation. I finished radiation in June and out of the clear blue sky one I was outside and realized my skin felt like I was being stung by bees and bitten by fire ants. As it continued, I realized it was heat - hot showers, hot flashes or the sun, that was causing it. It drives me totally nuts and there is no relief except the the A/C or standing directly under a fan.
I spoke to my doctor who sent me to an Allergist and he advised me that it wasn't allergies - that it may in fact be my anemia. I was always borderline anemic but after the chemo it just went haywire. I am waiting for test results to confirm. He said it's either anemia, the cancer has returned or my skin is still working out the chemo. I'm praying it's just the anemia. I've had 3 iron infusions and my blood count is still a 12 when the range is 12-18.
Sorry for the long post, I just couldn't believe I wasn't the only one. My oncologist looked at me like I was crazy but when I stopped the Anastrozole for 1 month and it was still happening, she realized this was not just a nuisance. If anyone finds out anything else, please post. I will post when I get my blood test results back.
Prayers to everyone and try to stay cool. I live in Florida and I pray everyday for the winter to finally show up.
Tay
Joined: Aug 2016
Thought I had bugs or something
I am glad to hear others are doing this. I am post menopausal. I itch like crazy and think a bug bite me and look at the spot and nope. I even had an exterminator come check the house thinking I got bugs. He said no, your house if fine. It's the after effects from chemo, no matter waht they say, too many of us have this for it not to be. I take benadryl and that helps. Continuing to fight fight fight like a girl. No one comes out unscathed, but our battle scars prove how brave we are. Roar ladies!
Joined: Jun 2010
No more itchy
Since ths thread jumped to the top again and since I started it in 2011, I just want to say I no longer have the itchies. In fact, I'd forgotten all about ever having them. Honestly, I can't remember when they went away, but they've been gone for a long long time, probably shortly after this thread started. I have absolutely no explanation but get it checked out if you have it and it's not normal for you.
Suzanne
Joined: Aug 2016
Itchy, prickly skin sensation
i too have this issue and it is painful! I finished chemo 3/30/16 and it started happening about a month later. I had four rounds of AC and 12 of Taxol. I asked my ONC and she said she had never heard of it and thought it was probably hormonal. I even told her that I had been googling and found other BC patients that were experiencing the same sensation with our skin when we got hot. I do not have to be directly in the sun at all. When it happens I feel painful needle like prickly/ electrical shocks almost all over my body. Even on my head. Then in areas where I perspire I get these tiny bumps under the skin. My only relief is to immediately get something cold on me. I can't even take an evening brisk without it flaring up.
i saw a Dermatologist because I wasn't happy with my ONC answer and she told me it is a form of Prickly Heat rash. She said it is not hormonal. You can get as you age, but more than likely mine was triggered by chemo. Since I have chemo in common with so many other women... I believe it is a lingering side affect. It is caused by nerve damage and not clogged sweat glands.
I do hope this goes away and soon. It makes exercising so difficult and the Texas heat is brutal for most of the year. But then again, it starts up even walking on a treadmill!!
Joined: Aug 2016
I have them now!
I've been dealing with this since April 2016. It started out as an intense itchy feeling, but went to a pins/needles feeling most of the day. I went to a dermatologist at the request of my oncologist, just to make sure I haven't developed any allergies. Well, come to find out I have truncal neuropathy, not from the chemo but from the radiation! It seems when I had my radiation, it hit my spine and inflamed the nerves from my breast line down to my knees! My difference is that mine hits me more when there is any temperature change to my body, be it cold to hot or hot to cold. A neurologist told me to get my Vitamin B levels checked and to have an MRI done on my spine to look for damage. He's telling me that it could possibly be permanent, but we'll see!
Joined: Aug 2016
Curel Anti-Itch shower gel!
Curel Anti-Itch shower gel! Worked wonders on the creepy crawley itch. It keeps the itch away for hours after use.
Joined: Feb 2017
Intense Itch during Hot Flash
I was 57 when diagnosed with IDC Breast Cancer. Beginning Dec 6, 2016, I started: 4 rounds of A/C (the Red Devil) , followed by 12 weekly rounds of Paclitaxel. I then had mastectomy of both breasts. (No radiation) After a hysterectomy eight years earlier, I had been on bioidentical HRT patches, but immediately stopped when I was diagnosed (as the IDC was estrogen positive). I immediately started having hot flashes, and they were worse during chemo... three an hour, followed by cold, accompanied by an intense itching all over. (I liken it to temporary poison oak rash.) Post-chemo, I was prescribed Letrozole (Femara) for the next five years. It is now ten months after my last chemo and I continue to have the hot flashes (one every 1.5 hours and less intense, so getting better) and to experience the itch (though less severe and generally more annoying on my back). I have come to a couple of conclusions: 1) I believe the itch is related to the chemo. I have searched the internet for other women experiencing itch during hot flashes, and only when I added the words "breast cancer" did I find others suffering from this. 2) I think it helps to rub your skin until the dead skin rubs off. Do this with slightly wet skin during a shower or bath. The dead skin will start to ball up and you can wash it off.
I am looking forward to the day when my hot flashes are less than five a day and no accompanying itch! What a relief that would be.
God bless us all.
Joined: Mar 2017
Heat and painful itching 2 years post chemo
Hi all! I finished chemo end of 2014 for TNBC followed by dbl mastectomy, radiation, hysterectomy due to BRCA1+. When I sweat, sit in a too warm tub or too warm shower, hot flash, or anything that makes me warm or sweat, I have the sensation of a thousand needles all over my body then it itches painfully without a rash. I too have asked my oncologist about this. I still see him every three-four months. He denies it has anything to do with chemo. My Gp agrees that is absolutely has something to do with chemo. I wonder if it relates to the drugs used in particular? I had eight rounds of cyctoxin/adriamycn with herceptin. Anyone having these side effects also have these chemo drugs?
All the best,
Gina
Joined: Aug 2016
Itch
I dont know why the ono's act like they dont think it is the meds. It says it right in the pamphlets. I had all the same meds as you adn I am finishing up the herceptin in July and I have those itches all the time. I use a mixture of a lotion over my whole body, vasoline, vit. E , and baby lotion mixed. I slather that on before I go to bed. keeps my skin soft. It helps. Taking benadryl helps some but watch out for leg cramps getting worse. The Herceptin does that too along with the wonderful bone pain. I try to stay away from pain killers but in the first week after the infusion, I got to take them and then I go down to Aleve or Tylenol. The itch comes and goes and I wonder if it is not caused by the stress our bodies have endured, the toxic chemicals coming out our pours. I dont know. My GP wondered it becuase of the stress is it a form of shingles trying to appear. I dont think so. Not all over your body. But she tried to be helpful. Lukewarm baths. Hot baths for the muscle pain. Walking like I am 80 sometimes. Looking it too. The anti-hormone has alot of the same side effects. I am not a happy camper and dont know if I can take 5 more years of it. Feeling very depressed and frustrated by it all.
Joined: Aug 2009
My suggestion would be to see
My suggestion would be to see a Dermatoloogist. They are the Specialist who deal with skin issues.
I did 4 DD A/C (Adriacycin/ Cytoxan) neoadjuvant and 12 weekly Taxol adjuvant. Had no issues like you are, but we are each so unique.
It is also possible that there is a new issue that has developed and not at all associated with any previous TX.
Do find out and get approprIate TX.
Winyan - The Power Within
Joined: Dec 2015
Obviously an SE of treatment...
...or there wouldn't be these posts about it! I get the itchy prickles everytime I have a hot flash. They are an annoyance, and itchy(!), but they only last as long as the hot flash. I was curious if they happened to anyone else which is why I searched and found this thread. At first the prickly-itchies were somewhat alarming but then I noticed a correlation between them and my hot flashes. I haven't even bothered mentioning the phenomenon to my docs, since I know they are related to my treatment. I am currently on anastrozole which is why I have the hot flashes (a known SE of aromatase inhibitors). I had IDC and did the entire poison-slash-burn protocol (ACT chemo, bilateral mastectomy, and rads). I got so tired of all the onc nurses and docs acting like it was the first time they'd ever heard about whatever SE I was having during chemo that I quit asking about stuff unless it was bad and I needed some sort of relief. I found I got more answers by reading these boards! :) I started taking anastrozole in September and it's now March, so it'll be interesting to see if the prickles happen this summer when I'm "hot" independent of the hot flashes.
Joined: Mar 2017
Me too - but not breast cancer
Hi, I came across this thread while Googling "pricking skin when hot following chemo". I thought I would let you know that my diagnosis was Follicular B Cell Lymphoma so my chemo drugs were totally different to those used for breast cancer treatment and I suffer the same dreadful prickling when I get hot. I understand patients not discussing these types of symptoms with their oncologist's and nurses as you can feel that the issue is not important enough or previous symptoms have been ignored or waved away as not a side-effect of chemo. I have felt this way. However, maybe this is part of the reason why the doctor may not have heard the complaints often enough to immediately accept it as a genuine side effect of chemo. Anyway, I am pleased to hear that I can expect this symptom to go away. All the best for ongoing good health everyone.
Joined: Sep 2017
KerryB
hope you are right that these symptoms will go away .. I messaged my oncologist again today to see if there is any creme that might help.
Good luck
Joined: Jul 2012
Prickly, itchy skin
Found this thread and, as everyone else, happy to see it is not just me. Had chemo for ovarian cancer in 2012 and developed this about 6 months after completing. It waxes and wanes but is particularly difficult in the summer. Overheating and direct sunlight seem to be my triggers. Will try some of the suggestions offered here. Thanks!
Joined: Aug 2017
Hurting, Prickly Skin
Right -- can't be the chemo. How is it that it never happened before the chemo and conitunes now 9 years later. I have learned how to be as cool as possible and can go a pretty long time before it hits, but I still have it. It is as if all of my nerve endings got fried during chemo. My entire body has to cool down before it goes away. It happens to my arms first - so I know to immediatly find a cooler place.. Applying cold water doesn't do it. Chemo does a lot of damage - seriously. Funny how many of us who had chemo have this issue.
Joined: Aug 2017
Same thing with me
Just wanted to chime in that I have the same thing and I'm trying to figure out how to treat it. I can't be outside pretty much...
Joined: Sep 2017
Gelainest
me either I have been inside all summer!!!! Outside not even 10 minutes and have to run inside to be in air conditironing.... dread winter when heat is on!!
Joined: Aug 2017
Prickly skin
I have been bothered with this problem too. My symptoms also started after by full cocktail of chemo drugs. I am now finishing up my herceptin ( one more to go, yahoo) infusion and am wondering if I will have this condition for a while longer. I too didnt mention it to anyone. On my next visit to the Ocon Doctor I will bring it up and mention that several others suffer from the same thing..
Joined: Aug 2016
Terral
Congratulations on finishing up the treatments. I just got done myself! It is a great feeling to know your done. I have no doubt that there is a connection to the chemo and the itching. I have made the decision to just be kind to myself and deal with it the best I can.
Please let us know what your docs response is.
Hugs,
Annie
Joined: Aug 2017
Intense Itching Insanity!
During Taxol, my soles and palms would itch so intensely that I would literally cry. I had to carry ice packs to numb my feet and hands throughout the day. Just thinking about how intense and insatiable this itch was makes me want to cry right now. But I have been off of chemo for a year, had my ovaries removed due to ER 100% BC and started Anastozole immediately afterward (I have stopped taking for the past 3 weeks as an experiment but am still having these itching attacks with my hot flashes). Ever since I had my ovaries removed and started the Anastozole, I get intense, insatiable, itching whenever I work out whether low, moderate, or high intensity workouts it still causes hot flashes and this insane itch. I believe it is due to nerve damage from Taxol. I saw something called Neuropathic Itch on NIH's website.
I have been explaining this to my ONCs since February and they keep referring to it as a "skin" thing and dry skin is a side effect of Anastozole. I promise this itch in NOT on the surface or any layers of my skin it is a subcutaneous itch!! It feels like my veins are itching all over my body. I try to ignore it and not complain, because after all, I got the "all clear" from my ONC team and there are no lesions or lumps in my mammograms and my blood test are great. I just need to know if this is a permanent part of BC recovery or if its menopausal or is it nerve damage that will be corrected as time goes on and I just need to wait it out a bit.
It so hard when you feel that people think you are insane because they are suggesting that you change lotions, soaps, and detergents or take an allergy pill or use a topical antihistamine and you will be okay. I wish they could understand that it is not that kind of itch and it is miserable. I have to literally stop what I am doing and keep perfectly still as to cool myself down enough to lessen the intense itch. If the doctors and researcher do not acknowledge this long term side effect, how can we get relief! The hot flashes are one thing, the itch is another all together.
Good know that I am not insane afterall and others are experiencing this problem, I just wish we get a solution!
"Warm" regards, literally,
Christiena
Joined: Aug 2016
Christiena, your not insane hon...
I have been done with the A/C chemo a long time and done with the Herceptin for a month now. I think all this lead to neuropothy in the worst way. My feet drive me bats.
I have lymphedemia in my arms. I have diabeties, and had neuropothy on left side prior to BC diagnosis. The chemo made it worse. Just intensified it to the max.
I had a hysterecomy back in 2010 and went through the hot flashes. 2016, the breast cancer, hormone pos. They put me on the Als back in Oct. 2016 and those first 4 mo. were awful with continuous hot flashes. They have now tapered off quite a bit. But I have all the other SE of it. bone pain, itching.
I dont know what is what. All I know is this is a crap shoot and many people have not a clue how hard this is on our bodies. I hope they never have to.
HUGS<
Keep fighting the fight.
Annie
Joined: Sep 2017
Itchy skin
i have ended chemo on May 23. I have been dealing with itchy creepy skin when I get warm and it stops when I cool down. I see many others here have the same issue .... this is the second time I have had cancer and did not go through this last time
Joined: Sep 2017
itchy skin
any of you that are experiencing the itchy skin did you have taxol? I did just wondering if that is the common denominator. This is crazy . There has got to be an answer to what it is. And a cure
good luck all
Joined: Aug 2016
i did not
I did not have taxol. I have the itchy skin.
Joined: Sep 2017
Apaugh
how long have you had the itchy skin? Is it getting less?
Joined: Sep 2017
Itchy
has anyone tried any lotions or creams to help? If so what did you use and did it help? The side effects of the chemo is crazy. Not to mention the chemo itself. I have been done for 4 months and now dealing with the creepy skin , hair still really short but is coming back , still some neuropathy in fingers and toes . Was on Gabapentin for that but stopped that 2 weeks ago thinking that is what caused the itchy skin, but still have it. It has been a rough year and want to get back to normal... if that's possible!!!
Joined: Aug 2016
Without looking it up (SE
Without looking it up (SE chemo brain) I think my high dose was over Sept of 2016 and then I went to Herceptin treatments until July 2017. My itchy skin started sometime during the high dose and it has not stopped. I dont think there is particular lotion for the cure, it is just keeping your skin soft that helps. Staying hydrated and not getting too warm. Trying to keep your stress levels down (LOL) and most of all praying for better outcomes.
Hugs
Annie
Joined: Sep 2017
Heat and itchy skin
I too have experienced itchy skin, but it turned into a rash. It has been awful. The dermatologist gave me some cream and it finally started to go away, but 5 days ago, came back with a vengence. It is so very frustrating. The back of my legs itch so bad. When I first got it and scratched so bad, my husband said I looked like I had been in an automobile accident as there was so much brusing. It just feels so unfair after going through surgery, chemo, and radiation for breast cancer then to have this happen. If anyone has any ideas on how to treat, please post them. Thank you and good luck to us all!
Joined: Feb 2018
Aloe vera gel seems to help
Hi, everyone. The same symptoms started for me in December, which was 5 months after finishing chemo (Taxotere, Carboplatin, Herceptin, Perjeta), 3 months after I started Tamoxifen, and 1 month after finishing radiation. I've been on just Perjeta and Herceptin since October and will finish in May. My diagnosis was for triple positive breast cancer, right side, one positive node.
I do think it's hormonal and heat related. It starts with feeling a little warm, like if I'm being active or wearing too many layers, and then bam, I'm *roasting* and I've got these nasty little itches all over.
I've tried a number of approaches. Keeping the house humid, using Neutrogena shower oil after showering, and keeping lotions on my arms, hands, and legs all seem to help keep dry skin at bay. It still isn't quite enough, though.
The thing I've found that will shut down an attack is aloe vera gel, which is usually on the same aisle with sunscreen and remedies for sunburn. The gel always seems slightly chilly, which feels great, and within a minute or so, the maniacal itching shuts down. I haven't tried keeping it in the fridge to make it even colder, but that might be worth a shot. It can dry kinda sticky, which some might find annoying, but I'm usually so glad to not be itching that I don't care. :-)
Another thing that I tell myself works is eating maybe half to 2/3 a cup of sorbet. If you eat it fast enough you get a rush of cold that normally would be unpleasant but is kinda nice when you feel the wave of heat coming on.
Good luck and positive thoughts to everyone. :-)
Joined: Aug 2016
I am all in for Sorbet
I agree with you and keep ice water with me at all times. Hot flashes and night sweats were so bad that I thought I was going crazy. You all know what I mean. Doc changed my meds up from Arimdex to Tomoxifen because of my bone damage. Hot flashes got worse. I was sleeping with a fan in my window blowing right over my bed. Now it is winter and did it in below 0 weather and did not care. I could of slept in a pup tent outside on the lawn and felt great. I was also freezing everyone in the house and it was making me sick with a head cold. So Doc suggested effexor and gabbipentin to combat the flashes. The effexor and gabbipentin has helped. I now take it in low dose effexor 37.5 and Gab 300 mil. one time a day ea. I still get some, always will I suppose, but they are not as intense and I can now just sleep with a fan in the room and the family is thankful for that. The itching has lessoned some now. I still use lotion all the time as the meds dry me out. Maybe we should all buy stock in lotions!
I put away all my sweaters, heavy coats, and such and just wear summer clothing all the time no matter the weather. And I try my best not to get stressed. Stress just sets me off like a rocket. That can be difficult to do but I try my best to avoid all the drama I can.
It is about me, I have to take care of me to survive this awful disease or I am not going to be here. So my family understand that and try not to stress me. I love them so much.
Hugs,
Annie
Joined: Jul 2018
Itching skin/ neuropathy
I was sure glad to find people with the same symptoms i have been experiencing. I mentioned this itching, burning, tingling sitution during my treatments, and after i was done with all my chemo and noone would listen. The oncologist herself shrugged her shoulders at me and the nurse I was crazy! After they do there part, they don't want to hear about any residuals from the meds I had my cancer in 2014 and I still have issues with it. I cant go in the sun, if i get into a hot vehicle, I have be careful with the water tmp. in the shower. As I am writing this i am researching this dilemna ........
Joined: Sep 2010
Itchy skin!
@ecurran7, I'm 8 years out of treatment but this has been the worst year for itching, seems like every summer I would start itching and I to thiught it was flees lol I have a dog in the house but no one else got bit then I thought it was what I was washing my clothes in changed that, but after 3/4 summers I realized it only happened when I got in the sun, but this summer is the worst and it's all from my knees down, but I had surgery own my shoulder last year and had to wash in hiberclens before surgery and I had a whole bottle left and I started washing my legs in that and it's drying the sores up because I had scratched so bad
Joined: Nov 2019
Found something that helps my prickly skin
My pin prickles happened whenever I had a hot flash Or would sweat. It started about one month after chemo ended. They were absolutely agonizing for nine months. I talked to my oncologist but he had never heard of such a thing and sent me to a neurologist to test for neuropathy. A friend of mine and I were talking about hair loss and she suggested I take the supplement hair, skin and nails. I started taking it and noticed that my pin prickles went away. I had seen a neurologist, had all sorts of different tests done. Only for him to say it was not a neurological problem. I have continued taking hair skin and nails and am almost pain-free. The days I forget to take the hair skin and nails the pin pickles come back as bad as they ever were. I still have hot flashes but they don't hurt. Before I felt like I had thousands of slivers or pins jabbing me all at the same time.
Joined: Oct 2017
What is this supplement
What is this supplement called?
Joined: May 2020
Prickly skin
Also have prickly skin issue. No rash, no hot flashes, but triggered by sun or heat (when cooking, etc). Just finishing breast cancer (Her2+) treatment: chemo (taxotere/carboplatin/perjeta, herceptin) last fall, then lumpectomy, then 5 weeks radiation. Continuing w/ Herceptin every 3 weeks until July. This SE just manifested - I think it's the Herceptin. Oat-based lotion helps. I'm going to also try aloe vera & hair-skin-nails supplement. What is brand name?
Joined: Jul 2016
Itchy skin
I have been having very strong periods of itchy skin. I didn't associate the AI med with itch.
The period started as nasal congestion and a constant itchy nose. Then, when nasal congestion was the strongest, the eyes also itched and were inflamed and congested. After a few days, my upper torso began to itch and I still feel a burning sensation in my skin, especially my back. Some days I can't sleep because, the more my skin sweats, the worse is the itchy period. I am using steroids (prednisone) to control attacks but I can't keep taking that pill.
Heat increases the itch and I live in the Tropic. I will tell the alergist doc to check on the AI. I was considering changing it because my feet are swollen and have constant pain. I don't want a thrombo in my legs and the insufficiency syndrome is developing with the AI.
Joined: Aug 2020
Prickly heat
Hi everyone
I had a lumpectomy last September then chemotherapy from November to March this year. A course of radiotherapy followed. I am now taking letrozole every day to inhibit hormone production but I too have prickly heat as the rest of you describe. It is absolute torture! Does anyone know if this is permanent? Will we ever be able to enjoy the sun again?