I Hate Dialysis Message Board
Dialysis Discussion => Dialysis: Transplant Discussion => Topic started by: UkrainianTracksuit on June 10, 2020, 02:20:41 PM
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So, what did your early skin cancer spots look like?
I've a spot on my face that has been there for around 3 months. At this point, I'm not saying it is a cancerous spot, but it is bugging me that it is still there after all this time. It's scabby and no matter what I do to it, it remains...well, scabby and a bit raised. It could simply be that I take an extremely long time to heal but the fact this thing stays the same is bothersome.
With the current situation, getting a hold of my GP hasn't been easy, and office hours have been significantly been cut. I have an appointment in 2 months.
I spoke about my concern with my local renal department and they advised it was a GP issue (as I knew) but "you'll have to wait over a year for a dermatologist appointment." I'm 95% sure if I told my transplant doc that the team there could arrange something sooner.
But, it goes back to the original topic. Not going to cause a fiasco over something harmless.
Anyway, what did it look like? What did it feel like? I can't get a great view of it as I have to use a mirror so touch is my best experience with this spot.
Any input, thanks.
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I've just recently been to a dermatologist for a checkup and was surprised to learn that I didn't have a cancerous spot because I have several odd spots that sound something like what you've described. Google "actinic keratosis" and see if that might describe what you are seeing as that is what my spots seem to be, "scabby and a bit raised".
I'm sorry you may have to wait so long for an appointment.
Maybe someone else on here can be more helpful!
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It sounds/looks similar. Thanks for that info.
When I google it, I see lots of people with severe sun damage. If I may so ask, did you have noticeable sun damage and spots in that certain area?
I don't have anything noticeable, but I wouldn't put it past the situation because it's in a place I probably missed sunscreen.
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Of course you may ask!
No, I do not have noticeable skin damage, but it is impossible to live to my age without acquiring any sun damage at all. The spots I have are on my back and are, oddly enough, always covered up my my oh-so-sexy one piece bathing suit, so I don't know why I would get spots there. I've had those spots since before my transplant.
Since my transplant, however, I've developed two more spots, one on each side of my neck. No doctor has ever even mentioned them, which is strange, but there you go. I suppose they recognized them as "AKs" and didn't feel the need to investigate further.
I've developed one more which actually bisects my tx scar, another area that never sees the sun's rays. Go figure.
I do use sunscreen regularly.
I hope this helps. If you have any other questions for me, feel free to ask!
Apparently, these "AKs" are common.
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I'm blonde, very fair-skinned, outdoorsy, and burned more times than I can count when I was a boy.
Mine was just a small, slightly raised, skin-colored mole near my ear.
Also, my dermatologist freezes off any moles that get irritated or bleed.
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How about the size? We're told to look for spots larger than a pencil eraser. I go to the dermo every year and so far everything I've been concerned about has been not cancerous. The NP freezes off a lot of spots if they bother me for which I'm grateful. I just last year realized that I have brown spots on my left hand because that's the one near the window when I drive. I can never remember to put sunscreen on my hands before I leave the house. The NP calls these "wisdom spots" but I'm not fooled. I try to avoid mirrors in general so I only recently realized I have some of those flat brown spots on the sides of my face. Sigh. Let us know how you make out.
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I had two derm exams at the same practice, but different MDs. One was standing in my underware for a 3 minute look-over.
The other done by this fantastic Vietnamese MD (MIT, Stanford, Harvard Med, Mass general fellowship) was completely different. Laid down on the table and had everything checked out from my scalp to between my toes and everything in between, then flipped over for the other side. Asked about a dark area on my cheek the size of a dime "harmless" - she then used a liquid N sprayer on it, and when the scab fell off the dark spot was gone.
There is a quality difference in these exams - be sure to get a derm who spends time and pays attention to detail. If (s)he doesn't at least poke around your hair to look at the scalp, consider upgrading.
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Thanks for all the responses.
All of this just augments the need to get this checked even more.
It's like MM said: you can't expect to live without accruing some sun damage. I've never had a sunburn and I avoided the sun for the most part (except for outdoor sports), but I did live on the Black Sea for some years, without sunscreen :banghead; and it was very sunny/hot. Stupid youth.
I have very few moles anywhere at all though I do look at them regularly to esnure they are okay. However, what you guys described here leads me to believe this should definitely be looked at. Pencil eraser sized, a bit raised, red scaly scabby. Even if it is an AK (I want to add 47...) at least there is some peace of mind.
My renal team managing here just tells me to check my own skin. Wear sunscreen. Wear a hat. Have not mentioned seeing the dermatologist probably because we don't have one! And then that leads to Simon Dog's suggestion here: This is socialized medicine here. I have no choice. Haha, I go where they send the referral. Sure, I can ask for a second opinion, but again... If they refer me out of town, that would be best as it would be to a major city centre.
So that's why I am going to ask my husband to take me to a private clinic out of town if things move awfully slow. I found one that does skin cancers and cosmetic procedures with good doctor information.
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No need for a special clinic - just book a derm exam with any decent board certified dermatologist. My transplant Neph offered me a referral to one in the hospital he works at, but I used one closer to home.
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UT, the aks on my back are all larger than a pencil eraser, but if they were to get bigger all of a sudden, I'd be concerned. So, size in and of itself is not the worry, rather, it's a change in size, I guess.
This is obviously something that will niggle at the back of your brain until you are checked out, so it might be worth getting it seen to at a private clinic if that will make things go faster.
Let us know how you get on, OK? I'm curious to know what you find out.
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Very small update:
My scheduled appointment got pushed back again so we will go the private clinic route. Hopefully COVID precautions doesn't interfere with that either!
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How frustrating! Still, thanks for the update.
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I hate the sun, always have, and always have avoided it. I can burn from exposure to moonlight. Which is why I like downtown. When I go out running, I cling to the shade of tall buildings.
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I hate the sun, always have, and always have avoided it. I can burn from exposure to moonlight. Which is why I like downtown. When I go out running, I cling to the shade of tall buildings.
Hello Enginist,
I am very sorry for you and the symptoms you describe.
Has your doctor checked-up on SLE/MCTD/Lupus ? Hating sun- and moonlight could mean, that your body does not like it and could this be connected to SLE/MCTD? Unfortunately SLE/MCTD can usually not be diagnosed that easily, as it is a very rare disease, which only shows-up during a severe flare-up. But you could help yourself by observing your BP and check-up if it rises due to sunlight and/or ultraviolet light & moonlight etc?
It might also help you to wear a hat with a large brim to protect your face & sun-glasses & cover your body by wearing long sleeves etc. and of course, use some SPF 50+ sun- cream
If you research on the Internet you might find that going for a run is not that advisable and research has shown, that a long gentle walk goes “a long way” to keep as fit as possible. Good luck and best wishes from Kristina. :grouphug;
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Hi Katrina. Welcome back. I'm glad that you decided to rejoin us.
No, I don't have lupus, and I'm not a vampire. My problem is that I have fair Irish skin. The solution for it is simple: stay out of the sun.
I know you like your little walks, which you have mentioned on previous posts. But I am an inveterate runner. There is nothing more exhilarating than high-intensity interval training, which really gets those endorphins flowing. And it helps to have good running music. I share with you your love for classical music, but when it come to running, I find myself more motivated by trance or house or EDM at 180 bpm. On good days, I can run forever.
Plus, I'm convinced that being a fitness buff has helped me ward off the worst effects of several illnesses, including sepsis and CKD. When I can't run any more, I'll know that I am done.
Again, let me say that your absence was noticed, and that long-time members like you bring value to the site.
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Hi Katrina. Welcome back. I'm glad that you decided to rejoin us.
No, I don't have lupus, and I'm not a vampire. My problem is that I have fair Irish skin. The solution for it is simple: stay out of the sun.
I know you like your little walks, which you have mentioned on previous posts. But I am an inveterate runner. There is nothing more exhilarating than high-intensity interval training, which really gets those endorphins flowing. And it helps to have good running music. I share with you your love for classical music, but when it come to running, I find myself more motivated by trance or house or EDM at 180 bpm. On good days, I can run forever.
Plus, I'm convinced that being a fitness buff has helped me ward off the worst effects of several illnesses, including sepsis and CKD. When I can't run any more, I'll know that I am done.
Again, let me say that your absence was noticed, and that long-time members like you bring value to the site.
Yes, it IS nice to see a post from Kristina! :thumbup;
I am not a runner, although I do like the idea of it, but I do like walking, hiking, swimming, and particularly gardening. When I say "gardening", I don't mean just watering my posies, rather, I'm talking hauling mulch and other rather heavy duty chores. I always wear sunscreen, but OMG, I sweat like a stuck pig with that stuff on. I have used sprays and creams and lotions and sticks, and I can't find any sun screen that won't make me overheat while working outdoors. Do you wear sunscreen, and if you do, can you recommend one to me? Or do you just stick to the shadows of tall buildings?
House and EDM work for me when I'm walking, so I understand that particular musical choice. I agree that keeping physically fit helps keep the worst symptoms of CKD at bay if you can possibly manage it. It's also the best mood lifter. Good for you!
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I use avoidance over lotion, but apparently you're not the only one having problems with their sunscreen, MM. According to a brief online search, Banana Boat makes a water-proof, sweat-proof SPF30 that is said to be highly breathable. Others recommend the KINeSYS brand or Coppertone Sport Ultra. There are probably others.
You don't need to be a runner to help your limbs stay limber. Any kind of activity that gets you off the couch will work, and you are not a slouch in that department. You also get some exercise from lifting those thousand-page novels you like to read.
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Oh no, you've got me started. I love talking about sunscreen! Every day, 365, even if I'm staying in the house, I sunscreen face/neck/chest/ arms and hands before getting dressed and reapply if outside more than just running to the car.
As they don't degrade after 2 hrs or burn my eyes and are easier on the environment, I try to use mineral only sunscreen on my face; my favorite of the less expensive is Australian Gold tinted spf 50. get it at CVS or Walmart for about $12. Dries matte, doesn't make you look like a pink ghost. I wear it almost every day year round. My favorite all mineral (pricier, not waterproof) sunscreen is Paula's Choice light daily defense spf 30. Lightly tinted; I'm not much of a makeup wearer but it looks natural. Waterproof sunscreens are harder to remove from your face; I find an oil based cleanser followed by a regular cleanser removes it best.
People love Elta MD all mineral face sunscreens, but I found the spf 44 sport one too greasy and stayed shiny. Would work if you had dry skin. The Australian Gold is a little drying if you tend to be dry skinned.
My favorite body sunscreen (which was chemical) was Coppertone foam but its been discontinued. There is a BananaBoat dry sport that is supposed to be less greasy. I've used dry sport sprays before, but had to go outside to spray it on as overspray makes your floors slick.
I swam every day when I was in Florida this past winter and wore long sleeved, high neck rash guard shirts from Landsend that cover arms/chest/back. Didn't find them sweaty at all, but I was wet! And a hat. Always a hat.
Don't forget the back of your hands. I carry little tubes of sunscreen in the car (the mineral ones don't break down in the heat) and my dash is all smudgy. By mineral, I mean zinc oxide and/or titanium oxide. Its formulated better than it used to be.
Sunshine is good for our bones and our mood! Enjoy.
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I honestly didn't get into the sunscreen habit until tx. My mother always advised to avoid the sun mainly for wrinkles and "you can see all the women who spent a lot of time in the sun because they have faces like shoeleather!" however I did train in the sun. Biathlon training means you are outside both in winter and summer. But, I was young and dumb, so stuck on some (ineffective, but looked cool) eye black and did my thing. And then, Black Sea life means you are exposed to the sun whether you like it or not.
But then, transplant happened and I got into sunscreen religiously. A big hat. Sheer cover ups. All that. I use Sisley Sunle˙a because it is non-greasy, no residue and moisturizers at the same time. It (or at least I thought) took care of my sun needs for running errands or going for walks. Sisley has an "after sun" product too and while it smells nice and "promotes the skin's natural defenses", it's most likely junk science. So says my rough patch... ::)
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I use avoidance over lotion, but apparently you're not the only one having problems with their sunscreen, MM. According to a brief online search, Banana Boat makes a water-proof, sweat-proof SPF30 that is said to be highly breathable. Others recommend the KINeSYS brand or Coppertone Sport Ultra. There are probably others.{/quote]
Cupcake mentioned Banana Boat, also, so I may check that out. Right now I use Neutrogena Ultra Sheer Body Mist for when I swim. It's "broad spectrum" which is supposed to be best, with an SPF of 70. I use it mainly because it has a "full reach design", meaning I can turn it upside down to spray on my back without it going wonky. For my face and neck, I just spray it into my hand and rub it into my skin.
When I'm gardening, I wear protective sleeves, not so much from the sun, but from thorns and such.
You don't need to be a runner to help your limbs stay limber. Any kind of activity that gets you off the couch will work, and you are not a slouch in that department. You also get some exercise from lifting those thousand-page novels you like to read.
edited to add: Sorry, I don't know what's going on with this post! I've tried messing about with the quote function, but it's still a mess. Apologies.
I was pretty couchy slouchy yesterday. I needed a day of rest. But yeah, my biceps are in pretty good shape from carting around Anna Karenina. :P
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Sorry about my above post. Something's goofy about the quote function. I've spent too much time trying to fix it to no avail. Apologies.
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Cupcake, you are so hard core! Well done you!
To be fair, I am pretty sure my perspiration problems stem from my tacrolimus. The patient information sheet that comes with it warns of this. I use different types of sunscreen for different occasions and for different seasons. Summers are problematic for me, and wearing sunscreen makes things worse, so I'm constantly having to towel my face off and then reapply my sunscreen. I do wear a visor when swimming if possible, but I do not wear a hat gardening or dioing anything else outside because all of that heat gets trapped in my head, and it makes me nuts.
So, I have to employ other techniques. When I'm in the garden, I follow the shade. I've tried wearing a hat, but it's always getting knocked off.
I'm of the opinion that any broad spectrum sunscreen with an SPF of at least 30 is effective if you remember to use it and remember to reapply it. And in my case, I have to remember to keep hydrated.
UT, I was the same. When I was a teenager, that was the era of using suntan oils to get the deepest tan possible, but now circumstances have changed! I hope you get your crusty bit looked at soon. It's frustrating having to wait.
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Cupcake, I just ordered a swim t-shirt from Land's End, not so much to deflect the rays but to conceal an unsightly scar.
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I love Land's End's tugless tank swimsuits. I've worn only those for at least a decade. I haven't ever bought one of their SPF suits (or T-shirts or anything), so I'd be interested to know how effective they are.
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At risk of sounding like a commercial for Landsend, they are supposed to be SPF 50+ and I would say they are at least. Enginist-I even wear one in the indoor pool as I think it hides my flabby arms and keeps my shoulders warmer if the ventilation is blowing. Plus, I think I look more like a Bond girl when I wear the one that is all black and zips up to my chin.
I was in the Villages this past snowbird season and probably about half of the water aerobics and water volley ball players wear some sort of rash guard shirt. Men and women. Just makes sense.
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I have no idea what's Land's End so sorry to crash that party, but MM, could you care to elaborate? This is familiar and I thought it was just my out of control hormones. Might have to dig up the papers from a box of Avagraf.
To be fair, I am pretty sure my perspiration problems stem from my tacrolimus. The patient information sheet that comes with it warns of this.
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I have no idea what's Land's End
1. The southwestern tip of mainland England (Cornwall county) [with apostrophe]
2. A multi-national clothing store based in the US and owned by Sears Holdings [without apostrophe]
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My wife has taken to wearing a rash guard as sometime in the last 10 years she started being much more skin sensitive. We think doxycycline for malaria preventative caused it. It feels like in the past couple of years rash guards became more popular and available.
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UT, I think I have been mistaken about the tacrolimus causing sweating. I've just reviewed all of my medication notes, and it is the patient info on prednisone that lists "excessive sweating" as a possible side effect.
After my tx surgery, I remember telling one of the nurses that I felt really hot but that it was not a feverish hot, rather, it was just a sweaty hot. She said, "Oh, that's the tac." At the time, I didn't know what "tac" was, but for all of these years, I'd been thinking that was the culprit. At least now I know!
Apologies for the misinformation on my part.
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Hi Katrina. Welcome back. I'm glad that you decided to rejoin us.
No, I don't have lupus, and I'm not a vampire. My problem is that I have fair Irish skin. The solution for it is simple: stay out of the sun.
I know you like your little walks, which you have mentioned on previous posts. But I am an inveterate runner. There is nothing more exhilarating than high-intensity interval training, which really gets those endorphins flowing. And it helps to have good running music. I share with you your love for classical music, but when it come to running, I find myself more motivated by trance or house or EDM at 180 bpm. On good days, I can run forever.
Plus, I'm convinced that being a fitness buff has helped me ward off the worst effects of several illnesses, including sepsis and CKD. When I can't run any more, I'll know that I am done.
Again, let me say that your absence was noticed, and that long-time members like you bring value to the site.
Hello enginist and many thanks for your kind reply and - if I may say so - I would like to mention, that - as a "Continental" I don't mind you calling me "Katrina" instead of my real name Kristina. But it has been pointed out to me that some of our American friends here mind very much if you call me "Katrina", because the name "Katrina" reminds them of Hurricane Katrina which, back in 2005, hit the US Gulf Coast and killed 1200 and cost about $125 billion in damage.
So, with respect to our American friends could you please call me by my real name to avoid any further distress?
I appreciate that you stay out of the sun because of your fair Irish skin and the only reason why I have mentioned SLE/MCTD/Lupus is because the symptoms you have described are almost identical to mine before I was diagnosed with SLE/MCTD. Because of that, I felt it my "human duty" to mention this because SLE/MCTD/Lupus is a very-hard-to-diagnose disease and, at the same time it is very deadly. In fact, it has been mentioned as the "Lady-killer", because nine out of ten patients happen to be female, but it also hits the male population very badly ...
The reason why I go for regular walks is because my kidneys first failed in the very early 1970's and, after their function recovered a little again, medics advised me to eat an easy digestible vegetarian diet and keep as fit as possible by going for "gentle walks". I was warned against any running because - according to the doctors at the time - running unnecessarily "wobbles" the kidneys up and down and since my injured kidneys were very fragile in their function etc., medics thought it a good idea to keep my kidneys as calm as is possible, especially because of my serious kidney-disease and to avoid deterioration for as long as is possible. Perhaps it was the right advise in my case, because, without dialysis I could keep my injured kidneys functioning - just about - for another 43 years.
Whatever you are going to decide, I wish you the best of luck and please check-up with your medics and I send my kind regards from Kristina. :grouphug;
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I lived in New Orleans for seven years, and still often visit, so maybe I unconsciously switch the names. I will make a sincere effort to refer to you as Kristina, a lovely name in its own right. However, if some people here are complaining about a harmless slip of the tongue, they should be grateful that they don't have far worse problems to complain about.
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However, if some people here are complaining about a harmless slip of the tongue, they should be grateful that they don't have far worse problems to complain about.
Yesterday there was a funny post on the Facebook group starting out, "Have any of you fallen pregnant well on dialysis." The post was updated to clarify that falling pregnant was common English in south Africa for becoming pregnant! Unfortunately she had to add the calcification because people automatically assumed her English language skills are bad or she had a slip of the tongue rather than that it might be a cultural difference. Anyway that was a funny learning experience!
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I lived in New Orleans for seven years, and still often visit, so maybe I unconsciously switch the names. I will make a sincere effort to refer to you as Kristina, a lovely name in its own right. However, if some people here are complaining about a harmless slip of the tongue, they should be grateful that they don't have far worse problems to complain about.
I'm going to cop to this so that there is no misunderstanding. During private messaging with Kristina, I made the observation that it was nice to see her post on IHD and that you, enginist, had posted a very charming "welcome back". She noted that you had been calling her "katrina" and that she thought that was a lovely name, that it was "continental" and even "Russian sounding".
I then explained that whenever I heard the name "Katrina", it reminded me of the hurricane, and I went on to explain how people were impacted. My mother's family is from Mississippi, and her parents, upon retiring, bought a small home near the beach in Long Beach. I spent many, many summers there. I remember when Camille hit and we were all so worried about my grandparents.
They had died long before Hurricane Katrina hit, but the house was still very much a part of the family. I told Kristina about the horrific damage as I was there 6 months after the storm, and it still looked like something in a bad apocalypse movie. My aunt had just bought a home in Gulfport, and the winds of the storm blew a container truck filled with frozen chickens onto her property. You can imagine what that was like.
Having lived in New Orleans for some years, I'm sure you have a story or two.
Anyway, I in no way was complaining, rather, I thought Kristina might be interested in this rather significant even in the history of a particular part of the US. While I was not "distressed" at all, it did bring back some sad memories, but I certainly did not think you rude or insensitive. I hope this clears things up!
Iolaire, I sometimes still use British words and idioms without realizing it, and I can get some weird reactions. She "fell pregnant" sounds nicer than "she got pregnant"!
Edited to add: To make this post relevant to the topic of skin cancer, both of my parents developed skin cancer in their elder years, my dad on the back of his hand (I never saw it), and my mom on her face. It was an oval shaped, black spot that was fairly large. Neither of them ever wore sunscreen or took any precautions at all. My dad liked running/walking, and my mom enjoyed gardening, so they both spent a lot of time outdoors...in Texas. So, I suppose it was inevitable.
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Katrina does sound Russia, as does Katerina. The former, unfortunately, has negative connotations, but I don't think that Kristina is anything like a hurricane.
Yes, I have some stories, but nothing like a truck of chickens jackknifed on the lawn. Although I did hear of some fraternity guys who rented a motel room in Biloxi during Camille. They wanted a hurricane party on the beach, but the storm hurled a sailboat though their window, killing four.
I wonder if skin cancer is considered an underlying condition.
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I remember the story of the frat boys in a Biloxi hotel. It was a true story.
Yes, skin cancer would be considered a pre-existing condition if you were to change insurers, who would price that in accordingly.
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Is there a problem with "sounding Russian?" :P Don't make me drop the gloves a second time in the same day over a similar thing!
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Is there a problem with "sounding Russian?" :P Don't make me drop the gloves a second time in the same day over a similar thing!
Hello Ukrainian Tracksuit,
Perhaps enginist might refer to me “sounding Russian” and that would be cleverly observed, since my late mother came from a White émigré family who had to leave Russia in 1917.
Kind regards from Kristina. :grouphug;
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In the last 15 years I have had a cancerous mole or pre cancerous removed every year. My symptom of these is a intense itching on my back in the area of the mole. In fact if I contact my Dermatologist with this symptom I usually get a appointment with in the week instead of a month. My problem is as a youth I had the same neon white skin I am cursed with today spend any time in the sun and I go from neon white to neon red and back to neon white in short order. This was made worse by the attitude of the 50’s and 60’s that get out of the house and into the sun as it’s good for you that every one had in that era.
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As it happens, Katrina is German in origin. Katerina, on the other hand, is as Russian as Anastasia, who was killed with her family by the Bolsheviks in Yekaterinberg. Kristina is Scandinavian, a variant of Christina, which ultimately is Greek in origin.
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Ugh, so, just to close this chapter then and sorry that I let it go so long without an update. Just had to find my bearings over the whole thing in yet another "I am fed up with 2020" moment.
It turned out to be cancerous, squamous cell carcinoma to be exact. Naturally, because I was assessed as high risk, the doctor went with the surgical route. Since it was on the side of my face, I am pretty glad it wasn't a large thing to remove and the doctor does work in a cosmetic clinic so he totally understood where I was coming from. Funnily enough, he said I was one of the least demanding patients they see. Haaaaaa....
After surgery, and to be safe, he prescribed fluorouracil (5FU). Pretty routine ointment for a short period. Back for a check-up next month.
I have to practice gratitude that I am able to have such medical care, but I am just fed up at this point.
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So, what did your early skin cancer spots look like?
Thanks for the update. Please would you upload an image of what the spot looked like? Feel free to crop it down to just the spot area. It would be good to see what you were concerned about now that you know it was skin cancer.
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Well, I'm certainly glad you caught it early, when it was small, and that you've got it taken care of. It must have been scary. Like Iolaire has said, I wouldn't mind seeing a photo if you happened to take one before it was removed.
This is just SO 2020! LOL!
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Ugh, so, just to close this chapter then and sorry that I let it go so long without an update. Just had to find my bearings over the whole thing in yet another "I am fed up with 2020" moment.
It turned out to be cancerous, squamous cell carcinoma to be exact. Naturally, because I was assessed as high risk, the doctor went with the surgical route. Since it was on the side of my face, I am pretty glad it wasn't a large thing to remove and the doctor does work in a cosmetic clinic so he totally understood where I was coming from. Funnily enough, he said I was one of the least demanding patients they see. Haaaaaa....
After surgery, and to be safe, he prescribed fluorouracil (5FU). Pretty routine ointment for a short period. Back for a check-up next month.
I have to practice gratitude that I am able to have such medical care, but I am just fed up at this point.
Glad to hear that you got the spot taken care of, UkrainianTracksuit! I haven't been on here in a while-with life happening and the pandemic and all. But, I did have two recent skin cancer surgeries. One was above my right eyebrow (3 weeks ago)-where they removed a Squamous Cell Carcinoma (7 external stitches and 4 internal stitches). Glad it was squamous rather than basal cell-as Squamous then to be more localized and easier to remove during a MOHS precedure. BTW, I had a biopsy done as soon as something showed up on my face-as I've had MANY skin cancers. The trick is to get them removed early!
That being said-I also had a basal cell removed from my right upper chest area (Two weeks ago) -That was biopsied in 2018! I let this one go too long-and I paid for it! (Malignant Excision and intermediate layered linear repair). It was weird that "normal skin" had grown over the top of the actual cancer-and it made an ugly bump on my chest, too!
Particulars:
Preoperative size: 1.8X2.0 cm
Margin: 5 mm
Excision size: 2.8X3 cm
Final length: 9.8 cm
As you can see to get the area closed up, the would area ended up being about 10 cm. Three sets of sutures, innermost at muscle area was proline (like fishing line) 5 sutures, second layer of sutures were 16...and outer most layer of sutures were 21 stitches!.
Now I have a nasty looking scar that goes from my right upper chest and ends at the base of my neck area. Oh well...I knew not to wait so long!In all I have had 20 MOHS procedures on my face and scalp area.
By the way, due to the 100's of basal cells that I've had-I was on the initial trials and subsequent prescriptions with Vizmodegib (Oral chemo pills for skin cancers-for multiple BCC-basal cell carcinomas). Vizmodegib has some nasty sde effects like most chemos-loss of taste, loss of hair and horrible muscle cramping. The longest I was on it was about 11 months. The last time I was on it was for 5 1/2 months...and couldn't stand the side effects any longer
I am lucky and I go to Mayo in AZ. The doc I see next month is one of the docs that developed Vizmodegib. The reason I am seeing him is to hope they have sometihng different I can try. If not, I will most likely go on the Vizmodegib from September to December.
I also use fluorouracil cream (5FU) which is a skin cream formula of chemo. I also use Imiquimod cream 5% as well.
I guess what I am saying is that you should get frequent checks if you are prone to skin cancers. It's a lot less painful! :)