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- January 1, 2018 at 3:44 pm
I am wishing everyone a very Happy New Year from an unusually chilly Arkansas! It is currently a balmy 4 degrees at my in-laws this morning, so I am definitely looking forward to getting back home to the Rock where the high will be a sweltering 25. Ha!I’m still digesting this article as I am not really sure what to make of it. On the one hand, it does seem odd that one would be better off waiting longer for SNB. However, I am taking the survival statistics with a grain of salt. The landscape of melanoma management has changed so dramatically in just a few short years that I am not sure disease-free, melanoma specific, and overall survival statistics which include those from 3-18 years ago are truly relevant. That being said, the phenomenon is definitely worthy of more research. This does not change my mind about wanting the SNB when I go for my WLE. Despite the fact that Clark levels are no longer used for staging, I personally feel they are very important when determining whether or not a person with thin melanoma should get SNB. My 1.0 mm melanoma was Clark level IV, so it has technically reached the reticulated dermis where blood and lymph vessels are located. For that reason, plus the higher mitotic rate of 4, SNB is really a no-brainer for me.
Thank you, Celeste, for posting this article. It is definitely food for thought. In my short time on this board, you and other regular posters have given me so much piece of mind. I still have melanoma, but I now have a much larger support network of people who have gone through the emotional rollercoaster that is melanoma. Wishing everyone a fabulous ride in 2018!
Laura
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- December 29, 2017 at 8:02 am
So I’m hearing you speak of casein, gluten, and inflammation, but smoking is fine? Thank you for the sound advice, but I shall respectfully disagree. I am happy you are doing well, but I would hope no one who reads this thread would take your initial post literally as it could easily be misinterpreted as misleading. You did, in fact, undergo medical procedures to treat your Mel. Regardless, I wish you good health and many blessings in the new year! -
- January 18, 2018 at 5:10 am
I am so sorry you are having to go through this. The waiting and the unknown are the absolute worst! I was diagnosed with mel at the end of December and my WLE is next Wednesday. The waiting is excruciating. Hopefully you just have a weird mole that decided to pop up and say hello. In any case, you’ve been proactive and are taking the necessary precautions. Sending positive vibes and big hugs to you!Laura
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- January 1, 2018 at 10:28 pm
No worries! We can all be a little too sensitive about our health and well-being especially when you’re dealing with something that could potentially kill you. I don’t think that’s necessarily a bad thing. That same passion and thirst for knowledge is the reason great strides have been made in melanoma management as well as other diseases!Thank you for the interesting tidbit about VitD levels and nail/hair growth. While it makes total sense, I’ve never thought about it like that! Is a Vitamin D level a special lab draw, or do they routinely check it after Mel diagnosis? I am almost positive I am deficient, and I would love to know my actual level. I will ask my surgeon about it when I see him on the 8th. I still have to establish with a dermatologist as this whole “You have melanoma” thing hit me like a ton of bricks. I want to arm myself with as much information as possible so that I can be my best advocate.
I will definitely look into boron supplementation. As a living organism, all we are is just a bunch of cells smooshed together in a very specific manner. So many things are required to make us “work”. When things (vitamins, minerals, pH, etc) get out of whack, so do we eventually. I think the main reason for the big warning on borax is misunderstanding of the actual chemical. Boric acid is toxic but borax is not the same thing. Or maybe because there can be some nasty side effects when consumed in large quantities? Who knows? I found a few sites which talk about how to use it in other ways as well as drinking the solution. I may have to try it. Very interesting indeed!
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- January 1, 2018 at 6:29 pm
I could very well be paranoid. No doubt. I’m just concerned as some studies have shown abdominal skin to drain to axillary nodes. Therefore epitrochlear nodes are indeed within the realm of possibility of what would be a distant metastasis. Is it more likely that node is enlarged for another unrelated reason? Absolutely, but the worry is still there. I was just wondering how they go about testing suspicious palpable nodes. -
- December 31, 2017 at 4:55 pm
Whoa Nelly. All I said was that your initial post was a bit misleading. I never once dismissed your other claims except for a finger-wag at your smoking.I have just recently been diagnosed and I have been doing as much research as I can to educate myself and to be able to make better choices. I absolutely agree with making dietary changes when diagnosed with any type of cancer. (Sure changes should have been made prior, but I’m human.) Vitamin D levels have been shown to be strongly associated with increased survival as well as disease-free survival in melanoma patients. I am learning more about the whole casein thing now. I’m not a huge milk lover but I can get down on some cheese, so that is definitely something for me to assess. For quite a while, I have felt our food is killing us. There are chemicals ranging from questionable to downright toxic in almost everything we consume or use on our bodies. I truly feel it is the biggest reason for the increased prevalence of all types of cancer in the past several decades.
And as far as UVB goes, I thought it was UVA rays such as those in tanning beds that were the nasty ones, but I don’t have a lot of knowledge on that subject.
I am truly sorry you feel people don’t take you seriously. I’m not totally sure why that is since most of what you have proposed has at least been moderately to vigorously studied. More studies are needed in some areas, but links of association have been made. I for one am making changes with the first one being the Vitamin D supplementation and just trying to eat cleaner. No way can I just go purely plant-based as some literature has suggested. I need meat, and no veganazi will ever make me believe I wasn’t meant to eat it! (Although organic and moderation are key.)
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- December 29, 2017 at 11:28 pm
Thank you so much! I agreed with your blog post about SNB being a no brainier. I am definitely going to ask for it if it isn’t offered. I just don’t think I could ever rest without knowing for sure. Even though my Mel was “thin”, it certainly doesn’t mean it hasn’t spread, especially given my Clark level of IV. I would just rather be certain (or as certain as one can ever be with melanoma.) Now if I can just stay off Google….but I can’t. I’m obsessed. I just want to be armed with as much current information as possible just in case Mel decides to throw me a curve ball.
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