My surprising journey from diagnosis to Mohs surgery...
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- Опубліковано 9 тра 2024
- In January I had the Mohs Surgery to treat a recent basal skin cancer diagnosis. Here is what my experience was like!
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My name is Samantha Wayne and I have been creating advocacy videos on UA-cam since 2009. This channel was formerly known as Live Hope Lupus and was created in order to start a community for those living with chronic illnesses. In September 2019, I transitioned to a plant-based diet and I have found my body is responding well to it. Along with my lifestyle change, I am learning to alter my focus more on the positive. My current content will focus on my healing journey, what food I am eating, and everyday life. I will still be posting an occasional update about my health. I hope you all are ready to join me on this crazy journey of healing. We are all learning how to navigate this life together. If you have subscribed, thank you! I appreciate your support and look forward to talking with you all in the comments.
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DISCLAIMER: This content within this video is not medical advice. The purpose of these videos are for general education and to share my own experience. This content should not be used to self-diagnose or self-treat any health condition. Please consult a healthcare professional before attempting anything in this video.
I had Basel cell carcinoma twice. It was on my nose, and my right ear. Now I have a more aggressive form of skin cancer on my jaw line. I know exactly what you are saying. Bless you sweetheart 😢
First of all - thanks for sharing your journey with all of us. I know it can be difficult going through with this or shall I say reliving this all over again(on camera). Just know that SHARING IS CARING and that you sharing your journey inspires others like myself to go through life and all it's difficult experiences good or bad. By you giving a bit exposing yourself and what you have or what you are going through helps others including myself to know that I or we are not alone in life and all it's battles.
Big thanks 🙏 Samantha for sharing your journey and essentially "You are not alone I am here with you always!"
So happy you made it through.
Blessings to you.
I'm so glad that you are okay and Hope you be healthy Always ❤
Thank you very much!
I am totally here to support you. I truly appreciate that you share your journey. It is so important that people realize what it is truly like.
I think the scar healing looks really good. There are wonderful products that you can you use to continue healing it. Sunscreen (which you already know about) is the best to protect from hyperpigmentation.
Sending positive energy
I’m totally here to support you, I just found your channel and I’m so glad I did💖
Didnt realise you tried the Protocol previously. Good Luck with your health.
Bless you, dear.
Thank you for you costochondritis tutorial, I’m devastated to hear you have cancer, I swear some people are put through these things perhaps as a Devine test from god to see if you see the silver lining and make the most of what you’re delt with 🤷🏻♂️ idk just a thought from someone who’s had a number of health issues
Thank you so very much for all you do for us ❤❤❤
Has your dermatologist talked to you about treating the scar? I needed my open heart surgery scar treated because it was turning into a keloid and hypertrophic in different spots. Anyway, they treat scars with steroid injections and I was surprised to learn it's the same thing as the steroid shot at the rheumatologist for lupus flairs! Fair warning it HURTS a lot worse than the numbing but the results are fantastic. Might be worth asking your dermatologist down the line if the scar bothers you or hurts.
hi sister i hope your will fine, prayers for you and dont be worried your face looks normal and beautiful after the biopsy,be strong ,prayers from a systemic sclerosis worrior!!
I have just been diagnosed with a basal cell carcinoma in just about the same spot. My history is one of autoimmune conditions - Hashimotos thyroiditis, Alopecia, Rosacea, PLE (sun allergy with urticaria). I've recently learned that photosensitivity can be autoimmune. It's difficult. I wish there was some form of treatment that was less invasive.
Sos muy valiente ❤
When I had my nose taken care of. I had to go back in four times, before they got it all. My ear was only twice. I believe my skin cancer came from years, and years of being in the sun, when I was young. Now I am 75, and I'm still going through it. We didn't know anything about any kind of cancers back then.. My father died of throat cancer, and my Mother died of liver cancer.
Hi..
So I just had mohs / forehead flap on my right lower side of my nose surgery two weeks ago, and I had my stitches removed, last Wednesday now I’m experiencing some numbness on my upper lip where my stitches were removed ..
Did you experience any numbness during your healing process?
You look really good! You really don’t notice.
Thank you!
Hi Samantha! How is your Costocondritis now?
❤❤❤❤❤❤❤❤!!!!
Didn’t you consider HSCT?
Hi Samantha, so sorry that you got basal skin cancer 🥲🥲🥲 Do you think taking Cellcept has something to do with that? Since one of the side effects of Cellcept is increasing the risk of getting cancer especially lymphoma and skin cancer.
Been diagnosed with Lupus SLE Lupus nephritis with ANCA vasculitis and taking prednisolone, plaquenil and Cellcept for 7 months now. I’m so scared of the side effects of the medication 😢😢😢
did you ever try Rituxam for your condition and if so, how did it work for you