Mohs Surgery Experience
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- Опубликовано: 19 мар 2023
- 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 RUclips 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.
Please my dear girl be strong ! ❤
😢😢 inshallah u gonna be healthy ❤
In Cuba used HEBERFERON for skin cancer, be healthy.
Thanks for the advice. I have Myasthenia GRAVIS.. I was diagnosed about 6 yrs ago and besides mestinon... Those 2 medications you just named are the 2 they had me try out instead of IVIG... however... They both made me violently I'll... And of course they never mentioned the side effects of the medication especially the cancer part. They never do .. with me .. anyway. They never explain shit. I had to do my own research with my MG when I left my 11 days in ICU after walking around.. barely alive for over year
Yeah, it is unfortunate but with most of our health experiences we have to figure out these things on our own. It is one of the reasons why I continue to advocate. I'm sorry you had to go through that! I was not aware of all the risks until I read the very fine print.
Do have continous muscle twitching????
Can I ask how long you were on the immunosuppressant? Was it imuran or cellcept?
I’m sorry. I joked with my dermatologist: @will there be anything left of me”. As I did a pointing finger inch worm across my eyes like the dance in pulp fiction.
WHY didnt you just put rick simpson oil on it?