Chemo in July - Let's support each other!
I will begin Chemo in July. This is all new to me. Anybody that wants some support, I'll be there for you. We can do this! If we could stay on the topic of our specific diagnosis and treatment, that would be great, but everyone is welcome to discuss. Together is stronger!
Comments
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Me to and I can relate to this newness. Where will you have your chemo? I will be going thru Baptist Hosital Kendal facility. I will be undergoing Caboplantin and Taxotere once a week every third week for six sessions. Then Herceptin weekly for a year. Guess pretty standard treatment for Stage1A, node negative, HER2+ breast cancer. Somewhere I will also take an oral hormone blocker for ten years. Once completed then radiation will follow at five days a week, time undetermined as of yet. I've been reading alot of the blogs and I'm really glad I did. Very helpful to know the reactions from the chemicals that we all must endure. I wish there was more on cold scalp therapy. I know insurance doesn't cover it, but it's really not that expensive on a monthly basis. The results are phenomal on keeping your hair during chemo. Process a little tedious, but once you jump on the horse and ride it I'm sure it will be easy peasy. I'm looking into it as my hair is almost touching the top of my buttocks and is thick with great body. Now that I'm getting older the silver is coming in beautifully. This is probably the least thing I should be focusing on, but since Fenruary I have made myself sick with worry, educating myself thru this process, trying to understand going natural verses chemotherapy, and making a final decision to get on with it. Well here I am ready to get it done and over with. Still scared but hopeful. Here we all go fighting together for the same reason! 🤓😇😉😃
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Thank you so much Maria for commenting. I'm determined to kick the devil in the tail with this sickness! How ironic after being in the medical field since I was 18 and never once thinking that I would get hit up the head with such a devasting disease. I always, always sacrificed my life in the field for all my patients, now I'm on the other end. Guess knowing what I know from behind the scenes it what scares me the most.
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Hi JMSusan and tsambile
JMSusna we have a very similar diagnosis, and tsambile we have a similar treatment plan.
I'm doing 4 rounds of TC, weekly Herception followed by a year of Herceptin every 3 weeks. Ive gotten one done so far (July 6th) and it wasn't nearly as bad as I anticipated.
Ive had minimal nausea, which I've kept at bay with Zofran. This week I do have flu-like symptoms, but I'm not sure if its related to chemo because I was a little sick when I started.
Glad to find you ladies, we can do this!
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