Hand and foot syndrome… anyone experience that?
Hi guys! Merry Christmas!🎁 I have 5 more treatments to go and now have hand/foot syndrome. Yayyyy! What are your experiences with this? My hands have started peeling and I have massive callouses on my feet now. I hate the feel of the working hands and feet creams and ordered udderly smooth. Hands get the tingling and burning swollen feeling and my feet as well for a couple days after treatment. Oncologist said it will get worse. I am wondering how worse with 5 weeks to go could it get for me and if I can prevent it? She hasn’t lowered my dosage. I don’t know if she will or not. The visiting nurse thought they might. Hanging in there though! Over the hump…
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Thank you! My son is my rainbow! 🌈 I just got the clearance to exercise so I am going work on getting down a couple more sizes and work on writing some songs! I am looking at this as an opportunity to just be! Its been a while since I could do that. I am so glad you made it to the other side. I couldn’t imagine being in the hospital that much. 4 days after my surgery was enough for me!
I love the "just be" part of that!
I have no personal experience with HFS... I guess I got lucky.
Here's some info about it I found:
https://my.clevelandclinic.org/health/diseases/24105-hand-foot-syndrome
Notice that 5FU is listed as one of the causes.
The article has some advice for treatment of symptoms.
Meanwhile, hang on! you'll get through it.
Last, a very Merry Christmas to you and yours!