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All TopicsForum: HER2+ (Positive) Breast Cancer → Topic: Cold Therapy Gloves and Booties to Combat Chemo Neuropathy

Topic: Cold Therapy Gloves and Booties to Combat Chemo Neuropathy

Forum: HER2+ (Positive) Breast Cancer —

Testing, treatment, side effects, and more.

Posted on: Oct 25, 2017 02:02PM

TreysRib wrote:

Hello,

Has anyone tried cold therapy gloves or booties during chemo to combat neuropathy? If so, what brand did you purchase and from which site. Thanks

Dx 9/21/2017, IDC, Right, <1cm, Stage IA, Grade 3, 0/1 nodes, ER+/PR+, HER2+ Surgery 10/12/2017 Lymph node removal: Sentinel; Mastectomy: Right; Reconstruction (right): Tissue expander placement Chemotherapy 11/14/2017 Taxol (paclitaxel) Targeted Therapy 12/4/2017 Herceptin (trastuzumab)
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Oct 25, 2017 02:24PM OCDAmy wrote:

TreysRib, They are pretty expensive. I just bring quart size zip lock bags and fill them with ice at the infusion center. I wear thin socks and rubber medical gloves. I only using during the taxotere infusion which is an hour and I only put my fingers and toes on ice. I start 15 minutes before and keep the ice on 15 minutes after. They give me washcloths at the center to place under the bags because they sweat but you could bring your own. I have had no neuropathy or nail issues.

Dx 2/2017, IDC, Left, 4cm, Stage IIB, Grade 2, 2/13 nodes, ER+/PR+, HER2- Chemotherapy Cytoxan (cyclophosphamide), Taxotere (docetaxel) Surgery Lymph node removal; Mastectomy: Left; Prophylactic mastectomy: Right; Reconstruction (left): Tissue expander placement; Reconstruction (right): Tissue expander placement
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Oct 25, 2017 03:07PM Legomaster225 wrote:

TreysRib, I used booties with gel packs on my feet. I bought them off Amazon for around $25 I think. They worked well. For my hands I just held a frozen water bottle or bags of ice. I did not experience any neuropathy. Whether it was the icing or just luck I'll never know but I was happy. I also drank slurpees or frozen cokes during treatment to kept my mouth cold. I just like them but maybe those helped as well.

Dx 12/3/2016, IDC, Right, 3cm, Stage IIB, Grade 2, ER+/PR+, HER2- Chemotherapy 1/19/2017 AC + T (Taxol) Dx 6/22/2017, IDC, Left, <1cm, Stage IB, Grade 1, ER+/PR+ Dx 6/22/2017, DCIS, Left, <1cm, Stage 0, Grade 1 Surgery 6/22/2017 Lymph node removal: Sentinel; Mastectomy: Left, Right; Reconstruction (left): Silicone implant; Reconstruction (right): Silicone implant Radiation Therapy 8/22/2017 Whole-breast: Breast, Lymph nodes, Chest wall Hormonal Therapy 10/17/2017
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Oct 25, 2017 05:14PM Meg101 wrote:

I've been using small ice packs that fold over my toes and fingers during infusions. The ice packs are called CryoMax. They stay frozen for eight hours with no dripping, sweating, or refreezing. I bought them through Amazon. The size I bought were 6 inch x 6 inch squares. There are 2 ice packs per box, so I bought 2 boxes (total of 4 ice packs) to cover both feet and both hands. The total cost was about $20. The infusion nurses loved them because they didn't have to replace any ice or clean any wet areas. In fact, the infusion center is considering buying them for all their patients so the nurses don't have to deal with hauling ice and mopping up when ice melts. You will have to specify the "CryoMax" brand when you search on Amazon. Hope this helps. Oh, just wear a pair of regular socks while icing.

Dx 7/14/2017, IDC, Left, 3cm, Stage IIB, Grade 2, 3/14 nodes, ER+/PR+, HER2- Surgery 8/11/2017 Lumpectomy: Left; Lymph node removal: Left, Sentinel, Underarm/Axillary Chemotherapy 9/18/2017 AC + T (Taxotere) Targeted Therapy Hormonal Therapy Aromasin (exemestane) Radiation Therapy Whole-breast: Breast
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Oct 31, 2017 11:41AM - edited Oct 31, 2017 11:50AM by jenglutenfree

meg101 - Thank you for the cryomax advice. Do you wear the socks under or over the packs?

JenGF Dx 8/18/2017, IDC, Left, 3cm, Stage IIB, Grade 2, ER+/PR+, HER2- (IHC) Chemotherapy 9/21/2017 AC + T (Taxol)
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Oct 31, 2017 02:38PM TreysRib wrote:

Thanks Meg 101. I ordered the packs from Amazon so I am ready to go. One question, do you use socks for your hands and feet? If not, what do you use for your hands

Dx 9/21/2017, IDC, Right, <1cm, Stage IA, Grade 3, 0/1 nodes, ER+/PR+, HER2+ Surgery 10/12/2017 Lymph node removal: Sentinel; Mastectomy: Right; Reconstruction (right): Tissue expander placement Chemotherapy 11/14/2017 Taxol (paclitaxel) Targeted Therapy 12/4/2017 Herceptin (trastuzumab)
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Nov 11, 2017 02:07AM Faithonfire wrote:

hi everyone, I know cold is all the rage in new therapy for peripheral neuropathy but I have only seen that work for patients new to the symptom in my experience under 6 months to a year. I have heard many happy stories of using snow layer in hats and socks with one hat snow and second hat after bathing to try to avoid hair loss with limited success but great for hot flashes at least!

Didn't work nearly as well as I hoped either, once it started falling out fast it was gone in under a week no matter what I did so I got a free shave and new wig at a fabulous salon that donates everything to patients and survivors every month and it's such an amazing gift to be able to be a part of it all I had to share the latest tidbits we talk about in what we all call living with it!

I'm unique on a few levels more than previously joked about with family and friends, and having genetic proof of that now I hope it helps others to adapt and heal the way my body is right now during chemotherapy treatments that doctors can't explain. Not only do I have active hair regrowth on taxol now, it turned from white to brown last 2 months without any fallout at all, patches are changing color as they get longer and thicker it's freaky!

I've had peripheral neuropathy in my hands and feet for over 12 years now and I am very blessed that it was rarely painful but gradual heat therapy always worked better for me than anything else I have ever tried. My skin does not burn only when it is cold but I cannot accurately determine temperature on my skin below my elbows so it is important to know personal limitations and risks to any type of therapy you plan to use during chemotherapy treatments that make symptoms flare on top of new ones!! My team was quick to address it and my results of therapy are amazing benifit to my quality of life I wanted to share with you all.

Bottom line is, I HATE being cold, even during hot flashes I want wind over cold because I was sensitive to it before but on chemo I feel like I need a plastic bubble with a temperature of 70 to cruise around in!

so it's more about what you find comfortable in your circumstances and practical and safe for your total care plan.i do enough damage with a scooter in a store I can't imagine how much fun a huge hampster ball would be!

Take care and best of luck to everyone

Dx 6/25/2017, IDC, Both breasts, Stage IIIC, ER+, HER2- Chemotherapy 7/13/2017 Abraxane (albumin-bound or nab-paclitaxel), Cytoxan (cyclophosphamide), Doxil (doxorubicin), Methotrexate (Amethopterin, Mexate, Folex) Chemotherapy 9/1/2017 AC + T (Taxol)
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Nov 14, 2017 01:06PM snowday123 wrote:

thank you for detailed info! So helpful.

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