Diamondm35

Activity

  • ld_105
    Welcome to What Next!
    April 2014
  • MarnieC
    Hi Diamondm35 - you asked me about juicing. I have a few recommendations on my website, but this article explains why it's so good for you and a few other tidbits. http://marnieclark.com/do-you-know-the-benefits-of-juicers-for-cancer-patients/ My best advice is to go with green vegies like kale, celery, cucumber, a little bit of pear to sweeten it a tiny bit, ginger, beet (fresh only), carrot and you could throw in some blueberries because research is showing they are great for triple negative breast cancer. Hope that helps!
    March 2014
  • banditwalker
    Hi diamondm, how is your radiation therapy going? I just posted a question about types of creams to use and saw you had also asked the same. Did you have any success with anything? And, are you burning at all? I start rads this Tues.
    Hope all is well.
    March 2014
  • Gabba
    DCIS is ductal carcinoma in situ, which means it is in the duct and is not invasive. Hope this helps.
    February 2014
  • Carool
    Dimondm35, just saying hi and hoping you are feeling okay. Best, Carol
    February 2014
  • TiffanyJ
    Hi Diamond, just wanted to check in with you. How are you feeling? Sounds like you got some great advice about taxol. I hope you are doing better, or that your doctor will work with you if you need more help. You made it thru the AC, just a few more weeks...you will be done soon!
    December 2013
  • CyndiLou
    I had 18 weeks of taxol and had to take a break at week 16 b/c it was to hard on my body and I needed to stop prior to surgery. I did have about a 6 week break and it was great! Yes, my hair fell out, my taste buds were AWFUL, I was running to the bathroom all the time, my bones ached and I did have abdominal pain. However, as crazy as this sounds I was able to keep myself in good moods by exercise. I went to the gym 2-3 times a week and would cut the grass weekly with a push mower. I took over the counter caltrate for the bone pain. Taxol affects your bones so you need to take something to help keep them strong. The exercise I did was only cardio like the climber, elliptical and the treadmill. 6 weeks after my surgery I added weights to my routine. I am now on day 17 of radiation and the fatigue is awful, but I am going to the gym still....ugh! I believe the exercise keeps the few white blood count and the red blood cells moving & gets you endorphins going. The YMCA has a 12 week free program for cancer patients. The gym I go to isn't the Y, but my trainer works with me and my journey and he keeps up with my blood counts, side effects and we make adjustments where & when needed. I did not go to the gym prior to cancer but am so glad I decided to do my part to kick cancer in addition to what the doctors said to do. Good luck to you as you battle through this. You will hit a wall, but take everything you can and u will get over it and it's much better on the other side.
    December 2013
  • GregP_WN
    Hello and welcome, we are glad you found us. Please feel free to join in the conversations. Here is a link to our cancer dx page for your type of cancer. Take a look at it to get you started on some information. You will notice at the bottom of that page 4 of our active users who have had that journey already, you may wish to contact them for their experience and wisdom. Also, I encourage you to go to the questions page now by clicking on the questions tab at the top of the page and post what is the most pressing issue you have right now. This will introduce you to the community and get you started on the help you need right now.

    https://www.whatnext.com/conditions/cancer/breast-cancer
    There are also subtypes listed on this page to narrow down the type of cancer to match your dx.

    Also, if you can take a few minutes and fill in some details of your journey so far, it will help others as they try to answer questions for you, it also helps others as they search through the data base to find someone like themselves. Confirming your email will allow you to receive updates and notices from the site when someone answers your questions or writes on your wall.

    Thanks for being with us and let me know if I can help you find any information on the site. After you have an opportunity to look the site over and see what great things there are here, we encourage you to invite your friends, family or anyone you know that may be helped by the connections on WhatNext to join the site also. Just click this link to invite them to join. http://www.whatnext.com/recruit-a-friend

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    GregP 3X Survivor
    Team WhatNext Community Mgr.
    December 2013
  • SueRae1
    welcome to WhatNext. I'm sorry you needed to find us, but now that you are here you will find the greatest bunch of supportive people whose combined knowledge is awesome. We can answer your questions, hear you vent and celebrate good news with you.
    I see you have begun exploring our site and look forward to learning more about you and your journey.
    December 2013
  • DaveWaz

    Welcome to the WhatNext family! The WhatNext family is made up of people like you who are looking for help or looking to help others. To help you along your journey the WhatNext family has put together a Beginner's Guide to Cancer that I highly recommend you check-out here: http://bit.ly/10BQKCi. Also, please do not hesitate to reach out to others or ask for help.

    Wishing you the best.

    David
    Founder, WhatNexter
    December 2013