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Lisa O

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Everything posted by Lisa O

  1. I would like to second Ry's post. Those last wishes go double for you Ry.
  2. I thought there was something wrong with my shoulder, like a torn tendon. It was the CT that diagnosed the lung cancer.
  3. I'm here! I've been in PT since March to build muscle and have a CT this Friday. Otherwise... status quo
  4. I thought lung cancer was already responsible for more deaths than breast cancer in women? Interesting about the herbs. I hope they lead to some quick meds.
  5. There are many different studies going many different ways. Some studies of late have shown that antioxidants do not necessarily protect cancer from chemo as many oncologists believe. My oncologist is fine with the diet and excercise part of the alternative/complementary path, but will not allow supplements while on chemo.
  6. Lisa O

    John

    Ry, My heart breaks for you. I know this is a tremendous loss for you and your family. You will all be in my prayers. Lisa
  7. There are a few posts on this in the alternative med forum. I think there may be some validity in the nutrition aspect of the diet. Some believe the restrictions are a bit harsh.
  8. I agree, this is very exciting. Be careful to check with your doc before taking the supplements that are out there though, because they interact with some meds and can cause bleeding or gi problems in the wrong combinations.
  9. Welcome Colleen! I hope you and NED have a long and happy time together.
  10. Linzy, I understand the fear. Even considering cancer is scary. Also remember, that even if it is inoperable lung cancer, many of us continue to do very well and stay stable for many years with all of the new treatments they are discovering. Keep positive and keep us posted.
  11. awesome! thanks for the heads up!
  12. From another melanoma and LC SURVIVOR, I am praying and betting you will battle this one off. I wish you the best.
  13. Lisa O

    Roll Call...

    Ry, This was a great idea. I have been looking for updates and am never sure where to look. I am thrilled to hear Hebbie's news and everyone is always in my thoughts.
  14. I have taken pieces of certain plans and diets throughout my diagnosis. I do not follow any plan to the extreme but I do eat cottage cheese and flax seed oil on the idea that it can only help. As for anything that may compromise treatment.... I leave that part out.
  15. I would guess that smoking marijuana as dealer's sell it to the general public poses more of a risk due to chemicals and impurities ingested through the lungs.
  16. Great advice Rich. My doc did not want me to take much more than a multivitamin with Iressa.
  17. That is a great article. Too many excercise enthusiasts are all or nothing. I really liked this article.
  18. Lisa O

    Please Think

    Bill, I am a caregiver and a survivor as both my mother and I have nsclc. I understand what you are saying and feel terrible that anyone here would feel the need to treat you with disrespect. I thought your post was framed respectfully and most of the responses were also respectful. We all need to treat eachother with respect... we are not the enemy... cancer is. If you have a request, people should allow you to vent it. If they disregard it, you can choose to ignore the posts. I did not feel you slammed anyone and I would hope that no one here would be mean to anyone else. In one way or another we are all in this together. Please try to remember that we are people and not statistics. If someone posts some disheartening news they may be looking for reassurance. I am sure and would hope that no one would post sad news for the purpose of bringing others down. If us survivors are not up for the job, perhaps someone else can step up to the plate. I hope so. That is what makes this community great.
  19. I love Curry for taste... but I have heard of people having some interactions with the supplements in large quantities. It is always good to talk to physicians about medical interactions if taking supplements.
  20. Lisa O

    Melissa Zagon

    Melissa was the first person I spoke with after being diagnosed. She was so helpful and such an inspiration. My heart breaks for her family. I will be forever grateful and inspired by the legacy she has left behind.
  21. I am glad you were able to enjoy your children Don. I am sorry you were missing Lucy.
  22. I understand as well. My doctor doesn't want all of the supplements during treatment. He agrees that some are very beneficial to the immune system when we are out of treatment but the supplements can affect chemo.
  23. When I was first diagnosed, every doctor told me horrible devastating news. I walked around in a fog and missed some of the joy that was available in the first few months. I am still stage four.... over four years later. What I have learned is to celebrate each moment. Doctors cannot tell anyone how much time they have. It is up to us to enjoy every minute of the time we have with family and friends. I can't give you a look into the future.... but I can tell you that you have your dad NOW... and you could easily have him for years to come. Either way, you will never get this moment back, so take pictures, eat pie, light candles and give hugs. Whether you have one day or thousands, that it what makes happiness.
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