CAMUL - Carol, Please check in when possible ..

VickiSam
VickiSam Member Posts: 9,079 Member

How are you feeling?  Disability issues still ongoing?   We are thinking about you ..

 

Vicki Sam

Comments

  • New Flower
    New Flower Member Posts: 4,294
    hi Carol

    Looking forward to hearing from you. I saw repy to Eileen's post hoping you have been doing reasobly well. 

    Hugs

  • SIROD
    SIROD Member Posts: 2,194 Member
    For Carol:

    I think of you daily and all you have been going through.  A short note to update us?

    Hugs,

    Doris

  • camul
    camul Member Posts: 2,537
    SIROD said:

    For Carol:

    I think of you daily and all you have been going through.  A short note to update us?

    Hugs,

    Doris

    I did this last nite, must not havr waited long enuf.
    Have seen med onco, pain mgt dr, and rad onco. med onco says tumor markers looked ok nothing to worry about, maybe do acupuncture/and massages 1-2 weekly. Paun doc took blodwork, came back low on vit b12 and hypothyroidissm again, made me appt w/ endo. Rad onco looked at last scan of left leg, says not stable as new metabolic/tumor activity in left leg.
    Having bone and ct/scan on Wed. She is concerned w/numbness in hands /feet as weell as whole body crampong. Med onco aagrees w/scans. Med dr. says take ritalin in am and lunchgime for exhaustion and sleeping aid at night. I say no, find out why so exhausted. Rad onco agrees, thinks something is not right as spine is so sore cant stay asleep. Wake up w/cramping and pain in legs aand spine.
    All agree, this may be as good as it gets, but checking it out none the less. .
    So a week from Monday I will have results of scans, and the following Monday I see my endocrinologist whom I love. All women now! They coordinated it all in about 15 minutes aand they have waited 3 weeks for notes from my med onco. I brought mine with me, but his office has not responded after 2 requests.
    I am hoping they can fix whatever, there is not much quality now.
  • Clementine_P
    Clementine_P Member Posts: 518 Member
    camul said:

    I did this last nite, must not havr waited long enuf.
    Have seen med onco, pain mgt dr, and rad onco. med onco says tumor markers looked ok nothing to worry about, maybe do acupuncture/and massages 1-2 weekly. Paun doc took blodwork, came back low on vit b12 and hypothyroidissm again, made me appt w/ endo. Rad onco looked at last scan of left leg, says not stable as new metabolic/tumor activity in left leg.
    Having bone and ct/scan on Wed. She is concerned w/numbness in hands /feet as weell as whole body crampong. Med onco aagrees w/scans. Med dr. says take ritalin in am and lunchgime for exhaustion and sleeping aid at night. I say no, find out why so exhausted. Rad onco agrees, thinks something is not right as spine is so sore cant stay asleep. Wake up w/cramping and pain in legs aand spine.
    All agree, this may be as good as it gets, but checking it out none the less. .
    So a week from Monday I will have results of scans, and the following Monday I see my endocrinologist whom I love. All women now! They coordinated it all in about 15 minutes aand they have waited 3 weeks for notes from my med onco. I brought mine with me, but his office has not responded after 2 requests.
    I am hoping they can fix whatever, there is not much quality now.

    Wishing for the best

    Carol,

     

    I am keeping my fingers crossed that they can find something to help restore some quality for you again.  I wish you weren't going through this.  You are a tough tough lady.

    Fingers crossed,

    Clementine

  • Jean 0609
    Jean 0609 Member Posts: 2,462
    camul said:

    I did this last nite, must not havr waited long enuf.
    Have seen med onco, pain mgt dr, and rad onco. med onco says tumor markers looked ok nothing to worry about, maybe do acupuncture/and massages 1-2 weekly. Paun doc took blodwork, came back low on vit b12 and hypothyroidissm again, made me appt w/ endo. Rad onco looked at last scan of left leg, says not stable as new metabolic/tumor activity in left leg.
    Having bone and ct/scan on Wed. She is concerned w/numbness in hands /feet as weell as whole body crampong. Med onco aagrees w/scans. Med dr. says take ritalin in am and lunchgime for exhaustion and sleeping aid at night. I say no, find out why so exhausted. Rad onco agrees, thinks something is not right as spine is so sore cant stay asleep. Wake up w/cramping and pain in legs aand spine.
    All agree, this may be as good as it gets, but checking it out none the less. .
    So a week from Monday I will have results of scans, and the following Monday I see my endocrinologist whom I love. All women now! They coordinated it all in about 15 minutes aand they have waited 3 weeks for notes from my med onco. I brought mine with me, but his office has not responded after 2 requests.
    I am hoping they can fix whatever, there is not much quality now.

    Thinking of you Carol

    You are in my thoughts and prayers daily. 

     

    xoxo,

    Jean

     

  • camul
    camul Member Posts: 2,537
    Jean 0609 said:

    Thinking of you Carol

    You are in my thoughts and prayers daily. 

     

    xoxo,

    Jean

     

    Jean, Olga,doris, vicki Sam and Clemintine, thank you.

    Responded last nite apparently didnt send. I am doing ok. Very frustrated. Saw my Med onco, Pain Management, and rad onco in the last week. Pain doc ran adl blood tests, was out of town til Wed. By 830a. she had faxed info to med onc, rad onco, and endo then called me to let me know the results. High sugar, B12 too low, I am hypothyroidism (endo called while I was on with her). She has requested 2x for report from new med oncologist, still no reply. I told her I brought blood copies to rad onc, she was going to go and get . Rad onc has scans for Wed. will have results Fri. will meet with tumor board Monday morning before seeing me. She does not like my lungs, sounds like fluid. Med onc says everything is ok because of tumor markers, yet ct scan in er 2 months ago showed metabolic tumor activity in left leg, calf and femur. When I asked he said tumor marker was ok, not to worry. Rad onco is hesitant on more radiation, thinks at thus point oral radiation may be best option. Asked about chance of paralysis if spinal column at c spine level gets comprimsed.She said if that happens, it would also affect breathing and I wouldnt we alive long enuf to worry as I wouldnt be able to breathe Decided with her, no ritalin /sleeping pills to give me energy. Better to find the cause. This may be as good as it gets! My orig. Onco was aggressive. Chemo, scans, oxygen, etc. Then as soon as I had to go on medicare, he stopped everything but blood thinners and Thyroid meds. His only option was hospice. New med onco is all for t markers, very conservatjive. He comes from NIH andnhas always worked in research and trials, has not spent much time w/patients but they say he is really informed on all new treatments. Rad onco said both are excellent doctors, just at oposite ends of the spectrum No one can give me a prognsois, but she will work with the e do, pain mgtdr and med onc ifi he responds to her requests

  • aisling8
    aisling8 Member Posts: 1,627 Member
    camul said:

    Jean, Olga,doris, vicki Sam and Clemintine, thank you.

    Responded last nite apparently didnt send. I am doing ok. Very frustrated. Saw my Med onco, Pain Management, and rad onco in the last week. Pain doc ran adl blood tests, was out of town til Wed. By 830a. she had faxed info to med onc, rad onco, and endo then called me to let me know the results. High sugar, B12 too low, I am hypothyroidism (endo called while I was on with her). She has requested 2x for report from new med oncologist, still no reply. I told her I brought blood copies to rad onc, she was going to go and get . Rad onc has scans for Wed. will have results Fri. will meet with tumor board Monday morning before seeing me. She does not like my lungs, sounds like fluid. Med onc says everything is ok because of tumor markers, yet ct scan in er 2 months ago showed metabolic tumor activity in left leg, calf and femur. When I asked he said tumor marker was ok, not to worry. Rad onco is hesitant on more radiation, thinks at thus point oral radiation may be best option. Asked about chance of paralysis if spinal column at c spine level gets comprimsed.She said if that happens, it would also affect breathing and I wouldnt we alive long enuf to worry as I wouldnt be able to breathe Decided with her, no ritalin /sleeping pills to give me energy. Better to find the cause. This may be as good as it gets! My orig. Onco was aggressive. Chemo, scans, oxygen, etc. Then as soon as I had to go on medicare, he stopped everything but blood thinners and Thyroid meds. His only option was hospice. New med onco is all for t markers, very conservatjive. He comes from NIH andnhas always worked in research and trials, has not spent much time w/patients but they say he is really informed on all new treatments. Rad onco said both are excellent doctors, just at oposite ends of the spectrum No one can give me a prognsois, but she will work with the e do, pain mgtdr and med onc ifi he responds to her requests

    Sending good thoughts

    Okay, we need a miracle. That's the new plan. A miracle. 

    Carol, you must be feeling so overwhelmed and fatigued and frightened. I'm sending all good thoughts, my positive energy, and some prayers and some imaginary hugs.

    xoxo

    Victoria

  • camul
    camul Member Posts: 2,537
    camul said:

    Jean, Olga,doris, vicki Sam and Clemintine, thank you.

    Responded last nite apparently didnt send. I am doing ok. Very frustrated. Saw my Med onco, Pain Management, and rad onco in the last week. Pain doc ran adl blood tests, was out of town til Wed. By 830a. she had faxed info to med onc, rad onco, and endo then called me to let me know the results. High sugar, B12 too low, I am hypothyroidism (endo called while I was on with her). She has requested 2x for report from new med oncologist, still no reply. I told her I brought blood copies to rad onc, she was going to go and get . Rad onc has scans for Wed. will have results Fri. will meet with tumor board Monday morning before seeing me. She does not like my lungs, sounds like fluid. Med onc says everything is ok because of tumor markers, yet ct scan in er 2 months ago showed metabolic tumor activity in left leg, calf and femur. When I asked he said tumor marker was ok, not to worry. Rad onco is hesitant on more radiation, thinks at thus point oral radiation may be best option. Asked about chance of paralysis if spinal column at c spine level gets comprimsed.She said if that happens, it would also affect breathing and I wouldnt we alive long enuf to worry as I wouldnt be able to breathe Decided with her, no ritalin /sleeping pills to give me energy. Better to find the cause. This may be as good as it gets! My orig. Onco was aggressive. Chemo, scans, oxygen, etc. Then as soon as I had to go on medicare, he stopped everything but blood thinners and Thyroid meds. His only option was hospice. New med onco is all for t markers, very conservatjive. He comes from NIH andnhas always worked in research and trials, has not spent much time w/patients but they say he is really informed on all new treatments. Rad onco said both are excellent doctors, just at oposite ends of the spectrum No one can give me a prognsois, but she will work with the e do, pain mgtdr and med onc ifi he responds to her requests

    cont.

    I truly believe that some of the differences also come from the atmosphre. Onco:#1, is one of the owners in a 'For-Profit' offce. I had every test and scan run, every new chemo, etc every new med,
    Med onco #2 has been way consevative. Scans every 4-6 months.
    Now it is all about quality!.

  • Pixie Dust
    Pixie Dust Member Posts: 424 Member
    camul said:

    cont.

    I truly believe that some of the differences also come from the atmosphre. Onco:#1, is one of the owners in a 'For-Profit' offce. I had every test and scan run, every new chemo, etc every new med,
    Med onco #2 has been way consevative. Scans every 4-6 months.
    Now it is all about quality!.

    PUT ON THOSE PINK BOXING GLOVES AND KEEP FIGHTING

    Carol, sorry to hear that you are having so much trouble and going through alot. I am glad you found 2 Docs that may be able to come up with a new treatment plan. Girl, put on those PINK BOXING GLOVES and keep fighting and we look forward to hearing from you about hitting this beast in its ???.    (HUGS AND PRAYERS)   Pixie

  • tufi000
    tufi000 Member Posts: 745 Member
    camul said:

    Jean, Olga,doris, vicki Sam and Clemintine, thank you.

    Responded last nite apparently didnt send. I am doing ok. Very frustrated. Saw my Med onco, Pain Management, and rad onco in the last week. Pain doc ran adl blood tests, was out of town til Wed. By 830a. she had faxed info to med onc, rad onco, and endo then called me to let me know the results. High sugar, B12 too low, I am hypothyroidism (endo called while I was on with her). She has requested 2x for report from new med oncologist, still no reply. I told her I brought blood copies to rad onc, she was going to go and get . Rad onc has scans for Wed. will have results Fri. will meet with tumor board Monday morning before seeing me. She does not like my lungs, sounds like fluid. Med onc says everything is ok because of tumor markers, yet ct scan in er 2 months ago showed metabolic tumor activity in left leg, calf and femur. When I asked he said tumor marker was ok, not to worry. Rad onco is hesitant on more radiation, thinks at thus point oral radiation may be best option. Asked about chance of paralysis if spinal column at c spine level gets comprimsed.She said if that happens, it would also affect breathing and I wouldnt we alive long enuf to worry as I wouldnt be able to breathe Decided with her, no ritalin /sleeping pills to give me energy. Better to find the cause. This may be as good as it gets! My orig. Onco was aggressive. Chemo, scans, oxygen, etc. Then as soon as I had to go on medicare, he stopped everything but blood thinners and Thyroid meds. His only option was hospice. New med onco is all for t markers, very conservatjive. He comes from NIH andnhas always worked in research and trials, has not spent much time w/patients but they say he is really informed on all new treatments. Rad onco said both are excellent doctors, just at oposite ends of the spectrum No one can give me a prognsois, but she will work with the e do, pain mgtdr and med onc ifi he responds to her requests

    Keep your center dear one

    My wish that your journey on this miserable road stays stress-free and comfortable. You have been there for so many of us and maybe you will recall your own words at those times for yourself

    Sherry

  • New Flower
    New Flower Member Posts: 4,294

    PUT ON THOSE PINK BOXING GLOVES AND KEEP FIGHTING

    Carol, sorry to hear that you are having so much trouble and going through alot. I am glad you found 2 Docs that may be able to come up with a new treatment plan. Girl, put on those PINK BOXING GLOVES and keep fighting and we look forward to hearing from you about hitting this beast in its ???.    (HUGS AND PRAYERS)   Pixie

    keep looking for the best and fighting

    Hi Carol,

    I am very sorry. Please continue your fight you has been giving me inspiration at my lowest moments. My markers are always behind compare to the imaging. We have returned to every three months schedule since cancer has become active again to monitor progression.

    I am interested to hear what your radiation oncologist will propose. Please ask for a consultation with orthopedic surgeon. My doc send me for consult to orthopedic surgeon who gave me a hope and support. I have mulctiple new areas of metabolic activity on my other side that are a big concern for fractures and my mobility.

    I am also going to see radiation oncologist next week to see what can be done for palliative care.  Probably we cannont radiate all of the areas, need to be selective for palliative care. i am currentey on Afinior 5 mg. 

    I am considering  an open lable clinical study  of palbociclib (PD-0332991),  CDK4/6  Bakersfield, CA. It suppose to be a oral new drug in combination with Femara. I know you cannot do Femara, still please talk to your family, it could be am option for you. If you are interested I will PM you contact info for the trial. This drug has imazing results and has been submitted to the FDA for approval two weeks ago.

    Sending you Positive thoughts and hugs

    Olga

  • Double Whammy
    Double Whammy Member Posts: 2,832 Member
    tufi000 said:

    Keep your center dear one

    My wish that your journey on this miserable road stays stress-free and comfortable. You have been there for so many of us and maybe you will recall your own words at those times for yourself

    Sherry

    I hate that you continue to struggle so much

    to find the right combination of whatevers to improve your quality of life.  Just wish I could make it all better.  I do continue to keep you in my thoughts and prayers.

    Hugs,

    Suzanne

  • VickiSam
    VickiSam Member Posts: 9,079 Member

    I hate that you continue to struggle so much

    to find the right combination of whatevers to improve your quality of life.  Just wish I could make it all better.  I do continue to keep you in my thoughts and prayers.

    Hugs,

    Suzanne

    Carol ...

    Sisters in PINK -- have circled around you, sending LOVE, Support, PRAYERS, Positive Thoughts, HOPE, and Magic Sprinkles...  We prayer relief comes to you, and sooner.

    You inspire so Many of Us!

     

    Vicki Sam

  • camul
    camul Member Posts: 2,537
    VickiSam said:

    Carol ...

    Sisters in PINK -- have circled around you, sending LOVE, Support, PRAYERS, Positive Thoughts, HOPE, and Magic Sprinkles...  We prayer relief comes to you, and sooner.

    You inspire so Many of Us!

     

    Vicki Sam

    Thanks Vicki Sam!
    I am trying to stay positive. Sometimes it is just hard. I am hoping that the scans Wedbesday will give some answers. It is always easier when I know what I am looking at. I have just been so frusstrated when I leave a doctors office with throbbing pain and the only thing they come up with is the tumor marker looked good. I just want to scream. I will get through it, just hoping that there is an answer even if it is'there is nothing we can do', but this is what is happening in your body!
    Glad you made it home safely. I love Cabo! That would have been quite the experience.One I am glad I have never experuenced. Will they ship your belongings?
  • VickiSam
    VickiSam Member Posts: 9,079 Member
    camul said:

    Thanks Vicki Sam!
    I am trying to stay positive. Sometimes it is just hard. I am hoping that the scans Wedbesday will give some answers. It is always easier when I know what I am looking at. I have just been so frusstrated when I leave a doctors office with throbbing pain and the only thing they come up with is the tumor marker looked good. I just want to scream. I will get through it, just hoping that there is an answer even if it is'there is nothing we can do', but this is what is happening in your body!
    Glad you made it home safely. I love Cabo! That would have been quite the experience.One I am glad I have never experuenced. Will they ship your belongings?

    When we Left with the clothes on our backs,

    that was it -- all belongs, went to the hundred's of looters --  No electricity, no power - so there is no way of keeping tabs on tourists, or personal belongings.

    In fact - at Cao airport - our pass ports were checked, and information written down on paper -- with a good old fashion pen. hahaha

    no access into the international terminal, as it was damaged by hurricane - we stood in streets, and tar mat for 18 hours - 92 degree weather, 90% humidity.

     

    Vicki