Update from Judy plus she wants to know if anyone has had a similar experieance
Comments
-
To my Sister, Judy
I can not answer this question but I am thinking of you, Don and Caitlin always. I pray for resolve to these issues and I admire your strength. Popi is praying for your family and would love to come meet you and Don. Please let me know if there is anything I can do, I am 1 hour away. Don is a HERO and tell him Team Popi is cheering him on... Love you guys-Lynn0 -
Freida & LynnFighting4Popi2 said:To my Sister, Judy
I can not answer this question but I am thinking of you, Don and Caitlin always. I pray for resolve to these issues and I admire your strength. Popi is praying for your family and would love to come meet you and Don. Please let me know if there is anything I can do, I am 1 hour away. Don is a HERO and tell him Team Popi is cheering him on... Love you guys-Lynn
Thank you so much. I was without the iPad today and I don't know how to copy and paste on the iPhone.
Doctor came in tonight and said the plan for tomorrow is to tap and drain fluid and send that off to pathology. Until the kidneys greatly improve they are unable to another ct scan. They are also going to another dialysis if the numbers are favorable for that. It really wiped him out today. They are at a loss as to the cause of this except they have said their worst fear is a recurrence but so far they have been unable to find it. The increasing soft tissue was not there in February but did show up in June (which I did not know until tonight) and it has also increased since June as evidenced in the MRI they did last week or over the weekend. They did say it could either be scar tissue or the cancer. They cannot get to it to biopsy.
This is tiring and frustrating so I sure hope something gives here pretty soon and can shed some light. They said if it is a recurrence he could not tolerate chemo in his condition. Their immediate goals are to get the fluid off and try to get him eating or at least able to tolerate the ng feeding. They do not want to do the TPN feeding unless they absolutely have to because that could add stress to the kidneys and he sure doesn't need that.
Don told me tonight that he doesn't want anything to happen here at the hospital. He wants to go home if he isn't going to get better. I would hope the right thing to do will become apparent very soon. I don't want to leave without answers but I want him to come home also. We built that home together from the ground up. I dug the footings and me and my uncle showed Don how to build the garage. We had our daughter there. If there is some good answer to be had I pray that God will show us and the doctors soon.
Hugs and FEC,
Judy0 -
My dearest JudyJReed said:Freida & Lynn
Thank you so much. I was without the iPad today and I don't know how to copy and paste on the iPhone.
Doctor came in tonight and said the plan for tomorrow is to tap and drain fluid and send that off to pathology. Until the kidneys greatly improve they are unable to another ct scan. They are also going to another dialysis if the numbers are favorable for that. It really wiped him out today. They are at a loss as to the cause of this except they have said their worst fear is a recurrence but so far they have been unable to find it. The increasing soft tissue was not there in February but did show up in June (which I did not know until tonight) and it has also increased since June as evidenced in the MRI they did last week or over the weekend. They did say it could either be scar tissue or the cancer. They cannot get to it to biopsy.
This is tiring and frustrating so I sure hope something gives here pretty soon and can shed some light. They said if it is a recurrence he could not tolerate chemo in his condition. Their immediate goals are to get the fluid off and try to get him eating or at least able to tolerate the ng feeding. They do not want to do the TPN feeding unless they absolutely have to because that could add stress to the kidneys and he sure doesn't need that.
Don told me tonight that he doesn't want anything to happen here at the hospital. He wants to go home if he isn't going to get better. I would hope the right thing to do will become apparent very soon. I don't want to leave without answers but I want him to come home also. We built that home together from the ground up. I dug the footings and me and my uncle showed Don how to build the garage. We had our daughter there. If there is some good answer to be had I pray that God will show us and the doctors soon.
Hugs and FEC,
Judy
You both
My dearest Judy
You both have been thru so much with so few answers.This poor man's strength must be at his limit and your caregiver skills are at a breaking point. I certainly know how you feel.
Thank God they are going to drain Don's fluid today. He can at least be a bit more comfortable I would hope.
I hope it is not, but if it is a recurrance then I know Don and you would want to be home.Hospice came to our house and made Vince more comfortable.
My heart is breaking for you and your family. If there were some magic words that I could say to make this all go away I would. But I know I can't.
I am so very sorry.
FEC FEC FEC FEC FEC.
No one deserves to go thru this.
LOVE to you and Don
Barbara0 -
Praying for that answer...JReed said:Freida & Lynn
Thank you so much. I was without the iPad today and I don't know how to copy and paste on the iPhone.
Doctor came in tonight and said the plan for tomorrow is to tap and drain fluid and send that off to pathology. Until the kidneys greatly improve they are unable to another ct scan. They are also going to another dialysis if the numbers are favorable for that. It really wiped him out today. They are at a loss as to the cause of this except they have said their worst fear is a recurrence but so far they have been unable to find it. The increasing soft tissue was not there in February but did show up in June (which I did not know until tonight) and it has also increased since June as evidenced in the MRI they did last week or over the weekend. They did say it could either be scar tissue or the cancer. They cannot get to it to biopsy.
This is tiring and frustrating so I sure hope something gives here pretty soon and can shed some light. They said if it is a recurrence he could not tolerate chemo in his condition. Their immediate goals are to get the fluid off and try to get him eating or at least able to tolerate the ng feeding. They do not want to do the TPN feeding unless they absolutely have to because that could add stress to the kidneys and he sure doesn't need that.
Don told me tonight that he doesn't want anything to happen here at the hospital. He wants to go home if he isn't going to get better. I would hope the right thing to do will become apparent very soon. I don't want to leave without answers but I want him to come home also. We built that home together from the ground up. I dug the footings and me and my uncle showed Don how to build the garage. We had our daughter there. If there is some good answer to be had I pray that God will show us and the doctors soon.
Hugs and FEC,
Judy
Praying that you will get that answer as to what to do.0 -
Man...JReed said:Freida & Lynn
Thank you so much. I was without the iPad today and I don't know how to copy and paste on the iPhone.
Doctor came in tonight and said the plan for tomorrow is to tap and drain fluid and send that off to pathology. Until the kidneys greatly improve they are unable to another ct scan. They are also going to another dialysis if the numbers are favorable for that. It really wiped him out today. They are at a loss as to the cause of this except they have said their worst fear is a recurrence but so far they have been unable to find it. The increasing soft tissue was not there in February but did show up in June (which I did not know until tonight) and it has also increased since June as evidenced in the MRI they did last week or over the weekend. They did say it could either be scar tissue or the cancer. They cannot get to it to biopsy.
This is tiring and frustrating so I sure hope something gives here pretty soon and can shed some light. They said if it is a recurrence he could not tolerate chemo in his condition. Their immediate goals are to get the fluid off and try to get him eating or at least able to tolerate the ng feeding. They do not want to do the TPN feeding unless they absolutely have to because that could add stress to the kidneys and he sure doesn't need that.
Don told me tonight that he doesn't want anything to happen here at the hospital. He wants to go home if he isn't going to get better. I would hope the right thing to do will become apparent very soon. I don't want to leave without answers but I want him to come home also. We built that home together from the ground up. I dug the footings and me and my uncle showed Don how to build the garage. We had our daughter there. If there is some good answer to be had I pray that God will show us and the doctors soon.
Hugs and FEC,
Judy
I have been praying for strength for you both. I'm really at a loss for words, but your courage as a wife and caregiver have truly been an inspiration to me. Hang in there, Don. Hang in there.
~Jayme0 -
prayers for youJReed said:Freida & Lynn
Thank you so much. I was without the iPad today and I don't know how to copy and paste on the iPhone.
Doctor came in tonight and said the plan for tomorrow is to tap and drain fluid and send that off to pathology. Until the kidneys greatly improve they are unable to another ct scan. They are also going to another dialysis if the numbers are favorable for that. It really wiped him out today. They are at a loss as to the cause of this except they have said their worst fear is a recurrence but so far they have been unable to find it. The increasing soft tissue was not there in February but did show up in June (which I did not know until tonight) and it has also increased since June as evidenced in the MRI they did last week or over the weekend. They did say it could either be scar tissue or the cancer. They cannot get to it to biopsy.
This is tiring and frustrating so I sure hope something gives here pretty soon and can shed some light. They said if it is a recurrence he could not tolerate chemo in his condition. Their immediate goals are to get the fluid off and try to get him eating or at least able to tolerate the ng feeding. They do not want to do the TPN feeding unless they absolutely have to because that could add stress to the kidneys and he sure doesn't need that.
Don told me tonight that he doesn't want anything to happen here at the hospital. He wants to go home if he isn't going to get better. I would hope the right thing to do will become apparent very soon. I don't want to leave without answers but I want him to come home also. We built that home together from the ground up. I dug the footings and me and my uncle showed Don how to build the garage. We had our daughter there. If there is some good answer to be had I pray that God will show us and the doctors soon.
Hugs and FEC,
Judy
We are praying for you. I'm sure each hour seems like days as you look for answers. My kids brought a favorite thing from home, to the hospital room while we waited for updates. It made my husband smile.0 -
Judy,JReed said:Freida & Lynn
Thank you so much. I was without the iPad today and I don't know how to copy and paste on the iPhone.
Doctor came in tonight and said the plan for tomorrow is to tap and drain fluid and send that off to pathology. Until the kidneys greatly improve they are unable to another ct scan. They are also going to another dialysis if the numbers are favorable for that. It really wiped him out today. They are at a loss as to the cause of this except they have said their worst fear is a recurrence but so far they have been unable to find it. The increasing soft tissue was not there in February but did show up in June (which I did not know until tonight) and it has also increased since June as evidenced in the MRI they did last week or over the weekend. They did say it could either be scar tissue or the cancer. They cannot get to it to biopsy.
This is tiring and frustrating so I sure hope something gives here pretty soon and can shed some light. They said if it is a recurrence he could not tolerate chemo in his condition. Their immediate goals are to get the fluid off and try to get him eating or at least able to tolerate the ng feeding. They do not want to do the TPN feeding unless they absolutely have to because that could add stress to the kidneys and he sure doesn't need that.
Don told me tonight that he doesn't want anything to happen here at the hospital. He wants to go home if he isn't going to get better. I would hope the right thing to do will become apparent very soon. I don't want to leave without answers but I want him to come home also. We built that home together from the ground up. I dug the footings and me and my uncle showed Don how to build the garage. We had our daughter there. If there is some good answer to be had I pray that God will show us and the doctors soon.
Hugs and FEC,
Judy
One of the worst
Judy,
One of the worst things about Ec is all the testing, waiting and not knowing what is going on. It is so exausting and this has been going on with you two, for a long time. Praying for that miraculous healing.
You and Don are in my thoughts and prayers,
Sandra0 -
Love and HugsJReed said:Freida & Lynn
Thank you so much. I was without the iPad today and I don't know how to copy and paste on the iPhone.
Doctor came in tonight and said the plan for tomorrow is to tap and drain fluid and send that off to pathology. Until the kidneys greatly improve they are unable to another ct scan. They are also going to another dialysis if the numbers are favorable for that. It really wiped him out today. They are at a loss as to the cause of this except they have said their worst fear is a recurrence but so far they have been unable to find it. The increasing soft tissue was not there in February but did show up in June (which I did not know until tonight) and it has also increased since June as evidenced in the MRI they did last week or over the weekend. They did say it could either be scar tissue or the cancer. They cannot get to it to biopsy.
This is tiring and frustrating so I sure hope something gives here pretty soon and can shed some light. They said if it is a recurrence he could not tolerate chemo in his condition. Their immediate goals are to get the fluid off and try to get him eating or at least able to tolerate the ng feeding. They do not want to do the TPN feeding unless they absolutely have to because that could add stress to the kidneys and he sure doesn't need that.
Don told me tonight that he doesn't want anything to happen here at the hospital. He wants to go home if he isn't going to get better. I would hope the right thing to do will become apparent very soon. I don't want to leave without answers but I want him to come home also. We built that home together from the ground up. I dug the footings and me and my uncle showed Don how to build the garage. We had our daughter there. If there is some good answer to be had I pray that God will show us and the doctors soon.
Hugs and FEC,
Judy
I've got nothing. I'm speechless at all that has been asked of you both. Know that you are in my thoughts and prayers constantly.
Call or txt if you like. You know I keep strange hours and would love to be here for you if it would help.
FEC! Lean us, Judy. Strength to you both.
Terry0 -
Oh I am so sorry to hearTerryV said:Love and Hugs
I've got nothing. I'm speechless at all that has been asked of you both. Know that you are in my thoughts and prayers constantly.
Call or txt if you like. You know I keep strange hours and would love to be here for you if it would help.
FEC! Lean us, Judy. Strength to you both.
Terry
Oh I am so sorry to hear that he has been having so many troubles. I will pray that the Dr's can find out what is going on, and also pray for strength for you both. This is a tough one and I am not sure what to say. Just know that we are all pulling for you guys. My husband was sent home on Hospice that is why I haven't written in a while. It is so hard for me to keep up with everything, and my daughter. God bless you guys0 -
Oh Judy, you are more thanJReed said:Freida & Lynn
Thank you so much. I was without the iPad today and I don't know how to copy and paste on the iPhone.
Doctor came in tonight and said the plan for tomorrow is to tap and drain fluid and send that off to pathology. Until the kidneys greatly improve they are unable to another ct scan. They are also going to another dialysis if the numbers are favorable for that. It really wiped him out today. They are at a loss as to the cause of this except they have said their worst fear is a recurrence but so far they have been unable to find it. The increasing soft tissue was not there in February but did show up in June (which I did not know until tonight) and it has also increased since June as evidenced in the MRI they did last week or over the weekend. They did say it could either be scar tissue or the cancer. They cannot get to it to biopsy.
This is tiring and frustrating so I sure hope something gives here pretty soon and can shed some light. They said if it is a recurrence he could not tolerate chemo in his condition. Their immediate goals are to get the fluid off and try to get him eating or at least able to tolerate the ng feeding. They do not want to do the TPN feeding unless they absolutely have to because that could add stress to the kidneys and he sure doesn't need that.
Don told me tonight that he doesn't want anything to happen here at the hospital. He wants to go home if he isn't going to get better. I would hope the right thing to do will become apparent very soon. I don't want to leave without answers but I want him to come home also. We built that home together from the ground up. I dug the footings and me and my uncle showed Don how to build the garage. We had our daughter there. If there is some good answer to be had I pray that God will show us and the doctors soon.
Hugs and FEC,
Judy
Oh Judy, you are more than welcome. I wish there was more that I could do for you but am happy I can do this little thing.
I hope you get some good news soon. I can't even begin to imagine how frustrating it must be to have been in hospital all this time (what is it - 4 weeks now?) and not have answers yet. I think my head would explode.
Did they say why you were not told about the increasing soft tissue back in June? Our doctors usually go over the reports with us and tell s anything like that, then after a few days the reports are available for us to read online. Being me, I always read them though I don't think Bill does. It just seems a little strange they would not have told you.
Don and you must both be exhausted. I do hope you get to go home soon.
You are in my thoughts constantly.
Hugs and FEC
Freida xx0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 121.8K Cancer specific
- 2.8K Anal Cancer
- 446 Bladder Cancer
- 309 Bone Cancers
- 1.6K Brain Cancer
- 28.5K Breast Cancer
- 397 Childhood Cancers
- 27.9K Colorectal Cancer
- 4.6K Esophageal Cancer
- 1.2K Gynecological Cancers (other than ovarian and uterine)
- 13K Head and Neck Cancer
- 6.4K Kidney Cancer
- 671 Leukemia
- 792 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 237 Multiple Myeloma
- 7.1K Ovarian Cancer
- 61 Pancreatic Cancer
- 487 Peritoneal Cancer
- 5.5K Prostate Cancer
- 1.2K Rare and Other Cancers
- 539 Sarcoma
- 730 Skin Cancer
- 653 Stomach Cancer
- 191 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.8K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards