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Member Since: August 17, 2008
Last Login: October 24, 2008
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Recent Posts by chipdog3

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Oct 24, 2008 10:22 am

Xeloda questions?

My mom is on her third cycle of Xeloda. 2 weeks on 1 week off. She takes 1,000mg daily. 1 am and 1 pm. On the weeks she takes the meds. her breast with the tumor in it feels uncomfortable and she feels a stretching sensation. Is this feeling the meds working or... She has breast cancer with lung mets. She was diagnosed in late JUne. She is using the udder cream for dry skin but, still gets little broken spots all over her skin. So I will look into some of the other suggestions on the dry skin on xeloda thread. She never had pain in the area of the breast until she started the meds. The Dr. said the tumor shrunk from 2 cm. to 1.7cm. So I guess this is good? Any suggestions will help. Thanks and good luck to all.

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 20, 2008 03:42 pm

Need Prayers for Our LuAnn

Wishing you well, you have answered every post I've ever written. I wish if there was a pain fairy she would come and take all yours away and leave you something very special in its place. Since its your fairy you can pick the something special. I hope your pain fairy shows up soon. Hugs and well wishes. Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 19, 2008 09:09 am

I'm probably thinking too much, but.....

I am unsure if this is something I read or heart from family. I think the family is contacted when the university or what ever is done with the  body. You can choose to have the  cremated remains returned to you for buial. so your family would still be able to visit your remains. I dont know if this is true thought I heard it somewhere.   Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 15, 2008 08:35 pm

mom has severe arm pain on xeloda

Saw doc today he said mom is good lungs and heart sound good. Will see onc next tuesday. So I guess for now all is well. thanks, Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 14, 2008 10:31 am

My doggie passed away from cancer on Monday

I am so sorry for the loss of your friend. You did the right thing I work for a vet and see these situations all the time. The best thing you could do was help him cross from this world to the next. No matter how many times this happens it never gets easier. Soon the sadness will subside and good memories of the past will become what you remember. I had to put my best friend to sleep 6 years ago. I have 2 other dogs now that I love to the ends of the earth. But, I will always remember my "Dagwood" I miss him still. He was not my first dog or my last but he was the best. So sorry again for your loss.  Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 14, 2008 10:23 am

mom has severe arm pain on xeloda

That is what I was worried about yesterday she has had congestive heartfailure before and does take lasix daily. But she really does look pretty swollen in her arms and legs. And trust me everything scares me. I am afraid every ache and pain is a sign of something more. Which is probably why I dont have any credibility with my mom. I am going to send my daughter in to see if she can get any more infor when she gets up. She is 17.  Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 13, 2008 10:41 pm

mom has severe arm pain on xeloda

When I went back down to check on mom she was in bed reading. I expressed my concerns and she refused to go to hospital she said it wasn't that bad anymmore and turned off her light to go to sleep' Sorry to have gotten everyone in an uproar I guess we will just wait and see. Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 13, 2008 07:59 pm

mom has severe arm pain on xeloda

Help my mom started xeloda on monday 1 pill am 1 pill pm. Right now she is crying and holding her arms saying they hurt so bad does anyone know if this is okay. I cannot call the onc till monday and I worry alot. Since she had her stress test she has been complaining about arm pain but now she is crying. How do I help? Also she said she ;has gained 5 pounds since yesterday. I am worried about her heart. Help calm my fears if you can. Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 13, 2008 06:24 pm

I wish mom would live life.

Her room is on a different floor and she is afraid to climb the stairs. It has been this way since my dad(stepdad) died 3 years ago. She used to come up to the kitchen every night for dinner but when he passed she stopped coming up. So I just take food down to her.Even though if she rode her chair to the front porch there is only one step to get in. She is not a big fan of t.v. and when I rent movies she says she doesn't feel like watching them. So its like throwing money away. The only thing she enjoys is going to the casino. My son has taken her twice since her cancer diagnosis. But now she worries about needing the money for bills. It has been so long since I have seen her do what makes her happy that I am unsure if even she remembers what that is. The kids and I try to play games with her and talk about the good times we have had camping and fishin and such but all those things were with my dad. Since he's been gone she really hasnt done anything. Well we all do the best we can thanks for all the help. well wishes,  Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 13, 2008 01:36 pm

I wish mom would live life.

We live in Toledo, quite a long drive from cincinatti, but thanks for the offer. I don't really think its depression since it is somewhat the way she has always been. I guess I just feel an urgency for her to do all the things she wants to do before time runs out. As for going out side she usually uses her electric wheel chair when she goes outside to read and it would be hard for her to get up off a swing. But the image was very relaxing. I wonder if the side effects out way the treatment. The docs dont seem to think there is much to do to help her and I wonder if the small amount of xeloda is worth the side affects. Dont get me wrong I am so proud that she is willing to fight. I am unsure if I would be brave enough to try. It seems like people alot smaller than my mom are taking alot more medicine. Oh well we see the onc nurse in 2 weeks then the dr. in 3 more weeks. How do they tell if the xeloda is working?  do they do more bloodwork or other tests? I guess they will let her know. I am trying to let go of the fact that I cannot fix this. So I hope I will be more help and less henderence.   Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 13, 2008 12:16 pm

I wish mom would live life.

Oh I would never push my mom to do anything and I will accept and agree with whatever she choosed. I will respect her wishes to the best of my ability and would never try to change who she is. I am her daughter so I have some of the same loner type feelings. I just feel sad sometimes when she seems all alone. We have never been a touchy feely family so during this time I would like to share more with her but, I feel it would just freak her out. I have bought her a couple of cards and just slipped them into her mail she has never said a thing about them. I also wrote her a letter thanking her for all she has done for me and my family and how much I love her. I will just let her lead from here and will not worry about her getting out. I will just offer like I always have and just support her. She is on a deparession medication that she called and got from her family doc the day she was diagnosed. So I guess if she needs me to do anything she will let me know or I can ask if I think I can help. Got it. Thanks for your imput.  Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 13, 2008 08:15 am

I wish mom would live life.

Mom started her xeloda on tuesday. Since then everday when I get home she is lying in bed reading. I have offered to get her something to eat but she says she already ate. She does have some food in her apartment type room and a microwave and fridge. But I never see any dirty dishes. Now she has lived here for over 5 years and so I usually know the signs of what she has been doing pretty easily. The kids have been getting her take out for lunch. I know the meds may  be making her not feel well, but I worry. I have asked if she is okay and she just keeps saying I don't think i'm sick. Since my step dad died 3 years ago she has only left that little apartment type room about once a month. It is attached to our home and I go talk to her like 20 times a day. The kids and my husband also check on her and just talk with her. Since the diagnosis of bc and lung mets she was of course leaving the room more often to go from doc to doc and test to test. But now she is back to just sitting in front of the computer or laying in bed reading a book. I had hoped that if anything "good" could come from this that maybe it would inspire her to get out more and live the 12 months she has left. She won't allow me to tell anyone she is ill so no one calls to check or her or just to chat. She has always been a loner and never really has had many friends and any friends she did have she has lost contact with since living in florda for 7 years then moving back to ohio 5 years ago. I ask her everyday if she wants to go and do anything, usually she is not even dressed all day so pushing her out the door is not an option. I also care for her mom who lives in a retirement apartment at age 89 and doesn't drive anymore. I take her to all Dr. appts. I take her to the grocery store every saturday. I do her laundry, banking and whatever else she needs to do that she doesn't do at her senior appartment. She plays cards 3 days a week, bingo, pokeno, and bunco. She also holds a card party in her apartment for a group of friends every 4th friday. They have pot lucks and partys and she seems content to me. I asked my mother on several occasions if she wanted to live someplace like this and she got so pissed off at me I will never ask again. I have offered to take her to a senior center to play cards which she loves to do, she says she can play the same games on computer. I guess I don't really have a question as much as I just wondered if there is anyway I can motivate my mom to at least enjoy the little bit of life she has left.          Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 10, 2008 06:42 am

Some answers from 2nd opinion.

Thank you for your suggestions. I know it is not right to be afraid of the meds but thank you for understanding that my fears are real. I will do the best to care for my mom until the end. I am unsure how much time she has but I will make the best of it for her. Fears or not. She knows the type of fears I have and I think she will understand. We went through the death and dying of cancer with my dad(Step-dad). He choose to not treat the brain cancer which was his 3d. So I did not have the fear of the meds because he was not on any. We did care for him in our home till he passed 3 years ago. Again thanks for the information I would not have thought about the plates and silverware but will work on that. I think that will help for future worries I would not have thought about. thanks again, Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Sep 7, 2008 03:34 pm

Some answers from 2nd opinion.

Well my mom saw a second onc last week. We quit seeing the first one cause all he would do was send her from surgeon to surgeon. all of whom would not do surgery. A little background about 2 months ago she was diagnosed with bc then lung mets or so we are told. This onc actually examined my mom to feel and see the bc lump for himself. He actually talked to her like a real person and asked what she wanted from him. After he talked with her at length about her expectations, thoughts and feelings. He left the room to view her films and  test results that we have been collecting for the last 2 months. He came in and told her she had  triple negative something or other. Which I gathered from him continuing talking is about as bad as it gets. He also said he was 90 % sure the lung spot was mets from the bc.He kinda said that the treatments available were not really going to help. He did offer to put her xeloda and see if it helps. We go back to see the nurse in 3 weeks then see the doc on 3 more weeks. At least  we finally got some answers as to what we are dealing with. Does anyone know if the xeloda will help her live longer or does it only help with the actual  tumor growth. I am afraid for her to take the meds. I am afraid to take antibiotics because of the side affects. So even having the chemo meds in the house scares me to death. I hope I will not be afraid to touch her for fear some of the meds will somehow get into my system. (I know I need therapy even to think such a thing but I do.) Anyway, I just had to get this out. I am not allowed to tell anyone we know she is ill and sometimes it drives me nuts to be able to share it with somone. Thanks for listening. Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 29, 2008 02:39 pm

Doc cancels moms surgery

The surgeon said the only way he would do surgery would be palliative. I don't really know what that means but he said something about the cancer being close to the skin and possibly breaking through the skin. So I guess that means if it comes through the skin they may have to remove it for sanitary or health reasons. We still don't have an appt. with the new onc yet. So I am assuming from all the posts that my moms bc has to be at least a stage IV to spread? My mom was excited to not have to have surgery I think it was her biggest fear. She seems like she is mostly worried about having pain. So far she doesn't have any pain from the bc or the lung mets. She does have COPD and sleeps with a breathing machine at night. She has very overweight and doesn't get any exercise except walking from the computer to the restroom. She uses an electric wheel chair on the rare occasion that she leaves home which is seriously once a month. Except for the trips to the doctor this last month. So far no onc has given us any other options other than surgical but all of the surgeons have said no to surgery. (The bc surgeon and the thorasic surgeon). When we talked with the bc surgeon he said she may or may not be a candidate for chemo or radiation. I never even knew you could be denied chemo and radiation. I sure hope we get an appt. with the new onc. soon and hopefully this one can give us some answers. I try to ask questions but mostly I  just get brushed off. I hope this new doc can help sort things out. Wish us luck.   Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 28, 2008 09:08 pm

Doc cancels moms surgery

Thank you all for all of the information and thoughts and prayers.  Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 28, 2008 10:34 am

Doc cancels moms surgery

why would the surgeon cancel the surgery if it needs to be done. She does have other medical issues. They said she has to have a stress test before they will even consider doing chemo or any other treatment. We saw a thoracic surgeon who said he would not do lung surgery because she would not recover from the surgery. It seems like every time we get new it information there are less and less options. She is about to shut down completely. I hope this other onc has a game plan because wondering aimlessly is driving me nuts. Thanks for your help, Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 28, 2008 06:45 am

Doc cancels moms surgery

My mom was scheduled for mastectomy on sept. 9th. Wed. the surgeon called and wanted her to come in for appt. He said because of the mets to the lung she would no longer be a candidate for the bc surgery. I guess when she kept saying say she wasnt going to have surgery she was right. He did recommend a new onc to see if she is a candidate for chemo or radiation. Wow i thought she was just thinking about not treating but it sounds like that might be her only choice. Its amazing how fast it goes from we can save your life to ummmmm we will see what happens. So i guess we are just on pause until we see the new onc. The only reason she agreed to see the new onc is it is a woman. Well I just wanted to vent a little. Mom said I should feel better now because she doesnt need surgery I am not sure if she understands the alternative. I am more worried now with the possibilty of no treatment available. I guess she was really scared of the surgery. Anyway thanks for listening.   Sandy

Posted in: Support & Community Connections + For Family & Friends of Those Who Have Breast Cancer, Created: Aug 27, 2008 07:06 am

Doctors!! Ughh!!

I feel the same way about the doctors. We have like 4 doctors that have no idea who is in charge. They send us from place to place to have this test and talk with this doc. I dont think anyone is in charge. My mom has to be cleared for surgery from a lung specialist the appt is 5 days after the scheduled surgey date. No one seems to get it when I tell them so I guess we just move forward. Good luck on getting your surgery I hope everything turns out well for you. Sandy

Posted in: Connecting With Others Who Have a Similar Diagnosis + Recurrence and Metastatic Disease, Created: Aug 27, 2008 06:55 am

CT guided lung biopsy

My mom is 66 she had a lung biopsy 2 weeks ago. it is like the other posters say. My mom actually hated the ct scan more because it was uncomfortable to keep her arms above her head. She said the worst part of the lung biopsy was laying on her stomach because of the location of the tumor. It really does take all day but the procedure it self took like half and hour. She did not have any collapsing of her lung and has been fine since. good luck and hang in there.  Sandy

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