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palves

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Everything posted by palves

  1. palves

    One year

    Thanks everyone. We just had a family day and that helped. Suprisingly my 15 yo spent time with us which was very nice. We got through it and now all the 1st's are over (I think). Paula
  2. palves

    One year

    Tomorrow is one year since my dad passed away. We had his unveiling in early June. Today we celebrated my daughter's 10th brithday. Some tears from my mom but we are doing ok. I just lit the candle. Tomorrow I thought my mom would want to spend it with me and my family, but she is going to the cemetary and then to a friends for dinner. Guess I should have suggested some plans rather than played it by ear. Oh well. Hoping she isn't too upset with me for not going to the cemetary with her - didn't know she was planning to go. Can't go because I have someone scheduled to come to our house at the same time. In general though I have no pulling desire to go there anyway - figure I can miss him and think about him from anywhere. Am I wrong? Paula
  3. Thanks everyone. I have been doing ok. Still a lot of second guessing. But I suppose thats normal. We have been surrounded bya lot of comfort the last few days. The next few will feel so strange I'm sure. I' m so used to running to do this or that, expecially the last 2-3 weeks. Kind of feel, empty, raw, not sure . want to crawl under the covers and hide for a few days I think. But mom, MIL, kids, I just can't .... I'll make it just need to take a step back and let the emotions rule for a bit. Paula
  4. of fighting my dad lost his fight Saturday morning around 4:30 am. About 2 weeks ago I took him to the ER because the tumor in the brain (met from the lung) had caused some additional coordination/balance problems and he had fallen and couldn't get up. The result was that there was really nothing left to do. The liver had mets that had increased, even with surgery or radiation functionality wouldn't necessarly come back. Decision was made to send him to rehab for a bit to see if he could get a bit more strength in his legs / arms to assist w/ transfers. he really wanted to go home. He went downhill from the time he got to rehab - needed oxygen (never needed it before), began to swell, and developed pneumonia. He really wanted to go home and we would have taken him home this week. I feel really horrible that he didn't get home and that he was alone last night (we weren't told before we left last night that it looked like this was it although we knew he was struggling). While the call at 4:30 was a surpris it really wasn't a surprise. Feeling all kinds of emotions sadnss, relief, and guilt ..... Thanks everyone for being there for the last few years, although I didn't write much, I did ask for advice on/off and everyone was so giving. Appreciate and love you all... Paula
  5. Thanks everyone for your great advice. I've called a number of hospices (thanks Ned) and have a few more to call. My mom called a few home healthcare agencies. Does anyone know if Medicare covers home health care if Hospice is also called in? Paula
  6. Hi - I need some help in figuring out what to do about hospice. We had someone come talk with us in the hospital from someplace, but now I understand there are more than 1 hospice type programs in each area. How do I go about finding out about the different hospices in a given area? I just did a search, but only came up with the visiting nursing association. So I'm not sure if I am searching for the right thing. The real question is what is given by each hospice program (and what one qualifies under the insurance plan) - is it standard to just be allowed up to 4 hrs per day of a home health aide? The one program we talked wtih said up to 4 hrs a day, and then another 4 potential from a combination of home health aide, spiritual advisor, volunteer and visiting nurse. How ofter should we expect a visiting nurse to come? We were also trying to fgure out if he goes into home hospice can he later switch to in patient hospice? He really wants to go home (he is in rehab now trying to get him to strengthen his legs). And I want to honor his wishes, but my mom cannot care for him. There needs to be a way to get someone to care for him 24x7 so that she does not have to. The only way that would be wold be for us to pay for it or for him to get admitted to to in patient hospice. Another question, for a home health aide - right now its pretty much taking 2 people to move him in/out of bed/wheelchair. Can one person realistically do this? How will that work if not, will he be bed bound then? Will my mother, me or my sibilings be required to be there at all times to help? My brother works, my sister is in school, and I'm job searching/interviewing and can't put that aside. I just feel so confused. Any advice is well appreciated. Thanks Paula
  7. Thanks everyone .. right now we have faxed the reports over to Sloan. Ginny thanks for the PA recommendation. I'm going to discuss that with my mom tonight. Thanks Bunny - got your PM. Definitely will check that out ...
  8. Anyone hear of Dr. Chandranath Sen out of St. Lukes? or Dr. Vivian Tabar out of Sloan Kettering? My dad has mets to the brain - cerebellum. Recommendation is to wait for blood spt to reduce on its own or possibly look for surgery. Need a 2nd opinion. Please provide any suggestons. Direct email is [email protected] Regards, Paula
  9. Anyone hear of Dr. Chandranath Sen out of St. Lukes? or Dr. Vivian Tabar out of Sloan Kettering? My dad has mets to the brain - cerebellum. Recommendation is to wait for blood spt to reduce on its own or possibly look for surgery. Need a 2nd opinion. Please provide any suggestons. Direct email is [email protected] Regards, Paula
  10. My dad has severe swelling possibly due to the chemo he is on. He is on diretics for it, but its not helping much. His protein levels also came up low? Has anyone experienced this? What did you do to raise theprotein levels? Is it dangerous? Are there any meds? Thanks in advance
  11. Can you PM and let me know if you are treated at Fox Chase or elsewhere and perhaps are you happy and who you see. Looking for alternatives. Thanks Paula [email protected]
  12. My thoughts are with Julia and Aarons family. This makes me so sad. If I had known I would have tried to visit - I don't live that far from there. A tragic loss. Paula
  13. palves

    John

    I am so sorry to hear this. Ry I always get such inspiration from you. Just know that I am thinking and grieving with you. My thoughts are with you and your entire family at this very sad time. Paula
  14. Anyone have any experience with these drugs in a trial situation? Dad has 2 possible trials that he can participate in (Phase 1) as the Alimta failed him. Trying to make a decision. Velcade seems promising - its been FDA approved I believe for multiple myeloma (sp?) Any thoughts well appreciated as always. Paula
  15. Mazel Tov and a L Shana Tova What a great way to start the new year
  16. my mom that is . Next Fri I am going to have a thyroid biopsy,. They do not think it really is anything, but better safe than sorry as there are now 2 suspicious areas. BUT the same week and the following week my dad has his scans, the appt to review the scans and decide appropriate action, an appt for a prostate test (his is enlarged), and an u/s for his kidneys (dr felt what is to be kidney stones which he has had before), and the following week my sister will be having minor surgery. I've kept this to myself so far (and some of my friends), but I might be in a situation where I need some help (my friends work so they can't take me to/from the hospital for my test) as my dh is already taking off 2 other days that week to deal with some other pressing matters ... I just told him that he can drop me off, pick me up - even though I'm uncomfortable with that, but ... Anyway, am I right to keep this from her?
  17. palves

    Weak moment

    Reading this last reply reminded me of something the rabbi said to the children of a friend of mine when Barbara died, he said "Everyone will say its going to be ok, its not going to be ok, its going to be different, and thats ok". So this too shall be different, and like the post before said you will find your new routine. It won't be the same, but it will be different, and thats ok too. Paula
  18. palves

    Weak moment

    Kelly - breathe ... take a breathe and back up from that ledge ... you will get through it - just like you have gotten through everything else this summer - 1 day at a time .. take some deep breaths .. you've been through the 1st day jitters before, you know the routine and I bet once you get into the classroom intuition and training will kick right in. You are a great teacher and leader and once you see the kids you will feel that excitement and love again. Right now your focus has been on everything else, but once you are back, well its like riding a bicycle. Your kids will be ok too - They too know what is expected from them, and TOGETHER you will make it work - your family is still a TEAM, even with mom missing,and you will work like one to get through tomorrow and the next day. Maybe if you put your thoughts down on paper it will help release some of that tension in your mind. Can you try to write out a plan for the morning? And if nothing else works I will (and I'm sure all your LC friends too) will be rooting for you and your team ... Can't wait to hear about how the 1st day goes and the kids you will meet this year ... One step, one day .. now go get some rest ... Paula
  19. when your little one (7 yo) says is Grandpa very, very, very sick? I'll be really sad if he died. Honestly I can't even remember exactly what she said, but it all started because we lost a family friend this weekend (who happens to be the mother of my daughters library teacher) and then we past a cemetary I went through this with my son when my dad was 1st diagnosed, but I've not really talked to my daughter much about it (she was only 3 when dad was dx and I guess now that I think about it Ryan was 8.5). And then she was so mean when she wouldn't kiss my dad goodbye (she is stubborn like this a lot of the time but usually to my ILs not so much to my family). And then my dad got angry. I'm just so sad tonight .... The rabbi suggests honesty and I told her that he is taking medicine to hopefully help him feel better and that if this doesn't work we will try something else (but I question that there is anything else). I'm just feeling very beside myself and I thank you all for just listening ... Paula
  20. palves

    Alimta

    Hi my dad had Alimta - not a favorable response - he is now on Tarceva Paula
  21. Ok - dad started on Tarceva - about 2 weeks ago - so far no effects. He said maybe he is getting something on his fingers, instead of acne on his face. Is that possible - is that a sign. I just hate this, and I hate asking my mom (and him) how he is doing and looking for signs of a rash. I'm just so scared that this is not going to work. I've got to find a way to go to the Dr w/ them next time around, but right now I have a meeting that same morning. Urghhhh. Anyone else have problems w/ their fingers? Paula
  22. palves

    Thoughts for Val

    Val - thinking of you and Andy during the start of this deployment, yet a bittersweet day for you. Reflect on your perfect day and hold your memories tight. Paula
  23. Congratulations to everyone. I'm so glad that everyone is doing ok. Jacob is over 5 lbs so that is great. And he is not too far behind his sister. Yeah !!!! I'm sure you have some happy grandparents as well. Give Randi a high five for us. Paula
  24. palves

    Prayers for Andrea

    Tomorrow seems like it will be I day for Andrea's twins - induction day. Lots of luck coming your way to you, Brian and your new bundles of joy. Paula
  25. Aaron - Mazel Tov on your appointment. I'm happy that you were able to take a negative experience and turn it into something wonderful. Only positive things here on out. Paula
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