Rosevalley - this is for you!
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Well it's Friday and after getting Gemzar on Wednesday I feel ok on Thursday and horrid on Friday. I puked up my coffee and cheese stick and took zofran. I feel awful. Still no word on the tumor markers. It's supposed to be 104 and is beastly hot already at 10am. Pity anyone with no AC. Looks like it will be a wipe out day of laying low. I was up off and on all night with terrible gas, flatus, burping that just lasted several times an hour all night. Felt like I would explode. Miserable. Gemzar comes at a price.
I did have something rather comical happen yesterday morning. I was sitting in the living room when I hear this screeching, screaming howling and just about flew out of my chair. It was hysterical and I knew it was my Siamese mix Emmy and I thought my goodness she has torn her leg off.. something very awful. Well I go in to the Family room to the patio door and she is on the inside poofed out having a hissy fit in epic proportions because there is a HUGE male grey cat with a red collar on the other side of the screen drinking out of her water bowl! Emmy is fiercely territorial and this just rocked her world. The nerve!! My other cat Zoey (old toothless and gimpy) was sitting there wide eyed like tell him Sista!! It was so funny. Good thing they couldn't get at each other it might have been an ugly cat fight. Anyway I had to escort the interloper out the side gate, how he fit through the bars is beyond me. He had to be 16 pounds, obviously a fat beloved friendly pet. No fear all curiosity. Then I let our dog out to further discourage visits... So today Emmy has circled the lot several times and searched the bushes and perimeter.... looking for any signs of the grey one! We have cracked up at how she is behaving! She won't soon forget this episode. Her nick name is Wilma Bird Killer... we try to keep her in our catio (8 x 5 enclosed screened in porch built by DH off a shed, cat tower, multiple perches and landing areas to climb and play, box and water. Emmy loves it out there and will go hang out inside even with the door open. It's her safe haven, there are sleeping pillows and kitty cup. Most of the time she lounges like a leopard hanging off the cat tower Queen of her domain. I know lots of you have cats so thought you might like the story.
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CA 15 Antigen jumped from 663 to 908 in the week off I had from Gemzar. This explains the puking and misery. I start puking at 850. It jumped 145 points up taking a break. Cancer is winning. Sigh.
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((((Rosevalley))))
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Oh nooooo. Many prayers for you sweet Rose.
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Rose - I love your cat v. cat story. They are so territorial.
Joining you in steaming heat here, I'd promised my 17 year old male persian that he would never get a lion-cut again, but at 100 degrees, he got one last week. He is now fur-ocious. Not really, as I have to carry him to his sandbox when he paws absent mindedly at my chinese rug and not the tile where a little pee won't matter. Sorry your TMs jumped and NV returned. We are rooting for you - August is nearly over. (()) Claire
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hey rose. I like your new goal of voting hooray no new brain Mets.
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Gentle hugs (((Rosevalley))) .
I'm sorry that the TMs are up and the N/V is back. I hope you get relief soon. Are the weeks on Gemzar better?
Keeping you in my thoughts and prayers.
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That lion Persian is hilarious! I bet he's more comfy in the heat. We took our border collie down and had her butt/tail and back legs shaved because of knots and matts. It was just too matted to untangle. So we shaved her. She was so embarrassed! She tucked her tail under and scrunched under like "no one look --- what have they done to my behind!" She's now filling out and back to being fluffy but she looked pretty silly there.
It was 104 here yesterday..ugh. that's too hot. Today 98-100,marginally better. I guess 2 days after Gemzar I need to expect to feel horrible I just puked and slept and felt flattened. Crashed and slept all day. Oy It's supposed to be an easy chemo.. really? It whoops my butt. May everyone have a good day. Thanks for your prayers and support. I would sink without it. Hugs and lovingkindness to all!
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Tomorrow we take our youngest to Deaf Church. I really can't believe that I am supporting my DD3 to go to this church. They are evangellical, literal bible interpretation, refuse to marry same sex couples, believe abortion is wrong no matter what the circumstances, are against death with dignity meds for cancer sufferers and are pretty much only for those whose beliefs match theirs. You may be able to marry who you want as the law of the land but not in their house. This is a HUGE church multiple services, hundreds of worshipers, entire blocks donated to medical and job skills, indigent care etc and the price is your soul and allegiance. It's also the only deaf game in town. They are against everything I hold near and dear- I am trying to be open minded but what do I tell my kid? Your relatives and your sisters best friends are going to hell because they are gay/lesbian? Your church says you are not to judge- leave that to God, accept as people but do not encourage? Really? Big of you that kind of attitude will promote family unity. Last service I sat there just speechless. I will die by death with dignity meds unless I die first of something faster. They will tell my kid Mom went to hell? There is a part of me that is amused since I don't believe in hell. There is not much I can accept and endorse with their brand of Christianity.
It is not the "loving all no exceptions" message I got from the New Testament I took in college. Anyway after years in a Quaker Meeting where woman had a voice in the 1600s and slaves were embraced, same sex couples married happily under Meetings and choice and mercy for the dying are sanctified, peace work- it's a real hard pill to swallow this brand of Christianity. Now that I am folded into Buddhism with my back ground I am left speechless. I tell my daughter her choice is her own, but be educated and thoughtful; think hard about what you are accepting. She is a smart kid and will figure it out. I have always believed it best to teach by example. Live what you believe and that will speak volumes more then a lecture. A sense of belonging and meaning and community is strong though, I hope it's worth it. Please no one take offense since I mean none and believe there are many paths up a mountain to the summit. Pick the path that speaks to you and follow it. Everyone has a right to choose.
This is one of the hardest things I have had to do. Thanks for listening to me ramble. You never know where life will lead,
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Rosevalley, thanks for showing us how it is for you and DD3!
I'm not a mom, so don't comment much on that, but I was certainly a rebellious teen searching for stability in an unstable world, culture, family and changing body. Ah, life-threatening illness and teenage hormones!
My parents were good liberals (what we call progressives, these days), so my rebellion looked like a search for truth in Buddhism, yoga and world religions/philosophies.
If I hadn't witnessed the perils of fundamentalism, I might have fallen for its assurances that all would be right in the world if I just followed their righteous rules.
Instead, I decided to join up with the 1960s and 1970s countercultures, hippies, activists, natural food folks and seekers.
Yet, I empathize with your daughter - her early life, physical and emotional challenges and years of you with breast cancer must give her some sense of how unstable and transitory the world really is. When change is the only constant, it's understandable that we seek stability through authorities promise us safety and certainty.
I hope this is just a stage for her and that she'll be inspired by how you've lived your life. What we see/perceive in others is so much more important than what they say. You are doing a great job as a mother...yours is a particularly tough situation and I so appreciate you sharing it with us.
Sending a warm cyber-hug for you today, my friend, Stephanie
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Thank you for your post Stephanie. We have always tried to have a welcoming home, accepting and embracing of differences and cultures. I was feeling like I abandoned all the principals that guided me. Still I know from some of the other deaf folk's comments and asking for clarification that they are more accepting in their views then the church. I do admire the indigent care and free clinics they offer the community here. I think you are right that my DD is seeking some certainty and reassurance when in reality life offers none. Change is constant. Hard to live with that when you are 15 and use a language that the main culture does not. It will work out in the end.
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hang on dear Rose, DD3 will do fine. She is lucky to be guided by your wisdom.
I try drinking corn hair tea whenever I am too bloated & it helps.
Mom put a handful of fresh almonds in a glass of water and wait a night before juicing half of it with the water.. İnteresting milky stuff, definitely not yucky.
Also does the same with the inside crust (lung-shaped) of chestnuts. Just the glass of water with it draining out the good stuff overnight and no juicing .. İt, too tastes ok. Botj worth trying.
Broth is the best food at this point. I dip a piece of bread and most of the time I am able to keep my stomach full.
Having seen 3000+ TMs, I am confident you do get benefit from Gemzar.. Worth the blah..
Hugs & love
Ebru
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The misery of vomiting and nausea. So sorry. You know your body so well. I'm delighted no brain mets. I'm amazed you are still kicking if you go back and read December/January. When does school start?
You are a wonderful mom. I'm sure your daughter will see the truth and light but may just need that rigidity right now.
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Rose, sorry you are having a rough time during the chemo break. I am hoping things will get better once you start up again, and that future breaks will be less difficult.
I keep thinking about all the goals you have set for yourself over the past year and how you've met each one. That is quite powerful. What's up next after school starts?
I have to admit that my church teaches a few things I just can't agree with. I struggled with it quite a bit years ago but realized that the good far outweighs the bad and that there are many others in the congregation who feel the same. People and churches can change over time. There is hope that bigoted minds can be reformed.
Hugs to you.
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Thank you for your support but this is beginning...to be an awful ride. One break from Gemzar and I am right back where I started. I am so miserable most of the time that I sleep just to get away from it. My shoulder hurts and my abdomen just aches and spasms with waves of gas and bloating. Terrible distention and pain. I ate 2 meals and pulled off fluid and felt awful. I just want to make it through to school starts and then I want to go to that wonderful place where I leave my cancer filled body behind. Peace for me... no more pain and misery. I will miss getting to vote for Hillary but I can't wait for November. The thought of more weeks of this makes me cringe with despair.
Noni I hope this Church changes some of its rigid views. Well I made my goal... September is in sight.
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rosevalley I have been keeping up with this thread and I'm so inspired by your strength as you go through this journey. As a fellow stage 4 sister but no as far long as you my mets are small in comparison. I was only diagnosed a year and a half ago with mets but the inspiration from those further along than myself is so helpful
Keep fighting!! sad to read the tumour markers are rising...
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Rosevalley, for as long as we've known one another, we've both been dying.
It seemed for those long months of December and January that you'd be flying free soon, but then life called you back.
You've made so many milestones with your family, showing up in incredible ways for those who rely on your wisdom, steadiness and physical presence.
You've shared some of your greatest challenges with us.
Of course we, I!, have come to love you deeply. You've allowed us to see you as you see yourself, your world as you perceive it.
There are few people in my life who've let me walk with them, Rosevalley.
You have and it's an extraordinary honor to share our journeys these months.
Our ascites adventures are so similar, while our personal lives and treatment (my no treatment) decisions have differed dramatically.
Yet, you've always welcomed me and I am grateful for you, our connection here.
Rosevalley, I do look forward to meeting up with you on the other side. I'd recognize you anywhere!
Yet, of all you've taught me over these months, the greatest is not to have expectations of what life and death will bring.
You've been pulled back so many times. And perhaps, when you surrender you will find yourself floating on a cushioned cloud of more life, until life is done with you.
I write this knowing that my surrender to death has buoyed me along into more life, though a very changed one - filled with sleep and loving kindness.
Rosevalley, I wish you floating, sleep, loving kindness and assurance that you've been a remarkable presence in my life and the lives of so many who love you.
And I 100% accept and support your wisdom and clarity in choosing the moment and method of your passing.
Do let us know when the time comes and our healing meditations of love and light will carry you over.
caring and crying, Stephanie
xxx
xxx
Life is a very narrow bridge between two eternities. Be not afraid.
RABBI NACHMAN OF BRASLAV
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I woke up at 3 and spent time losing my dinner. What a way to wake up. After vomiting I managed to get back to sleep. I am tired. I am weary and accept that the cancer has infiltrated my bowels, stomach and gut. The MRI said that while there was no brain involvement there was increased skull mets, increased cervical penetration in the vertebrae and no doubt the aching in my humerus on the left is cancer. I have had it irradiated already. So I have a steady diet of zofran, reglan and oxy. The cancer diet with tea and clear boost. Yum yum. No one cry at my passing it will be a joyful release - a setting free of the spirit. Be free of cancer.... fly on.
Thank you for your support I wouldn't have made it this far with out it. :-) Stephanie that's a really pretty song.
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Totally selfish crying today - anticipatory grief, Rosevalley.
Who understands this ascites and implanted drain thing better than you.
I will walk you to the end and bid you free to fly - rejoice in your joyful release!
loving kindness, Stephanie
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Oh Rose, I sure wish there was something that I could say or do to make you feel better. Like Stephanie has said, you are a great inspiration to all of us and we have grown to love and care about you a lot. I pray for peace for you. We will all walk you to the end.
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Rose, I don't know what to say except that I am thinking of you, wishing you peace, comfort and no pain. You have had such a lasting impact on so many of us on these boards. For that, thank you.
The no crying / celebrating only is a great way to commemorate your life. I have always wanted the same.
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I pray for peace for you, Rosevalley.
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Yes we will miss your grit and determination. But so wish you relief from unrelenting nausea and vomiting.
You are an inspiration and you have more than earned the right to peace.
Thank you.
Fly free.
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Did you see where the police tried to stop a speeding car (N. Carolina -no mention how fast) and the driver pulled into his driveway got out and was signing to the officer and they shot him dead. He was a married father of 2 and deaf with limited speech. I can just imagine what happened the cop yelled "stay in your car hands up" and the man heard nothing and followed nothing and they killed him. My DD3 wants to learn to drive. She is profoundly deaf, non verbal, no speech. I am making my DH promise me he will make her take a place card that says DEAF KID LEARNING TO DRIVE. I might insist he write it on the windshield, since I won't be here. These kinds of incidents keep me up at night. So many things to wrap up. (((hugs)))
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Sending loving thoughts your way.
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Rose - A dear friend has a son with cerebral palsy. He does not speak much, though his mom can understand him. He communicates mainly through sign language. He does drive and has a sign language only sticker on his back windshield and carries a card explaining things in case he gets stopped. He is in his fifties! He is amazing and I'm so glad to know him.
My mom passed before I started kindergarten. I've always felt her spirit. There have been several times that I felt she communicated important life things to me that I had no way of knowing otherwise. I consider her my 24/7 guardian angel.
Gentle hug to you sweet mama.
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Rose, I'm heartbroken by the loss of the Deaf father of two in NC. It's sad that so many police encounters are now "shoot first, ask questions later."
I have similar fears for my autistic son. Although he is high-functioning, he does get stuck and will not always follow directions. Fortunately, my son is never alone, there's always a family member or a staff member with him at the group home (just placed). However, to protect him further, we will be registering him with the county's special needs registry.
I like the "sign language only" sticker on the back windshield and carrying a card explaining things. That would be useful for many special needs people. There are many groups for parents and children with special needs, who will have many more resources for you.
Because my son will always need a guardian,I've been looking into these folks: https://plannj.org/wp-content/uploads/2016/04/PLAN... Their mission: "Who will care for my loved one when I'm gone"
Worrying about my son keeps me up at nights as well. Finding the right resources can help. Wishing you peace as you make your plans for DD. Sending much love and prayers, Madelyn
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Mominator our DD1 is MR/Autistic and Deaf, mild CP. She is also high functioning has a job and activities. She is in a fantastic group home and they are wonderful with her. Good luck with your son's placement I hope he has great success with it. Autism is both a blessing and a curse. It helped my DD1 take her limited cognitive skills and concentrate them on reading and writing, which she does at 3rd/ 4th grade level. Pretty good. I know other DD kids only without the autism, same IQ range, who can't write and read as well. Glad I am not the only Mom up thinking what happens after I am gone.
About 3 or 4 years ago we also got the special citizen registry to give descriptions and photos of non verbal DD adults in our town of 150K. My DD1 was number 5 in their list! She used to wander and thankfully stopped. It gave me a little peace of mind. They started this registry after a really tall young black autistic teen got lost, didn't respond to commands by Portland police and they shot and killed him. I think the young man was only 15 but very tall, adult sized and had never spoken. There was outrage and they started the special citizens registry. My DD1 and DD3 are both deaf and neither talk, ASL only. My youngest is just deaf and can learn to drive but all kids can make mistakes! I will look to see how to get a Nonverbal /ASL only bumper sticker or window decal.
Farmerlucy- thank you for your shared story. I am glad to hear your friend's son is 50 and drives and gets around. It's great to hear that. I worry about my youngest learning to drive. I will try to be her guardian angel and spirit watch. How very sad your Mom died when you were so little. I cherish the time I have had to see my kids grow. When they are babies is special, toddlers... I dearly love 4 year olds. When they are 10 and 11 and are so serious.. then teens are kind of a mixed bag. Then they are in college and fun again. So many different ages to love.
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Good morning Rosevalley,
Thinking of you this morning and sending hope for peace and days without pain and cancer reminders. Rest seems like a reasonable wish.
You achieved your goal of September and DD3 seems to have found a place to feel spiritually safe for now. Your spirit has gone to deeper waters, far beyond the need for narrow pathways.Thank you for the wise counsel and inspiration when they were needed most.
By your side in spirit...(((( ))))
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