Best Of
Re: Ladies in their 30s?
Hi!
I’ve been reading these for months (and have found them so comforting!), but haven’t posted anything yet. I was diagnosed de novo in December of 2020 at 34. No genetic component and no family history of breast cancer. Currently stable (yay!), but obviously dealing with all the physical side effects of this horrific disease and especially the mental health impacts these days…
I am in Houston, and I don’t know a single person my age who is also metastatic. It is so lonely and isolating. Everyone else I know is having babies, making career moves, buying bigger houses, and just “living their best life.” I want to celebrate them, and at the same time I am so sad about everything that’s been stolen from me. I would love to connect with others here just to know I’m not alone. And if anyone is close to the Houston area (or travels to MDA), please let me know!!
I am also curious if anyone is thinking about or has pursued surrogacy after being diagnosed metastatic. I had gotten married 7 months before diagnosis, and we were hoping for a family. I have so many feelings about this. The short version is that I don’t know if I can bring a child into this world knowing I likely won’t get to raise it. But at the same time it’s my husband’s life too, and he really wants kids. I would love to chat with anyone going through/who has gone though this.
Looking forward to connecting here!! And hoping for a 2022 filled with good health for all of us who are facing this ❤️
Re: Ladies in their 30s?
Hi ladies it’s me again. I just wanted to see if anyone has had this issue. Recently I went to see my gynae and she said I have endometrial thickening despite being on Lucrin/ Lupron for past couple of months. I’m being monitored for the endometrial thickening and she is saying I might have to do a d & c after I’m done with chemo for my lung met that was discovered through a routine pet scan. I still have 2 cycles left,
I’m just feeling like one after the other when does it end! It feels so unfair at 30 I have to face all these problems when all of my friends are either pregnant or giving birth. It upsets me that I might never have the chance. How do I just accept this ordeal that life has thrown at me. I feel happy for my friends that are expecting but it just hurts me to know that it might not be in my future ever. Holding onto a miracle and just taking it a day at a time.
Any advice would be appreciated.
Re: Ladies in their 30s?
nikisworld- so sorry you find yourself here. 25 is young to have to deal with this disease...30 is very young for stage 4...I’m sure there are lots of thoughts and feelings surrounding your dx. I just wanted to chime in and say welcome and offer a little hope...although I was older and am older now...I was dx stage 4 at 34 years old and I am now 41 1/2! I have no words of wisdom or what to do or not to do...this disease is simply about finding the right drug for your specific cancer...I will pray that you find the magic combo and things go as well as possible! Sending hugs.
Re: Ladies in their 30s?
hi all, I was diagnosed with stage 2 triple positive breast cancer at 25. Just found out last week that there is a met to the lung which was confirmed to be the same cancer from the breast. I’m currently 30 years of age. I’m struggling with the uncertainty of life ahead and unknowingly how everything’s going to turn out. Emotionally I’m a mess. Feels like my whole world has fallen apart
Re: Ladies in their 30s?
Hi Ladies! I'm 34, dx stage IV from the get go in 2011 with Mets to bone. In 2018 I was dx w/ liver Mets and in 2019 lung mets. I've been on a handful of treatments in my years and had radiation more times then I can count. I think my hands and feet are the only places I don't have bone mets. This last year has been particularly rough as I fractured my T-12 and coccyx last fall. This place on my spine had been treated with both standard radiation as well as cyber knife before fracturing and expelling bone fragments to the surrounding area. Even Chicago surgeons don't want to touch me and said only if my symptoms start affecting QOL. I have weakness in my rt arm, a tremor in my left and pain in the general area. I had to give up my job as a dialysis tech to take an office job after that due to safety and lifting restrictions. I also broke my hip in January (thanks for failing hard and fast ibrance!). I'm just getting ready to go back to work. This despite not being as severe an injury has been the longest I've taken to recover. Each one seems less and less likely I will bounce back to being able to work and care for myself. I just started Gemzar about 2 months ago. Lots of fatigue, dry mouth, dry skin. White cells plummit on it though so we switched my schedule to two on one off otherwise I never made the 3rd treatment. Otherwise not too bad.
Re: My Husband, My Life, My Love, My Family, My Cancer
Sorry the storms made you feel crappy, but glad they brought cooler temperatures. Being able to go outside, even just to sit and look at the sky and the trees and flowers is a definite mood booster. Hope the experts can create an effective plan for your back pain.
Does your MO stop Ibrance while you're on augmentin? I had it for 3 weeks for my recent bout with diverticulitis and my MO had me stop Kisqali for that time. Have my first regular 4 week bloodwork today and hoping the numbers are still in the normal range despite the Kisqali "vacation".
Re: My Husband, My Life, My Love, My Family, My Cancer
@wren44 Reporting for pocket duty. Prayers for the day to be over quickly and that all is well. You need a lot of pockets with all the gals supporting you. You got this!!!!
I sure am immune compromised. Years of MS treatments and of course Ibrance now. Neuo said he will not add any other treatment plan at this time. I rejoiced. Just tired of one bottle after another of antibiotics. The salivary gland blockage came back. 7 days of augmentine. Last month diverticulitis. 10 days of antibiotics. Month before, UTI. You get it.
The weather did change here. Much cooler after tremendous storms rolled thru. I feel crappy as the storms lasted all day. I find my legs super weak right now. Get to see Neuo Tuesday and the Pain Management clinic on Thurs., to see if an epidural will aide with severe back pains. PT and cortisone did not work.
In pockets for all my sweet friends. May your days be pain free and your spirit bright.
Re: Anyone starting brand drug, Enhertu?
@more_cowbell. It's so interesting how people react so differently to treatments. I suppose it depends on what they'd been through before. I had very few issues with Ibrance, Truqap, and now Enhertu. My hair loss started before my second infusion, so maybe that won't be a thing with you. However, I have not had any nausea issues. My fatigue hasn't come back since my fifth infusion (just finished my seventh). My onc says it's possible that it just takes a while for people to adjust to new treatments. So I might be done with side effects (?!). My hair is growing back. Peach fuzz, but I don't have completely bald patches anymore. I hope you keep your hair and your nausea gets better as time goes on. My first set of scans while on Enhertu were good. Bone mets still NEAD and liver progression is stable, so I hope I can keep on Enhertu for a long while. Not sure what my next line would be.
Re: Elacestrant (ORSERDU)
Hi, I am new here as well. Just started Orserdeu about 2 weeks ago. So far just lots of fatigue.
Taking a down day today. It is a beautiful day in the Pacific Northwest.
I also have a new grandbaby due this week. Number 3 and this one is a girl!
Hope everyone is managing well and finds some enjoyment and heart opening.
Re: Elacestrant (ORSERDU)
Hi all,
New here…..started Orserdu about 2.5 months ago. Doing well with little side effects.
I am ESRU1 mutation, and did not tolerate Kisquali & Verzenio.
Saw by wonderful oncology team yesterday, and am so thankful everyday for such wonderful care. I told them, "I see this cancer treatment is almost like an 'art form'". What to take, when, the continual dance of it all. When to intervene and when not to.
I was initially dx in 2003. ILC (I found it). Double mastectomy ( in situ in other breast). AC & tamoxifen.
Fast forward, October 2023….in a car accident. Fractured sternum on CT scan. Went home, read COMPLETE report next day. Last sentence, Intermittent scherlotic bone metastatic cancer. NO ONE told me. If I would not have know the meaning, I would be just cruising along. I believe everyone is free to choose their beliefs, but I gotta tell you ladies the Holy Spirit was ALL OVER this one. I also developed two pulmonary embolisms after accident and drove myself to hospital. The doctor told me "I got chills when I read your file". Thank you Jesus
Kisquali & Verzenio sent liver enzymes through the roof. ESRU 1 mutation, so now on Orserdu.
Thanks for reading & listening. Hugs to all, C