Confirmed
Spinal Metastasis with cord compression - To say I'm terrified is an understatement. I have no words.
Comments
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I can't bring myself to update my dx line.. lovely, denial starting already.
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Finallyoverit.....Sending big hugs to you
💚💛💜
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Thank you. I'm numb with fear.
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Lord, have mercy. I'm so sorry.
Deep breath...you'll get a plan in place with your team and start walking through this one step at a time. It's overwhelming now, and we all know what that feels like. But you can do it, one foot forward.
We've got your back with prayers and good wishes.
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I'm so sorry.
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My MO says we have options so that helps a bit but not exactly the news anyone should hear, esp in their early 40s.. like way early. No one deserves this.
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Finallyoverit. I totally get the numbing fear. Try to get some anxiety meds and know there are many treatments available. Prayers and gentle hugs.
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big hugs to you finallyoverit. I'm so very sorry you got this news. Stupid disease!
Nancy
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holding you in the light. I'm so so sorry to hear your news
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Thank you ladies. I will post more once I begin to wrap my brain around this but wanted to thank you all for the support. Means more to me right now than I can say.
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sorry to hear of your diagnosis. I was just told I have a recurrence. I also had my first diagnosis in October 2013. I will be praying for tou
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Thank you ladies. My head is still spinning.. no idea which way is up at this point. Had emergency spinal surgery and just trying to recover. Still numb with fear
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I know where you are and I am so sorry you had to join us. Deep breathes and know that its a long game now and that there are many many options and treatments for us. I had thought it would be just like last time - where I had the freight train of chemo hit me - but treatment options are a lot less dramatic, Something I am just getting used to. That pesky strap line can wait too!
I get a huge amount of support from this board, but I also joined a local support group and find the support and info or just plain nods and understanding I get is invaluable.
I wish you a comfortable recovery from your surgery. Put some of the stage 4 threads into your favorites - I follow the Ibarance and Liver mets ones closely. I hear there's a great bone mets one too.
With love and e-hugs
Sarah
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Finallyoverit, wishing you a smooth recovery from surgery. Gentle hugs to you.
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Finallyoverit, I've been where you are. Concentrate on getting well from the surgery, and think long term. You'll feel better once you get over the "shock and awe" period, but it will take some time. I was lucky enough to spend mine under the influence of percocet as I recovered from my fusion.
Once you start cancer treatment life will return [somewhat] to normal.
PM me if I can help!
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Ack! Stupid disease. I hate cancer. Hoping you recover quickly and have s plan in place soon
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I'm so sorry to hear this. Be kind to yourself during this difficult time.
My thoughts and prayers are with you. XO
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Prayers for treatment to kick those buggers to the curb! Assuming you've been on hormonals, maybe a switch to another one should be in order.
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Finallyoverit So so sorry. Just wanted to share a friend of mine who had been cancer free for a number of years had BC metasasize to her spine so seriously they gave her weeks to live. They aggressively treated the cancer and I remember her telling me she prayed for three years. That was six years ago and she is doing fine with ongoing treatments. Her life is full and there no reason to believe she won't continue to do well. Hugs
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Finallyoverit...sorry for what you're going through. How are you doing? I just found out Thursday that I have a spinal cord lesion that has been causing horrible neuropathy from waist down. Fortunately, it doesn't look like there is spinal cord compression, but only nerve compression at this time, but surgery will likely come soon. I know little more at this point...will meet with my oncologist on Tuesday and then a neurosurgeon. First thought they could treat with rads, but I already had rads very close to this area on spinal mets last spring. Very scary stuff, indeed! I was humming along with all prior mets to lungs, liver and bones (MANY!) resolved with rads, chemo and hormonal therapy since spring of 2016, but alas, there was an intruder unseen! Rats! Keep us posted on your recovery!
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Bbecksoon - just seeing your message. I stayed away from the forums for a while. I'm hanging in there.. still a lot of numbness in one of my legs, but I'm able to get around. I hope your docs were able to come up with a treatment plan for you.. I agree, very scary stuff.
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Thank you everyone for your kind words. They mean more to me than I can say.
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I'm really sorry to read this, sending you hugs, thoughts and best wishes.
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I am so sorry to hear this, but stay strong and never give in to this hateful disease. Lots of prayers and thoughts your way.
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Hoping you tolerate the treatments well and that they get you to NED
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Hi I was just confirmed too. October 5th . Wishing you the best!
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ihopeg - you and me both! Was confirmed Mets on Oct 5th! Still haven't completely processed the news, I have some good days, and some not great...I have rad consult for my spine met next week...good wishes and best of luck to you! Let's fight this horrible disease!!
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So sorry for your DX. I had 10 rad treatments to my left sacrum/iliac for pain and 5 tumors. Pain was immediately relieved and tumors have shrunk along with kisqali/letrozole pills. Started treatment in March and will have my 3rd pet/Ct scan in November to monitor my response to treatment. Good luck. Hugs and peace
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finallyoverit,
I'm so sorry. I'm thinking of you and sending you healing and courage. This is the toughest time, this shock.
Love to you.
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