Hi I'm new, looking forward to sharing and learning more about MBC. It will help to know I have friends .....we are in this together! Great comfort in feeling I;m not alone!
Flatrock17
Hi I'm new, looking forward to sharing and learning more about MBC. It will help to know I have friends .....we are in this together! Great comfort in feeling I;m not alone!
Flatrock17
Hello and welcome, sorry you need to join us. This is a wonderful place to find understanding and support.
I remember when I was first diagnosed I felt like I was the only person in the world with mbc then I found this group and it's been a life line 😊
Welcome. I was diagnosed bone Mets June
2018. Ibrance and anastrozole with modest side effects. Still active. After hearing this crushing news, my 3d cancer dx since 2004, I was very low for a month. Then, oddly, I realized I wasn’t going to die right away and that mood lifted. I see a counselor, take CBD tincture with low THC for anxiety, and rely on the support of the wonderful women I found here. Good luck.
Hello and a warm welcome to this amazing group. I don’t know how I can get through this illness without the wonderful, kind and compassionate people on this board. You will be okay here.
Maria
Hi and welcome. I'm quite new here too, diagnosed in April this year, and Im so glad I found this group. There's so much support and a lot of information on things like diet and what to expect with the meds etc. Real people experiencing the same ups and downs and the myriad of feelings we all have. I hope it helps you as much as its helping me. Sending positive thoughts your way, stay strong and take care. Xx
Welcome to the group nobody wants to be a part of! I'm also new to the group and newly diagnosed and have found this group an amazing support during my first few weeks.
welcome & sorry you needed to join us in the MBC club...this site does though make it a bit easier to cope & know that you're not alone in this.
I joined the club in January 2019, and I've been helped numerous times when it comes to weird symptoms or what not. Sometimes that help is just to lend and ear, so to speak and reassure me that I am not on an island.
Welcome to the site sorry for the diagnosis. You can get great support and information here from people who truly understand what you are going thru.
Welcome! This is a great site with amazing women who give encouragement and share info and experiences.
It's a Godsend to help you know you are not alone.
You are definitely not alone and this site is a wonderful support system. We all understand what you are going through. Please reach out whenever you have questions or just need to vent!
Kim
Welcome, sorry your here. This is definitely a great group who are positive and very supportive. We're in this together. xo
Robin
All of the above - like what everyone else has said. I've been living with metastatic breast cancer since 1998. The only online support back then was a list server where you could send an email to a central source and then receive emails back in response. Things have changed a ton since then. I find that FaceBook has been a great place to connect with others on a daily basis. Not sure if you're on FB -- some people avoid it at all costs -- but the MBC community is strong there.
Welcome! I'm sorry you're here though. You will find a lot of support, answers to questions, opinions and a place to vent/rant if needed. We all have different diagnoses and approaches to treatment, ie: conventional, alternative, complimentary, etc. You're definitely not alone.
Hi Flatrock17!
Welcome! I was diagnosed MBC de novo with mets June ‘16...I just realized this will be my 4th summer in the infusion room! 😱
Oh well I guess it’s my new normal!
Perjeta/Herceptin every 3 weeks...but so far it’s still working! 😀
Welcome. I am sorry you had to join, but I know you are in a great group.