hi all,
i'm clare, and was also diagnosed on 27th oct '15. apologies firstly for grammar, i've broken the keyboard .....
i've had a right mastectomy, chemotherapy, radiotherapy and was on letrozole and zoladex until recently changed to exemestane following investigation of a bone lesion.
i'm signed up for fridays event and looking forward to meeting people in similar circumstances - i'm a worrier and hoping to gain some tips to manage my anxiety
clare xx
Hi Everyone.
My name is Lex and im coming from Newport. I was diagnosed December 15 and i underwent chemo and a lumpectomy. I then found out I was a BRCA carrier so went and had risk reducing surgery. Lost all my confidence so looking forward to meeting others and hearing your stories x
Sarahm,
Hi, I think I have sent you a private message! I am not familiar with this site. Wondered if you wanted to meet up on the train? Gay xxx (womble)
Hello Ladies,
So lovely to read all your posts so far, really looking forward to Friday 3rd and meeting you all.
I'm Amanda, I live in Cardiff, was diagnosed a week before Christmas 2014! I had 2 lumpectomies, axillary lymph node clearance, chemox6, radio x15 (breath hold) and have been taking a daily tamoxifen since August 2015. I constantly worry about developing lymphedema and am looking forward to the group on that. I still feel like I have chemo brain, nearly 3 years down the line 😂
Have safe journeys to Cardiff and see you all on 3rd,
Amanda X
Thanks Louise, I'll be interested in knowing how you are getting through it all. Look forward to meeting you. xxx
Hi All
So nice to hear from you all and all the different experiences, which I'm sure we'll share more over the weekend.
I'm Sue from Cardiff. I was diagnosed in Aug 2016 and have gone through chemo, surgery, radiotherapy and recently had my ovaries removed to make me post-menopausal. I've just started on Letrozole. I'm thinking of returning to work next Spring, and quite scared about it!!!
Look forward to meeting you soon....
Sue xx
Hi Clare,
The implant will gradually dissolve over the four week period so will be all gone by the time of your next injection.
Gay xxx
Hello,
Me too! I was diagnosed last Nov. I've had mx, chemo and radio, Now on zoladex and letrozole. I have been back at work for 2 months.
I am very much looking forward to this but feeling quite nervous too.
Anybody coming from the Swansea/Bridgend direction?
xxx
Hello
I'm really looking forward to this event, but quite nervous also - I find that since all my treatment I'm very anxious and nervous around a lot of people. I know it'll fine ultimately 🙂
See you all soon,
Cwtches xx
Hello Everyone,
I am currently 7 weeks post surgery and just started my second round of chemo. I am looking forward to meeting everyone at this event and be able to share experiences with each other.
I have found that there are not only physical but emotional barriers that I did not anticipate and hoping that I come away finding ways to handle them, along with in any way I can, be of support and laughter for others in similar situations.
Look forward to seeing you all.
Hussana
xxx
Looking forward to meeting everyone next weekend.
I'm Sarah and I've got my final round of chemo on the Monday after the BCC event. Still got surgery and rads to go (as well as 10 years of hormone pills, etc!). I'm looking forward to the surgery workshop in particular as I'm still feeling confused about surgery options with my operation date looming in early December.
I'll be getting the train from Temple Meads on the Friday morning if anyone is coming from through Bristol and fancies a chat on the train.
x
Hi everyone,
My name is Jo and I'm going to the event in Cardiff next weekend. I've just finished chemo and about to start radiotherapy. I'm looking forward to meeting other people with a shared experience - and having some fun! I'm particularly looking forward to the laughter workshop!!
I'm interested to hear who else is planning on going.
See you there!
Jo