Good morning ladies Thought I would pop by and say hi to you all. Good to see that most of you are doing well and sending hugs to those of you that are still going through it with treatment and medication side effects. I’m just coming to the end of my Radiotherapy. Have 2 more left out of 20. Although it’s nowhere near as bad, physically, as chemo I have been surprised by the effect it has had mentally. I think it’s a mixture of the travel, tiredness and being around other people in a far worse state. It’s been 9 months since diagnosis so also feels like a long hard slog! I just wanted to comment on your post re the Herceptin and sty’s Marilyn. I’ve never suffered with them before but have had a couple of small ones and I am on Herceptin so wonder if there is a link?? I do seem to suffer with my eyes now. I went to the opticians last week and she said they were very dry. She recommended that I use hycosan eyedrops indefinitely. Asked her if it was due to chemo and she said medication and hormonal changes are both factors so double whammy there then!! You may have noticed our Dec forum has gone a little quiet. We have set up a Facebook messenger group as we have been arranging our meet up so really excited about that 😁 Sarah, I hope you don’t mind me asking but me, hubby and kids age 17 & 15 are going to Bristol/Bath at the end of the month for a few days. Never been before so wondered if you have any recommendations for ‘must do’s’. Loved all your pics of the street art. Sending you all love and 🤗 🤗 🤗 xx
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