I hope you're all coping and doing as well as you can.
Sorry to barge in from the other side of the world but I have an English based query.
I have triple negative Inflammatory beast cancer and nearing completion of about a year and a half of chemo with a mastectomy and axillary clearance and good margins. Thankfully I've responded well to treatment but unfortunately chemo just didn't quite eliminate the thing.
Protocols indicate that I should have radiotherapy very soon but I also suffer from Systemic Lupus Erythematosus which in the past has been seen as massive contraindication as it might trigger a nasty re - activation of the lupus which for me tends to damage vital internal organs.
I've found a radiation oncologist here who's very respected, senior, experienced and to be honsest - is the only one I've found who believes radiation is worth the risk for me.
He's based his opinion on what looks like brand new Lupus / radiotherapy observational data from a Dr Gillian Ross from the Royal Marsden Hospital who he spoke to.
My question is a bit weird - but has anybody come across this lady in their travels and have any opinion or feedback about her ? - and / or the Marsdon Hopital ?
Please feel free to private message me if you'd prefer - and know anything you say is utterly confidential and won't be shared or quoted anywhere.
Thanks.
Written by
Freckle1000
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the Royal Marsden is said to be the premier cancer centre of England. Or the UK. Or Europe?? Doctors go there for their onco training (and presumably surgical cancer training though Iβm not so sure about that).
I know nothing of the doctor you named, though,
Iβm sure you would be as reliant as anyone could be on thatβs doctors thoughts, and I really feel for you.
Please do post back here (or pm me) when youβve made your decision. And then again when youβve recovered.
ps. thanks also for putting the Royal Marsdon into a local English context. It's really helpful. It is a somewhat freaky situation to have one Dr's opinion and the prestige of a hospital being very singled out as a guide. The fact that my radio - oncologist went to the effort of seeking an opinion from there - according to my local Drs ππ€ seems to be an indicator that I should trust him too ?
Maybe try posting on Lupus Uk site , you might find someone with similar issues or they might recognise Dr Gillian Ross from the Royal Marsden Hospital .
A big hello weathervane ! ππHow have you been ?
As you can see I've been a bit of a mess but I'm doing a lot better now.
That is a VERY good idea !
Once I get a bit more oomph I'll do just that.
When I was first diagnosed with the cancer I was told radiotherapy wouldn't be an option - so I had a browse of old Lupus UK posts and contacted ( cant remember her name ) a medical info person there - who sent me lupus / radiation literature. It looks like one (or two) people went ahead with radiotherapy despite being told they couldn't - and it went well.
Fun fact - I learnt today that plaquenel and radiotherapy doesn't mix. ( Rheumy )
And from my renal specialist - localised radiotherapy should be ok but whole body - not so great.
As for the oncologists - their opinions are very polarised, emotive and adamant.
I had no idea how much the treatment decision making is up to the patient in oncology. Its very different.
I have SjΓΆgrenβs and get rituximab infusions. I had a lumpectomy and radiotherapy without any major issues, oncology and rheumatology did liaise . Only issue was the delay in next rituximab. The radiotherapy is quite targeted and other parts of body can be protected.
Itβs enough for you having lupus without having to worry and research about this . I hope you get get it sorted and receive the treatment you need. Take it easy and look after yourself, best wishes xxx
hi lm in the UK and found her straight away with a google search still at the Royal Marsden you may have to try to get to her through the hospital but does both private and NHS good luck and keep in touch if you want me to do more research for you at this end
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