Hi All
i am having RAI at the Christie at the beginning of September so start my two week LID tomorrow.
Has anyone on here had treatment at Christie? What are the facilities like? What did you take with you? How long were you in?
sorry for all the questions just curious
Hi there my surgery was the 7th May and due to Covid there has been a delay with getting to RAI but still within the six month window
Hello, I had my RAI at The Christie last year. I think the rooms have all just been redecorated by the Butterfly Thyroid Cancer Trust, but TBH the room was fine. Here are some photos of my room:
I was in for two nights. I'd followed some guidance on here which said to shower twice a day to help get rid of the radiation and so my levels were pretty low the day after the tablet, and had reduced enough that I didn't need any restrictions when I came home. I had the low dose, so it might be a bit different if you're having a higher dose. I took my ipad and phone in. I think they ask you to leave any magazines in that you take in with you. Clothes wise, just take some comfy pjs/ loungewear and they will give you guidance about how to wash it separately when you get home.
I don't know if you've read about damage to your saliva glands after RAI? Everything I'd read before told me that the hospital would give you lemons/ sharp sweets to suck. This didn't happen at The Christie and my saliva glands are damaged so I'd recommend that you take some sharp sweets in with you (or lemons) to encourage your saliva glands to work.
The staff were really lovely.
Hope it all goes ok.
I think the delay has been due to Covid and because of all the cancers this is considered low risk as long as you have the treatment within six months
The RAI definitely damaged them, but they do still work. It just means my mouth is dry most of the time so I drink a lot of water, but having a dry mouth means that my gums get sore and I have to look after my teeth a bit more. I've been prescribed a special toothpaste and that seems to be helping.
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