Chelsea14Ian Posted June 17, 2023 Author Share Posted June 17, 2023 Back home yesterday evening. This may help.Like most undergoing Radiotherapy. You need f50 sun cream and aftersun later.Think it was Tuesday suncream due to sweating got in my eyes.Sore for hours.I asked in boots if there was one for eyes. Thanks to a chap he looked on line. (See) photo not cheap, £20 but it works well only need a little.I put some on my forehead and eyes. 1 Quote Link to comment Share on other sites More sharing options...
vanessan Posted June 17, 2023 Share Posted June 17, 2023 This is a sunscreen actually produced by the dermatologist and skin cancer surgeon who dealt with my problems a few years back. The website is altruistsun.com but you can also get it from Amazon. Very reasonably priced too. Quote Link to comment Share on other sites More sharing options...
Chelsea14Ian Posted June 20, 2023 Author Share Posted June 20, 2023 I had my last treatment yesterday afternoon. I have a phone consultation today with Zac JP.Then one on Friday from Addenbrookes. Once again very pleased with the care given to me.Hoppfully that will be a good present for Marina. Who's birthday it is Friday. A few photos of my musk,used for my Radiotherapy. 5 Quote Link to comment Share on other sites More sharing options...
addicted Posted June 20, 2023 Share Posted June 20, 2023 Hope the treatment is totally successful Ian and you can put this glitch behind you. Fingers crossed. Carole 1 Quote Link to comment Share on other sites More sharing options...
Chelsea14Ian Posted June 20, 2023 Author Share Posted June 20, 2023 Zac my Consultant phoned me this afternoon. Still will speak to someone from Addenbrookes Friday. Zac will arrange for a follow up MRI in a month's time.Im okay side affects not to bad. 6 Quote Link to comment Share on other sites More sharing options...
Chelsea14Ian Posted June 23, 2023 Author Share Posted June 23, 2023 Spoke with Addenbrookes.Like Zac they asked about side affects. Thankfully not to many.The main ones head aches.One odd thing Monday evening. We were having dinner.Both my fore fingers and index fingers,stuck together and I had to move them apart. The Doctor thinks that's the Steroids which I stopped by Tuesday. She couldn't tell me if the Cancer has gone. A Follow l óMRI next mp th.Tjen see Zac August. Quote Link to comment Share on other sites More sharing options...
chrisdobson45 Posted June 23, 2023 Share Posted June 23, 2023 All the very best Ian, it looks like you have the best of the best looking after you. I am undergoing radiotherapy at present, 10 months after surgery as "it" has returned. The worst part of my treatment was the fitting of the rectal spacer last week. Why is it that every time I'm in theatre, on my back, with my legs apart, there's a few young nurses around? 2 Quote Link to comment Share on other sites More sharing options...
Chelsea14Ian Posted June 23, 2023 Author Share Posted June 23, 2023 There always are.When I had the chop.I was told just a little prick.Oh you mean the injection! I hope all goes well with you. 1 3 Quote Link to comment Share on other sites More sharing options...
Chelsea14Ian Posted July 15, 2023 Author Share Posted July 15, 2023 Not quite this time. On the first of July I came via Ambulance to James Paget with poor breathing. Lots of tests,they ruled out things like pneumonia, it was my COPD. My breathing improved during the day and they let me home .I was still under the care of the hospital and I recorded my obs and a nurse phoned me each day.I took my Antibiotics and steroids.After a few days I was a lot better.Then a few days ago my obs were not good again so yesterday evening I phoned 111,after questions then sent an Ambulance back to JP more tests.I am on low levels of oxygen (1 lt ). One consultant thinks its what he called a low grade infection. So more antibiotics and steroids for two weeks. They hope to send me home tomorrow, providing my obs are not to low when walking. Who have I 😡 upset? As for Cancer. As far as I can tell moving in the right direction. A few headaches and little lightheaded times.That could also be my breathing. 6 Quote Link to comment Share on other sites More sharing options...
SwanR Posted July 15, 2023 Share Posted July 15, 2023 Sending you my very best wishes that you’re feeling better and home soon Ian. I have a close family member with COPD so I’m familiar with some of the effects when all is not well. 1 Quote Link to comment Share on other sites More sharing options...
addicted Posted July 15, 2023 Share Posted July 15, 2023 Sorry to hear this Ian. Let's hope they let you out not just for good behaviour but because you're on the mend. As ever thoughts with you and Marina. Carole 1 Quote Link to comment Share on other sites More sharing options...
Ray Posted July 15, 2023 Share Posted July 15, 2023 Keep strong Ian 👍 1 Quote Link to comment Share on other sites More sharing options...
DAVIDH Posted July 15, 2023 Share Posted July 15, 2023 Best wishes Ian. Not long before the season starts and your beloved team starts to perform to its true potential under Pochettino. Something to look forward to while you're getting kicked around in the close season. 1 Quote Link to comment Share on other sites More sharing options...
Chelsea14Ian Posted July 18, 2023 Author Share Posted July 18, 2023 Sunday never happened. In my bay there was five of us.Four due to go out.None of us due to the Doctors strike.Which was a blessing in disguise My stats were low.Checks on my stats early yesterday morning off oxygen had improved a great deal,then saw the consultant who said I could go home. off oxygen. My low level infection is an infection in my windpipe.Still on steriod for nearly two weeks and antibiotics for a week.So again a very worrying time for the both of us.It certainly worried me more the the Cancer oddly. 1 2 Quote Link to comment Share on other sites More sharing options...
SwanR Posted July 18, 2023 Share Posted July 18, 2023 No one wants to be in hospital but I hope the time has allowed you to recover a bit and get the right treatment. A difficult time for you and the family. I hope there’s brighter days ahead. 1 Quote Link to comment Share on other sites More sharing options...
kpnut Posted July 18, 2023 Share Posted July 18, 2023 Oh Ian, life certainly throws more than your fair share at you. Keep positive and similar to what Jean said, an enforced rest might be a blessing in disguise. 1 Quote Link to comment Share on other sites More sharing options...
Chelsea14Ian Posted July 18, 2023 Author Share Posted July 18, 2023 Yes and no , not complaining,but l was in three wards. Two of which linked to a & e.Friday to Saturday no sleep.Saturday to Sunday slept well.Sunday to Monday poor sleep.At home up at 06.50.For me a good night's sleep.The worse thing was the worry of not improving and a life on oxygen. What I found out which no one told me before. Oxygen and COPD are not good partners. Co2 levels can increase which can be dangerous for COPD suffers.I will still be checked on daily for the next two weeks. 1 1 Quote Link to comment Share on other sites More sharing options...
Gracie Posted July 18, 2023 Share Posted July 18, 2023 Trying to sleep in Hospital is awful, they wake you up to do your obs every couple of hours and then the ruddy cleaners come in at silly 0 clock Take care Ian, you are so brave and strong, all the best to you both x 1 Quote Link to comment Share on other sites More sharing options...
JawsOrca Posted July 18, 2023 Share Posted July 18, 2023 Glad you home pops.. at least you can come and see me now... I'm still chuffed I got a free helicopter ride! 20230715_192354.heic Quote Link to comment Share on other sites More sharing options...
Chelsea14Ian Posted July 18, 2023 Author Share Posted July 18, 2023 Well Alan thankyou.Me yoi to JP via Ambulance. You to NN via helicopter. Still can't carry on taking the mick me head butting Ludham Bridge. Yes we're pop down to the hospital this afternoon. Hope all goes well. 1 Quote Link to comment Share on other sites More sharing options...
OldBerkshireBoy Posted July 18, 2023 Share Posted July 18, 2023 1 hour ago, Chelsea14Ian said: Still can't carry on taking the mick me head butting Ludham Bridge. You sure about that? Friends and family can be wicked you know. 😁 Quote Link to comment Share on other sites More sharing options...
Chelsea14Ian Posted August 2, 2023 Author Share Posted August 2, 2023 I've set up a just giving page in aid of the Macmillan coffee morning. I'm doing the coffee morning at our house on the 29 September 2023 from 10.00am to 1.00 pm. I'm doing coffee and cakes ,snacks with a raffle ,and donations.I hope a few of my Macmillan nurses can attend. I attend coffee mornings each month at JP.They've been very helpful to me and have become good friends .I understand most of you won't be close to me on that date. However all are welcome just pm me for our address or if possible please donate to my just giving page Macmillan is a charity that helps some many people with Cancer. Thankyou Ian 4 2 Quote Link to comment Share on other sites More sharing options...
Chelsea14Ian Posted August 3, 2023 Author Share Posted August 3, 2023 I had a MRI,monday last week and will speak with my Consultant on 22 August.Hopefully I will have good news.If not I will take it as it is comes.Friday last week and over the weekend my oxygen levels dropped very low,with dizzy spels. I Had bloods on Monday Thankfully my windpipe infection has cleared,however I'm back on steroids for about a month and a half. 2 Quote Link to comment Share on other sites More sharing options...
YnysMon Posted August 3, 2023 Share Posted August 3, 2023 Good luck for 22nd August Ian. 1 1 Quote Link to comment Share on other sites More sharing options...
Chelsea14Ian Posted August 4, 2023 Author Share Posted August 4, 2023 On 02/08/2023 at 14:00, Chelsea14Ian said: I've set up a just giving page in aid of the Macmillan coffee morning. I'm doing the coffee morning at our house on the 29 September 2023 from 10.00am to 1.00 pm. I'm doing coffee and cakes ,snacks with a raffle ,and donations.I hope a few of my Macmillan nurses can attend. I attend coffee mornings each month at JP.They've been very helpful to me and have become good friends .I understand most of you won't be close to me on that date. However all are welcome just pm me for our address or if possible please donate to my just giving page Macmillan is a charity that helps some many people with Cancer. Thankyou Ian Sadly I've had a number of problems with the just giving page.Ive tried to resolve the problem,without success. So please don't attempt to donate to my just giving page.I will soon close this page. 1 Quote Link to comment Share on other sites More sharing options...
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