Cancer · Fundraising · Living with Cancer · Melanoma

Its May – Melanoma Awareness Month and Time for the Skipathon

Living scan to scan can take its mental toll and as you know I have been on a bit of a rollercoaster over the last few months.  As my last scans had showed an indeterminate anomaly with a chest lymph node on my scan I was feeling slightly nervous as I headed to the Marsden for my latest results last Friday.  It sometimes feels like turning up at the teachers door for exam results not knowing if you have managed to scrape past or not, except in this case the results can have a much more fundamental meaning as there may be no resits. This may sound over dramatic but I felt rattled to the core earlier this year after my experience earlier in March plus I also saw from 2 other friends who also had stage 4 melanoma just how quickly things can change and they are sadly no longer with us.

I am a glass half full person and live every day to the fullest as my Dad taught me that and cancer has made me even more determined that that’s how I’ll be living my life. I used to be worrying about deadlines for work or what I’d be wearing to the next party but that all falls into insignificance when you are waiting to hear if you’ll sill be alive and kicking in 3 months time.  Of course no one knows that but living with not one but 2 cancers means my odds are not ones you would be betting the house on. Saying that and with my positive hat on I am still here four years on from that stage 4 melanoma diagnosis and that almost certainly wouldn’t have been the case 10 years ago. So my trip to the Marsden on Friday was a good one, my latest scan results are all good, there is no issue now with the chest lymph node and my Oncologist was correct it was likely due to the COVID vaccine. I left the hospital armed with cycle (months) 42, 43 and 44 of the wonder targeted drugs Debrafenib and Trametinib looking a bit like a Mexican drug lord and felt elated to be passing go for the next 3 months.   Thank you as always to the fantastic melanoma team and also a big thank you to the radiology team. I am a frequent flyer at the Marsden for scans I haven’t counted the number I have had but it is a LOT. The radiographers are amazing calming the patients, chatting to you knowing your name as they see you there so often and putting you at ease while understanding you  are going through a stressful experience. They are then reporting on the scans in super speedy turn around time so that everything is ready for your doctor by the next appointment. They are some of the unsung heroes at the hospital and often go under the radar when they play such a key role in your overall care and deserve a big thank you.

With the lockdown starting to lift in the UK I have been beyond excited to catch up with friends and family. It has felt so special to see people in person and such a treat to go out and eat dinner. It was also lovely to get out of London and see the hiking gang and those simple things that you used to take for granted are really a special treat. We are also in countdown mode for our trip north of the border after 3 cancelled trips from the autumn through Xmas plus we have had to postpone our planned trip to the Outer Hebrides until next year, however, we are all set to head there later this month and cant wait to see the gorgeous parentals and family.

As we reach the start of May it’s Melanoma Awareness Month and Team Shomelanoma are kicking off the Skipathon Challenge starting today May 1. It’s going to be a lot of fun, we’ll be skipping for 10 mins every day and there’s going to be some funny videos and pics to share.  I have to say a HUGE thank you to everyone who has signed up for the challenge and a big mention to Christchurch and Holy Trinity Primary School where my lovely friend Avis Hawkins is Head Teacher and approximately 400 of the children there will be joining the Skipathon for the month to help raise funds for melanoma research at the Royal Marsden. Having seen some of them practicing their skipping this week they are looking pretty good.  We’ll be sharing some fun photos and videos throughout the month so look out for them, we are beyond excited to get going well some more than others David will be getting his new skipping rope out of the bag tomorrow and attempting to skip for the first time in many years, look out for that video.  Full details of the skipathon .

https://www.justgiving.com/fundraising/shomelanomaskipathon

I also have to say a BIG thank you to gorgeous friends Chris Lloyd and Nicki Millward who both took part in the virtual Royal Parks Half marathon on April 11. Chris ran along the banks of the Thames with David alongside him on his bike for moral support. As many of you know Dave is a regular at the Royal Parks half marathon (he is featured in the Marsden Progress Magazine this month) but he is saving himself for the next Royal Parks half marathon in October so that he can get his running back up to speed. Jane and I were on our bikes too in the support crew and Chris finished in a good time under 2 hrs. Nicki was running close to home in the Malverns and also did an excellent time of 1 hr 54 Thank you to both of them and everyone who supported their amazing effort.

If you would like to join any of the upcoming fundraising challenges or organize your own please let me know. I will be doing a full update on the melanoma research projects the funding is supporting  in an upcoming blog.

As the weather starts to heat up in the UK we will no doubt see the excitement of the British public stripping off as soon as they see the sunshine. Remember that UV damage is cumulative and to protect you skin and stay out of the mid day sun. Most importantly don’t get burnt and if you do notice any changes to any moles or new skin lesions get them checked out by a GP or dermatologist. The motto is if in doubt get it checked out and don’t delay.   Melanoma UK is an excellent source of the key warning signs to look out for

https://www.melanomauk.org.uk/the-abcde-rule

Thank you as always for all of your support. I’ll be back soon to report on a full update on the Skipathon next month.

Cancer · Fundraising · Living with Cancer · Melanoma

Its December 2020 – The Forgotten 2nd Cancer

We have arrived in the final month of 2020 and for many of us I am sure we will be glad to see the back of 2020. What a contrast to Nov/Dec 18/19 when I was fortunate to go on the adventures of a lifetime to Argentina and Peru. I have had the photos pop up for the last month to give me a reminder of those amazing trips. Back in reality the latest national lockdown has ended and we are feeling hopeful about a trip to Scotland to see family over Christmas. But first it is December and back to Marsden HQ.

As some of you may recall 4 years ago I discovered that along with melanoma I also had DCIS (precancerous breast cancer) found in my right breast. As if dealing with one cancer wasn’t bad enough there was also a second to contend with. At the time, I had a horror month of a lot of tests and appointments at different hospitals across London with different doctors and several opinions and the situation only improved after all my medical care was all moved to the Royal Marsden. Shortly after this, the melanoma advanced to stage 4 and the precancerous breast cancer was put on the back burner as the melanoma was treated as high priority.  As my Oncologist explained to me its all about managing risks. Last month I received a reminder to go for a mammogram so it was time to revisit and check up on the forgotten 2nd cancer.  

I had a mammogram 10 days ago and a follow up appointment to review the results. My doctor said the mammogram looked very similar to 4 years ago which I took as positive but there was one area of thickening that they wanted to double check so they were sending me for an MRI, ultrasound and biopsy. I have to admit that I left the hospital with my head in a bit of a tailspin.  As I have been so focused on melanoma for the last 3 years and have felt very fortunate that it has been brought under control and for the last 2 years I have been able to live a fairly normal life with minimal side effects from the drugs I am on.  I was feeling that a Pandora’s box had just been opened and the December factor was about to rear its ugly head.

It just happened that last week, my regular melanoma scans were also scheduled so it was a week of almost daily trips to the Marsden. I had an MRI scan of the chest; this was an uncomfortable experience as you are face down breasts in cones and arms over your head as you go into the scanner.  After lying still in that position for half an hour, I came to the conclusion that this made the brain scan seem relaxing and I never thought I would be saying that. On Wednesday, I had my body CT and MRI of the brain plus blood tests which proved to be a challenge as one of the veins in my arm burst.  Feeling stressed, I left the Marsden and headed off for lunch with my good friend Liz and chatting with her helped to calm me down. It is amazing what a bit of lunch and a cup of tea can do for you so big thank you Liz as by the time I returned to get the blood tests done again in the afternoon it was quick and successful and I was able to head home for the day.

On Friday morning it was back to the hospital for an ultrasound and biopsy of the right breast.  I spoke to the doctor and she told me that the MRI scan of the right breast had shown up 2 very tiny lumps which they were going to biopsy.  On the ultrasound they could only see one of the lumps so they did the biopsy and now I have to wait for the results later this month on to see what happens next. On Friday afternoon I was having my regular clinic appointment with my Oncologist to get my latest melanoma scan results and this was making me feel very nervous. I had a quick walk up and down the Kings Road to calm myself down before returning to the hospital. You are not allowed to have partners with you at the hospital just now due to COVID restrictions so there was no rockstar husband by my side. I just had to put the big girls pants on and get on with it and this is sometimes easier said than done. I took big inspiration from the amazing Bowelbabe who has recently been documenting her latest surgery on social media and thought if she can be getting through this on her own without any fuss then I can get on with getting my scan results.

It was good to see my Oncologist and nurse in person (well masked up)  as consultations have all been over the phone due to COVID. But since I was already in the hospital then it made sense for me to get my scan results in person rather than rushing home to wait for a phone call.  I was delighted to hear that the melanoma CT and MRI scans were good and 3 years on from started my targeted drugs Debrafenib and Trametinib my melanoma is under control and I was told as far as the melanoma is concerned we are in the best place possible. I felt a huge relief that at least it was good news. The other positive is that as both of my Doctors are at the Marsden then they will talk to each other if I do need further treatment following the results of the breast biopsy. I left the hospital feeling in a better mood although I do have to admit my delight was slightly tainted by the fact I have to wait for the results of the biopsy and what happens next.

At this point I have to say a big thank you to the teams at the Royal Marsden. I know that in the time of COVID it has been hugely challenging for staff and patients.  I know I am very fortunate to be treated by such wonderful teams and there is a village of them from the security guards on the door to the receptionists, cleaners, radiologists, pharmacists, nurses and doctors everything has been handled efficiently and quickly so whatever is next I know I am in the best hands and that is hugely reassuring.  

Since the last blog when we were just a week away from the Giants Causeway Challenge like all other events it was postponed to next year. It was disappointing as we had been training hard and were looking forward to it. But next year we will be back onto the challenge cause and raising more funds for the team at the Royal Marsden. If you are interested to join us we have a number of challenges planned for 2021 including a team at the Royal Parks Half Marathon, the Giants Causeway Big Hike in July and the Blenheim Triathlon in September.  If you would like to join us or plan your own challenge please let me know and thank you as always for all of your support.

Last month, the Duke of Cambridge laid the foundation stone to mark the building works of the new Royal Marsden Oak Cancer Centre, which will be a state of the art cancer research facility, based at the hospital in Sutton. The new facility will bring together over 400 researchers under the same roof as patients and clinicians in spaces designed to encourage collaboration and to put patients at the heart of research. The building is due to open in 2022 and you can find out more here. https://www.royalmarsden.org/blog/hrh-duke-cambridge-lays-foundation-stone-state-art-cancer-research-facility

In addition, I made my first billboard appearance on one of the hoardings going around the building.  I haven’t seen it yet but ones of the girls at the charity kindly sent me a picture. As the saying goes it’s never too late to make it onto a billboard.

In the meantime, I have been out and about staying active and doing some hikes during lockdown to keep myself sane and stay fit and well preparing for the next adventure. Enjoy the run up to Xmas and I’ll be back soon with more Shomelanoma updates.