Beginning My Return to Normality (Almost)
(To read my cancer story from the beginning start here – April / May 2018 – You Have Cancer)
Christmas 2018 was great
I even managed to eat some turkey, roast potatoes, honey roast root vegetables, sprouts, etc. the only real struggle were the pigs and blankets – Sausages, bacon, ham, bread and a few other things would remain a struggle for a few months yet.
Straight after Christmas I had weekly trips to Coventry for the nurse to pull out about an inch of the pack from my neck each week and redress it, by now though I was feeling well enough (and confident enough) that I would drive myself and go on my own π
I was also at the stage where I was only seeing my support team once a month, my oncologist once a month and my consultant once a month (usually tying in seeing my support team on the same day as seeing my oncologist or consultant) which meant that once my neck was sorted I was only having to go to Coventry once a fortnight for the next 2 or 3 months.
The weekly pack treatments were a doddle, I didn’t feel a thing when she was pulling it out and on the last week when she pulled the last bit out I was expecting to have stitches but no it just seals up on it’s own the nurse told me.
With my neck sorted, infections finally cleared I could begin my Lymphatic treatment.
My consultant had made an appointment for me but unfortunately it was in Nuneaton a good 10 miles further North than Coventry (I was 30 miles south of Coventry)
It was about then that I found the MacMillan Cancer Support Community which I joined and asked a question about Travelling so far for treatment.
It was suggested I contact my GP, I then did a bit of research and found there was a specialist Lymphoedema clinic at the Myton Hospice at Warwick
I emailed them explaining my circumstances and asking if I could be treated there instead of Nuneaton and was pleased to receive a reply later that day asking for more information.
I sent them all they asked for and said to leave it to them to contact Coventry hospital and get everything set up.
A week later a nice lady at Myton Hospice in Warwick had arranged everything and my 1st appointment was to be in Warwick in the 1st week of February π
I also went for my gym assessment at the end of January, was weighed, body fat measured, fluid retention measured etc.
I was now 10 stone 12, body fat slightly high, fluid slightly high but well within a healthy range and within a healthy BMI
I was given an exercise plan, basically just 3 pieces of equipment for the 1st 6 weeks whilst I was having my assessment; 10 minutes on treadmill, 10 minutes on Exercise bike and 10 minutes on an arm spinning machine.
My cancer story continues here – Lymphatic treatment and having my PEG out
Recent Posts
- My Christmas Tree From Christmas 2018
- Nothing to Worry About
- Just Muscle and Fat
- A New Lump to the Collection
- 3 Years After Operation for Jaw Cancer
- 3 Years After Being Told I had Jaw Cancer
- Still Wobbling On
- 2 Years on from Hearing I Had Cancer
- Early 2020
- The Last Months of 2019
- The Summer of 2019
- Be Careful with the Suntan Lotion
- Getting Ill When Recovering from Cancer
- How Stupid is the Tax Credit System Cancer Sufferers
- 12 Months on From Being Told I Have Cancer – A Brief Summary
- Can a 16 Plus Stone Man Become Anorexic
- Cancer Free and no more PEG
- Lymphatic treatment and having my PEG out
- Beginning My Return to Normality (Almost)
- Will I be Home for Christmas 2018
- Swelling, Lumps and Puffiness The Cancer is Back
- No More Radiotherapy
- Last Couple of Weeks of Radiotherapy
- The Bad Radiotherapy and Chemotherapy Weeks and Back in Hospital
- Early Stages of Radiotherapy
- Radiotherapy β Whatβs all the fuss about?
- My 1st Radiotherapy and Chemotherapy Sessions
- Back at home, the calm before the storm
- Having a Radiotherapy Mask Made
- Drips, overnight feeds and blood transfusions
- Back in Hospital
- 2 days at home then a near trip in the Air Ambulance
- Removing the elastics and going home
- Stitches out, Temperatures and Infections
- Time to try solid foods
- It’s Not Me You Want to Thank
- 3rd operation of the week
- The Infections and that Damned Heat
- Back on the Ward
- I Never Liked Lifts
- My 2nd Operation in a Week
- My 1st night after my operation
- The Day of the Operation
- My 1st Night in Hospital
- Pre Op Arrangements
- Having a Feeding Tube Fitted – Percutaneous Endoscopic Gastrostomy (PEG)
- Telling Your Family You Have Cancer
- Coventry Warwick Coventry
- April / May 2018 – You Have Cancer