Its been a week since my final Proton Therapy treatment
Its taken a long time to get to this stage since my original diagnosis in February
There have been some big up and downs along the way
I have kept this blog as a form of diary to myself as well as information for relatives and friends who I hope have found useful
It is difficult to remember times and dates of the various events so the blog has been my memory prompt
There are are lot of people to thank who have helped and supported me through this period
The NHS have generally been great with a few exceptions
The GP surgery unfortunately took way longer than they should have to realise that my repeated visits to them need further investigation. Eventually I was sent to the hospital for further investigation
The hospital investigations revealed I had a Clival Chordoma
Whilst undergoing treatment at Addenbrooke's Hospital I found the consultants, surgeons and most of the nursing staff were very good. Although my nursing care after my second operation was below par
Work were understanding. I was under the threat of redundancy just before my first op so was worried that I would soon not have a job. I was advised day before op that my job was secure
From the very beginning of the consultations with the neuro team there was mention of Proton Therapy. Much depended on the surgery outcome as to whether I could even be considered for this treatment
After the surgeries and whilst recovering I was put forward and accepted for treatment in Jacksonville Florida at the University of Florida proton centre. We had 2 weeks to pack up and leave the UK for the best part of three months
The difficult decision was what to do with the children. Our youngest boys James and Joshua would be finishing their primary school and starting their secondary school in the period we would be away. Our eldest Thomas would be starting his final yr
After much heartache we decided this was a critical period in their schooling and to miss these periods of school would be tough
Also what would they do in Jacksonville ?. With me off to treatment every day they would have a lot of bored time. Luckily we had the help of my sisters Clare and Anne who shared the bulk of care for the boys. Also thanks to Andy, Kelly and gang. Sue and Dave. My nephew Matthew and Niece Rachel and of course my mum who all did their bit in looking after the boys
We had many many offers of help and we appreciate the kindness of you all
And so to Proton
The kindness and professionalism of all the staff at the proton centre was amazing. They put a lot of effort to make it a community we were encouraged to join in and take part if we wanted to
We enjoyed the events we attended and the things we did ourselves - we needed to keep busy
We ganged up with a group of fellow patients and careres mainly from The UK
Many thanks to those fellow Brits (you know who you are) we meet who helped to make our time in Jacksonville easier. We had good times with them. We already miss you and good luck with your journeys
And so to the future. It all starts afresh. I will be having scans periodically to ensure no regrowth. They say if there is no change for 5 yrs I am cured. Ill drink to that
A blog documenting the progress of my treatment of the Chordoma Cancer
Wednesday, 25 September 2013
Saturday, 21 September 2013
Wednesday, 18 September 2013
The lunch bunch
As a Graduate of the Proton treatment I joined other Graduates, Alumni, newbies, patients and carers at the lunch bunch
A lunch laid on every wednesday at the centre
I got up and said a few words about my "journey"
I will attempt to put a few words on here in the next few days describing that journey and the feelings and experiences
A lunch laid on every wednesday at the centre
I got up and said a few words about my "journey"
I will attempt to put a few words on here in the next few days describing that journey and the feelings and experiences
Tuesday, 17 September 2013
Ringing the Chimes - Treatment complete
Today was my last day of treatment at the University of Florida Proton Institute
Some Vid and pics of me ringing the chime of hope - Aud's Chime
Some Vid and pics of me ringing the chime of hope - Aud's Chime
My time has come to ring this chime
A simple sound - a simple sign
That tells the world this is my time
To cherish the health that I will find
(Sue Anderson)
A simple sound - a simple sign
That tells the world this is my time
To cherish the health that I will find
(Sue Anderson)
Click pics to enlarge
We had a few friends - fellow patients and carers over in the evening for a celebration Chinese meal
Monday, 16 September 2013
Pool day and Barbera Jean's
Saturday, 14 September 2013
Georgia - Jekyll Island
We had a trip out to the state of Georgia about an hour or so north of Jacksonville to a place call Jekyll Island Famous as a retreat for rich business people who also built their own mansions the likes of the Goodyears, Rockefellers, and Vanderbilts see The Jekyll Island Club
Click to enlarge pics
Julie with Bill and Mary Ann |
Julie and Mary Ann |
Thursday, 12 September 2013
Biscottis for afternoon cake and goodbye to fellow UK proton patients and carer's
Ronnie and Ted have finished their treatment and are off home this weekend
We went for a afternoon cake fest at Biscottis to say farewell
we will be the next to go in our "group"
Click to enlarge
We went for a afternoon cake fest at Biscottis to say farewell
we will be the next to go in our "group"
Click to enlarge
3,2,1.................I will be done
Only 3 more treatments
Friday, Monday and Tuesday
Hopefully we can get an early flight home
Friday, Monday and Tuesday
Hopefully we can get an early flight home
Tuesday, 10 September 2013
Loooong day at the Proton centre - but the end is in site
I had an treatment time of 11:30 am. So got their 10:45
On monday you have your vitals done by a nurse and a short consultation by the doctor
The proton gantry I use (red) was running about half an hour behind so we managed to see the doctor at around 11:35 - great I thought we would be off early
The time passed 12 and I popped down to the gantry to see if there was a problem
It turns out they got my time wrong and it should have been 2:30
Also the machine was playing up so there was further delay
I did not get treatment until after 4pm
There were a few more patients from the UK having their first day today so had a chat with them about our mutual experiences
Everyone naturally has a story to tell of their journey so far
We are all grateful of the fact the NHS recognise and fund this treatment for our disease
After today I have six more treatments - counting down the days
We are hopeful we can get out flight moved forward so we can get home soon after treatment finishes
On monday you have your vitals done by a nurse and a short consultation by the doctor
The proton gantry I use (red) was running about half an hour behind so we managed to see the doctor at around 11:35 - great I thought we would be off early
The time passed 12 and I popped down to the gantry to see if there was a problem
It turns out they got my time wrong and it should have been 2:30
Also the machine was playing up so there was further delay
I did not get treatment until after 4pm
There were a few more patients from the UK having their first day today so had a chat with them about our mutual experiences
Everyone naturally has a story to tell of their journey so far
We are all grateful of the fact the NHS recognise and fund this treatment for our disease
After today I have six more treatments - counting down the days
We are hopeful we can get out flight moved forward so we can get home soon after treatment finishes
Sunday, 8 September 2013
Farewell to Seb and Sue
We went to Perfect rack billiards to say farewell to fellow brit patient Seb and his family who are on their way home this week
Seb played some music as it was open mic night at the bar
His brother and girlfriend also played a set
I had a beer (don't tell my doctor)
We had a lovely evening
Seb played some music as it was open mic night at the bar
His brother and girlfriend also played a set
I had a beer (don't tell my doctor)
We had a lovely evening
Saturday, 7 September 2013
Out on the town
Friday, 6 September 2013
Thursday, 5 September 2013
The 1 in 3 million gang
At the moment there are 4 of us at the proton centre from the UK all with Clival Chordoma
Considering how rare it is what are the odds of 4 of us being treated at the same time at the same place
Ronnie and Ted have just completed their treatment and I have about 8 to go and Sue round 15 to go
Click to enlarge
At the completion of treatment you ring the chime to commemorate
Considering how rare it is what are the odds of 4 of us being treated at the same time at the same place
Ronnie and Ted have just completed their treatment and I have about 8 to go and Sue round 15 to go
Click to enlarge
Ted, Ronnie, Me and Sue. The Clival Chordoma four |
At the completion of treatment you ring the chime to commemorate
Ronnie ringing the bell |
Ted Ringing the bell |
More Brits abroad |
Wednesday, 4 September 2013
Brits abroad
Some of my fellow British patients and carers. At the Proton centre
Tuesday, 3 September 2013
Proton resumes
After a long weekend here due to the Labour day holiday on Monday the Proton centre reopens
Only 12 more treatments to go (edit only 11 to go. After a meeting today with Dr Malyapa we found out I am having 41 treatments not 42 as I had previously thought)
The end is in sight
Only 12 more treatments to go (edit only 11 to go. After a meeting today with Dr Malyapa we found out I am having 41 treatments not 42 as I had previously thought)
The end is in sight
Monday, 2 September 2013
Labour day weekend
They live just north of San Francisco and flew down to South Carolina to see Lisa's Mum and brothers for couple of days then drove down to see us for the weekend
Friday we went out for a meal at Cap's on the water
Click to enlarge pics
Julie |
Lisa and Peter |
Julie and Lisa |
Peter and me gurning |
Saturday we went up to Kingsly Plantation and down the road had lunch at the Sand Dollar
In the afternoon we drove onto the beach at Huguenot Park and had a swim in the sea
After a siesta at home we had a meal at Maggianos Little Italy near where we live
Lisa Peter and Julie @ Kingsley plantation |
Peter and Lisa at Maggianos |
Sunday we had a stroll along Ponte Vedra inn and club beach (where Peter and Lisa were staying) followed by lunch in the golf club
Peter and Lisa then left for Orlando for their flight home tomorrow
Julie and I relaxed on the beach for the afternoon
We had a great weekend
Lisa and Peter |
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