Its bye to my motorhome

After days of agony yes .no yes  .no. We have decided its time to let our loved motorhome go. We cannot  deal with maintaining it. We had a  nice few days last weekend but realised that camping is no longer for us. Now this new Marsden trial is to intense. So I am waiting feedback from a dealer. Now we have made our minds up it has to go.

I must start today to  empty it ,so much stuff in it. But all good things and that!.

A Diary Of A Mesowarrior Living with #mesothelioma #asbestos — A visit to the Assessment and Admissions ward The Royal Marsden







My tuesday appointment went well.

We had to go to Assessment and Admissions this time as Im going to have a Port fitted on my Birthday next Tuesday

Thats a great present –Not !!

I had a PICC Line last trial but Sepsis hid in the plastic and kept knocking me out at each infusion so a Port was thought to be better for me this time around.

I didn’t know it would be more involved and I have to go next Tuesday with a dressing gown and slippers and I will be given anaesthetic so I had to be assessed that Im fit enough. of coarse I passed all the tests  so Im ready now.

Off I went for a hot chocolate and up to see my team in Oak Ward where Rex took my bloods for the last time through my poor worn out vein.

Surprise though as my worn out vein has grown a new one. Rex explained this was called Collateral Circulation







Collateral circulation is a network of tiny blood vessels, and, under normal conditions, not open. When the coronary arteries narrow to the point that blood flow to the heart muscle is limited (coronary artery disease), collateral vessels may enlarge and become active. This allows blood to flow around the blocked artery to another artery nearby or to the same artery past the blockage, protecting the heart tissue from injury.

Well this can also happen when we damage our veins like mine are through 10 years of being used for all the Chemo and drug use for Mesothelioma.

The new vein worked so well we were OOing and Ahhing.

I saw the doctor and we talked about how tired I was over the weekend, my eyes and how they had got better and my Itching Oh Boy!! the Imminotherapy Itch is so hard. Always scratching especial when warm in bed at night.

Then we went and had some lunch but back again for that long boring wait in the waiting room for the blood results.

I did ask if we could go home but was told that as we lived in Whitstable they wouldn’t be able to call us back if anything was wrong, so Ray fell asleep waiting. The HYPER Trial can alter your blood count and you get to many white cells so I have to build the red cells up.

Anyway at 2 pm I finally got the go ahead that I was good to go and we drove back home.

Another long day.

But we are now free until Tuesday

A diary of a Mesowarrior Living with #Mesothelioma #asbestos — A whole week of visits to The Royal Marsden






A quick catch up for the week.

It has been a case of travelling daily to the Marsden for my Injection for the Hyper Trial.

This is hard a round trip of 160 miles each day is time consuming especially when your only in for a jab and then out again. What we mesowarriors do to stay in a trial is amazing really but the unsung hero is the carer. Ray never moans he gets up early and drives even if he does catch up with sleep when we are in the waiting room. Im sure other patients that dont know us must think Ray is the patient bless him!!

Wednesday was different as we carried on into London to the Foundations head office at 99 Gresham Street and had a brilliant board meeting with so much accomplished. The research grant has been chosen by the Board of Doctors and so we will announce and present very soon.

The bank is all sorted and Virgin is our chosen Just Giving so we are really set up now and happy.

We had to travel back to the Marsden and pick the car up, got home had dinner it was time for bed as we had to get up again to travel back to the Marsden again.

2 years of trail is beginning to seem a long time. I pray we see shrinkage at next scan.

Then my eye started playing up so we had to travel Friday to Ashdown near Epsom for the Eye specialist to examine my eyes.

He said that all the chemo and Immunotherapy is now telling and my age as well isnt helping. All I can do is find drops that help and really use all day long.

Ray and I slept most of Saturday we needed to catch up and now we have just to visit the next two Tuesdays to  have blood tests just to watch how Im tolerating the drug. It has been passed on mice but we have to prove humans can cope with it.







Yes Im a guinea pig but there is no alternative there ?



What a day.

Marsden day . A later start because they made appointment for Mavis`s eyes. we got  jab at 10 am free to go. But a taxi booked for 1.45 to go to Epsom Hospital. so we sat around waiting. At lat  1.45 Taxi arrived, Nice chatty driver we arrived at 2.20 booked in.

2.25 called in to see dr. Very nice informative  consultation.  2.40 all done back to Marsden 3 pm  paid for paring  left for home. 5 pm got home. Mavis has put cream in her eyes now she says she cant see.

Never rains but it pours.

Busy ole day

Early start ,off to Marsden. Mavis ECG was good Next she got her injection and we were done. But  we had to get taxi to Sutton Stn. The Train to London Bridge then taxi to  our meeting. That lasted from  12 to nearly 4 pm then Taxi back to London Bridge,Train back to sutton ,Taxi  back to  Marsden to collect car then my 70  mile  trip home. Shattered. Ready for Marsden again in the Morning.

First Injection Day

Another early day at the Marsden. Journey  wise it was a good one we arrived early. had a Hot Chocolate and then booked in. We were surprised it was  bloods  again. But  we got the first  injection drug. Mavis was dreading it. But good ole Rex put her fears at rest. What a star he is. After the jab we had to wait 2 hours but then we were free to  leave. So  it was not a bad day. I dropped off when  a nurse  gently woke me. I jumped out of my skin. But tomorrow is a bit later start so we get 2 hrs longer in bed. We  have a board meeting so we will need to  be completed quickly. Then its a Taxi and a Train into London.


It was  the usual early  day up at 4.30 am  get ready for Marsden walk poor half asleep louis up the lane in the dark. But  M25  was good today we arrived at  just a little after 7.30. Went for a coffee well hot chocholate really.

Bloods done early Doctor early but more forms to sign. Now we wait for blood results . They were ok now we have to wait for  Bi op. But a hitch  no  forms signed  to agree to it. But  later we escourted to radiology. We met  her before . I asked if I can come in . Of course you can. Get mr nye a chair she said. Iwas sat while Mavis got comfy on the table. Did you want to come sit  closer  she asked. Yes please I said so she pulled my chair  right up to the table. She explained everthing very clearly  she was so lovely and understanding. I held mavis hand throughout the procedure as they took 6 segments for a bi opsy. mavis was so brave. Afet she was wheeled back to the ward  we had to stay 2 hrs to make sure all was well. We got  back home at 4.30pm. Tomorrow is another day. Hope its not as long but she gets the first  injection of the new drug. She was told that there are several tumours clustered. But  they are not yet as large as her first ones and they are slow growing and that  things dont look so bad.

So its WTS.