Posts Tagged ‘Myeloma’

Request from Megaphone UK for Volunteers for their Leafletting Campaign

October 2, 2022

I got this from the left-wing canvassing organisation, the Megaphone earlier this morning. I’m afraid I can’t volunteer, because I’m simply too ill. It’s not just the myeloma, I’ve also come down with a stinking cold. This is one of the reasons I haven’t posted much over the past few days. Despite my inability to join the campaign, I’m putting the message up here for any readers of my blog who would like to.

‘David,

Cutting costs, keeping the heating off, and doing without essentials: the cost-of-living crisis is already stretching people to the limit.

That’s why the Prime Minister’s budget announcement was so disappointing. The budget delivered tax breaks for bankers and big business, when we need real support for families.

On November 2 in London, we’re going to lobby our MPs and demand a better deal for workers. 

But first, we need to get the word out.

Will you sign up to organise a leafleting event in the next fortnight at a train station near you?

I will hand out leaflets

We know that between work, family, and other responsibilities, people already have a lot on their plates. 

But it’s important for MPs to hear directly from as many of us as possible. 

By leafleting our community, we can spread the message that only working people can deliver change and pressure the government to actually listen — and act.

Last June, we leafleted 92 places around the country. This time, we’re trying to hold even more events to reach half a million people. Will you organise one of them?

Yes, sign me up

Don’t worry if you haven’t done this before — organising a leafleting event is pretty simple and rewarding. 

You’ll join hundreds of other people who are stepping up and speaking to their local communities. 

Sign up here, and you’ll receive everything you need to get started.

Hope you can join us,

Anthony, 

Megaphone UK’

Out of Hospital for Myeloma Treatment

July 7, 2018

Way back on the 18th of last month I posted that I was going into hospital for 2 1/2 weeks for the intensive dose therapy for myeloma. Myeloma is a type of blood cancer, which causes anaemia, loss of calcium, and attacks the bones and kidneys. Since about a decade ago it’s been treated with a number of drugs, which avoid the side-effect of traditional chemotherapy. I was diagnosed with the disease last September.

However, after that phase of the course of treatment has finished, they then call you in for a more intense course of treatment to drive the disease further back into remission. Your own stem cells are removed, ready to be returned to you to jump start your own immune system. You are also called into hospital and put in isolation. In Bristol’s BRI you are given your own room. You have a piccline inserted running from your bicep to almost to your heart, through which they administer the drugs. They then give you a dose of malophan, the drug that they originally used to treat the disease.  The next day, they also give you back your own stem cells, and a few days later they also give you back the platelets they removed.

Throughout the whole period you are carefully monitored, given drugs, both in pill form and in infusions to deal with the effects of the cancer treatment. The doctors see you every day to see how you’re coping. If you have problems eating, you may also a nutritionist, while a physiotherapist will also visit to advise you on gentle exercises if you are weak.

I shudder to think how much all this would cost under the private insurance system in America, which the Tories  and New Labour so much admire, even while they’re prating about how much they ‘treasure’ the NHS.

They released me yesterday, and it’s good to be home. The treatment has, however, left me as weak as the proverbial kitten, with a sore mouth, and diarrhoea. I’ve been prescribed and given mouthwashes and drugs for some of these effects. The booklets for the treatment state that it may be 2/3 months, or even 5-6 months, before you make a complete recovery. So don’t expect very much energetic blogging!

I cannot fault the treatment given by the medical and the ancillary staff. They were professional, friendly, courteous and reassuring. I found the treatment very difficult, but they were at pains to say, ‘This is not the ‘new you’. You will recover.’ And it can be very interesting talking to the ancillary staff, some of whom were non-White immigrants, and hearing their stories and perspectives. The NHS certainly has benefit from the skills and dedication brought to it by its medical professionals and ancillary staff from across the world, whether Asia, the Caribbean, Africa, or eastern Europe. And the health service is suffering because many of these are being forced to return home, or look elsewhere for work, because of Tweezer and Brexit.

I’m afraid I haven’t been blogging very much while in hospital, despite my best intentions. Their wifi system simply wouldn’t let me. The hospital wifi system was insecure, so that anyone geographically near me could see my passwords if I went to a site that require them. So the system simply refused to let me on after I posted up those couple of pieces to the blog about George Galloway winning his libel battle against the Torygraph, and New Labour’s desperate policy to stop NHS hospitals owning and operating their own MRI scanners, as opposed to leasing them from private firms. So I spent my time in bed trying to read an SF novel by the awesome Paul McAuley, and re-reading a few old copies of Private Eye and Clive James’ The Crystal Bucket. This last is a collection of James’ old TV reviews from the 1970s from the Observer. James started out as a radical socialist, and then move right, eventually ending up in the Torygraph. An intellectual, with a tendency to show off, he nevertheless took trash culture very seriously, at a time when many intellectuals did dismiss television. One of the jokes about it used to be ‘Why is television a medium? Because it’s neither rare nor well done’. Which is true of a lot, but not all. And James stated that heartfelt trash culture was worth far more than bad high art, like Michael Tippet’s A Child Of Our Time. The ’70s were also the  decade of the Vietnam War and the horrors of the CIA coup in Chile, George Kissinger’s support of genocidal, murderous dictators across the world as part of the campaign against Communism, Watergate, and TV dramas about the Holocaust, all of which he reviewed, along with Star Trek, Dr. Who, Miss World, the World Disco-Dancing Championships, the footie and the athletics. Quite apart from more highbrow productions of Shakespeare, intense dramas, and the horrors of the classic BBC series, I, Claudius, set under the deprave reign of Caligula.

He also reviewed an interview with the old Fascist, Oswald Mosley. Mosley was the leader of the British Union of Fascists in the 1930s, and a series of successive Fascist movements after the Second World War. He was very definitely persona non grata for many years, until he partly rehabilitated himself with the publication of his autobiography, My Life.  He then got a job doing book reviews for the Telegraph. Mosley was a fan of Mussolini and then Adolf Hitler. When Mussolini was overshadowed by Hitler as the great Fascist dictator, Mosley changed the name of the BUF to the ‘British Union of Fascists and National Socialists’. He corresponded very amicably with the Nazis, although claimed during the War that in the event of an invasion of Britain he would not serve as this country’s Quisling, the traitor leader of Norway. And in the interview the old thug constantly denied being an anti-Semite, claiming that the attacks and violence were instead all the fault of the Jews. All the while making it clear that he still identified them with the ‘money power’, which was secretly ruling from behind the scenes. James said of him that he didn’t so much proclaim anti-Semitism as embody it. There’s much to blog about in James’ TV criticism from this period. I especially want to do a piece about this interview with Mosley to show the difference between real anti-Semites, and those decent people, who have been smeared as such by the Israel lobby, New Labour and the Tory press. People like Jackie Walker, Ken Livingstone, mike, my brother, Tony Greenstein and so many, many others. Absolutely none of whom are in any way, shape or form anything like the real Nazis and anti-Semites, like Mosley or the characters now crawling out into public view from the Alt-Right and Libertarians.

I spent part of yesterday evening trying to answer the various comments that had built up on this blog over the past few weeks. I really appreciate all the messages of support and encouragements to get well and get blogging soon! It was really great and encouraging to read. I feel fortunate that I have people like you all following my blog.

I’m still quite ill at the moment, but I hope to pick up and carry on blogging as far as I can. And I hope you all are enjoying good health, and haven’t suffered too much from the heat these past weeks. With luck, it shouldn’t be too long before it’s business as usual. I hope.

 

 

Going Into Hospital Tomorrow for Myeloma Treatment

June 18, 2018

This is to let you know that tomorrow I will be going into hospital for about 3 weeks for intensive treatment for myeloma. This is a kind of blood cancer, in which the bone marrow produces toxins called paraproteins. These can cause anaemia, and damage the bones and the kidney, as well as leading to loss of calcium. I was diagnosed with it September-October last year after a routine blood test by the doctor revealed I was slightly anaemic. She referred me to the haematology department of Bristol’s BRI, who commenced treating me.

This is usually done for 6-8 months using a variety of drugs, which are different from those regularly used to treat cancer, and which don’t have some of their side effects, like hair loss. This meant going to the hospital once a week for an injection of the anti-cancer drug, and taking a variety of drugs, including an antiviral, to control the side effects. Most of these were pills, though one of the drugs was an anti-coagulant, which had to be taken twice a day by injection.

After this drug treatment has reduced the paraproteins as far as possible, they then take you into hospital for intensive treatment using the conventional cancer drug. This damages the immune system. In order to get it back up and running, they take stem cells from your own blood, store them, and then give them back to you. This consolidates the effect of the previous cancer treatment, and adds more time to the period of remission before the myeloma returns. I’ve already had my stem cells collected, which took a whole day connected to something similar to a dialysis machine. I’m due to be given the drug, and then the stem cells this week. I’m then due to spend the next several weeks in isolation at the BRI to protect me from disease while my immune system is still weak, and so that they can monitor me and make sure that the stem cells are properly taking hold.

I’ve received excellent care from the staff at Bristol’s various hospitals, not only the BRI, but also the hospitals in Southmead and Whitchurch. You are allowed to bring books and DVDs into hospital, as well as use laptops. I shall be taking a laptop into hospital with me, and hope to continue blogging while I’m there, if I can. If I can’t, for some reason, this is why.

I was in hospital being given a phosphate infusion as part of the anti-myeloma treatment the Sunday last year, when the CAA, the Sunday Times and the other right-wing papers libelled Mike as an anti-Semite and Holocaust denier, which infuriated me at a time when I could well have done without it.

I also understand that a number of other people have also been diagnosed with myeloma after random, routine blood tests. I’d therefore advise people to make sure that they have these done, even though they can appear to be an inconvenience. It could save them from more serious health problems later on.