Information about the music video

Flowers for Jonas

I’m glad to see you here.
On the subpages, you’ll learn how my BluJo project came about. Why this project?

I’m Jonas’s dad and I look after him day and night. All the photos and footage used in the YouTube music video are real, and every word of my song is true and reflects my personal experience. Everyone should be able to clearly recognize the AI-generated parts. With my video, I want to help make ME/CFS as well-known as cancer or migraines. So that the countless cases of mistreatment and misdiagnosis—which have cruel consequences for patients and their families—will finally come to an end.
I won’t make any money from my videos. If you’re able to, please donate to ME/CFS research:
https://mecfs-research.org/en/support/
https://www.omf.ngo/ways-to-donate/
So that Jonas and all the others suffering so terribly from ME/CFS can have a chance at life again. Thank you!

I’ve written most of the text on this website using DeepL. Just so you know, there might be mistakes or slightly awkward phrasing in there. Sorry about that. “kite” instead of a “dragon” anywhere? That would be a typical one, as ‘drachen’ means both ‘kite’ and ‘dragon’ in German – and DeepL didn’t realise that this wasn’t a ‘kite site’.

Just ME (icke) – with Bernabé guitar and with La Palma in the background – and of course, no kites.
FAQs below or contact info@justme-icke.com

Dragoduction

View from Jonas’s hospital room at the BDH Clinic in Waldkirch

Last changes

Making-of-Video finished.

“Flowers for Jonas” is also available on Spotify, Apple Music and all major streaming platforms.

On May 9 in Freiburg, at Augustinerplatz, I performed “Blumen für Jonas” live. Sorry folks, all in German. But at least this shows you that I can actually perform my own music. It’s not AI. Flawed, but human. Video (song ‘Blumen für Jonas’): https://youtu.be/xshErWENxDE

Watch music video

The music video in all its versions – and perhaps even more?

Just ME (icke) on Youtube

FAQ:

What is ME/CFS?

Imagine you had severe migraines. Every ray of light, every sound causes you terrible pain. Your digestion goes haywire and new symptoms keep cropping up. You never know what the next day will bring. If you summon all your strength, you can manage to get things done in your daily life. But you usually pay a high price for it: you’re completely wiped out afterwards, often not until the following day. You’re forced to lie in bed in agony. And it goes on and on, getting worse and worse. Your doctors tell you you’re healthy and that you shouldn’t make such a fuss, and that you should do more exercise. If you’re unlucky, you’ll end up in a psychiatric ward straight away. You can find more detailed information online. For example, at https://www.omf.ngo/what-is-mecfs/.

Are you looking for help?

You’ll find most of my experiences in this PDF brochure (in English). Finding a good doctor for ME/CFS is extremely important, but it’s often like looking for a needle in a haystack. Get in touch with a support group in your area. Here in southern Germany, near Freiburg, there are actually several support groups, such as the Initiative ME/CFS Freiburg. Without the support of so many people, including our GPs, Jonas would probably no longer be alive.
The German website lists the main patient organisations in the German-speaking world here. I’m afraid I’m not in a position to say which ones apply to your country.

How did Jonas become so seriously ill?

Jonas probably has a genetic predisposition to ME/CFS and had previously contracted the Epstein-Barr virus. In late 2013, he came down with an infection. The fever subsided, but he was left with persistent weakness, and further symptoms such as gastrointestinal and swallowing problems, as well as headaches, began to emerge. He had to give up all his hobbies, such as acting and jogging. A gastrointestinal infection triggered another downward spiral in the spring, and countless tests and doctor’s appointments followed. It was traumatic to have doctors suggest that he was merely imagining it all and wasn’t actually ill. The treatment at the university hospital in 2014 was pure horror and is symbolically depicted in the music video. He was still able to walk in. He came out emaciated to 41 kg, with five pressure ulcers and an antibiotic-resistant Pseudomonas infection. At home, together with our wonderful GP Dr Schwald, we managed to pull him back from the brink of death over the following six months. But it was a real close call. I have created a PDF file with lots of details (in English); further information can be found on the subpage Jonas.

Why are most doctors unfamiliar with ME/CFS? Why so little investment?

Chief Physician Prof. Gerner explained this clearly in Freiburg in 2024 (Youtube-Video, in German). I also discuss this on page 17 of my P DF brochure on Jonas (in English). The fact that scientists and doctors alike cling to false beliefs for so long is known as the Planck principle. Seen in this light, ME/CFS is indeed a major psychological problem: in the minds of doctors who have been treating ME/CFS incorrectly for decades. I, too, refused to accept at the very beginning that Jonas had ME/CFS. Until I realised that my wife Andrea was right about it.

The fact that a country as wealthy as Germany has failed to fund research and care for ME/CFS for many decades is a disgrace in itself, given the sheer number of people affected and the immense suffering involved. But it’s also financially foolish: the costs of ME/CFS in Germany alone are estimated at 64 billion euros—year after year! See the ME/CFS Research Foundation on this topic, as well as studies in other countries, e.g., for the U.S. by Solve M.E. Investing so little in research and care hurts everyone. If your house is on fire, you don’t hesitate to call the fire department just because their response costs money. Even if you don’t know exactly what can still be saved.

I don’t have any money to donate. What can I do?

Ask your doctors what they do for ME/CFS patients. If they don’t know about ME/CFS – why not? How can a doctor not know about a condition that leaves millions of people around the world so terribly ill? In Germany alone, the number is estimated to be as high as one million! You wouldn’t know it to look at most of them, because they aren’t as severely affected as Jonas.
See if there are any ME/CFS sufferers in your neighbourhood. Even if you can just take some of the daily household chores off their hands, you’ll be helping to break the downward spiral of ME/CFS.
Most importantly: talk to friends and family about the issue. Raise awareness.

Is that an AI video?

No. While 30% of the video contains elements generated by AI video generators—such as the dragons—nothing was used as-is without editing. For the most part, these scenes are a mix of video clips I shot myself, effects, and AI elements. I explain this in the making-of video. The song is AI-free—you can tell by my imperfect voice. And all the photos in this video are real. I also used a lot of old videos I shot myself. They’re unedited, except for the painstaking quality enhancement I did using DaVinci Resolve In the AI video disclosure, I have listed the scenes in which AI was used. The Tech/AI page also provides a general description of the use of all technical tools, including artificial intelligence.

In summary: AI junk is created by greed. People want to make money quickly with little effort or original ideas of their own. Providing the tools for this brings a lot of money to a select few. For me, AI makes it possible to bring my ideas to life, and in some cases, I use generative AI only as a supplement. I don’t make money from videos; I’m a non-profit.
AI-junk creator = 90 shallow videos a day.
AI as art = 1 video with an original plot in 90 days—in my case.

Is JustMe (icke) an artist? An influencer?

There are plenty of people who sing in public and really ought to give it a miss. Comedians, for example. It’s quite possible that many will say the same about me. But people sing so little in Germany that it sounds really bad when they do. So I don’t stand out that much. I just enjoy music. I don’t need to be an artist. Even if ‘Just ME’ is my ‘stage name’. And influenza is an illness, that’s all there is to it. More info on the subpage JustMe/Dragos.

Isn’t the video a bit silly for such a tragic illness?

I don’t know how Jonas manages to cope with the constant loneliness and darkness, along with all those terrible symptoms. Perhaps he makes up fantasy stories when he’s feeling better? – There are already plenty of excellent documentaries that show the misery of this illness. But I can well understand that someone who wants to relax on YouTube after a hard day’s work isn’t in the mood for such serious videos. It is precisely these people I want to reach with my video. And to highlight the stark contrast between Jonas’s zest for life – if only he could! – and his cruel daily reality.

Will there be more videos?

There’s more to come – that much I can reveal. Subscribe and hit the bell at https://www.youtube.com/@JustME-icke to find out. And there’s already plenty about Jonas online; see my list on the Jonas subpage.

There’s far too much going on in the video at once; no one with ME/CFS could watch it, could they?

That’s intentional. I want to spark curiosity and I want people to watch the video several times. So that the complex messages about ME/CFS get across. Not ME/CFS sufferers – they can barely watch the video, but they know the score anyway – but healthy people who are used to ‘demanding’ videos. Whether it’s details about Jonas’s taste in music, a dragonfly moving across the top of the screen, or an ironic reference to the dragon playing the bongos: I want to reach as many groups as possible who have hardly ever watched ME/CFS documentaries before.

Are there any positive experiences reported by ME/CFS patients in hospitals?

Yes. In autumn 2025, the BDH Clinic in Waldkirch took excellent care to accommodate Jonas’s high sensitivity to sensory stimuli (noise, light) and other needs. As well as is even possible in a standard clinic. Unfortunately, however, this is still the exception. As can be seen in the video in the hospital section, this is still how things usually go today – and it’s often much worse! For the care of ME/CFS patients, it will depend on the medical profession as a whole finally taking on board the findings regarding ME/CFS. I have described why this is so difficult on page 17 of Jonas – (No) Life with ME/CFS.

Questions about the project: Why? How do you go about it? Technology? Organisation?

This is covered on the subpages Project BluJo and Tech/AI, as well as in the making-of video https://www.youtube.com/watch?v=KN4w6p3fCZg

Information about the music video

Flowers for Jonas

Lyrics & Meaning

Who is Jonas?

Equipment used

Last changes

Watch music video

FAQ: