It was a courageous and hopeful thing Ren did to periodically post these video updates for the ME community. It was also life saving for him. A Dr saw these videos and offered him a stem cell transplant if he could make his way to L.A. It gave him the first marked improvement in his health, and set him on a path to recovery. I think his sharing these videos with the world has kept him grounded, and offered hope to others with similar conditions.
This beautiful young man deserves every ounce of his success and I’m so glad to have found his music to share this amazing journey.. I don’t think anyone has worked harder to get where they are today… Ren is a true inspiration to so many, truly beautiful inside and out.. x
Bless young baby Ren! He’s such an inspiration to us all. He’s just amazing and I’m so glad he made these videos because they can teach us so much about our own selves. I love him and he’s taught me so much 🫶🏻🙏🏻💜!!!!
Thank you for supporting Ren in his quest of finding answers.. For others. ❤ Yes it can be hard to watch for some and maybe it's hard for Ren to see himself this way but there's two sides to every coin as Ren has said himself.. If anyone is willing to show the good bad and the ugly then it's something to be admired and inspired by. I have upmost respect for Ren 💖 and through doing this he did find answers for himself maybe not what he wanted to hear but he it gave him more determination to fight knowing who his real enemy was. Lots of love goes out to anyone suffering alone ❤️💕🥰
Thank you @sampanther8854 for your understanding of the benefit of sharing these videos. My daughter, who has had ME since 1994, was following Ren back when he was making them, and writing a blog, I believe, and for her, it felt like they were fighting through their illness together, and she wasn’t alone with it. She is now completely bedridden and cannot cope with watching anything that Ren is doing, although I have been able to quietly tell her a little bit. Over the years, Ren has given my daughter and myself unfailing hope for the future, and she truly believes that one day, when scientists find the key to unlock ME, that she too will rise like a Phoenix. Huge thanks to Ren for keeping this record, and thank you again Pete for sharing with us ❤❤
My daughter has been living with CFS since she was 17. Empathise with you so much. She is now 32, has two small children and'managing' her life. She is happy, but the condition has made her life so much smaller. You are awesome and able to speak for so many people who are not able to articulate how they are doing everything they can to just cope every day. Anita was much better when she was pregnant and breastfeeding, strangely, and doing well now. I wish we had an a n swer. Your music is phenomenal
I have such respect for Ren throughout this very bad time before his stem cell transplant. I would hold him and hug him. I’m so proud he battled his way through it to get to where he is today even still having treatment.
I totally get this. Lyme/ autoimmunity sucks! Hugs 🫂 I am in this space but it’s a total rollercoaster. It’s hard to believe this is the same man he is today. Hugs young ren 💚🦠💚🦠
It was a courageous and hopeful thing Ren did to periodically post these video updates for the ME community. It was also life saving for him. A Dr saw these videos and offered him a stem cell transplant if he could make his way to L.A. It gave him the first marked improvement in his health, and set him on a path to recovery. I think his sharing these videos with the world has kept him grounded, and offered hope to others with similar conditions.
This beautiful young man deserves every ounce of his success and I’m so glad to have found his music to share this amazing journey.. I don’t think anyone has worked harder to get where they are today… Ren is a true inspiration to so many, truly beautiful inside and out.. x
Bless young baby Ren! He’s such an inspiration to us all. He’s just amazing and I’m so glad he made these videos because they can teach us so much about our own selves. I love him and he’s taught me so much 🫶🏻🙏🏻💜!!!!
Thank you for supporting Ren in his quest of finding answers.. For others. ❤ Yes it can be hard to watch for some and maybe it's hard for Ren to see himself this way but there's two sides to every coin as Ren has said himself.. If anyone is willing to show the good bad and the ugly then it's something to be admired and inspired by. I have upmost respect for Ren 💖 and through doing this he did find answers for himself maybe not what he wanted to hear but he it gave him more determination to fight knowing who his real enemy was. Lots of love goes out to anyone suffering alone ❤️💕🥰
Thank you @sampanther8854 for your understanding of the benefit of sharing these videos. My daughter, who has had ME since 1994, was following Ren back when he was making them, and writing a blog, I believe, and for her, it felt like they were fighting through their illness together, and she wasn’t alone with it.
She is now completely bedridden and cannot cope with watching anything that Ren is doing, although I have been able to quietly tell her a little bit. Over the years, Ren has given my daughter and myself unfailing hope for the future, and she truly believes that one day, when scientists find the key to unlock ME, that she too will rise like a Phoenix.
Huge thanks to Ren for keeping this record, and thank you again Pete for sharing with us ❤❤
Bless him
My daughter has been living with CFS since she was 17. Empathise with you so much. She is now 32, has two small children and'managing' her life. She is happy, but the condition has made her life so much smaller.
You are awesome and able to speak for so many people who are not able to articulate how they are doing everything they can to just cope every day.
Anita was much better when she was pregnant and breastfeeding, strangely, and doing well now.
I wish we had an a n swer.
Your music is phenomenal
Prayers of hope and restoration for Ren ❤
I have such respect for Ren throughout this very bad time before his stem cell transplant. I would hold him and hug him. I’m so proud he battled his way through it to get to where he is today even still having treatment.
❣️🦇❣️🦇❣️🦇❣️
🪽🤍🪽
Why are you filming Rens pain
I'm not filming Ren's pain. He uploaded these himself in order for other people to understand the difficulties and issues with chronic illness.
He wanted people to see his journey through his illness. It made him feel better
I totally get this. Lyme/ autoimmunity sucks! Hugs 🫂 I am in this space but it’s a total rollercoaster. It’s hard to believe this is the same man he is today. Hugs young ren 💚🦠💚🦠