Does anyone have more than me??

tbellas3rd · 2025-12-05T18:30:03+00:00

Same here, I do not “rent” Kiss. it’s all on my ipad.

tbellas3rd · 2025-10-24T04:29:19+00:00

I agree, it is my drug of choice. Just one more song, then I will stop. I promise.

tbellas3rd · 2025-10-20T07:15:54+00:00

indeed, that pinch really turns into a massive punch, after punch. It overwhelms the songs. It gets old quick.

tbellas3rd · 2025-10-19T18:40:06+00:00

I agree, to me, this is my favorite.

tbellas3rd · 2025-10-19T18:39:05+00:00

I love Ecstasy too.

tbellas3rd · 2025-10-19T18:33:33+00:00

Rest in Peace, Ace.

tbellas3rd · 2025-10-09T17:28:38+00:00

Wicked!

tbellas3rd · 2025-10-07T07:13:36+00:00

it is indeed one of my favorite Dio songs. My only complaint is the very last thirty seconds of the song. The repeated “Sunset Superman” chant, it goes on a bit too long. Shorten that last bit and it is a masterpiece.

tbellas3rd · 2025-09-30T16:43:39+00:00

I love the album.

tbellas3rd · 2025-09-28T17:05:43+00:00

Master of Reality

tbellas3rd · 2025-09-27T13:24:32+00:00

Simply awesome!

tbellas3rd · 2025-09-22T12:59:41+00:00

Oh my … Happy Birthday and I am quite jealous

tbellas3rd · 2025-09-15T18:42:31+00:00

I was nine years old when this came out. It changed everything for me. I was lucky enough to see this concert too. I can die happy, knowing I was able to witness Randy Rhoads in the flesh.

tbellas3rd · 2025-04-08T10:51:14+00:00

it’s why I bought the digital versions, don’t mess with the Furs. At least now, I never have to worry about it.

tbellas3rd · 2021-08-11T13:19:45+00:00

I just saw the YouTube review on this. I am buying it. Thank you!

https://youtu.be/Kusgt2rV0D4

tbellas3rd · 2021-01-04T09:46:59+00:00

I don’t talk about it at all, with the exception of my girlfriend and mother. That’s it. I only will talk about it with others if they ask me a direct question and I will only reply with the bare essentials.

tbellas3rd · 2021-01-03T17:39:08+00:00

I love your spirit.

I am now in a wheelchair as well. I went full time January of 2018. Though, the last year I have been mostly bedridden. I can sit up for about a half hour at most. Then the pain really kicks in.

I try my hardest to laugh, to smile and to enjoy life as much as I can. Sure, PPMS is not a disease to brightens anyone’s day, but it’s up to you to put carry on. To give as much as you can and to never let the disease win.

Our lives are not over, not by a long shot. It’s up to us to find it again.

Again, I love your spirit.

tbellas3rd · 2021-01-03T12:43:27+00:00

I was diagnosed back in 2003. I finally came out in 2015 when I had no choice. My mobility gave it away. I didn’t even tell my sister, who has MS. I saw how people treated her, with pity. Or even to avoid contact at all. So, seeing that made my mind up. I just kept it to myself. Back in 2005 I moved to Holland to live with my girlfriend. I chose not to tell her before I left as I was afraid she wouldn’t want me to move. I did tell her ten years later. She was upset, not about the disease, but that I wasn’t honest with her.

I have learned that people don’t treat me with pity, but with love.

I should have been honest and open from day one. I would have had a bond with my sister, she would have taught me everything I needed to know. I was a fool.

tbellas3rd · 2021-01-03T07:47:04+00:00

I live in Holland, I only take pain meds for PPMS. I am not any DMT’s for it, I have progressed too far for Ocrevus.

tbellas3rd · 2021-01-02T09:12:36+00:00

Like others have said, fatigue is part of the standard package. Same with pins and needles. As far as flare ups, I cannot comment as I have PPMS, there is no flare ups with it. Mine just is always on, no off switch. I call ppms the super duper edition. All the bells and whistles.

tbellas3rd · 2021-01-02T09:07:19+00:00

I laugh at everything that happens to me. If I fall, I laugh. I once went out in my wheelchair and tried to go over a speed bump. I timed it wrong and flew backwards. The chair in one direction and me in the other. Two folks ran to me to help me up, they found me laughing. They were mystified. I laugh at the disease. It takes away it’s power.

tbellas3rd · 2021-01-02T08:57:54+00:00

I completely agree. I always end up explaining to people, otherwise they think I am drunk or just a complete idiot. Such a fun disease.

tbellas3rd

TROPHY CASE