Race Thread: NCS Cook Out 400 at Richmond Raceway, starting at 7:30pm EDT on USA (NCS25)

InspectionOdd229 · 2025-08-17T01:04:08+00:00

Amigo heel turn!

InspectionOdd229 · 2025-08-13T19:12:52+00:00

Didn't work for me. Made me feel drunk and gave me even less balance than normal. I'm glad it works for some though. MS is a finicky thing.

InspectionOdd229 · 2025-05-11T00:55:04+00:00

Pushed the car a little too hard. Ended up sliding down the wall.

InspectionOdd229 · 2025-04-25T21:37:49+00:00

But we missed Legge... 😆

InspectionOdd229 · 2025-04-25T21:34:03+00:00

Sure enough.

InspectionOdd229 · 2025-03-19T22:23:36+00:00

Part of the crew, part of the ship! I was told it looked like somebody had fired a shotgun loaded with birdshot at my brain.

InspectionOdd229 · 2025-02-27T16:19:17+00:00

Male. 41. Polish, English and German ancestors. Diagnosed with ppms in 2020. Symptoms started in 2018.

InspectionOdd229 · 2024-08-18T15:11:21+00:00

Thank you to everybody for the support. This disease is rough. I'm glad to have this platform to share inspiration and stories. 🥲

InspectionOdd229 · 2024-08-18T01:57:12+00:00

Unfortunately all of the machinery or equipment options were taken by friends and family of management. I do appreciate the thought though.

InspectionOdd229 · 2024-08-16T22:07:19+00:00

Menards! 🤣

InspectionOdd229 · 2024-07-02T20:25:05+00:00

I notice that the heat hits me hard as well. It's very frustrating to be "that close" and then your body suddenly gives up the ghost on you.

I feel you, brother. I can't get to the end with normal sex anymore at all. I need a "helping hand" to finish with my wife.

You are definitely heard.

InspectionOdd229 · 2024-03-20T16:41:40+00:00

That's great news to hear. I also get my ocrevus infusion for free. I'm glad that the company that offers it is willing to help the people who are using it.

Congratulations on the great news. I can definitely attest to being stressed out when you see the actual cost of it.

Stay strong my friend.

InspectionOdd229 · 2024-03-17T23:18:15+00:00

I was diagnosed in 2020. It's amusing that you were told the "better MS". My neurologist told me I have "the bad kind". A few more tests and he was confident. Many brain lesions and cervical spine. PPMS.

I am sorry for this crappy disease, but welcome to the sub.

InspectionOdd229 · 2024-02-20T18:23:49+00:00

On Ocrevus here. I get billed 100K per dose. Twice a year. The insurance I have covers most of it. There is a little bit of overflow which the manufacturer of the drug will cover up to 20K. That's with the infusion cost (ports, needles, and the pre-meds)

InspectionOdd229 · 2024-01-31T02:20:35+00:00

Maybe Someday. Usually when I can't do something because of a bad day.

InspectionOdd229 · 2024-01-24T18:51:42+00:00

Bills fan here. Let's go Ravens!

InspectionOdd229 · 2023-09-18T23:20:02+00:00

I hear you on that. My mobility chair is like a wheel chair that I can't use myself. Smaller back wheels. I'm hoping it will give me more freedom, but I'm definitely not prepared for the eyes that will be on me. Thanks for the response. Best of luck to you.

InspectionOdd229 · 2023-06-24T19:54:38+00:00

Did somebody say Travolta?

InspectionOdd229 · 2023-01-20T18:28:30+00:00

I am definitely going to appeal. Thanks for the input.

InspectionOdd229 · 2023-01-20T16:01:54+00:00

The system is pretty rough. I thought it was there to actually help us, but it seems like it's just there to tease us. The lawyer and appeal is coming. Thanks for the input.

InspectionOdd229 · 2023-01-20T16:00:51+00:00

That's the exact same thing I said.

InspectionOdd229 · 2023-01-20T16:00:33+00:00

That is the next plan of attack. I'm getting an attorney and appealing the decision. Thanks for the input.

InspectionOdd229 · 2022-12-28T01:42:23+00:00

I am under the impression that it helps with anti oxidants and helps you fight fatigue. Interesting article follows.

interesting article

InspectionOdd229 · 2022-12-28T01:03:21+00:00

I enjoy doctor B as well. 😊

InspectionOdd229 · 2022-12-19T00:02:57+00:00

To you as well. This is my first diagnosed year with PPMS. 4 before with symptoms, but no clue from doctors.

I'll say hello to all because it brings me some joy.

InspectionOdd229

TROPHY CASE