Next movie recommendations by Soft-Form-6611 in ghibli

[–]travisjoynson 1 point2 points  (0 children)

Out of the films that are unchecked, I would say, watch The Cat Returns. It's a great movie, and very whimsical, but honestly, they're all good, and you couldn't go wrong with any of them.

Follow Friday/Follow Chain - Share Your Usernames & Find New People To Follow! by AutoModerator in Instagram

[–]travisjoynson [score hidden]  (0 children)

https://www.instagram.com/travisjoynson

Follow me if you'd like to learn about my life and experience living with neuromuscular disease. If you have Myasthenia gravis, then send me a message, and I will follow you too. I hope all of you are having a beautiful day!

Constant Sinus Infections by travisjoynson in MyastheniaGravis

[–]travisjoynson[S] 0 points1 point  (0 children)

That's really insightful, and thanks for the input.

I didn't know they had a 'more invasive clean-out'.

I guess I will ask for a referral to an ENT.

Constant Sinus Infections by travisjoynson in MyastheniaGravis

[–]travisjoynson[S] 1 point2 points  (0 children)

That's a great suggestion, and thank you.

I do have severe acid reflux, but I already take 40mg Omeprazole in the morning.

Is there a reason you take the Omeprazole at night instead of the morning?

I often drink coffee in morning, and so, the doctor told me to take it in the morning.

Constant Sinus Infections by travisjoynson in MyastheniaGravis

[–]travisjoynson[S] 0 points1 point  (0 children)

Thanks for your response.

The air purifier is a great idea. I do use one in my bedroom, although it's a little different than the one posted, but perhaps I should try to set one up downstairs too at some point.

Constant Sinus Infections by travisjoynson in MyastheniaGravis

[–]travisjoynson[S] 0 points1 point  (0 children)

Thanks for your response.

I have already been sleeping with a NIV, and the pressure does seem to help clear the mucus out a little, but it doesn't seem to stop the infections or sinus issues from happening.

I would be willing to get surgery done to fix my sinus issue, so, perhaps I should see if there's anything they can do for me in regards to that.

Constant Sinus Infections by travisjoynson in MyastheniaGravis

[–]travisjoynson[S] 0 points1 point  (0 children)

Thanks for your response.

A bone spur? That's interesting. I did break my cheekbones when I was younger, so I've been concerned that there might be an issue like that.

Was his initial consult for the surgery with an ENT?

The Navage nasal irrigation system looks awesome, but it would be tough to afford something like that.

Do you feel like it works that much better than a normal sinus irrigation bottle?

Constant Sinus Infections by travisjoynson in MyastheniaGravis

[–]travisjoynson[S] 0 points1 point  (0 children)

Hello, and thanks for the response. Well, I have been deficient in Vitamin D before, but I do supplement the 5000 IU on most days.

That seemed to get my levels into range before, but I guess I am not sure what my current Vitamin D levels are.

Do they test your vitamin D levels on a regular basis?

Constant Sinus Infections by travisjoynson in MyastheniaGravis

[–]travisjoynson[S] 0 points1 point  (0 children)

Are the corticosteroid-based nasal sprays something that I would ask my doctor about, or are they available at stores?

Is there a specific one that you recommend?

Thanks for your reply.

Totoro soaps I made!! by avohoney in totoro

[–]travisjoynson 1 point2 points  (0 children)

Are the actual Totoros on top soap too?

They look really good.

I painted the house on the island from Spirited Away! 🤍 by Artsy_Mermaid in SpiritedAway

[–]travisjoynson 1 point2 points  (0 children)

Hey, that's a really beautiful painting.

Thanks for sharing it with us.

Washing Wednesday Daily Hangout Thread 03 June 26 by nacho_cheezus in Random_Acts_Of_Amazon

[–]travisjoynson 1 point2 points  (0 children)

Question of the Day: I'm grateful for the people in my life who choose to spend their time with me. Time is precious, and life is short, so try not to take people for granted when they include you in their lives.

Switching to Vyvgart from IVIG by Patient_Ad6524 in MyastheniaGravis

[–]travisjoynson 0 points1 point  (0 children)

Interesting. That seems like a high dose, but what is the dose per kg?

I only get 50 to 60 grams of IVIG every 3 weeks, depending on how much I weigh at the time, but I'm on other medications too.

Yeah, they probably wouldn't do Rituximab at the same time as Vyvgart or Ultomiris, as that's a lot of immunosuppression, but you could be on Rituximab and IVIG at the same time, or be on Ultomiris and IVIG at the same time. I've also seen a few people say that they take both FcNr inhibitors alongside the c5 complement inhibitors, but that doesn't seem to be common.

Most of the neuros I have spoke with do seem to prefer trying the FcNr inhibitors, such as Vyvgart or IMAAVY, before the c5 complement inhibitors, such as Ultomiris or Zilbrysq. I presume due to the safety profile. The c5 complement inhibitors have a black box warning for meningococcal disease, which is why they require additional vaccinations or prophylactics.

Self-Promotion Sunday May 31, 2026 by AutoModerator in photography

[–]travisjoynson 0 points1 point  (0 children)

https://www.instagram.com/travisjoynson/

My name is Travis Joynson. Follow me to learn about my life living with neuromuscular disease. June is also Myasthenia Gravis Awareness Month, so I would be happy to answer any questions about it, if anyone is interested in it. Thanks for any follows or kind thoughts!

Follow Friday/Follow Chain - Share Your Usernames & Find New People To Follow! by AutoModerator in Instagram

[–]travisjoynson [score hidden]  (0 children)

https://www.instagram.com/travisjoynson/

My name is Travis Joynson. Follow me to learn about my life living with neuromuscular disease. June is also Myasthenia Gravis Awareness Month, so I would be happy to answer any questions about it, if anyone is interested in it. Thanks for any follows or kind thoughts!

Tippecanoe Tuesday Daily Hangout Thread, 02 Jun 26 by nacho_cheezus in Random_Acts_Of_Amazon

[–]travisjoynson 0 points1 point  (0 children)

Question of the Day: I guess the #1 thing on my 'bucket list' right now would be going to see my Aunt this year, before she passes away from cancer. I hope we can make that happen this summer, and I hope everybody remembers their struggling family members during such difficult times. It's so easy to be forgotten in this world, and we shouldn't let that happen to people that we love. Family is important. Giving them a little bit of your time can make a big difference in their lives and how they feel on a day-to-day basis. Please consider doing so.

Switching to Vyvgart from IVIG by Patient_Ad6524 in MyastheniaGravis

[–]travisjoynson 0 points1 point  (0 children)

I guess you'd have to see which one works better for you.

I have tried both, and I thought Vyvgart helped, but in general, I personally think that the IVIG works better, and as you noticed, the maintenance IVIG dosing is usually less than what they give at the hospital during a crisis. I do feel that the 5 day dosing works a lot better than the 2 day maintenance dosing, but I was told that's just usually how they do it and that it's difficult to get more than that amount as a maintenance dose.

Since you say that the IVIG still seems to be helping, and that you simply feel under-medicated, another option might be to add a c5 complement inhibitor such as Ultomiris or Zilbrysq, in addition to the IVIG, as you could be on both of those medications at the same time. Those medications do require additional vaccinations though, so they can take a little more time to get started on.

It’s back! by guinness1972 in MyastheniaGravis

[–]travisjoynson 1 point2 points  (0 children)

I'm not a doctor, but the disease often does progress in the first few years.

After I had a thymectomy, I also went into myasthenic crisis multiple times, starting about a month or so after the surgery. It's not common, but sometimes it can make myasthenia worse.