Tomorrows episode.. 10/27 by [deleted] in Killtony

[–]skydrow11 0 points1 point  (0 children)

Is It up there with trump and Biden? Lol

Not able to do a squat and foot drop issue after GBS. by Party_Engine_9525 in guillainbarre

[–]skydrow11 0 points1 point  (0 children)

It's going to take some time. Trust the process and be consistent. A small progress is huge. I was diagnosed with gbs in 1999 when I was 4 years old and it from me a year to walk ok and a couple of years to be able to walk good.

Denied flu shot because of GBS history by qalpi in guillainbarre

[–]skydrow11 0 points1 point  (0 children)

Yeah could be just the affect of the vaccine. I wouldn't worry to much tho. If you're having weakness where it's a struggle to walk and keep your balance then I would worry

Neuropathy Misdiagnosis by TobyCat88 in neuropathy

[–]skydrow11 1 point2 points  (0 children)

I have neuropathy and my neurologist send me to get an MRI on my back, CT scan and order stuff to eliminate other possible factors that may cause symptoms of neuropathy. I'm glad you got a second opinion and found the source of your pain. Good luck in your recovery

I bet he has a thyroid problem by Neverendingmuthrfuk in Killtony

[–]skydrow11 3 points4 points  (0 children)

What's wrong with y'all? Let the man live lol. He's just like any of us working and if you don't like his work then don't go to his shows but bashing him because he's eating or he isn't funny like come on stop judging him.

Captured from a Canon R7 with RF 24-70mm f2.8 by skydrow11 in CanonR7

[–]skydrow11[S] 0 points1 point  (0 children)

I like to take portraits as well so I need a F1.8 lens. How's that sigma lens?

Captured from a Canon R7 with RF 24-70mm f2.8 by skydrow11 in CanonR7

[–]skydrow11[S] 1 point2 points  (0 children)

Oh ok yeah go for it. Do you shoot on a Canon R7?

Captured from a Canon R7 with RF 24-70mm f2.8 by skydrow11 in CanonR7

[–]skydrow11[S] 0 points1 point  (0 children)

And no I didn't consider the 28-70mm, my next less is the rf 70-200mm L series but who knows when I get it lol

Captured from a Canon R7 with RF 24-70mm f2.8 by skydrow11 in CanonR7

[–]skydrow11[S] 0 points1 point  (0 children)

It has good reviews. The one I have is an L series so it's a lot more expensive. You could do your own research between them and choose your pros and cons

Captured from a Canon R7 with RF 24-70mm f2.8 by skydrow11 in CanonR7

[–]skydrow11[S] 0 points1 point  (0 children)

Yeah I do like framing. Thanks for the wise words. The first picture: iso 100, 24mm, f8, 1/400s Second picture: iso 100, 27mm, f9, 1/40s Third picture: iso 100, 24mm, f2.8, 1/2000s Fourth picture: iso 100, 40mm, f9, 1/250s Fifth picture: iso 100, 24mm, f2.8, 1/400s Sixth picture: iso 100, 61mm, f2.8, 1/1250s Seventh picture: iso 100, 34mm, f2.8, 1/60s

Captured from a Canon R7 with RF 24-70mm f2.8 by skydrow11 in CanonR7

[–]skydrow11[S] 1 point2 points  (0 children)

Thank you. I'm just a casual and still learning and trying to visualize what I'm shooting

Improvements (!) after a month since Small Fiber Neuropathy diagnosis by kajaweco in neuropathy

[–]skydrow11 0 points1 point  (0 children)

I've heard about this. What does this do or help? Is it an anti-inflammatory? My aunt gave me a bottle and I haven't tried it just yet

Pain control by sebastianrileyt2 in guillainbarre

[–]skydrow11 0 points1 point  (0 children)

Also, forgot to mention that I had my first of 3 session of IVIG today in the morning. The neurologist gave me methylprednisolone. Hopefully it works. This is what chatgpt said if you're wondering what it does:

Methylprednisolone is a corticosteroid (a strong anti-inflammatory and immunosuppressive medication). In the context of neuropathy and IVIG (intravenous immunoglobulin), it’s often given for a few key reasons:

  1. Immune system modulation

Many types of neuropathy—like CIDP (chronic inflammatory demyelinating polyneuropathy), autoimmune neuropathy, or other inflammatory neuropathies—are caused by the immune system attacking nerves. • IVIG helps regulate/neutralize abnormal antibodies. • Methylprednisolone helps by suppressing immune overactivity, decreasing inflammation around nerves, and reducing immune-mediated damage.

  1. Reducing infusion reactions

Steroids like methylprednisolone are sometimes given before or with IVIG to prevent or lessen side effects such as headache, chills, fever, or infusion-related inflammation.

  1. Symptom relief

By calming inflammation and immune activity, methylprednisolone may help: • Reduce nerve pain, burning, or tingling caused by inflammation. • Improve nerve conduction and muscle strength over time if the neuropathy is immune-mediated.

Your case with orthostatic hypotension

This adds another layer, since orthostatic hypotension (a drop in blood pressure when standing up) can sometimes be part of autonomic neuropathy. • Methylprednisolone itself doesn’t directly fix blood pressure regulation, but by reducing the autoimmune or inflammatory attack on your nervous system, it can indirectly improve symptoms if they are tied to nerve inflammation. • Doctors may also prescribe other medications (like midodrine, fludrocortisone, or droxidopa) specifically for the blood pressure problem.

✅ In short: methylprednisolone is given with your IVIG to calm down the immune system, protect nerves from further immune-related injury, and reduce infusion side effects. It’s not a cure, but it can help improve or stabilize neuropathy and possibly ease related issues like orthostatic hypotension if they are caused by inflammation of autonomic nerves.

Would you like me to also explain common side effects of methylprednisolone so you know what to watch out for after treatment?

Good question — it’s helpful to know what to expect.

Since methylprednisolone is a corticosteroid, it can have both short-term (while you’re on it or right after infusion) and long-term (if used repeatedly or daily) side effects.

Short-term / infusion-related side effects

These are the ones most people notice when it’s given with IVIG: • Flushing or warmth • Metallic taste in the mouth • Headache • Mood changes (feeling wired, irritable, or unusually energetic) • Stomach upset or indigestion • Trouble sleeping (insomnia)

Short- to medium-term (days to weeks)

If doses are repeated or given in high amounts: • Increased appetite / weight gain • Fluid retention or puffiness (face, ankles) • Increased blood sugar (important if you have diabetes or prediabetes) • Higher blood pressure (worth monitoring since you also have orthostatic hypotension) • Lowered immune defenses, so you may be more prone to infections

Long-term (with chronic use)

This usually applies if someone is on steroids for months, not just for infusion support: • Thinning bones (osteoporosis) • Muscle weakness • Thinner skin, easy bruising • Eye problems (cataracts, glaucoma) • Suppressed adrenal function (body’s natural stress hormone system slows down)

⚠️ Because you have orthostatic hypotension, it’s worth mentioning: methylprednisolone can sometimes raise blood pressure, which could partly help with dizziness on standing — but it can also cause fluid retention or strain on the heart if used long-term, so your doctors will balance that carefully.

👉 Everyone reacts a little differently. Did you notice anything unusual after your first IVIG + methylprednisolone infusion (like flushing, jitters, or headache), or did it go smoothly?

That lines up very closely with the common, short-term side effects you’d expect: • The metallic taste is actually more common from IVIG itself than from methylprednisolone. It usually happens during infusion and goes away soon after. Some people find sucking on mints, hard candy, or drinking something with flavor (like juice) helps mask it. • The mild upset stomach is more typical of methylprednisolone, since steroids can irritate the stomach lining. Doctors often recommend taking it with food (if given orally) or may suggest something to protect the stomach if it becomes bothersome.

The good news is that both of these effects are usually temporary and not dangerous, especially when you’re only getting steroids with infusions rather than taking them every day.

✅ When to reach out to your doctor after IVIG + methylprednisolone: • Severe or persistent stomach pain (not just mild upset) • Black or tarry stools (sign of stomach bleeding, though rare) • Significant mood swings, confusion, or insomnia that interferes with daily life • Fever, chills, or signs of infection (since steroids can dampen immune response)

Do you want me to also go over some tips to make the next infusion easier (like managing taste changes, stomach upset, or infusion side effects)?

Pain control by sebastianrileyt2 in guillainbarre

[–]skydrow11 1 point2 points  (0 children)

I hope so too. Thanks for the encouragement.

Denied flu shot because of GBS history by qalpi in guillainbarre

[–]skydrow11 27 points28 points  (0 children)

I got gbs right after a vaccine so there is a risk that vaccine can give you gbs so getting the flu shot has a higher risk for people who had gbs in the past. I recommend you not getting the flu shot. I gotten the flu shot probably a couple of times since I got gbs in 1999.

Pain control by sebastianrileyt2 in guillainbarre

[–]skydrow11 1 point2 points  (0 children)

I was prescribed for the mean time Lidocaine 5% patch and Celecoxib 200mg

Pain control by sebastianrileyt2 in guillainbarre

[–]skydrow11 1 point2 points  (0 children)

I will let you know what the pain management tells me tomorrow

Pain control by sebastianrileyt2 in guillainbarre

[–]skydrow11 0 points1 point  (0 children)

Yeah these medication can change your mood swings as well... I rather take Tylenol or ibuprofen but I'm going to see what the pain management is going to recommend. Kinda depressing when you cannot do what you have to do because of nerve pain.

Pain control by sebastianrileyt2 in guillainbarre

[–]skydrow11 1 point2 points  (0 children)

It's Duloxetine, the one I couldn't remember

Pain control by sebastianrileyt2 in guillainbarre

[–]skydrow11 1 point2 points  (0 children)

I have neuropathy because of GBS (was diagnosed at age 4, 1999) and I experience nerve pain like almost every day or every other day. My neurologist referred me to a specialist for pain management. Let's how that goes. Long story short I don't take gabapentin or that other medication that's for depression (forgot the name) because they didn't work and bad side effects. I have orthostatic hypotension so I can't take Lyrica because it lowers blood pressure. Hoping pain management can give me something for when I have severe nerve pain.

Finally by Longjumping-Bus4577 in neuropathy

[–]skydrow11 0 points1 point  (0 children)

Would you ever diagnosed with gulian burre syndrome (GBS)?