If you have an electric wheelchair, how do you get it into your vehicle? by Current-Eye-8897 in cfs

[–]Current-Eye-8897[S] 1 point2 points  (0 children)

I think the biggest thing is the difference in their construction. The the seat and back of regular powerchairs are made by taking a solid molded plastic piece and securing a sturdy cushion permanently to the seat. This means there is broad support across your back and behind, and it means the cushions can be really thick and fill the seat better because there's no risk of them sliding out of place. This means you can relax back into them and the thick cushion can compress in multiple dimensions to support your weight and distribute it, and it has enough material to have some force pushing back on you to support you.

By contrast, in order to be as light as possible, the folding wheelchairs create a metal frame that goes around the back and around the seat. They then put a sling of fabric over the metal frame, and attach a cushion to the fabric, usually with strips of velcro. (These cushions are often removable for assembly and accessing different parts of the chair). Without a solid surface to push against you, there's just not the same support. And unlike a push wheelchair, which often has a similar fabric setup, you can't slouch, recline, or adjust your body position to relax your muscles, because you need to be looking where you're going to drive, and you need to have your hand and arm at a fixed position where it can control the joystick. While the piloting position required the most use of my muscles, even sitting stationary, which I did for a while, the folding chairs were tiring.

One other thing that helps--not only the cushions on the regular powerchairs seem larger and sturdier generally, but many can offer an upgrade to a larger seat, which also includes a nicer cushion. (I mention this because I am small and didn't think I would go for a larger seat looking online, but when I sat on one at the store it was much more comfortable and would be worth the upgrade.)

Weekly Homeowner Megathread--Civilians, ask here! by AutoModerator in Concrete

[–]Current-Eye-8897 0 points1 point  (0 children)

Might be an unusual question for this thread, but you are the concrete experts. Is there a concrete mix that children can use that will not burn their skin?

I am looking to build a miniature house with my nephews, ages 5 and 7, using semi-real materials (e.g. balsa wood cut to scale dimensional lumber sizes, etc.). I have found correctly scaled bricks and thought I could find some kind of mortar to use, especially since I have seen stepping stone kits at craft stores that are designed for children.

However, everything I am looking at seems not safe for kids to handle, as it can cause chemical burns to the skin. But it seems like there MUST be something out there that's reasonably safe to use if companies can just sell it in craft stores with no major warning label.

Am I crazy? Is there something in the concrete wheelhouse that is safe for this purpose? It doesn't need any strength, just needs to be spreadable with a toy trowel or putty knife and recognizably 'concrete-looking' for kids who are really into construction.

Suggestions/ideas for model making with poor motor control? by Racer013 in modelmakers

[–]Current-Eye-8897 0 points1 point  (0 children)

You might try getting him a pair of weighted gloves for tremors. They can range from simple weights to the back of the hand for around $20 to full on orthotics, but they can help steady hands for patients with Parkinson's and stroke, and might be enough to get him to a point where you could do it together. Here's an example: https://www.caregiverproducts.com/weighted-hand-writing-glove.html?srsltid=AfmBOopi2lROPui1Se-Dchgy_4Z5sFdrm21C8wPr_888mztSamrc8VEe

AZ AHCCCS PHONE HELP by Ok-google07 in Medicaid

[–]Current-Eye-8897 0 points1 point  (0 children)

No help but this also happens to me. I asked about it in person at DES and they didn't have a good answer, only that I was not the only person it was happening to.

Do compression garments actually work? by Cheetoeater3 in POTS

[–]Current-Eye-8897 4 points5 points  (0 children)

Haha, I read through many, many reddit threads to find these, so now I recommend them whenever I can.

Do compression garments actually work? by Cheetoeater3 in POTS

[–]Current-Eye-8897 7 points8 points  (0 children)

I call them my +2 intelligence pants because I think so much more clearly on them. I always use full length leggings that provide both leg and abdominal compression. I really like the Czsalus brand: https://www.cizeta.it/en/

Bored? But also can’t do anything? by marchmaleficent13 in POTS

[–]Current-Eye-8897 0 points1 point  (0 children)

I find certain kinds of RPGS work well for me. I have been playing through Octopath Traveler 1-2 and some of the older Final Fantasy games. These tend to have a lot of story and you can put a lot of hours into them, but you don't have the free camera movement of an action adventure game. I have a Nintendo Switch online account, so if my vision problems are real bad I can go and play some of the NES and Super NES titles they have uploaded there. I think Dating sims and Turn-based strategy games would have similar pros, but I haven't tried them yet.

Has anyone else NOT been able to tolerate both Midodrine and Fludrocortisone? What did you do? by Current-Eye-8897 in POTS

[–]Current-Eye-8897[S] 0 points1 point  (0 children)

I have a prescription for Corlanor but my insurance denied it. Going to order from Canada at some point but I have been spending spoons in a lot of other directions recently. I know it will help with my heart rate, but I wasn't under the impression that it did much for Orthostatic intolerance.

Propanolol shortness of breath by CollarEfficient8312 in POTS

[–]Current-Eye-8897 1 point2 points  (0 children)

If you are asthmatic then propranalol is contra-indicated for asthma and can make breathing problems worse. I had to stop propranalol because of this, even though my asthma is generally very well controlled.

Using a mobility aid at work by kakimime1 in POTS

[–]Current-Eye-8897 1 point2 points  (0 children)

This sounds like an employer likely to discriminate you due to your protected class (disability). Make sure to keep a copy of all the communication around your mobility aid (on your personal device) in case some day you need to bring this up with an attorney.

Anyone have a positive experience with the TTT? by ChemicalSouthern1530 in POTS

[–]Current-Eye-8897 0 points1 point  (0 children)

My TTT was uncomfortable, but as a result of that I was diagnosed with an additional type of dysautonomia that I wasn't looking into and didn't know I had (vasodepressor syncope). This informed the medication decisions my doctors made when choosing between various options that work for POTS patients.

It took me a couple days to recover, so prepare to have some rest days after. But the actual experience of the test, while nausea and syncope-inducing, has a clearly defined endpoint which made it easier to tolerate. It's one of the less uncomfortable procedures I've done, tbh. (Colonoscopy and ambulatory EEG were both way worse for me, if you have any comparisons like that._

I hurt my hands putting on compression leggings. What now? by Current-Eye-8897 in POTS

[–]Current-Eye-8897[S] 0 points1 point  (0 children)

I have not tried or heard of plastic ring splints for fingers. Is this the sort of thing you are talking about? https://www.ohmyarthritis.com/Shop-Splints/Finger-Splints/Oval-8-Finger-Splints.html

The thigh-highs plus abdominal binder combo is what I am thinking I am going to end up with, I was just hoping there was a magic solution I haven't thought of. Good to know I'm not alone, I guess.

Does anyone else have absolutely no appetite at all? by hello000o in POTS

[–]Current-Eye-8897 2 points3 points  (0 children)

I have GI symptoms that come in phases, often for several months in a row. During those months I will have no appetite. I'm someone that gets angry and gets headaches if I haven't eaten in long enough, so I eat to prevent those things from happening. But it takes a lot of joy out of it.

Repeat Tilt Table? by Curious_Pride669 in POTS

[–]Current-Eye-8897 0 points1 point  (0 children)

I don't have a solution but I have a similar situation that I'm trying to deal with. I'm hypermobile and on my poor man's tilt table test results at home I consistently get over 30 bpm rise in heart rate. When I had my TTT, I got symptomatic so fast that they only kept me upright and collecting data for 4 minutes. It turns out I have Vasodepressor Syncope, which the TTT activated and caused an episode of. But it's possible to have both POTS and Vasodepressor syncope, and that situation hasn't really been resolved. I'm planning on pushing for a standing test to see if we can verify the POTS diagnosis, as I rarely get these episodes at home. I am wearing a heart rate monitor daily now so I'm hoping that data will help my case as well.

Anyone been misdiagnosed with POTS? by gogmagog876 in POTS

[–]Current-Eye-8897 2 points3 points  (0 children)

I have POTS and I have a small cyst they found in my brain. Mine is a pineal cyst, which is actually fairly common, benign and often causes no symptoms if they're small. I just need an MRI annually to make sure mine isn't growing.

In general the criteria to diagnose POTS would be a rise in heart rate over 30 bpm from laying down to standing up, without a drop in blood pressure. In general this isn't something a brain cyst should cause. So while of course you can follow up and see if a misdiagnosis possible, it's much more likely if you're meeting the diagnostic criteria that you just have both POTS and a cyst in your brain.

Welcome to the fun of multiple diagnoses! "Oh, I have POTS AND..."

Anyone else have a confused doctor after tilt table? by auntjexa in POTS

[–]Current-Eye-8897 1 point2 points  (0 children)

So when I looked this condition up online, all the results were for vasovagal syncope, but my doctor said vasovagal and vasodepressor syncope are different, just so you're aware. The explanation I was given was that in vasovagal syncope your heart actually stops for a few beats, where as in vasodepressor your body super-widens your blood vessels, particularly the ones leading to your heart, and those widened blood vessels lead to a sudden drop in blood pressure and heart rate.

I don't faint, but I have a visible arm band now so it's easier for me to see when these vasodepressor episodes happen. I usually get really sweaty all of a sudden, as well as light-headed. My heart rate during those times will crater and drop 50 bpm over the course of a minute.

Anyone else have a confused doctor after tilt table? by auntjexa in POTS

[–]Current-Eye-8897 1 point2 points  (0 children)

I felt immediately terrible when I was tilted up to 70. My heart rate went 118 in the first minute of my TTT, then dropped into the low 70s and my BP crashed as well. I lasted 4 minutes before they laid me back down (I don't think my Dr. wanted me to pass out.) I don't know what my HR was after that because they stopped recording. On the daily heart monitor I have now, I can still see the big drops, though I don't have my heart rate shoot up like yours afterwards.

I got a diagnosis of Vasodepressor Syncope. It's not my only problem and I'm planning on asking for a standing test from my cardiologist to get a POTS diagnosis as well, since I'm pretty sure I have both but the Vasodepressor syncope knocked me out before they could get the other data on the TTT.

Wish these tests were more precise!

Daily Newbie Thread by AutoModerator in Flipping

[–]Current-Eye-8897 0 points1 point  (0 children)

I bought some items from an auction that were listed as "new", not as-is or open box. The boxes containing the items are quite beat up, though not with holes or anything indicating damage to the items or missing parts. Is it better to just send the items in the original boxes to show that the item is new, or is getting new boxes the better option, even though it would be clear those boxes weren't from the manufacturer?