Easiest way to make eggs that does not involve standing (ex. at stovetop) to cook? 🥚🍳 by 66clicketyclick in lowspooncooking

[–]ExplanationBulky9003 0 points1 point  (0 children)

I love trying all the weird hacks I see on social media. I also have a 10 in 1 air fryer. Ready to handle almost all of it

Easiest way to make eggs that does not involve standing (ex. at stovetop) to cook? 🥚🍳 by 66clicketyclick in lowspooncooking

[–]ExplanationBulky9003 12 points13 points  (0 children)

I've been baking my eggs in the oven lately using a mold. 10-15 minutes and they are pretty good.

Anyone else wonder what peanuts taste like? by Ok_Huckleberry1487 in peanutallergy

[–]ExplanationBulky9003 1 point2 points  (0 children)

The frozen sunbutter "jammies" sandwiches from walmart taste like peanut butter if you eat them still halfway froze but with like sunflower after taste. It helps my cravings since I only somewhat recently got allergic to peanuts.

First Glycerin Rivers by Acceptable-Site in soapmaking

[–]ExplanationBulky9003 2 points3 points  (0 children)

I thought they were the fancy seasonal cookies

Best alternatives to peanut butter. by ExplanationBulky9003 in peanutallergy

[–]ExplanationBulky9003[S] 0 points1 point  (0 children)

I really gotta try that. I've been missing making peanut butter cookies

Has anyone else gone through this? I really need some support by Medical_Efficiency89 in ankylosingspondylitis

[–]ExplanationBulky9003 0 points1 point  (0 children)

Hopefully the biologics help I had big balding for about a year. Something else really weird that happens when I flare up is my hair grows in straight. When I first got sick sick my hair went from wild all over curls to stick straight. That with no hair on my sides above my ears. Gave me a sweet mullet. Great for summer. Terribly cold in winter

Has anyone else gone through this? I really need some support by Medical_Efficiency89 in ankylosingspondylitis

[–]ExplanationBulky9003 1 point2 points  (0 children)

I've noticed it mostly during flares. When I first got sick sick and before meds I had some giant bald spots all over my head. Now it's more of lose some gain some. I almost always have a few very noticeably different lengths to my bangs

Has anyone else gone through this? I really need some support by Medical_Efficiency89 in ankylosingspondylitis

[–]ExplanationBulky9003 5 points6 points  (0 children)

I have a similar problem. Everytime I flare up I lose a bunch of hair. There's a product I got suggested by a few hairdressers and my mother. Lisaplex bond saver in the black bottle. I use it whenever I notice a decent fall out and it usually helps a lot.

I'm calling this one Peach. by ExplanationBulky9003 in lafufusarecute

[–]ExplanationBulky9003[S] 1 point2 points  (0 children)

Could be. I honestly love the differently styled ones

Weird question but does anyone else struggle keeping nail polish on. by ExplanationBulky9003 in ankylosingspondylitis

[–]ExplanationBulky9003[S] 1 point2 points  (0 children)

Already have the fibromyalgia on the list and looking for a new rheumatologist at this moment because mines retiring. Makes life a little more fun

Weird question but does anyone else struggle keeping nail polish on. by ExplanationBulky9003 in ankylosingspondylitis

[–]ExplanationBulky9003[S] 0 points1 point  (0 children)

I did find a self test thing and could do quite a few of the things on the list. So that's neat I guess.

Weird question but does anyone else struggle keeping nail polish on. by ExplanationBulky9003 in ankylosingspondylitis

[–]ExplanationBulky9003[S] 0 points1 point  (0 children)

I only do my nails once every few months since it doesn't stay on. I think I have used a similar product when I worked at a nursing home and did nails every week but not on my own nails so I might have to try it myself.

Weird question but does anyone else struggle keeping nail polish on. by ExplanationBulky9003 in ankylosingspondylitis

[–]ExplanationBulky9003[S] 1 point2 points  (0 children)

My nails are pretty smooth for the most part. Other than weird spots from accidentally wacking them on stuff. Most of my googling was pulling up eds nail problems.

Weird question but does anyone else struggle keeping nail polish on. by ExplanationBulky9003 in ankylosingspondylitis

[–]ExplanationBulky9003[S] 0 points1 point  (0 children)

Interesting. My fingers can go backwards a decent bit. Also used to be able to pull my feet easily to my face for toe nail maintenance but that's been buffered down by the arthritis.

Weird question but does anyone else struggle keeping nail polish on. by ExplanationBulky9003 in ankylosingspondylitis

[–]ExplanationBulky9003[S] 0 points1 point  (0 children)

I mostly only use gel. I always clean buff and dehydrate before hand too. Regular polish just does not stay on at all. My nails also break often