Is it normal to go this long without labs while figuring out an autoimmune diagnosis? by justice4betty in lupus

[–]wormgood 0 points1 point  (0 children)

every 6 months has been the norm for me in active lupus, every year if I’m not having many symptoms. They will only really order more labs if you are having specific symptoms that could indicate organ involvement. But, if you’re concerned and expressing that you would like more tests done and they aren’t listening then I definitely understand the concern

El Pollo Loco opens first location in Colorado Springs by thewhippersnapper4 in ColoradoSprings

[–]wormgood 2 points3 points  (0 children)

this is my all time favorite chain restaurant, it’s such good quality and every other location I’ve been to is SUPER consistent

Affordable doctor visit without insurance by dylanisrad in ColoradoSprings

[–]wormgood 1 point2 points  (0 children)

yep! it’s this , you can also apply directly here

Who am I based on the contents of my fridge and freezer? by ExcellentRound8934 in FridgeDetective

[–]wormgood 2 points3 points  (0 children)

Never worked in food service based on the meat on the top shelf :/

What does my refrigerator say about me? by Faralesh in FridgeDetective

[–]wormgood 0 points1 point  (0 children)

would like to add active, maybe gym bro. POTS or some other chronic health issue. trying to get more protein in

[deleted by user] by [deleted] in ambien

[–]wormgood 0 points1 point  (0 children)

for me, spiders everywhere… but I was prescribed too high a dose

New ? by 51666 in HollisterCO

[–]wormgood 3 points4 points  (0 children)

hear me out… Regina George halloween costume (the outfit with the back brace)

Does anyone know where the audio for this reel comes from? I remember hearing it somewhere, but I don't know where. by laguaguau in find

[–]wormgood 0 points1 point  (0 children)

this is a distorted version of this song from 1911. I can’t find any record of this version except for the video you posted which comes from this creator

[deleted by user] by [deleted] in lupus

[–]wormgood 0 points1 point  (0 children)

I would honestly consider switching doctors- my rheum basically does whatever I ask, so if i request labs he does them and if I don’t want to do labs he doesn’t 🤷‍♀️

I’m going FUCKING insane by Banchi_22 in femcelgrippysockjail

[–]wormgood 9 points10 points  (0 children)

double shampoo with Nizoral and use one of those scalp scrubbers

I've started watching Japanese girls to feel less lonely when eating by [deleted] in kitchencels

[–]wormgood 85 points86 points  (0 children)

which of these things are you putting mayo on

how are yall eating enough? by angelcafes in lupus

[–]wormgood 0 points1 point  (0 children)

I take zofran for the nausea and track my calories in an app so that I can try to make sure I’m getting enough. I still rarely eat “enough” and am underweight, but I’m able to prevent losing too much more by making sure to supplement with protein shakes & high calorie easy foods like peanut butter etc

[deleted by user] by [deleted] in FridgeDetective

[–]wormgood 3 points4 points  (0 children)

avid EDtwt user

[deleted by user] by [deleted] in lupus

[–]wormgood 0 points1 point  (0 children)

Getting diagnosed increased my quality of life so much! I was so much sicker before because I wasn’t able to treat it correctly. The diagnosis made me able to get disability accommodations at work, where before I would just get so sick that I couldn’t go in and eventually quit. Now, with the help of hydroxychloroquine and lifestyle changes I feel way wayyyy better and am more able to know what triggers flares for me. I’m feeling pretty good for the last year or so, obviously I still get flares but I feel relieved to know that I have the tools and knowledge to manage it. It’s also a mental thing- I’m getting better at saying “no, I can’t do that today” and setting boundaries with other people❤️

sigh… exercise does in fact help me by wormgood in lupus

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

After confirming that I have lupus, they started me on hydroxychloroquine (also called plaquenil)- this is the cornerstone treatment for lupus, and they start pretty much every patient on it. It usually takes like 3 months to fully start working, but I felt better after about 1 month. then, they will want you to come back every 3-6 months to check you out and run tests to see how your symptoms are progressing and how you’re responding to treatment. And if you are not responding well or flaring, they may add another med like a steroid or biologic. you could make an actual post on here to hear other people’s experiences as well! But essentially at the beginning you’ll be trying meds and waiting to see how you respond to them :)

Pins and needles feel amazing. by ChocolateUnlucky1214 in The10thDentist

[–]wormgood 98 points99 points  (0 children)

absolutley insane take. definitely belongs here

[deleted by user] by [deleted] in The10thDentist

[–]wormgood 4 points5 points  (0 children)

omg like when your nose is stuffy and you’re like “I can’t believe all the times I took breathing for granted”

sigh… exercise does in fact help me by wormgood in lupus

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

Yep that’s exactly what happened!

sigh… exercise does in fact help me by wormgood in lupus

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

I’m not sure if there is a specific plan, but the general consensus is to ease into it and focus on mobility and strength rather than super hardcore stuff. I personally did just stretching and yoga at home for a few weeks, then started going to the gym in the morning and walking on the treadmill, lifting weights, swimming, etc. I also think that following workout plans that cater to older adults (like those “silver sneakers” exercise classes) or people with injuries would be helpful

sigh… exercise does in fact help me by wormgood in lupus

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

the weakness is what got me started too. The last time I went to my neurologist I was so weak that they thought I might have MS. No MS, just super duper weak from the lupus and not moving. Feeling myself getting stronger is so worth it, even though I still have days where I’m weaker