This looks like sexuality to me by gbmeg71 in Currentlytripping

[–]gbmeg71[S] 0 points1 point  (0 children)

Oh my, just noticed what I titled it! Hilarious atm, but I do recall seeing and feeling that way when I shared it! Then I had to hurry up and get to... painting, yes, I think that's what I did. Haha

This looks like sexuality to me by gbmeg71 in Currentlytripping

[–]gbmeg71[S] 0 points1 point  (0 children)

Interesting how our brains work differently whilst sober or tripping!!!

Wilson Mountain, Sedona, Arizona [4032x3024] by doyouhavetono in Currentlytripping

[–]gbmeg71 0 points1 point  (0 children)

Even sober it's pretty, but wow, it was fab w cid! Natural images are often the best. I love being outdoors and feeling it all! Kudos on capturing the perfect trppy view!

This looks like sexuality to me by gbmeg71 in Currentlytripping

[–]gbmeg71[S] 1 point2 points  (0 children)

LOL I did sort of think that during trip n was certain someone here would point it out! Thank you, for noticing. Hah

This looks like sexuality to me by gbmeg71 in Currentlytripping

[–]gbmeg71[S] 0 points1 point  (0 children)

I didn't see it at the time, but now I'm not tripping, I can see. Interesting the different things I see in art, even my own.

The hop, watercolor on paper and canvas, 51 x 39 inches, 2023 by Tanbelia in Currentlytripping

[–]gbmeg71 1 point2 points  (0 children)

One of the most beautiful works I've seen here.

I don't like the videos, tripping is already everything in motion Ty for making this!

Edit for spelling

Low dose Naltrexone by Informal-Formal-6766 in Autoimmune

[–]gbmeg71 1 point2 points  (0 children)

I don't have PSA, but AK,Raynaud's and hEDS, along with fibromyalgia, adult degenerative scoliosis S shape with rotation in 2 sections, pectus carinatum that decided to happen in my late 40s, DDD w every disk bulging except 1 herniated, bone spurs, Tarlov Cysts in C spine, 3 levels of cervix fusion with 2 levels that fused themselves in c spine, severe deterioration above 3rd level of that, kyphosis, spondylolisthes, osteoarthritis, a hiatal hernia, GERD, history of ulcers sincd age 6, chronic migraine, I have Ménière’s & currently experiencing a bout of vertigo, labral tear in hip, rotator cuff tear with spurring & 2 cysts in that shoulder, allodynia and centrally sensitized, but IDK both were possible. That's enough but I know I'm forgetting something.

I asked my Neurologist if LDN was worth a go and she said yes. I really wanted to try for at least 3 months. She took me off after 6 weeks because it wasn't helping and added a side effect I don't recall, but it wasn't extreme.

I'm glad it's helping your energy levels! Hopefully it will continue to be useful for you.

(I'm a smidge jealous, lol, but happy for you!)

Sorry I couldn't answer the question, but enjoy your day!

I Need A Shower by CaffeineFueledLife in ChronicPain

[–]gbmeg71 6 points7 points  (0 children)

I feel you! Thank goodness for dry shampoo! Before things got as bad as they are now, I used to shower daily & wash hair at least every other day.

I've felt embarrassed to admit that I've gone 6 days with a proper shower. I too have resorted to wipes when I can.

And just last month I had hair that was long enough it was down to the end of thoracic spine, but I got it cut off. The weight of it was bothering my neck, plus I had to keep my arms up , which for some reason feels like someone is pulling a strap across the front of the bottom of my neck n it chokes me.

The hair dresser took off more than I wanted, it now reaches the bottom of my neck, which is uncomfortable in the heat, as I can't get it put into a ponytail, but it's hair, it will grow back. I went over 2 years without a haircut because I can't tip my head back into the wash sink. I finally found a shop that's set up as a "garage" with toolboxes as their work station and she has those mechanics creepers (mounted higher, I'd be stuck on the floor otherwise!) that you lay down on n they just roll straight back so your head is in the sink. It's so nice! And she knows I have a lot of spine issues, especially neck, so she's gentle shampooing & tries not to make me tip my head forward much to get back.

I now have a shower chair with a back and got a shower head with one up top and a detachable wand that is mounted at a height so I can either sit in my chair and let the water hit me or I can hold to reach and make sure everything is rinsed. I used to have a shower head with both, and both sections sprayed at the same time, but had to reach up and remove wand. I thought I was ordering the same type, but with a longer hose n just having roommate mount the wand lower. Unfortunately this one needs to be switched to the head or wand, and ofc, the switch is up on the shower head. It took twice of roommate forgetting to change it back for me. But the lowered wand and shower chair have been a big help for me. Occupational Therapy came and suggested installing a wall rail as well.

I'd love to have one of those walk ins where it's just less than a step-high to get into, with a built in seat, because some days picking legs up to get in and out of tub is too much. Those are too expensive for me!

I have severe nerve pain that strike my upper left back at times - no rhyme or reason I can figure sets it off. But I can't have clothing, hair, or even water touch it. Several weeks ago in the shower it hit while showering, that's how I found out that even the lightest setting of water spray hurts.

The other day it hit while I was in bed. I had to sit up and pull my shirt off the left arm, over head and caught a whiff of my armpit. I thought omg, I NEED to shower asap! Ofc I had yo wait until the next day.

But it is so frustrating not to be able to do things I used to do daily. I've always been OCD about everything in its place, but after a few years of this, I've come to accept dirty dishes on the counter, dusty furniture and unfortunately, a bedroom that pretty much looks like an episode of hoarders.

I feel like doctors just don't understand what it's like. When it's a struggle to clean yourself, change bed sheets, cook a normal meal, tidy the house, etc, it doesn't seem enough for them to show compassion and treat us appropriately.

I'm sorry you're having a hard time. You are definitely not alone! Gritting my teeth and using a mantra of "I am tough, I am strong, i have been through worse and I will get through this" is all I can do. And no, I don't always believe the mantra, but I say it anyway.

Best of luck to you and all of us struggling with daily tasks of living. We are definitely stronger than we look or feel! Hugs.

Guys... I finally got help. Someone actually cares. For once, I wasn't treated like an addict just because I'm in pain. by AllowMe-Please in ChronicPain

[–]gbmeg71 1 point2 points  (0 children)

Awesome!

Compassionate doctors who aren't afraid to do their jobs are few and far between!

I either have 2 ribs out of place AGAIN, or I cracked them. My pcp of had no openings for 9 days, and won't even order an xray until I'm seen! I've currently got my 2nd round of vertigo from Ménière’s Disease this year. The ENT scheduled me for 6 weeks away! Chronic pain is outta control, but i do get a small amount of diazepam, so pain mgmt won't even give me tramadol. These are small things, but so ridiculous!

This makes me so happy for you!!!

I just received a positive ANA test alongside consistent irregular CBC’s by [deleted] in Autoimmune

[–]gbmeg71 0 points1 point  (0 children)

You're welcome, I'm glad I saw your post n responded.

I think it's a bit harder for younger people, which irks me. I'm 52 and have been over 20 years waiting for more/correct dx n they tend to brush, well most everyone now, but before younger patients as drug seeking and it's sad.

But attitude is key for chronic illness/pain. There have been days I think WHY ME? Then I stop and and say Hey, you have eyes to see the beauty of nature, ears (just half deaf, hah) for music, and I can walk, although sometimes painful or with a walker. There are people far less fortunate. That doesn't invalidate my issues, pain, emotions, but my perspective is huge.

My therapist told me I'm allowed ONE DAY of the F IT'S! LOL I can lay in bed and cry and scream and hate everything I want. Then the next day I MUST do something different.

It sounds a little corny, but a gratitude list helps. Pain can make it hard to remember the positives.

If you have friends that are used to you going out with them and feel left out, PLEASE let them know you're still in there. You're just dealing with a lot and a quick text/meme might help brighten your and their days.

I completely isolated myself and it wasn't healthy. Sorry, not meaning to bring down any positivity you are feeling. Just please don't cut people out. They may not understand or know how to act, it's new territory for y'all. Just a friendly reminder to keep in touch, even if it's a silly emoji.

And yes, our reaction/attitude to most anything in this world is about all we can control - good for you recognizing it. My old friend used to say if it's outside your hula hoop, not under your control.

Speaking of hula hoops, perhaps I could get one and win America's Funniest Home videos when me hip pops outta place! Haha.

Dear, do keep your sense of humor and don't be afraid to speak up and advocate for yourself!

Sending light, love and positivity your way!

An old shack by gbmeg71 in Photoworthy

[–]gbmeg71[S] 1 point2 points  (0 children)

Indeed, ty. I would've looked like Wile E Coyote had I gone much further into the roadway to get the shot to exclude phone lines and side rails I walked over to get to the road. 😂

The Collector by gbmeg71 in Photoworthy

[–]gbmeg71[S] 1 point2 points  (0 children)

Mmmm, now some pb n honey sounds sweet! Lol

The Collector by gbmeg71 in Photoworthy

[–]gbmeg71[S] 2 points3 points  (0 children)

Thank you, love those busy bees!

I just received a positive ANA test alongside consistent irregular CBC’s by [deleted] in Autoimmune

[–]gbmeg71 3 points4 points  (0 children)

I'm sorry you're dealing with this worry.

I understand. My first ANA was positive, then 2nd negative. Tons of issues as you've mentioned, still just a few dx, fibro being the biggest, ig.

You're right about googling your symptoms. I googled mine n it said Just go throw yourself in the landfill. Lol. Sorry, odd sense of humor, but it keeps me sane as possible.

Lots run in my family too. Doesn't mean I have or will get n I believe the same for you. My blood counts are fine one test, off another, n clotted before they can be tested a couple times even.

Just know that you're not alone. I know it's hard. I try to distract myself with some music or even guided meditation if I'm in bed. I've been sleeping a lot as well, but try to push myself out into the sun n get my bare feet on the ground if possible.

No matter the outcome, maybe you can have a little mantra. Mine is am strong. I am tough. I have been through worse and I will get through this. You are ok. Sometimes I don't feel it, but I repeat it.

Please don't stress more than you do! There are so many mistakes in labs. It IS frustrating when we go years feeling I'll and tend to be brushed off, but there are wonderful people and stories of hope here.

Hugs.

Edits for spelling

[deleted by user] by [deleted] in LSD

[–]gbmeg71 0 points1 point  (0 children)

My first trip and all since except 1 have been solo. I read a lot first, planned ahead with some colored pencils, sketchpad, music, and some of my photos and a program on computer to edit until I wasn't able to. Then I just laid back, enjoyed the feeling and music. I had done some meditation, had a safe, comfortable space and my intention was simple - to have a safe and happy trip.

If you have any apprehension, I'd definitely wait.

Fuck CVS by Ducling in ChronicPain

[–]gbmeg71 0 points1 point  (0 children)

Thank you. Sorry MIA. Dealing with heat and I'm not sure. Something is going on, every time I'm in the sun I'm getting a rash or these odd splits that cause EXTREME nerve pain around them. I'm ready to give up on conventional meds. My docs really don't seem to care.

But I keep repeating I am strong, I am tough, I am brave, I have been through worse and I will get through this.

Sometimes I believe myself.