Greenheart Stables
02:25:05 Green|Gren|Grenlin
You know I got myself thinking, younger me four years ago would be so excited with how far my stable has come. Its a nice feeling even if it took me three years to understand showing lol
SUMMER OF PEARLS
02:23:14 
<3
Executive Stables
02:20:37 Executive/Lyssa
Summer
Yep definitely😅
ShowJumpingChampions
02:20:15 SJC | Haley
She never does that well and I just wanted to finish the explore once lol.
SUMMER OF PEARLS
02:19:49 
@executive now you know i am just kidding right when i ask...did your thoughts come out as neigh neigh whinny? :)
ShowJumpingChampions
02:19:46 SJC | Haley
My Sub-Par brave horse spooked once five moves from the end -_-
SUMMER OF PEARLS
02:18:42 
mm hmm
Executive Stables
02:18:12 Executive/Lyssa
Sorry my brain is awake but sluggish after our thanksgiving lunch🤣
Executive Stables
02:17:41 Executive/Lyssa
Or maybe that sorry, lol I was thinking for the horses
The Old Gods
02:17:22 Void Malign
that's the horse training
Blue Diamond
02:17:17 Bluey
mine is 369972
Executive Stables
02:17:15 Executive/Lyssa
Their for tracking training, the bars
Blue Diamond
02:17:08 Bluey
stable number
SUMMER OF PEARLS
02:16:43 
what do the 6-digit numbers i am seeing on other pages, mean? like, 211222?
SUMMER OF PEARLS
02:14:41 
ok nevermind i figured it out
Greenheart Stables
02:10:37 Green|Gren|Grenlin
Well a sky phenomenon is a better way to call it lol
Legendary Stables
02:10:22 Legendary/Lyssa
Ooooh nice!
Greenheart Stables
02:09:54 Green|Gren|Grenlin
@Lyssa
Its a type of cloud phenomenon! Back when I owned her mother it was based off her and her fathers names
Legendary Stables
02:08:57 Legendary/Lyssa
Wow! I have less than that altogether in my savings
Legendary Stables
02:08:25 Legendary/Lyssa
Green,
Was just roaming through your barns(my favorite pastime is just seeing yÂ’allÂ’s horses) how did you come up with her name? -HEE Click-
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Fibromyalgia Advice January 4, 2022 06:56 PM


Kingfisher Cove
 
Posts: 874
#952634
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I've been dealing with joint pain and fatigue for over a year now and since my blood results came back normal my rheumatologist told me my symptoms could fall under fibromyalgia.

I wanted to see if anyone here has experience or advice on how to handle the symptoms of fibromyaglia; namely joint pain. I have a lot of joint pain in my fingers and the cold seems to make it worse.


Edited at January 4, 2022 06:59 PM by Silver Isle Eventing
Fibromyalgia Advice January 4, 2022 07:09 PM


WildWillow
 
Posts: 2131
#952637
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I have/had it! It was a long, long struggle trying to figure out what exactly I had and cycled through many different diagnoses.
My joint pain became so bad I was in a wheel chair. Hot compresses or cold (whichever your body prefers) can be a big help and yoga too. If you're sensitive to exercise, go really really slow. Like five minutes of exercise, then six a week later and so on. It feels tedious but it helps.
And don't be hard on yourself! I am someone that has a really hard time just allowing myself to rest without feeling like I should be doing something. Stress can make fatigue and joint pain much worse. So make sure to schedule in some self love and relaxation time. Don't push yourself - allow your body to dictate what it can do. Pushing will only be worse in the long term.
I pushed myself really hard last week and now I'm majorly paying the price.

Also, this was the big one for me - ask your doctor about Celiac & Gluten Sensitivity along with Chronic Fatigue Syndrome (CFS). After several years of no answers, we found out I was sensitive to gluten (likely Celiac as I tested positive via genetic testing but no official diagnosis as I do not want to go back on gluten for ~6 months to get an accurate blood test). My gluten sensitivity had been causing my joint pain, fatigue, and brain fog all those years without anyone having an idea that could have been the answer. My rheumatologist was stunned and now screens her patients for Celiac if they're showing fibromyalgia sympyoms. I was severely deficient for most nutrients which only made the issues worse - this was also caused by my gluten sensitivity.

Now, five years post adopting a very gluten free diet, I rarely if ever have any joint pain - only present at times of stress. I am extremely sensitive to pain and touch though. I still struggle daily with fatigue due to my CFS and headaches but it's definitely letting up. And my vitamin levels still are iffy - I was previously on ~70 supplements and now I'm just down to a handful.

My PM's are always open. :)

Edited at January 4, 2022 07:10 PM by WildWillow

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