@chass.gpjourney: #gasteoparesis #sclerosingmesenteritis #chronicillness

LaceyLeeAnn :

Feel this. I know it’s hard. I have lupus. It’s learning how to live with the new you and discovering who you are now.

Mary Aldridge :

I’m being put on hospice Monday.

Teresa Swanson :

I understand 💯 it's ridiculous I am in pain 24 hours a day even with medication having tkr 8 12 then have to get the other one done

Nathan North141 :

The burning, aching, throbbing, sharp, and electrical sharp type of pain throughout the body, all at once, is so painful, yet unless you have fibromyalgia, you cannot understand what torment we go through each second, minute, hour, day, week, month, and year. No relief for at least a minute to catch our breath is suffocating. Sharp electrical pain that makes a leg or arm go flying. The distrust of not dropping what we hold in our hands as what we hold now falls to the floor. The endless nights of exhaustion, but we cannot fall asleep or find that night's comfortable sleeping position. Never the same from night to night, causing frustration and anxiety, depression, and a sense of hopelessness. Let’s not mention the pain and nausea when the weather changes. The stronger the storm, the more intense the pain. Thoughts- tons of thoughts racing and bouncing in our mind- are endless noise that is unrealistic to turn off. The guilt comes crashing down on the moments, events, and time we spend with our family and friends, let alone the stranger who might come around. So, in the midst of the chaos described, can there really be a solution when nothing we have tried has worked to suppress the pain, even for a moment? The elusive solution that doesn't bring relief.

✨ Just a gal with WiFi ✨ :

It’s so okay and actually necessary to grieve the changes.🖤 Totally understand you, been sick for a while and the ups/downs are so hard to navigate.

sacredragemedia7 :

I’m sorry. It’s so hard. I know. 💔💔💔

Shy butterfly 🦋 Gen ❌71 :

I fight every day what I don’t talk about stay with me I have COPD complete respiratory failure dioxide with chronic bronchitis and emphysema asthma

Jessie :

the thing that really pisses me off is this is my 1 and only life and it is miserable and painful and not what I dreamt of

🌻💛amanda💛🌻 :

🫂. CRPS 🧡 & Endo 💛 girlie here….. fully understand this level of grief all too well 🥺

MimiBranham❌️ :

I feel you hon, keep your head up. Your not alone 💜

SimplySam 💚 :

I sit with you ❤️‍🩹 chronic illness warriors

🏳️‍🌈Megan 🆘🇺🇸 :

Sending hugs

Roxie Foxy the Kitten ❌ 50 :

I truly understand friend I fighting too sending hugs

Pamela Kaia :

We don’t make it out of this do we. No one makes it out of this.

Charlene powers :

I’m going to that my last throwing family member immediate and I’ve all died of cancer. I’ve held four hands and she’ll be fit and I can’t take no more.

tangieayers :

I was diagnosed a couple years ago with a rare autoimmune. It makes our life more tricky, and it’s never the same again… but that doesn’t have to mean horrible. It’s reminded me to slow down and care for myself. I hope you’re starting to feel better.

🧂🍳👻Brandy💪🏻🐘📚🤓 :

That’s one of the hardest parts sending you hugs 🥰🥰

🧡BrittBrat🧡 :

We got this!!!

Beck :

I had to do it also and even though things are crazy and worse I’m sure seeing more doctors is not it ❤️✌️🤞

alysa-mae :

I hate it I have gastroparesis and the medicine that will help insurance doesn't want to cover

Jenn :

I was dxd in 2022 and i grieve the life i used to have all the time! I’m adjusting slowly. It gets easier.

Heather :

It’s the hardest thing to do. Is mourn the person we once were isn’t coming back.

HeatherKann Homestead :

Theresa :

And yet we still stand. We still stand....

sherihorn03 :

hugs prayers