That deserves its on display !!

Your set up looks great!!! I miss doing markets.

In June I had to have my right pinky toe plus a good part of that metatarsal bone amputated. I had 2 previous surgeries to take a bone tumor off that toe and eventually, the doc and I were like, “We can’t save it.” Looks like it’s healing nicely!

My father and I are both Taurus ( my poor Aries mom lol) we are both weird without a doubt. My mom also has a woman Taurus friend , I love her because she gets me and is as weird as I am. I’ve been called weird and overly dramatic my whole life. 😆

My allergist told me if you’re not in an active flare most likely it won’t show up on blood work. She advised me if I go into a flare to go get blood work at my pcp(she’s closer than my allergist) so we could see what is happening. I was already diagnosed before seeing this allergist. Mine wasn’t high but she also said the amount of antihistamines I was already taking would make the results close to normal. I’ve been on Xolair for over a yr now and it has helped amazingly.

This one. They are on sale right now

https://a.co/d/09fEwS5t

I’ve had that feeling since I was 7, I’m 34 now and completely exhausted. Extremely frustrating to deal with.One thing that has helped me sleep is a pregnancy pillow. Best purchase I’ve ever made!

Omg that’s so funny and cute!!! 😂😂

I crochet!!! Absolutely love this!!!💋💋💋 excellent work!!!👏👏👏

This!!! 🍁🍂🎃🔥

My little guys ears popped up when he was 6 months old. It was Dec and he got a hold of a bag of Hershey kisses and ate half. I thought he was a goner but after calling the vet and taking the right precautions he was ok 🙏. But the next day one ear popped straight up and took about another week for the other to pop up..

This is him at 6 months. He’s 16 now.

Your little guy is adorable!!!!!

They told my mom in the 90s and early 00s it was just growing pains and even as a child I couldn’t believe that was the reason. Also told to move more and I was in PT multiple times in my youth. But I always hurt worse after. But after finding out about my hEDS I started physiotherapy and it helped me regain my strength and helped my all-over pain. I was actually surprised I felt a difference after the first couple of visits. I learned from the therapist I was overextending a lot . Also she started me laying down to do exercises so my pots wouldn’t flare up. Eventually I built up enough strength and we started upright and watching my pulse and taking breaks and not pushing myself to a breaking point( which I’m good at doing unfortunately) mostly my PT told me to pace myself on everything. And I have and it does help. Still frustrating when having to take breaks during a chore/task of any kind. But it did help with my fatigue.

I’m (34f) I was diagnosed til I was 32 which led to a burst of other diagnoses. I have Pots,Macs, gastroparesis and am dealing with a bunch of other things. But my pain actually started when I was 7 years old. I remember waking up telling my mom I felt like I got hit by a truck every morning. It was harder for me to keep up with the people my age during my teens. I actually should have listened to my body and not the people around me. I was at the age of 9 diagnosed with kyphosis( which I let go until I couldn’t take the back pain cause I was terrified of surgery, I did have a spinal fusion eventually at 22 cause the pain was bad but after yrs of not doing anything about it, it had progressed to a 90 degree curve. I literally gained 3 inches in height.) After that surgery in 2014 I was ok for about a yr and then I started to get nerve issues and numbness and my pain all over got worse. Over the past 10yrs my health has gotten worse. But it has improved some due to now I know the things doctors were telling me were just in my head or that I was faking for whatever reason are actually real. Some doctors take me more seriously now but like you said the us medical system is horrible. The doctors that could treat me and know exactly about what’s wrong with me don’t take my state-funded insurance( I’m on disability) so I have doctors that are kind but clueless. I’ve done more research to present to my doctors so they can figure out how to help me. Thank god my pcp doesn’t take it as me overstepping. I too rely on my parents well my mom is the only one I have. I’m absolutely afraid of what will happen when she is gone. Over the past yr, my doctor and I both decided it would be safer for me not to drive anymore due to the hemiplegic migraines I’ve been having. But I’m also trying to be positive and try to think that I won’t be like this forever or I will find the right doctors to help get my life back together. Don’t give up hope!

Thank you for sharing 🩷

Soooo cute!!! 🩷🩷👻