Does anyone here struggle to make friends? Or wishes there was an easier way?
Does anyone here struggle to make friends? Or wishes there was an easier way?
Has your POTS a gotten worse with other CI?
I’ve had like 12+ CI diseases develop in the past yr-I’m overwhelmed & dying my mum doesn’t get it nor do the other kids…I just want to hide
Summer
Does heat make your POTS worse? If so, what have you found that helps? I am in Georgia and almost completely disabled during the summer.
I just made a group called Teen and Adolescent Ill is anyone interested in joining?
After a 4yr battle against TPN I finally went home on full term #TPN #Gastroparesis #CysticFibrosis #childrenshospital
I was just diagnosed yesterday with Ehlers-Danlos-4
I have a very long history of so many different surgeries. I have had a lot of problems
Just too many right now to get into. I would love to write a short story about my Journey to this point. I have been through a lot I’m really just trying to understand this.. It has been a very long road Thank you ne I will add a picture soon.
I’ve had gastroporesis for 15 yrs. I’ve been on domperidone and PPI’s for the reflux. I’ve had SIBO 5 times. How did you decide to get a feeding tube?