My almost 14 year son has ulcerative colitis (similar to Crohn's disease). He has taken meds for three years and lived a normal life but about four months ago things changed. He's been in a lot of pain so we are switching to an IV treatment plan. Today is his first one! We have to travel to Vancouver for the procedure at BC Children's Hospital. We return in two weeks to do it again, then four weeks and then hopefully every 6-8 weeks from then on. Here's hoping it works!
Oh I hope he gets better and the treatment works well. So sorry to learn this, I know he wants to feel better quick. Medical science is pretty amazing, I'm sure it will help him!
Oh dear that is a sad situation for him to be in. I very much hope it all turns out to be worthwhile treatment and brings some comfort and happier days.
Nothing is worse than to watch your child in pain. Sending prayers that this new treatment works for him as the doctors hope. Tough thing to deal with at that age.
If you don't mind, I am going to pray for Gage that the treatments will not only work, but that he won't need all of those treatments to correct the problem!
Oh Man. Sorry to hear about his struggle. Fortunately modern medicine has come a long way. Hopefully they can get him back close to normal. Good luck Kim.....
Sending warm thoughts and prayers your way, my son has JIA so I completely understand what it feels like to watch your child suffer in pain with a chronic illness :0/. I really hope this corse of treatment works for your boy xoxo warm wishes again
I know that seeing your child struggling with an illness is one of the most difficult things for a parent to cope with. Sending you, your son and your family good thoughts, strength and courage.
Oh the poor guy. My niece has Crohn's and I have numerous digestive problems that are now almost under control with diet but I can empathise completely. The pain can be unbearable at times. I hope these treatments do the trick and he can get back to the activity he's used to xx
I wonder if this treatment is available in England... know a young fellow crippled by this condition! Good to hear about the treatment-not good to hear he has to have it!
Sending gentle and loving hugs to you and your son. I have lupus and arthritis, take daily meds via tablets and have chemo infusion every 6 months. Had 4 sessions and no great improvement yet. But we have to keep our fingers crossed. 💚
It tough to see young ones in the hospital but if the treatment works it'll be worth it. Sending positive vibes and goodwill your son's way. Let him know we're all rooting for him. :)
Sending all my best wishes.
Glad you are still taking photos as you go along.
Great pov!
Kelowna
My BIL lives kind of near you in Woss.