We are coming up on our one-year anniversary of our endoscopy. There’s very little drama now: we’ve got this. But we still have to jump through the GP visit hoops, and the Pediatrician hoops, and the GI Clinic hoops, and the blood monitoring every six months and and and…….
Flash back to this week and our visit to our GP. He is a great guy. He has seen me since I met my husband, handed me off to capable (sort-of, but that’s another story) OB-GYN’s and two babies later. He is ten years older than us, and grounded in sports medicine. He is wonderful. He is a comfortable GP based in West Vancouver with a practice in Yaletown. You get the picture.
When I first brought our issues to him, he was dismissive and textbook at best. He did his job, just didn’t listen. He put down A’s gastric issues to lactose, and told us to cut out milk. What he didn’t account for was THIS parent’s ability to go beyond the obvious and question the underlying stuff. WHY was he suddenly lactose intolerant? WHY was he so moody and pimply and grumpy and not HIM? This was not my child.
After two nights of midnight tummy troubles, I took A to our local clinic. We saw the on-call Doctor, and he looked at A and looked at me, and asked a bunch of questions, and ordered a bunch of tests.
Getting the tests back, my clinic Doctor looked at me and said “Dollars for doughnuts, this kid has Celiac disease, but we need to do further tests. I’m 99% certain. Now it’s up to your GP.”
Damn.
He was right. We pursued the diagnosis, went back to the GP, waited patiently for our endoscopy, got our positive endoscopy, and pursued a lifestyle we were suspect of all along.
Flash-forward to this week and our meeting with our GP. He had said that he wanted to follow us alongside the Pediatrician and monitor the GI clinic. Fine. Fair. I brought him the exhaustive blood test from the GI clinic. I explained that I was happy with his results, but that his iron and Vitamin D were a tad on the low side. I now knew how to read blood test results. I asked him if we needed to up his iron or D. I was concerned about his absorption rate.
And then he looked at me and offered what he could best do: an apology, of sorts.
He said: “You know, we aren’t trained to look for these sorts of things: we look at your symptoms and start from the beginning…” and petered off. He acknowledged that the Pediatrician was the best individual for the job (as he had clinic privileges at Children’s and a direct line to the GI clinic) and that he wanted to follow A in his journey, but that he was not necessarily equipped to handle it.
Now, I can accept his humanity. Now I can accept him with his inadequate diagnoses and lack of blood tests, and my frustration at me educating a health care provider. Now I can show him what to look for, and what to test for. Now I can sit by and accept his platitudes to my son about becoming an advocate for the cause in the face of educating the greater public.
Now.
We have this, this new lifestyle. We are in the 2.0 version of this auto-immune disease. We continue to educate family that this is not a “phase”, that he will not grow out of it like pimples or bad hair cuts or otherwise. That this is a life issue – not a choice, but a style.
Now.
I accept his apology, in all of it’s glaring inadequacies and inability to account for our voices.
Now.















