My son has just been diagnosed with Chrons desease. We are still doing tests to determine the severity and the kind exactly.
Can anyone give me any real life advice about how to deal with this and what to expect initially and down the road.Things i have read on the net are quite scary in regards to treatment and surgeries and side effects of the treatment😣.
I am also suffer from RA and his father has coriasis,extended family has many cases of auto immune disorders,so it isnt a surprise ,its just really devasting coz he is a child.
Any info will be much appreciated.