be your own advocate. It’s going to take time to figure out what’s best for you, and you’ll have days where you don’t want to stick to the plan. Just know it’s okay to have some off days and don’t apply pressure to yourself to do more than you can.
One tip I would tell someone who has recently been diagnosed with HS is that if you have pain, to acknowledge it instead of putting it aside and ignoring it. If I could say anything to an HS Hero who is struggling, I would tell them that I know it is hard but to keep fighting and they will get through it just fine.
Telling people was the best thing I could have done. I have not had any negative reaction to having HS, and if someone I know did say something mean or negative to me about it, I would not keep in touch with them. Simple as that!
Healthy living has been the biggest factor in the treatment of my HS. I tried other medical routes (ie. anti-biotics, Humira, etc). It wasn’t until I saw a Naturopath and was tested for food sensitivities that I made some major life changes and noticed a difference in my HS!
get yourself referred to a Dermatologist who has experience treating HS. There are many more treatments available now compared to when I was first diagnosed and a Dermatologist can tell you about them. Have faith and work with them through this.