eightball776
Well known member
Gosh, @eightball776! You are describing my life! It is all so overwhelming. I guess the journey that most of the TMS programs teach— learning to love ourselves and be patient with ourselves—is one of our challenges. Motivation is really hard when I focus on my failures. I get super sluggish. All hope goes out the window. But when I get in that magic zone of enjoying the present moment with no judgement, I get peace. It’s such a relief to feel it, even briefly. All things are possible. We have to believe it. Nurture the hope.
Most of us do focus on the negative. Hell, everyone does, some are just better at hiding it. I do feel like my TMS is especially stubborn because unlike my back pain years ago that could actually come & go, when all of this garbage lights a fire under the Crohn's, almost nothing can stop it. The additional "no hope" part comes from waiting to be healthy to do X, until the waiting turns into years. The "just do it" eventually became no longer possible, in part at times due to to my TMS's favorite one, the "enteropathic arhritis" (really just means inflammatory arthritis from Crohn's). A large % of CD patients also have joint pain everywhere during flares, or anytime. Prednisone stops it cold (before it turns you into a monster & breaks your bones - always wonder what % of TMS patients see relief from corticosteroids), and certain TNF something or others from biologic meds. It's not a surprise that chronically ill may have a much larger % of depression than other folks (it does).
I only describe it here to go back to the chicken or egg..another mind-f**k of real pathology, tissue damage, lost bone density....Then the autoimmune process & especially the meds for it, whack out your hormones & all of the muck we're talking about floats into & takes up residence in the conscious mind, essentially paralyzing it, and that "all or nothing" mentality becomes a lot more of nothing. Over the years I've been much more harmed by the treatment than the disease. It was the Prednisone that stunted my growth & made me insecure which led to other failures.
Then gratitude is what we're supposed to practice. I should have a ton of it. I have 2 friends dying - one at stage 4 lung cancer, the other ALS. I talk to them & they both show empathy for ME, and I just feel like an ass for my lack of gratitude. When we ruminate on all of our failures & spend all of our time in the past - it's easy to see why, the past was so much better than the present - we can't stay present, which we must. Even look at the future once in a while... but like every time travel movie, if you stay in the past too long you get stuck there.
Another time I was in a bad rut, I felt hope about my ability to change a situation (hated my job), once I started working on my MS, I felt a lot better. Of course in hindsight it was a huge waste of time & had no effect except another $40k in debt). That's the way out of the hamster wheel though, starting to do the things we CAN control, while stopping the worrying or lamenting what we can. Oh, and accept that it can't all be fixed in a day, which gets A LOT harder to do the older we get. This was probably more for my therapist. I just can't afford one.