Finalized in 2025, but there could be confusion…
My blog has been around for ages now and throughout postings folks will encounter my mentioning of my “ex” and of being divorced. I did not officially divorce until 2025, but in my heart and mind, we were divorced since our marriage ended after years of heartache. We did separate for years. Then the economy being what it was and still is, and my battle with ME/CFS, along with the needs of our three children converged as the most defining considerations. After reflecting on what outcomes we needed to nurture, we realized we needed to move back under the same roof in order to launch our children successfully. We literally were unable to legally divorce until 2025, but we gave each other room to pursue other relationships should the opportunities arise.
When we separated, we both felt confident my illness would still give me room to work and move us along to a finalized divorce before too long. However, confidence does not cure chronic illness and my health took a nose-dive the likes of which cornered me into working from the home and limited the time I could invest even in working from the home. I went through the cycles all ME/CFS folk go through where I would establish a fairly reliable baseline of possible activity and then life would pull the rug out from under me and leave me without a baseline, clinging to the couch for weeks or months at a stretch. Divorce became an elusive though sure outcome.
ME/CFS, and any chronic illness, catapults folks into challenging and nearly impossible life situations like the one I reference here where divorce is delayed for, gulp, two decades. If you have relatives or friends suffering serious chronic illness, be there for them. See them. Affirm their challenges and do what you can to help carry the burden. Know, too, that simply “going on disability” is not often an option and has been particularly challenging for ME/CFS folks since it has taken the medical community decades and decades to simply begin to acknowledge ME/CFS as a very real and non-psychogenetic illness. What does this mean? Note the words used here: Acknowledgement of legitimacy has begun and there are still far more uninformed physicians than informed. Medical neglect devastates many of the ME/CFS population and reaches into the legal work of seeking rightful financial relief. Those deciding whether or not ME/CFS is legit enough to warrant disability benefits are influenced by those who still suffer the terrible and often willful ignorance that leads to the abandonment of millions suffering with this real and debilitating disease. So, if the medical community still needs to catch up, the legal professionals deciding disability benefits will often not legitimize the need either. Then there’s the whole issue of whether or not spousal support from divorce will provide just enough financial support to block all possibility of receiving disability. The standards are galling. Navigating the possibilities exhausts and discourages the already weary, and is often weathered without help from friends or family. Be the exception if you’re able to be and roll up your sleeves in commitment to understand, bear witness and be with those sidelined by any chronic illness. The impact of ME/CFS is insidious and extensive, isolating and obstructing lives to the point of often complete alienation. Resolving divorce and income needs with such considerations is tricky work.
Meanwhile, should you be one of those who notes the strange and seeming inconsistency of my mentioning being divorced years and years ago, and then finally declaring our actual move to legally do so in 2025, you’ve likely scratched your head in confusion. You should understand why now. Life challenges can be surreal, and though divorce can take place often times before the actual legal act, legal marital dissolution is a powerful, needful spiritual and physical work. Don’t tread lightly into protracted separation. If you can avoid the limbo of not quite married/not quite divorced without wrecking the well-being and housing of those involved, do it. But plenty of people must continue to live under the same roof due to financial impossibilities. If you’re one of those unfortunately trapped, my heart is with you. Hang in there and get help in any way you’re able to do so.
