Fibronaut At Home

It’s 2 o’clock in the morning…

…or TMI and Vampires continued.

I’m reading a very steamy anthology titled “12 Shades of Surrender”.  My hubby is very happy about this.  Let me explain how this works.  I read something naughty and he actually gets to enjoy the reason he “bought the cow” in the first place.  The mood struck, I couldn’t get my muscles or my mind to shut off, so I went for it.

I only have myself to blame this time for my sex-induced insomnia.  Thankfully, I’m now embracing my fibro-vampirism ( says that vampirism is a word.  Google Chrome’s spell-check can suck it!).  I let the three-year-old stay up late tonight so she should sleep in which will allow me to sleep in.  Theoretically.  I may have just jinxed this theory by writing about it.  My older two are don’t have school tomorrow, so they will be at my beck-and-call tomorrow.  Double jinx!  Dammit!

If you have fibro and you aren’t taking advantage of your insomnia to blog or launch a stealth-sex-attack on your partner, what is the point?  If you are going to be awake in the middle of the night anyway, why not do something productive?  As long as you stay away from sharp objects and heavy machinery, you are good!

Fibro-vampires unite!


Advice Please

I’m still waiting to hear on my disability appeal.  According to the disability company, they have reached out to my doctor and he hasn’t responded and according to my doctor’s office, they haven’t heard anything.  I just don’t know what to do.  We have no money and going to this doctor is already problematic because he is so far away.  My hubby drives me to my Mom the night before appointment, which is 3 hours round-trip and then my Mom takes me to my appointment and drives me home with is another 3 hours round-trip for her.  I just don’t know if it is worth it to continue seeing this doctor.  What to do?  I’m pretty close to just finding another doctor but with the appeal process being an ongoing thing I don’t want to chance them denying me again while I’m in between appointments.  That is what started this whole mess.  Also, the doctor I’m seeing now charges $50.00 any time he has to fill out disability paperwork, which is not in our budget at all and would be a monthly expense if I was re-approved.  The thing I really like about him is that he thinks outside-the-box in regards to this illness and has helped me more than any other doctor I’ve seen.  Ugh.  I hate this.



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