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Today I was feeling sorry for myself but I got over it; there is too much turmoil in this country to be feeling sorry for myself. I’m grateful for the things I still have and can do, even though I’m bedridden I still have my arms, hands and fingers I can still use. Now, enough about my current situation; I’m going to tell you what happened to me while I was in the hospital for almost 3 months. Last New Year’s Eve I was admitted into the hospital with a UTI infection and I was treated with Intravenous brain blood barrier Antibiotics for a week. Then in February I ended up with another UTI infection and was treated for a whole week with the intravenous blood brain barrier antibiotics. Again in March, I became incoherent and had seizures and was once again admitted into the hospital for a septic infection for three weeks this time. Once again they treated me with a brain blood barrier antibiotic. All in all before all of this, I was constantly suffering with spasticity, muscle spasms, re...
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Change the affect.

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I recently got my hair shaved! My MS has now made it impossible to brush my hair. I tell you, since, I never realized how much effort it took out of me for such a simple task and now it's amazing how much energy I have now that I don't have to deal with my hair. I'm bedridden now and it sucks. I still try to stay in tune with today's modern chic way of life. I'm only in my forties so I should maintain how I look even though I can't use my legs anymore. You ladies hear me right? Being overweight doesn't help either so you know I got to work harder to look good these days! Don't get me wrong, I'm not ashamed living large! BBW are everywhere and look great working what their mother gave them. Also, I've noticed that just making yourself look "pretty" makes you feel like getting outside and sharing your beauty! That's when I started selling AVON products from the comfort of my home. I can't go to the people so I bring them to me thr...
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Stabbing Pins & Needles

These past few weeks I've been dealing with such incredible pain along with annoyance.  Anyone who has MS and has dealt with "pins & needles" anywhere in their body know how annoying it is trying to get anything done while your limbs are being constantly attacked by stabs of pins & needles.  My neurologist says it's just a discomfort having pins & needles but I feel it incapacitates my normal way of living, it's not just a discomfort for me.  Given the fact that he gave me a prescription for Gabapentin to help soften the constant attacks, I've read that this medication is for people with epilepsy.  I wonder if taking this pill will cause more damage for me than good.  It's a shame how we must use only government approved prescribed drugs while the illegal naturally earth grown herbs, which actually have no deadly side effects, are banned from being used.  I have to say that while taking Gabapentin alone, it hasn't helped nor stopped the pai...
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