Tuesday, August 18, 2009

Going to the MS Clinic Tuesday and More

I am going to the MS Clinic tomorrow (Tuesday) to talk to them about my needs not being met right now. Despite the amazing outpouring of support from several family members and friends on a daily basis, I am still overwhelmed and exhausted and they unable to keep up with what needs to be accomplished. I am hoping it is a productive meeting where I can get some additional help and support.

I also received an email from my state representative and they want to speak with me regarding some difficulties I have encountered receiving assistance with food stamps and Medicaid.

I still have a million things on my plate, many of which are long overdue and my energy level is zero, not to mention the pain, fevers, spasms etc. When I read the message boards from other patients talking about this disease being a "Monster" I know what they mean. I have no job, I have no assistance, I have no money, and I have less than zero energy.

I told my state representative that I would be advocating for those with MS ongoing. The challenges are many. My core body temperature continues to fluctuate around the clock, every day. It averages a 4 degree swing right now daily. Every day, slowly 4 degrees up, then 4 degrees down. It is like having the flu without the vomitng.

About My Blog

This is my personal blog. It details my own personal experiences with MS, as well as other ramblings about my life. I am NOT a medical professional and cannot offer advice or opinions of a medical nature. If you need medical atention, please contact a physician or, in emergencies, your nearest hospital emergency room. MS has many faces, and every single patient has his or her own unique experiences and challenges.

The links I provide are things I think may be of interest to those with MS or their friends and family for further research, and does not constitute an endorsement.