krbunn
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- Cathy and I are heading to Vanderbilt for more PLEX for me. We arrive on Monday to have the vas cath surgically inserted, then 5 days of inpatient plasma exchange.Here is a new video I did this afternoon.http://www.youtube.com/watch?v=TdF3KTRRx5E...
- I have some new post on my blog at http://krbunn.blogspot.com/ and some new videos on YouTube at http://www.youtube.com/user/drbunnThey deal with Myasthenia Gravis, Small Fiber Neuropathy Fasciculations, and Loss of Two Friends.--Kerry
- I have not posted much in a while, just some simple drive-by-posting. This is a great group and I enjoy being a part of it. You are all a blessing to me. Thanks for your prayers, support, and encouragement.Things are still gone fairly well for...
- I completed my 27th Plasma Exchange last week. I have a video at http://www.youtube.com/user/drbunn where I demonstrate the effectiveness of this last PLEX on my system. You may find it interesting.The video is entitled... 2012-02-08 Twenty-Seventh...
- My Myasthenia Gravis has worsened lately. I talked with the neurologist late last week and began the process of approval for additional plasma exchange. Everything is ready. I have the vascular catheter inserted in the morning (Tuesday). After that,...
- Today marks one full year out-of-work for me. I have several new posts on my blog that are too long to post here.I want to thank everyone for their prayers, support, and encouragement over the last year.--Kerryhtttp://krbunn.blogspot.com
- Have any of you had problems with cough medicine containing DM?I caused me real problems.--Kerry
- It was about this time last year that Cathy, myself, and my neurologist made the decision to take medical leave from my position as Senior Pastor of First Baptist Church of Ringgold GA in January of 2011. That medical leave would end with my...
- My SSA disability was approved this week. I applied in April, was turned down, filed an appeal and approved on appeal. The worsening breathing issues, chemotherapy, whole-body small fiber neuropathy, all the test, and extensive treatments with no...
- I emailed my neurologist at Vanderbilt on Tuesday about possibly doing another pulmonary workup at Vanderbilt because of my continued breathing difficulties. I have a good local pulmonologist, but there is value in having all tests and doctors at...
- The second Cytoxan infusion went well last Friday, October 7. No problems with side-effects. So far, the Cytoxan has been less problematic for me than IVIG or PLEX.Thanks for the prayers and support everyone!krbunnkrbunn.blogspot.com
- I start IV Cytoxan on September 9, 2011 at Vanderbilt for refractory Myasthenia Gravis and Small Fiber Neuropathy. I will be blogging about my experience at krbunn.blogspot.comThanks for all the prayers and support from this group!Kerry
- Just returned home from Vanderbilt and the Neurologist. The plasma exchange does not seem to be effective any longer . . . so I will not have any more plasma exchanges. Tomorrow's exchange is canceled. I had twenty-two exchanges in just a little...
- Does anyone else have voice problems?Does your voice problem sound similar to mine?My neuro said it does not sound typical for MG. Any thoughts?Check this video link for an example of my...
- About to have my 20th PLEX tomorrow. Will also be starting on a weekly PLEX schedule.Other information too long to share here. Those interested can go to my blog at http://krbunn.blogspot.comI also have a new video uploaded to...