TwitchyGambler
Well-known member
So today I was doing a training at a school and I saw my cousin. She is my dad's first cousin and my second. To give you a little background on those who don't know me my dad was diagnosed with BFS by Dr. Rivner in 1994 (he's duly noted in the ALS community and on all the major ALS sites)( at the ALS clinic in Georgia. I was told mine was probably Fibromyalgia but my neuro did say my twitches were benign. My neuro asked me if I had any Cherokee in my family and I said yes my great grandmother was straight off the Natalahalia Reservation. He said then that I inherited this from her. He said people of the Cherokee descent have lots of twitching and other sensory issues. So anyway I kind of walked up to my cousin and said so I know this is strange but we have the same grandmother and I was wondering if you have twitching. She looked at me funny and I told her what was going on and to my suprise my cousin - her sister is having a lot of the same issues that I am. She twitches a lot and sometimes she passes out right after she has a twitching spell. My cousin gave me her number and i am going to call her tomorrow. My cousin also informed me that her sister is going to the Cleveland CLinic December 15th. I have heard some of you mention that clinic on here. THen my cousin told me her daughter complains a lot about twitching and it really annoys her. Her daughter is 22 and I am sure has never googled her symptoms. She said that Jacq has complained for the last couple of years about annoying twitching. I thought how odd. This makes 5 of us that have this issue. I wish we could pinpoint this issue. I know its BFS to some degree but its really so much more. Not saying its deadly or debilitating but its something else with it. Wondering how many of you have BFS in your family?