Guest guest Posted April 5, 2004 Report Share Posted April 5, 2004 Hi Krista, We're going through the same thing except that Asher (3) had his biopsy done in mid-January. I e-mailed at Dr. Shoffner's last week just to ask when I should expect the results (mid-April will be 12 weeks). She was very nice and told me that Asher's last lab test was being run on 4/8 and I should expect a report in 2-3 weeks following that. Her e-mail address is: jessicahicks@... Don't hesitate to e-mail her. They don't seem to mind at all. Anne R Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 5, 2004 Report Share Posted April 5, 2004 > Hi, my name is Krista I have a son who is five and we were told in > 2000 that he has CP and has abnormal white matter and two years ago > we found out that it is progressive and most of the damage was in the > cerebellum. That's when his nero told us that she thought it was > Mito. We did a muscle byopsy that summer in Grand Rapids MI(june of > 2002)and it took a year to get everything back. It told us nothing. > (it was frozen) The doc's then said that they were going to send > everything to Dr. Shoffner. We saw Dr.Shoffner in December and did > another muscle byopsy he told us that it would take 8 to 12 weeks for > the results from his muscle byopsy to come back. I'm sure you all > have felt the same way but it will be 13 weeks on the 17th of April > and I am checking the mail hoping to get something or when the phone > rings I hope that it might be his office wanting to make an appt to > come back and talk with him about the results. My question to any > body who wants to respond is, how long did you wait and how were you > contacted by Dr. Shoffner? Was it by phone, mail, or through your > local nero. Should I be calling by now to see how things are > progressing or should I wate? I really hope that it doesn't take > another year to get stuff back from the labs. He also wanted to look > into a couple of other degenerative disease. Is there anyone that > can help me with this? > > Thanks so much. > > Krista > Mother of Skyler (5) not yet diagnosed hi krista! my name is davonne and i have a 16month old daughter who just seen dr.shoffner on march 30,2004. he did not do a muscle biopsy, just a office visit. he didnt feel a muscle biopsy was needed because karlee has severe grey and white matter disease. she had a muscle biopsy here {knoxville,tn} on january 14 and it was sent to dr. shoffner frozen and i got her results from our neuro here on march 12, he said she has complex 1 and 4 defeciency. when we seen dr.shoffner last week he didnt feel like there would be any helpful treatment. then on this past friday he called and left a message on my machine that he wanted to do a fresh biopsy. so i feel like i am on a huge rollercoaster mentally and physically. i would call every day to see if the results were back. i wish you the best. i dont know much about this disease, i am trying to find out everything i can. good luck, davonne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 5, 2004 Report Share Posted April 5, 2004 > Hi, my name is Krista I have a son who is five and we were told in > 2000 that he has CP and has abnormal white matter and two years ago > we found out that it is progressive and most of the damage was in the > cerebellum. That's when his nero told us that she thought it was > Mito. We did a muscle byopsy that summer in Grand Rapids MI(june of > 2002)and it took a year to get everything back. It told us nothing. > (it was frozen) The doc's then said that they were going to send > everything to Dr. Shoffner. We saw Dr.Shoffner in December and did > another muscle byopsy he told us that it would take 8 to 12 weeks for > the results from his muscle byopsy to come back. I'm sure you all > have felt the same way but it will be 13 weeks on the 17th of April > and I am checking the mail hoping to get something or when the phone > rings I hope that it might be his office wanting to make an appt to > come back and talk with him about the results. My question to any > body who wants to respond is, how long did you wait and how were you > contacted by Dr. Shoffner? Was it by phone, mail, or through your > local nero. Should I be calling by now to see how things are > progressing or should I wate? I really hope that it doesn't take > another year to get stuff back from the labs. He also wanted to look > into a couple of other degenerative disease. Is there anyone that > can help me with this? > > Thanks so much. > > Krista > Mother of Skyler (5) not yet diagnosed hi krista! my name is davonne and i have a 16month old daughter who just seen dr.shoffner on march 30,2004. he did not do a muscle biopsy, just a office visit. he didnt feel a muscle biopsy was needed because karlee has severe grey and white matter disease. she had a muscle biopsy here {knoxville,tn} on january 14 and it was sent to dr. shoffner frozen and i got her results from our neuro here on march 12, he said she has complex 1 and 4 defeciency. when we seen dr.shoffner last week he didnt feel like there would be any helpful treatment. then on this past friday he called and left a message on my machine that he wanted to do a fresh biopsy. so i feel like i am on a huge rollercoaster mentally and physically. i would call every day to see if the results were back. i wish you the best. i dont know much about this disease, i am trying to find out everything i can. good luck, davonne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 7, 2004 Report Share Posted April 7, 2004 Hi, My younger son was first diagnosed with CP also. My two sons had muscles biopies on 12/18/2003 and we did not get a final response until March 25, 2003. It is hard to wait, but sometimes the muscle samples go out to several different labs.. Hang in there... Marie > Hi, my name is Krista I have a son who is five and we were told in > 2000 that he has CP and has abnormal white matter and two years ago > we found out that it is progressive and most of the damage was in the > cerebellum. That's when his nero told us that she thought it was > Mito. We did a muscle byopsy that summer in Grand Rapids MI(june of > 2002)and it took a year to get everything back. It told us nothing. > (it was frozen) The doc's then said that they were going to send > everything to Dr. Shoffner. We saw Dr.Shoffner in December and did > another muscle byopsy he told us that it would take 8 to 12 weeks for > the results from his muscle byopsy to come back. I'm sure you all > have felt the same way but it will be 13 weeks on the 17th of April > and I am checking the mail hoping to get something or when the phone > rings I hope that it might be his office wanting to make an appt to > come back and talk with him about the results. My question to any > body who wants to respond is, how long did you wait and how were you > contacted by Dr. Shoffner? Was it by phone, mail, or through your > local nero. Should I be calling by now to see how things are > progressing or should I wate? I really hope that it doesn't take > another year to get stuff back from the labs. He also wanted to look > into a couple of other degenerative disease. Is there anyone that > can help me with this? > > Thanks so much. > > Krista > Mother of Skyler (5) not yet diagnosed Quote Link to comment Share on other sites More sharing options...
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