Guest guest Posted August 16, 2005 Report Share Posted August 16, 2005 Just a reminder to people about Dr. Dobbs genetic study. He is getting very close to finding this gene but he just needs more participants in the study. Especially people with multiple affected family members. He had a lot of good preliminary contacts with people from the group but not very many people have followed through with actually getting their blood drawn and sending it to him. If any of you guys have made inital contact with him but are missing information that you need to get this done, please let me know. You can email me directly at jagrindon@... Also, please, anyone who is new, or who wants more information about this, please contact me. I would also like to get some feedback from anyone who has actually been in touch with him, like if you have received sufficient information, if they are keeping in contact with you and if you have actually been able to participate etc. thanks, allison Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 16, 2005 Report Share Posted August 16, 2005 Just a reminder to people about Dr. Dobbs genetic study. He is getting very close to finding this gene but he just needs more participants in the study. Especially people with multiple affected family members. He had a lot of good preliminary contacts with people from the group but not very many people have followed through with actually getting their blood drawn and sending it to him. If any of you guys have made inital contact with him but are missing information that you need to get this done, please let me know. You can email me directly at jagrindon@... Also, please, anyone who is new, or who wants more information about this, please contact me. I would also like to get some feedback from anyone who has actually been in touch with him, like if you have received sufficient information, if they are keeping in contact with you and if you have actually been able to participate etc. thanks, allison Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 17, 2005 Report Share Posted August 17, 2005 I had said I'd be more than happy to help out, but never heard back from anybody. Let me know what I need to do - and we'll for sure do it. FYI - Zach is the only known person in either family to be born with clubfoot. Holly Zachary 7/27/02 Right C/F Treated by Dr. Ponseti DBB Nights Only > Just a reminder to people about Dr. Dobbs genetic study. He is > getting very close to finding this gene but he just needs more > participants in the study. Especially people with multiple affected > family members. He had a lot of good preliminary contacts with people > from the group but not very many people have followed through with > actually getting their blood drawn and sending it to him. If any of > you guys have made inital contact with him but are missing information > that you need to get this done, please let me know. You can email me > directly at jagrindon@y... Also, please, anyone who is new, or > who wants more information about this, please contact me. > > I would also like to get some feedback from anyone who has actually > been in touch with him, like if you have received sufficient > information, if they are keeping in contact with you and if you have > actually been able to participate etc. > > thanks, > allison Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 17, 2005 Report Share Posted August 17, 2005 I had said I'd be more than happy to help out, but never heard back from anybody. Let me know what I need to do - and we'll for sure do it. FYI - Zach is the only known person in either family to be born with clubfoot. Holly Zachary 7/27/02 Right C/F Treated by Dr. Ponseti DBB Nights Only > Just a reminder to people about Dr. Dobbs genetic study. He is > getting very close to finding this gene but he just needs more > participants in the study. Especially people with multiple affected > family members. He had a lot of good preliminary contacts with people > from the group but not very many people have followed through with > actually getting their blood drawn and sending it to him. If any of > you guys have made inital contact with him but are missing information > that you need to get this done, please let me know. You can email me > directly at jagrindon@y... Also, please, anyone who is new, or > who wants more information about this, please contact me. > > I would also like to get some feedback from anyone who has actually > been in touch with him, like if you have received sufficient > information, if they are keeping in contact with you and if you have > actually been able to participate etc. > > thanks, > allison Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 17, 2005 Report Share Posted August 17, 2005 Holly, Thanks for the feedback, right now he is solely needing families with 2 or more affected members. They are getting so close to pinpointing the gene, it is really more and more important to get families with multiple instances to participate. I do appreciate your interest and I'm sure Dr. Dobbs does as well, I am sorry that no one got back with you. It is interesting to note that in a lot of cases when people start doing a little digging, they find that there is an uncle or cousin or someone else who also had clubfoot but for some reason it was just not common knowledge in the family; or even that the person's family never had a definite diagnosis. These are the cases that could lead to this breakthrough! So...if anyone has any inclination to start talking to family members, calling hospitals, etc. to find out if that one cousin who " used to wear those little turned out shoes on a bar " actually had clubfoot -- please do, Dr. Dobbs would really be appreciative. Thanks, > > Just a reminder to people about Dr. Dobbs genetic study. He is > > getting very close to finding this gene but he just needs more > > participants in the study. Especially people with multiple > affected > > family members. He had a lot of good preliminary contacts with > people > > from the group but not very many people have followed through with > > actually getting their blood drawn and sending it to him. If any > of > > you guys have made inital contact with him but are missing > information > > that you need to get this done, please let me know. You can email > me > > directly at jagrindon@y... Also, please, anyone who is new, or > > who wants more information about this, please contact me. > > > > I would also like to get some feedback from anyone who has actually > > been in touch with him, like if you have received sufficient > > information, if they are keeping in contact with you and if you > have > > actually been able to participate etc. > > > > thanks, > > allison Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 17, 2005 Report Share Posted August 17, 2005 Holly, Thanks for the feedback, right now he is solely needing families with 2 or more affected members. They are getting so close to pinpointing the gene, it is really more and more important to get families with multiple instances to participate. I do appreciate your interest and I'm sure Dr. Dobbs does as well, I am sorry that no one got back with you. It is interesting to note that in a lot of cases when people start doing a little digging, they find that there is an uncle or cousin or someone else who also had clubfoot but for some reason it was just not common knowledge in the family; or even that the person's family never had a definite diagnosis. These are the cases that could lead to this breakthrough! So...if anyone has any inclination to start talking to family members, calling hospitals, etc. to find out if that one cousin who " used to wear those little turned out shoes on a bar " actually had clubfoot -- please do, Dr. Dobbs would really be appreciative. Thanks, > > Just a reminder to people about Dr. Dobbs genetic study. He is > > getting very close to finding this gene but he just needs more > > participants in the study. Especially people with multiple > affected > > family members. He had a lot of good preliminary contacts with > people > > from the group but not very many people have followed through with > > actually getting their blood drawn and sending it to him. If any > of > > you guys have made inital contact with him but are missing > information > > that you need to get this done, please let me know. You can email > me > > directly at jagrindon@y... Also, please, anyone who is new, or > > who wants more information about this, please contact me. > > > > I would also like to get some feedback from anyone who has actually > > been in touch with him, like if you have received sufficient > > information, if they are keeping in contact with you and if you > have > > actually been able to participate etc. > > > > thanks, > > allison Quote Link to comment Share on other sites More sharing options...
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