Guest guest Posted June 1, 2011 Report Share Posted June 1, 2011 Can you check with Dr. Gockel and see if she has arranged for any docs in the US to collect the samples? I have been in touch with her before and I know she was trying to arrange with Dr. Luketich, Patti and it seems someone else but I'm not aware it's done. That's my issue - I'm more than happy to 'donate' a swab of blood but it's the getting it to Germany part that's the hold up. Thanks for keeping us posted. for anyone considering the psychosocial survey - it only took me about 20 minutes - there's a few quirky translation things and a few questions about distance that are in km instead of miles - had to really think that one through!! Glad to know someone is doing something! ~ in NC > > Heres another good study going on. > Dear patient, > We are dedicated to research into the biological and environmental causes of achalasia, and would like to > invite you to take part in our scientific study, conducted by the University Hospital of Mainz, Germany. > For our molecular genetic investigation, only a small blood probe is necessary. Almost 400 patients have > participated already, and this will be the largest study on genetics in achalasia worldwide. We would be > very thankful, if you participate. Your contribution will be a large step to further characterize the etiology > of achalasia, which is still largely unknown. > Please find all information on the leaflet attached, and feel free to ask us further questions regarding the > study by e-mail: > achalasie@... > With kind regards, > Yours Sincerely > Ines Gockel, M.D > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 1, 2011 Report Share Posted June 1, 2011 I contacted the email address about the genetic study, I was advised there is no way to participate from the USA as of this time. They may include us in about a year. Quote Link to comment Share on other sites More sharing options...
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