Guest guest Posted May 9, 2012 Report Share Posted May 9, 2012 Glen, I don't have any information to offer as far as symptoms go, but I just want to give you a standing ovation. Thank you for all your hard work. It would be a great honor to meet you someday (I think we live fairly nearby). > Hi everyone, > > I'm Glen B Schallman, new to the group and a 53 year survivor of PMG and a HYPOTHALAMIC HAMARTOMA which is inoperable....looks like I'm the oldest living survivor. do any of the children and young adults that have PMG experience the symptoms that I have??? tingling on right side of head/face, TIA's, numbness hands and feet, headaches, and chronic cough????? I live in the Seattle area and can be contacted at or cell . and by the way I am involved with the NBTS (NATIONAL BRAIN TUMOR SOCIETY), the ABTA (AMERICAN BRAIN TUMOR ASSOCIATION and HOPEFORHH.ORG . I for 6 days have been in Washington D.C. participation in the RACE FOR HOPE and have been on Capital Hill talking, advocating to congress about brain tumors, brain deformities, conditions (PMG) and I think they are going to start recognizing us all now!!! WOW!!!! gave them our site www.pmgawareness.org<http://www.pmgawareness.org/> so let us see what happen here on Capital Hill in the near future. I do travel the U.S. meeting brain tumor survivors for HOPEFORHH.ORG and would like to meet PMG survivors. plus I participate in the epilepsy walks, and brain tumor walks.. I am participating in 13 walks this year. you can follow me on facebook or email me at turtlebrain@... > > GLEN B SCHALLMAN > 53 YEAR SURVIVOR OF PMG and a HYPOTHALAMIC HAMARTOMA. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 9, 2012 Report Share Posted May 9, 2012 Glen, you are such an amazing person! We are so happy to have found you! Keep up the amazing work you are doing! From: polymicrogyria [mailto:polymicrogyria ] On Behalf Of Wilbur Sent: Wednesday, May 09, 2012 4:07 AM To: polymicrogyria Subject: Re: QUESTIONS FROM A 53 YEAR SURVIVOR???? Glen, I don't have any information to offer as far as symptoms go, but I just want to give you a standing ovation. Thank you for all your hard work. It would be a great honor to meet you someday (I think we live fairly nearby). On May 8, 2012, at 4:13 PM, " GLEN SCHALLMAN " <turtlebrain@... <mailto:turtlebrain%40msn.com> > wrote: > Hi everyone, > > I'm Glen B Schallman, new to the group and a 53 year survivor of PMG and a HYPOTHALAMIC HAMARTOMA which is inoperable....looks like I'm the oldest living survivor. do any of the children and young adults that have PMG experience the symptoms that I have??? tingling on right side of head/face, TIA's, numbness hands and feet, headaches, and chronic cough????? I live in the Seattle area and can be contacted at or cell . and by the way I am involved with the NBTS (NATIONAL BRAIN TUMOR SOCIETY), the ABTA (AMERICAN BRAIN TUMOR ASSOCIATION and HOPEFORHH.ORG . I for 6 days have been in Washington D.C. participation in the RACE FOR HOPE and have been on Capital Hill talking, advocating to congress about brain tumors, brain deformities, conditions (PMG) and I think they are going to start recognizing us all now!!! WOW!!!! gave them our site www.pmgawareness.org<http://www.pmgawareness.org/> so let us see what happen here on Capital Hill in the near future. I do travel the U.S. meeting brain tumor survivors for HOPEFORHH.ORG and would like to meet PMG survivors. plus I participate in the epilepsy walks, and brain tumor walks.. I am participating in 13 walks this year. you can follow me on facebook or email me at turtlebrain@... <mailto:turtlebrain%40msn.com> <mailto:turtlebrain@... <mailto:turtlebrain%40msn.com> > > > GLEN B SCHALLMAN > 53 YEAR SURVIVOR OF PMG and a HYPOTHALAMIC HAMARTOMA. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 10, 2012 Report Share Posted May 10, 2012 hey , where are you located? Re: QUESTIONS FROM A 53 YEAR SURVIVOR???? Glen, I don't have any information to offer as far as symptoms go, but I just want to give you a standing ovation. Thank you for all your hard work. It would be a great honor to meet you someday (I think we live fairly nearby). On May 8, 2012, at 4:13 PM, " GLEN SCHALLMAN " > wrote: > Hi everyone, > > I'm Glen B Schallman, new to the group and a 53 year survivor of PMG and a HYPOTHALAMIC HAMARTOMA which is inoperable....looks like I'm the oldest living survivor. do any of the children and young adults that have PMG experience the symptoms that I have??? tingling on right side of head/face, TIA's, numbness hands and feet, headaches, and chronic cough????? I live in the Seattle area and can be contacted at or cell . and by the way I am involved with the NBTS (NATIONAL BRAIN TUMOR SOCIETY), the ABTA (AMERICAN BRAIN TUMOR ASSOCIATION and HOPEFORHH.ORG . I for 6 days have been in Washington D.C. participation in the RACE FOR HOPE and have been on Capital Hill talking, advocating to congress about brain tumors, brain deformities, conditions (PMG) and I think they are going to start recognizing us all now!!! WOW!!!! gave them our site www.pmgawareness.org<http://www.pmgawareness.org/<http://www.pmgawareness.org/>> so let us see what happen here on Capital Hill in the near future. I do travel the U.S. meeting brain tumor survivors for HOPEFORHH.ORG and would like to meet PMG survivors. plus I participate in the epilepsy walks, and brain tumor walks.. I am participating in 13 walks this year. you can follow me on facebook or email me at turtlebrain@...<mailto:turtlebrain%40msn.com><mailto:turtlebrain@...<mai\ lto:turtlebrain%40msn.com>> > > GLEN B SCHALLMAN > 53 YEAR SURVIVOR OF PMG and a HYPOTHALAMIC HAMARTOMA. > > Quote Link to comment Share on other sites More sharing options...
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