Guest guest Posted May 24, 2010 Report Share Posted May 24, 2010 ISOP needs your help. ISOP found out last wk. that we are now responsible for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET) to the U.S. This was not the original plan as we were hoping to have more help from the CO Hospital…Unfortunately, the hospital is brand new and hasn’t even opened its doors yet….They were not expecting this last minute opportunity (once WI. cancelled) and do not have the funds for business class airfare in their budget. This last minute monkey wrench has put ISOP approx. $3000 short for airfare cost and this will probably be Dr. M’s last ET Tutorial. This CO. conf is essential in helping children on the west coast….The region needing properly ET trained docs the most! ISOP cant let $ be the downfall of this conf.! We only need $3000 to help more children on the west coast……Which will in turn help children everywhere. Can anyone out there help? ISOP will take anything you can spare $10, $20, $50, $100, $1000! Remember, all donations are tax deductible and are going straight towards airfare…. Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure to give sponsorship credit to the parents on this group. Lets show the medical community exactly what Parent Demand is! If you have any ideas on how to help ISOP make this happen, please call me direct. Thanks gang! HRH (303) 507 2485 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 24, 2010 Report Share Posted May 24, 2010 and Everyone, I know everybody is strapped for money these days, we all feel it, but we will donate what we can! It all adds up! Dr. Mehta's hands on, vast wealth of experience and knowledge is SO precious, and we would have been lost without her and ISOP!!! She is now in her 80's, right? This is crucial to get her here, at least this one last time! Does ISOP get all of the money through the Facebook causes donations? If not, please let me know, and we won't use it, we'll mail a check directly. I am trying to think of fundraising ideas, too. Bexon and we are eternally grateful to Min Mehta. Heidi, Bexon's Mommy, (2 and a half years old, in 7th cast from Salt Lake City Shriners, currently down from 62 degrees to 19.7 in cast) From: Hyatt <heather@...>infantile scoliosis treatment Sent: Mon, May 24, 2010 9:13:22 AMSubject: ALL CAST Members ISOP needs your help. ISOP found out last wk. that we are now responsible for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET) to the U.S. This was not the original plan as we were hoping to have more help from the CO Hospital…Unfortunately, the hospital is brand new and hasn’t even opened its doors yet….They were not expecting this last minute opportunity (once WI. cancelled) and do not have the funds for business class airfare in their budget. This last minute monkey wrench has put ISOP approx. $3000 short for airfare cost and this will probably be Dr. M’s last ET Tutorial. This CO. conf is essential in helping children on the west coast….The region needing properly ET trained docs the most! ISOP cant let $ be the downfall of this conf.! We only need $3000 to help more children on the west coast……Which will in turn help children everywhere. Can anyone out there help? ISOP will take anything you can spare $10, $20, $50, $100, $1000! Remember, all donations are tax deductible and are going straight towards airfare…. Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure to give sponsorship credit to the parents on this group. Lets show the medical community exactly what Parent Demand is! If you have any ideas on how to help ISOP make this happen, please call me direct. Thanks gang! HRH (303) 507 2485 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 24, 2010 Report Share Posted May 24, 2010 Where can I mail a check to. Together with any amount we can make this happen!Amy J Sent from my Verizon Wireless BlackBerryFrom: NIck Guthe <nickguthe@...>Date: Mon, 24 May 2010 10:44:36 -0700 (PDT)<infantile scoliosis treatment >Subject: Re: ALL CAST Members and Everyone, I know everybody is strapped for money these days, we all feel it, but we will donate what we can! It all adds up! Dr. Mehta's hands on, vast wealth of experience and knowledge is SO precious, and we would have been lost without her and ISOP!!! She is now in her 80's, right? This is crucial to get her here, at least this one last time! Does ISOP get all of the money through the Facebook causes donations? If not, please let me know, and we won't use it, we'll mail a check directly. I am trying to think of fundraising ideas, too. Bexon and we are eternally grateful to Min Mehta. Heidi, Bexon's Mommy, (2 and a half years old, in 7th cast from Salt Lake City Shriners, currently down from 62 degrees to 19.7 in cast) From: Hyatt <heatherinfantilescoliosis (DOT) org>infantile scoliosis treatment Sent: Mon, May 24, 2010 9:13:22 AMSubject: ALL CAST Members ISOP needs your help. ISOP found out last wk. that we are now responsible for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET) to the U.S. This was not the original plan as we were hoping to have more help from the CO Hospital…Unfortunately, the hospital is brand new and hasn’t even opened its doors yet….They were not expecting this last minute opportunity (once WI. cancelled) and do not have the funds for business class airfare in their budget. This last minute monkey wrench has put ISOP approx. $3000 short for airfare cost and this will probably be Dr. M’s last ET Tutorial. This CO. conf is essential in helping children on the west coast….The region needing properly ET trained docs the most! ISOP cant let $ be the downfall of this conf.! We only need $3000 to help more children on the west coast……Which will in turn help children everywhere. Can anyone out there help? ISOP will take anything you can spare $10, $20, $50, $100, $1000! Remember, all donations are tax deductible and are going straight towards airfare…. Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure to give sponsorship credit to the parents on this group. Lets show the medical community exactly what Parent Demand is! If you have any ideas on how to help ISOP make this happen, please call me direct.Thanks gang!HRH(303) 507 2485 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 24, 2010 Report Share Posted May 24, 2010 We are absolutely here to help you out ! We have decided to hold a lemonade stand in the center of town during the annual Memorial Day Town Wide Tag Sale, this Saturday. Cole and I went and got a slot donated for Saturday from 9-4. We built a Lemonade Stand (super easy), and bought some lemonade, brownie mix, cups and napkins. We are going to try to replicate this again during weekly concerts in the park and I will try to solicit donations for these products. If you want to see what we did and how we did it check out our website http://web.me.com/jennifer.leggett/Site/Coles_Lemonade_Stand.html (I know it is blank now but I will post stuff when Cole goes down for a nap at 3:00 EST). I hope we can raise some money to help out ISOP! Jenn Mommy to Cole, 2.5 years old, 1st brace from Rochester, 2 degrees laying down out of brace, down from 47, after 10 months and 5 casts. > > ISOP needs your help. ISOP found out last wk. that we are now responsible > for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET) > to the U.S. This was not the original plan as we were hoping to have more > help from the CO Hospital.Unfortunately, the hospital is brand new and > hasn't even opened its doors yet..They were not expecting this last minute > opportunity (once WI. cancelled) and do not have the funds for business > class airfare in their budget. This last minute monkey wrench has put ISOP > approx. $3000 short for airfare cost and this will probably be Dr. M's last > ET Tutorial. This CO. conf is essential in helping children on the west > coast..The region needing properly ET trained docs the most! ISOP cant let > $ be the downfall of this conf.! We only need $3000 to help more children > on the west coast..Which will in turn help children everywhere. > > Can anyone out there help? ISOP will take anything you can spare $10, $20, > $50, $100, $1000! Remember, all donations are tax deductible and are going > straight towards airfare.. > > Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure > to give sponsorship credit to the parents on this group. Lets show the > medical community exactly what Parent Demand is! > > If you have any ideas on how to help ISOP make this happen, please call me > direct. > > Thanks gang! > > HRH > > (303) 507 2485 > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 24, 2010 Report Share Posted May 24, 2010 Yeah….Jenn u da’bomb! This is fab!!! What a great idea..I was thinking we could all forward the link to Coles youtube piece to everyone we know, as well….You did such an amazing job and the video actually states that ISOP needs to raise funds for Junes ET Tutorials! Can you forward the link to CAST again for anyone willing to forward to friends/family…(?) It’s a great awareness tool and may actually help us to raise the funds we need! Thank you. HRH From: infantile scoliosis treatment [mailto:infantile scoliosis treatment ] On Behalf Of genericallyloud Sent: Monday, May 24, 2010 12:03 PM infantile scoliosis treatment Subject: Re: ALL CAST Members We are absolutely here to help you out ! We have decided to hold a lemonade stand in the center of town during the annual Memorial Day Town Wide Tag Sale, this Saturday. Cole and I went and got a slot donated for Saturday from 9-4. We built a Lemonade Stand (super easy), and bought some lemonade, brownie mix, cups and napkins. We are going to try to replicate this again during weekly concerts in the park and I will try to solicit donations for these products. If you want to see what we did and how we did it check out our website http://web.me.com/jennifer.leggett/Site/Coles_Lemonade_Stand.html (I know it is blank now but I will post stuff when Cole goes down for a nap at 3:00 EST). I hope we can raise some money to help out ISOP! Jenn Mommy to Cole, 2.5 years old, 1st brace from Rochester, 2 degrees laying down out of brace, down from 47, after 10 months and 5 casts. > > ISOP needs your help. ISOP found out last wk. that we are now responsible > for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET) > to the U.S. This was not the original plan as we were hoping to have more > help from the CO Hospital.Unfortunately, the hospital is brand new and > hasn't even opened its doors yet..They were not expecting this last minute > opportunity (once WI. cancelled) and do not have the funds for business > class airfare in their budget. This last minute monkey wrench has put ISOP > approx. $3000 short for airfare cost and this will probably be Dr. M's last > ET Tutorial. This CO. conf is essential in helping children on the west > coast..The region needing properly ET trained docs the most! ISOP cant let > $ be the downfall of this conf.! We only need $3000 to help more children > on the west coast..Which will in turn help children everywhere. > > Can anyone out there help? ISOP will take anything you can spare $10, $20, > $50, $100, $1000! Remember, all donations are tax deductible and are going > straight towards airfare.. > > Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure > to give sponsorship credit to the parents on this group. Lets show the > medical community exactly what Parent Demand is! > > If you have any ideas on how to help ISOP make this happen, please call me > direct. > > Thanks gang! > > HRH > > (303) 507 2485 > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 24, 2010 Report Share Posted May 24, 2010 Heidi, You are so good with writing stuff up why don't you make up an email we can all forward to family and friends Including the mailing address to mail in a check. If you have any free time. You just have a way with words. , I will get something in the mail this week. When is all this needed by? TashaMommy of 5 year old twin boys- and Fort Worth, Texas is treated at Texas ish Rite Hospital in Dallas, TexasSeries of 6 casts for 14 months followed by bracing since September 2007You can read 's story at.... http://www.infantilescoliosis.org/stories.html From: NIck Guthe <nickguthe@...>infantile scoliosis treatment Sent: Mon, May 24, 2010 12:44:36 PMSubject: Re: ALL CAST Members and Everyone, I know everybody is strapped for money these days, we all feel it, but we will donate what we can! It all adds up! Dr. Mehta's hands on, vast wealth of experience and knowledge is SO precious, and we would have been lost without her and ISOP!!! She is now in her 80's, right? This is crucial to get her here, at least this one last time! Does ISOP get all of the money through the Facebook causes donations? If not, please let me know, and we won't use it, we'll mail a check directly. I am trying to think of fundraising ideas, too. Bexon and we are eternally grateful to Min Mehta. Heidi, Bexon's Mommy, (2 and a half years old, in 7th cast from Salt Lake City Shriners, currently down from 62 degrees to 19.7 in cast) From: Hyatt <heather@infantilesc oliosis.org>infantile scoliosis treatment @groups. comSent: Mon, May 24, 2010 9:13:22 AMSubject: [infantile_scoliosi s] ALL CAST Members ISOP needs your help. ISOP found out last wk. that we are now responsible for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET) to the U.S. This was not the original plan as we were hoping to have more help from the CO Hospital…Unfortunately, the hospital is brand new and hasn’t even opened its doors yet….They were not expecting this last minute opportunity (once WI. cancelled) and do not have the funds for business class airfare in their budget. This last minute monkey wrench has put ISOP approx. $3000 short for airfare cost and this will probably be Dr. M’s last ET Tutorial. This CO. conf is essential in helping children on the west coast….The region needing properly ET trained docs the most! ISOP cant let $ be the downfall of this conf.! We only need $3000 to help more children on the west coast……Which will in turn help children everywhere. Can anyone out there help? ISOP will take anything you can spare $10, $20, $50, $100, $1000! Remember, all donations are tax deductible and are going straight towards airfare…. Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure to give sponsorship credit to the parents on this group. Lets show the medical community exactly what Parent Demand is! If you have any ideas on how to help ISOP make this happen, please call me direct. Thanks gang! HRH (303) 507 2485 Reply to sender | Reply to group | Reply via web post | Start a New Topic Messages in this topic (2) Recent Activity: New Photos 1 Visit Your Group MARKETPLACE Stay on top of your group activity without leaving the page you're on - Get the Toolbar now. Get great advice about dogs and cats. Visit the Dog & Cat Answers Center. Get real-time World Cup coverage on the Toolbar. Download now to win a signed team jersey! Switch to: Text-Only, Daily Digest • Unsubscribe • Terms of Use .. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 24, 2010 Report Share Posted May 24, 2010 Jenn, What a great idea! I didn't read your email all the way through and went to see the stand. I'll check back later. Good luck....hope you guys do great! TashaMommy of 5 year old twin boys- and Fort Worth, Texas is treated at Texas ish Rite Hospital in Dallas, TexasSeries of 6 casts for 14 months followed by bracing since September 2007You can read 's story at.... http://www.infantilescoliosis.org/stories.html From: genericallyloud <jennifer.leggett@...>infantile scoliosis treatment Sent: Mon, May 24, 2010 1:03:01 PMSubject: Re: ALL CAST Members We are absolutely here to help you out ! We have decided to hold a lemonade stand in the center of town during the annual Memorial Day Town Wide Tag Sale, this Saturday. Cole and I went and got a slot donated for Saturday from 9-4. We built a Lemonade Stand (super easy), and bought some lemonade, brownie mix, cups and napkins. We are going to try to replicate this again during weekly concerts in the park and I will try to solicit donations for these products. If you want to see what we did and how we did it check out our website http://web.me.com/jennifer.leggett/Site/Coles_Lemonade_Stand.html (I know it is blank now but I will post stuff when Cole goes down for a nap at 3:00 EST). I hope we can raise some money to help out ISOP!Jenn Mommy to Cole, 2.5 years old, 1st brace from Rochester, 2 degrees laying down out of brace, down from 47, after 10 months and 5 casts.>> ISOP needs your help. ISOP found out last wk. that we are now responsible> for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET)> to the U.S. This was not the original plan as we were hoping to have more> help from the CO Hospital.Unfortunately, the hospital is brand new and> hasn't even opened its doors yet..They were not expecting this last minute> opportunity (once WI. cancelled) and do not have the funds for business> class airfare in their budget. This last minute monkey wrench has put ISOP> approx. $3000 short for airfare cost and this will probably be Dr. M's last> ET Tutorial. This CO. conf is essential in helping children on the west> coast..The region needing properly ET trained docs the most! ISOP cant let> $ be the downfall of this conf.! We only need $3000 to help more children> on the west coast..Which will in turn help children everywhere. > > Can anyone out there help? ISOP will take anything you can spare $10, $20,> $50, $100, $1000! Remember, all donations are tax deductible and are going> straight towards airfare.. > > Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure> to give sponsorship credit to the parents on this group. Lets show the> medical community exactly what Parent Demand is! > > If you have any ideas on how to help ISOP make this happen, please call me> direct.> > Thanks gang!> > HRH> > (303) 507 2485> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 24, 2010 Report Share Posted May 24, 2010 You're so sweet, Tasha- I'd love to! I'll write something and post it. I am also thinking I might haul some stuff I don't use anyomore to the second hand trendy store and see what I can get for it. Worth a try! Heidi, Bexon's Mommy, (2 and a half years old, in 7th cast from Salt Lake City Shriners, currently down from 62 degrees to 19.7 in cast) From: Tasha Fontenot <ryanswalk@...>infantile scoliosis treatment Sent: Mon, May 24, 2010 11:41:29 AMSubject: Re: ALL CAST Members Heidi, You are so good with writing stuff up why don't you make up an email we can all forward to family and friends Including the mailing address to mail in a check. If you have any free time. You just have a way with words. , I will get something in the mail this week. When is all this needed by? TashaMommy of 5 year old twin boys- and Fort Worth, Texas is treated at Texas ish Rite Hospital in Dallas, TexasSeries of 6 casts for 14 months followed by bracing since September 2007You can read 's story at.... http://www.infantil escoliosis. org/stories. html From: NIck Guthe <nickguthe (DOT) com>infantile scoliosis treatment @groups. comSent: Mon, May 24, 2010 12:44:36 PMSubject: Re: [infantile_scoliosi s] ALL CAST Members and Everyone, I know everybody is strapped for money these days, we all feel it, but we will donate what we can! It all adds up! Dr. Mehta's hands on, vast wealth of experience and knowledge is SO precious, and we would have been lost without her and ISOP!!! She is now in her 80's, right? This is crucial to get her here, at least this one last time! Does ISOP get all of the money through the Facebook causes donations? If not, please let me know, and we won't use it, we'll mail a check directly. I am trying to think of fundraising ideas, too. Bexon and we are eternally grateful to Min Mehta. Heidi, Bexon's Mommy, (2 and a half years old, in 7th cast from Salt Lake City Shriners, currently down from 62 degrees to 19.7 in cast) From: Hyatt <heather@infantilesc oliosis.org>infantile scoliosis treatment @groups. comSent: Mon, May 24, 2010 9:13:22 AMSubject: [infantile_scoliosi s] ALL CAST Members ISOP needs your help. ISOP found out last wk. that we are now responsible for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET) to the U.S. This was not the original plan as we were hoping to have more help from the CO Hospital…Unfortunately, the hospital is brand new and hasn’t even opened its doors yet….They were not expecting this last minute opportunity (once WI. cancelled) and do not have the funds for business class airfare in their budget. This last minute monkey wrench has put ISOP approx. $3000 short for airfare cost and this will probably be Dr. M’s last ET Tutorial. This CO. conf is essential in helping children on the west coast….The region needing properly ET trained docs the most! ISOP cant let $ be the downfall of this conf.! We only need $3000 to help more children on the west coast……Which will in turn help children everywhere. Can anyone out there help? ISOP will take anything you can spare $10, $20, $50, $100, $1000! Remember, all donations are tax deductible and are going straight towards airfare…. Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure to give sponsorship credit to the parents on this group. Lets show the medical community exactly what Parent Demand is! If you have any ideas on how to help ISOP make this happen, please call me direct. Thanks gang! HRH (303) 507 2485 Reply to sender | Reply to group | Reply via web post | Start a New Topic Messages in this topic (2) Recent Activity: New Photos 1 Visit Your Group MARKETPLACE Stay on top of your group activity without leaving the page you're on - Get the Toolbar now. Get great advice about dogs and cats. Visit the Dog & Cat Answers Center. Get real-time World Cup coverage on the Toolbar. Download now to win a signed team jersey! Switch to: Text-Only, Daily Digest • Unsubscribe • Terms of Use .. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 24, 2010 Report Share Posted May 24, 2010 That is a great idea Heidi. With money tight for us right now too, I may sell some stuff as well. I will help in any way I can. Thanks for the idea. Joanmom to Hayden 339 degrees down from 62After 4 casts, now in a brace 23 hours/dayTreated at ish Rite Hospital Dallas, TX From: NIck Guthe <nickguthe@...>infantile scoliosis treatment Sent: Mon, May 24, 2010 2:03:37 PMSubject: Re: ALL CAST Members You're so sweet, Tasha- I'd love to! I'll write something and post it. I am also thinking I might haul some stuff I don't use anyomore to the second hand trendy store and see what I can get for it. Worth a try! Heidi, Bexon's Mommy, (2 and a half years old, in 7th cast from Salt Lake City Shriners, currently down from 62 degrees to 19.7 in cast) From: Tasha Fontenot <ryanswalk (DOT) com>infantile scoliosis treatment @groups. comSent: Mon, May 24, 2010 11:41:29 AMSubject: Re: [infantile_scoliosi s] ALL CAST Members Heidi, You are so good with writing stuff up why don't you make up an email we can all forward to family and friends Including the mailing address to mail in a check. If you have any free time. You just have a way with words. , I will get something in the mail this week. When is all this needed by? TashaMommy of 5 year old twin boys- and Fort Worth, Texas is treated at Texas ish Rite Hospital in Dallas, TexasSeries of 6 casts for 14 months followed by bracing since September 2007You can read 's story at.... http://www.infantil escoliosis. org/stories. html From: NIck Guthe <nickguthe (DOT) com>infantile scoliosis treatment @groups. comSent: Mon, May 24, 2010 12:44:36 PMSubject: Re: [infantile_scoliosi s] ALL CAST Members and Everyone, I know everybody is strapped for money these days, we all feel it, but we will donate what we can! It all adds up! Dr. Mehta's hands on, vast wealth of experience and knowledge is SO precious, and we would have been lost without her and ISOP!!! She is now in her 80's, right? This is crucial to get her here, at least this one last time! Does ISOP get all of the money through the Facebook causes donations? If not, please let me know, and we won't use it, we'll mail a check directly. I am trying to think of fundraising ideas, too. Bexon and we are eternally grateful to Min Mehta. Heidi, Bexon's Mommy, (2 and a half years old, in 7th cast from Salt Lake City Shriners, currently down from 62 degrees to 19.7 in cast) From: Hyatt <heather@infantilesc oliosis.org>infantile scoliosis treatment @groups. comSent: Mon, May 24, 2010 9:13:22 AMSubject: [infantile_scoliosi s] ALL CAST Members ISOP needs your help. ISOP found out last wk. that we are now responsible for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET) to the U.S. This was not the original plan as we were hoping to have more help from the CO Hospital…Unfortunately, the hospital is brand new and hasn’t even opened its doors yet….They were not expecting this last minute opportunity (once WI. cancelled) and do not have the funds for business class airfare in their budget. This last minute monkey wrench has put ISOP approx. $3000 short for airfare cost and this will probably be Dr. M’s last ET Tutorial. This CO. conf is essential in helping children on the west coast….The region needing properly ET trained docs the most! ISOP cant let $ be the downfall of this conf.! We only need $3000 to help more children on the west coast……Which will in turn help children everywhere. Can anyone out there help? ISOP will take anything you can spare $10, $20, $50, $100, $1000! Remember, all donations are tax deductible and are going straight towards airfare…. Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure to give sponsorship credit to the parents on this group. Lets show the medical community exactly what Parent Demand is! If you have any ideas on how to help ISOP make this happen, please call me direct. Thanks gang! HRH (303) 507 2485 Reply to sender | Reply to group | Reply via web post | Start a New Topic Messages in this topic (2) Recent Activity: New Photos 1 Visit Your Group MARKETPLACE Stay on top of your group activity without leaving the page you're on - Get the Toolbar now. Get great advice about dogs and cats. Visit the Dog & Cat Answers Center. Get real-time World Cup coverage on the Toolbar. Download now to win a signed team jersey! Switch to: Text-Only, Daily Digest • Unsubscribe • Terms of Use .. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 24, 2010 Report Share Posted May 24, 2010 Ok I have the website up about how we are doing out lemonade stand. I am still finishing up the stand and will update the pictures when It is complete. http://web.me.com/jennifer.leggett/Site/Coles_Lemonade_Stand.html Also here is the youtube video our family made. Any questions, just let us know! Jenn Mommy to Cole, 2.5 years old, 1st brace from Rochester, 2 degrees laying down out of brace, down from 47, after 10 months and 5 casts. > > Heidi, > You are so good with writing stuff up why don't you make up an email we can all forward to family and friends > Including the mailing address to mail in a check. If you have any free time. You just have a way with words. > > , I will get something in the mail this week. When is all this needed by? >  Tasha > Mommy of 5 year old twin boys- and > Fort Worth, Texas > is treated at Texas ish Rite Hospital in Dallas, Texas > Series of 6 casts for 14 months followed by bracing since September 2007 > You can read 's story at.... http://www.infantilescoliosis.org/stories.html > > > > > > > > > ________________________________ > From: NIck Guthe <nickguthe@...> > infantile scoliosis treatment > Sent: Mon, May 24, 2010 12:44:36 PM > Subject: Re: ALL CAST Members > >  > > and Everyone, > > I know everybody is strapped for money these days, we all feel it, but we will donate what we can! It all adds up! Dr. Mehta's hands on, vast wealth of experience and knowledge is SO precious, and we would have been lost without her and ISOP!!! She is now in her 80's, right? This is crucial to get her here, at least this one last time! > > Does ISOP get all of the money through the Facebook causes donations? If not, please let me know, and we won't use it, we'll mail a check directly. > > I am trying to think of fundraising ideas, too. Bexon and we are eternally grateful to Min Mehta. > Heidi, Bexon's Mommy, (2 and a half years old, in 7th cast from Salt Lake City Shriners, currently down from 62 degrees to 19.7 in cast) > > > > > ________________________________ > From: Hyatt <heather@infantilesc oliosis.org> > infantile scoliosis treatment @groups. com > Sent: Mon, May 24, 2010 9:13:22 AM > Subject: [infantile_scoliosi s] ALL CAST Members > >  > ISOP needs your help. ISOP found out last wk. that we are now responsible for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET) to the U.S. This was not the original plan as we were hoping to have more help from the CO Hospital…Unfortunately, the hospital is brand new and hasn’t even opened its doors yet….They were not expecting this last minute opportunity (once WI. cancelled) and do not have the funds for business class airfare in their budget. This last minute monkey wrench has put ISOP approx. $3000 short for airfare cost and this will probably be Dr. M’s last ET Tutorial. This CO. conf is essential in helping children on the west coast….The region needing properly ET trained docs the most! ISOP cant let $ be the downfall of this conf.! We only need $3000 to help more children on the west coast……Which will in turn help children everywhere. > Can anyone out there help? ISOP will take anything you can spare $10, $20, $50, $100, $1000! Remember, all donations are tax deductible and are going straight towards airfare…. > Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure to give sponsorship credit to the parents on this group. Lets show the medical community exactly what Parent Demand is! > If you have any ideas on how to help ISOP make this happen, please call me direct. > Thanks gang! > HRH > (303) 507 2485 > > > Reply to sender | Reply to group | Reply via web post | Start a New Topic Messages in this topic (2) > Recent Activity: * New Photos 1 > Visit Your Group > MARKETPLACE > Stay on top of your group activity without leaving the page you're on - Get the Toolbar now. > > ________________________________ > > Get great advice about dogs and cats. Visit the Dog & Cat Answers Center. > > ________________________________ > > Get real-time World Cup coverage on the Toolbar. Download now to win a signed team jersey! > > Switch to: Text-Only, Daily Digest • Unsubscribe • Terms of Use > . > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 25, 2010 Report Share Posted May 25, 2010 You might want to see if members have air miles they can donate. We are no help as we have chase Disney miles... Unless Min wants to go to Disney. It takes 25000 Amex miles for a round trip ticket in most cases. Sent from my iPhoneOn May 24, 2010, at 11:13 AM, " Hyatt" <heather@...> wrote: ISOP needs your help. ISOP found out last wk. that we are now responsible for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET) to the U.S. This was not the original plan as we were hoping to have more help from the CO Hospital…Unfortunately, the hospital is brand new and hasn’t even opened its doors yet….They were not expecting this last minute opportunity (once WI. cancelled) and do not have the funds for business class airfare in their budget. This last minute monkey wrench has put ISOP approx. $3000 short for airfare cost and this will probably be Dr. M’s last ET Tutorial. This CO. conf is essential in helping children on the west coast….The region needing properly ET trained docs the most! ISOP cant let $ be the downfall of this conf.! We only need $3000 to help more children on the west coast……Which will in turn help children everywhere. Can anyone out there help? ISOP will take anything you can spare $10, $20, $50, $100, $1000! Remember, all donations are tax deductible and are going straight towards airfare…. Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure to give sponsorship credit to the parents on this group. Lets show the medical community exactly what Parent Demand is! If you have any ideas on how to help ISOP make this happen, please call me direct. Thanks gang! HRH (303) 507 2485 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 25, 2010 Report Share Posted May 25, 2010 Jenn, Just checked out the pics, boy, that is SO cute! Who could resist an adorable boy in a brace and his cute pregnant Mommy? If you could bottle your energy, I would buy a few cups! : ) Let us know how it goes! Heidi, Bexon's Mommy, (2 and a half years old, in 7th cast from Salt Lake City Shriners, currently down from 62 degrees to 19.7 in cast) From: genericallyloud <jennifer.leggett@...>infantile scoliosis treatment Sent: Mon, May 24, 2010 1:23:00 PMSubject: Re: ALL CAST Members Ok I have the website up about how we are doing out lemonade stand. I am still finishing up the stand and will update the pictures when It is complete. http://web.me.com/jennifer.leggett/Site/Coles_Lemonade_Stand.htmlAlso here is the youtube video our family made. http://www.youtube.com/watch?v=VrRXvehD4-sAny questions, just let us know!JennMommy to Cole, 2.5 years old, 1st brace from Rochester, 2 degrees laying down out of brace, down from 47, after 10 months and 5 casts.>> Heidi, > You are so good with writing stuff up why don't you make up an email we can all forward to family and friends > Including the mailing address to mail in a check. If you have any free time. You just have a way with words.> > , I will get something in the mail this week. When is all this needed by?>  Tasha> Mommy of 5 year old twin boys- and > Fort Worth, Texas> is treated at Texas ish Rite Hospital in Dallas, Texas> Series of 6 casts for 14 months followed by bracing since September 2007> You can read 's story at.... http://www.infantilescoliosis.org/stories.html> > > > > > > > > ________________________________> From: NIck Guthe <nickguthe@...>> infantile scoliosis treatment > Sent: Mon, May 24, 2010 12:44:36 PM> Subject: Re: ALL CAST Members> >  > > and Everyone,> > I know everybody is strapped for money these days, we all feel it, but we will donate what we can! It all adds up! Dr. Mehta's hands on, vast wealth of experience and knowledge is SO precious, and we would have been lost without her and ISOP!!! She is now in her 80's, right? This is crucial to get her here, at least this one last time!> > Does ISOP get all of the money through the Facebook causes donations? If not, please let me know, and we won't use it, we'll mail a check directly.> > I am trying to think of fundraising ideas, too. Bexon and we are eternally grateful to Min Mehta.> Heidi, Bexon's Mommy, (2 and a half years old, in 7th cast from Salt Lake City Shriners, currently down from 62 degrees to 19.7 in cast) > > > > > ________________________________> From: Hyatt <heather@infantilesc oliosis.org>> infantile scoliosis treatment @groups. com> Sent: Mon, May 24, 2010 9:13:22 AM> Subject: [infantile_scoliosi s] ALL CAST Members> >  > ISOP needs your help. ISOP found out last wk. that we are now responsible for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET) to the U.S. This was not the original plan as we were hoping to have more help from the CO Hospital…Unfortunately, the hospital is brand new and hasn’t even opened its doors yet….They were not expecting this last minute opportunity (once WI. cancelled) and do not have the funds for business class airfare in their budget. This last minute monkey wrench has put ISOP approx. $3000 short for airfare cost and this will probably be Dr. M’s last ET Tutorial. This CO. conf is essential in helping children on the west coast….The region needing properly ET trained docs the most! ISOP cant let $ be the downfall of this conf.! We only need $3000 to help more children on the west coast……Which will in turn help children everywhere. > Can anyone out there help? ISOP will take anything you can spare $10, $20, $50, $100, $1000! Remember, all donations are tax deductible and are going straight towards airfare…. > Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure to give sponsorship credit to the parents on this group. Lets show the medical community exactly what Parent Demand is! > If you have any ideas on how to help ISOP make this happen, please call me direct.> Thanks gang!> HRH> (303) 507 2485> > > Reply to sender | Reply to group | Reply via web post | Start a New Topic Messages in this topic (2) > Recent Activity: * New Photos 1 > Visit Your Group > MARKETPLACE> Stay on top of your group activity without leaving the page you're on - Get the Toolbar now.> > ________________________________> > Get great advice about dogs and cats. Visit the Dog & Cat Answers Center.> > ________________________________> > Get real-time World Cup coverage on the Toolbar. Download now to win a signed team jersey!> > Switch to: Text-Only, Daily Digest • Unsubscribe • Terms of Use> .> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 25, 2010 Report Share Posted May 25, 2010 , Just saw this and we will send whatever we can. We need her here! Chad And Catie <chadandcatie@...> wrote: >You might want to see if members have air miles they can donate. We are no help as we have chase Disney miles... Unless Min wants to go to Disney. It takes 25000 Amex miles for a round trip ticket in most cases. > >Sent from my iPhone > >On May 24, 2010, at 11:13 AM, " Hyatt " <heather@...> wrote: > >ISOP needs your help. ISOP found out last wk. that we are now responsible for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET) to the U.S. This was not the original plan as we were hoping to have more help from the CO Hospital…Unfortunately, the hospital is brand new and hasn’t even opened its doors yet….They were not expecting this last minute opportunity (once WI. cancelled) and do not have the funds for business class airfare in their budget. This last minute monkey wrench has put ISOP approx. $3000 short for airfare cost and this will probably be Dr. M’s last ET Tutorial. This CO. conf is essential in helping children on the west coast….The region needing properly ET trained docs the most! ISOP cant let $ be the downfall of this conf.! We only need $3000 to help more children on the west coast……Which will in turn help children everywhere. > >Can anyone out there help? ISOP will take anything you can spare $10, $20, $50, $100, $1000! Remember, all donations are tax deductible and are going straight towards airfare…. > >Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure to give sponsorship credit to the parents on this group. Lets show the medical community exactly what Parent Demand is! > >If you have any ideas on how to help ISOP make this happen, please call me direct. > >Thanks gang! > >HRH > >(303) 507 2485 > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 25, 2010 Report Share Posted May 25, 2010 , Just saw this and we will send whatever we can. We need her here! Chad And Catie <chadandcatie@...> wrote: >You might want to see if members have air miles they can donate. We are no help as we have chase Disney miles... Unless Min wants to go to Disney. It takes 25000 Amex miles for a round trip ticket in most cases. > >Sent from my iPhone > >On May 24, 2010, at 11:13 AM, " Hyatt " <heather@...> wrote: > >ISOP needs your help. ISOP found out last wk. that we are now responsible for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET) to the U.S. This was not the original plan as we were hoping to have more help from the CO Hospital…Unfortunately, the hospital is brand new and hasn’t even opened its doors yet….They were not expecting this last minute opportunity (once WI. cancelled) and do not have the funds for business class airfare in their budget. This last minute monkey wrench has put ISOP approx. $3000 short for airfare cost and this will probably be Dr. M’s last ET Tutorial. This CO. conf is essential in helping children on the west coast….The region needing properly ET trained docs the most! ISOP cant let $ be the downfall of this conf.! We only need $3000 to help more children on the west coast……Which will in turn help children everywhere. > >Can anyone out there help? ISOP will take anything you can spare $10, $20, $50, $100, $1000! Remember, all donations are tax deductible and are going straight towards airfare…. > >Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure to give sponsorship credit to the parents on this group. Lets show the medical community exactly what Parent Demand is! > >If you have any ideas on how to help ISOP make this happen, please call me direct. > >Thanks gang! > >HRH > >(303) 507 2485 > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 25, 2010 Report Share Posted May 25, 2010 Just some more ideas... June is National Scoliosis Awareness Month. Last June I sold ISOP bracelets as a fundraiser. This year we're holding a garage sale June 3-5 with a portion of the proceeds benefiting ISOP. ~Noah 4 1/2 years old9 months of casting in SLC; Currently on 2 years of bracing at 6* in braceAnd Mariella 15 months old - resolved Infantile Scoliosis infantile scoliosis treatment From: jennifer.leggett@...Date: Mon, 24 May 2010 18:03:01 +0000Subject: Re: ALL CAST Members We are absolutely here to help you out ! We have decided to hold a lemonade stand in the center of town during the annual Memorial Day Town Wide Tag Sale, this Saturday. Cole and I went and got a slot donated for Saturday from 9-4. We built a Lemonade Stand (super easy), and bought some lemonade, brownie mix, cups and napkins. We are going to try to replicate this again during weekly concerts in the park and I will try to solicit donations for these products. If you want to see what we did and how we did it check out our website http://web.me.com/jennifer.leggett/Site/Coles_Lemonade_Stand.html (I know it is blank now but I will post stuff when Cole goes down for a nap at 3:00 EST). I hope we can raise some money to help out ISOP!Jenn Mommy to Cole, 2.5 years old, 1st brace from Rochester, 2 degrees laying down out of brace, down from 47, after 10 months and 5 casts.>> ISOP needs your help. ISOP found out last wk. that we are now responsible> for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET)> to the U.S. This was not the original plan as we were hoping to have more> help from the CO Hospital.Unfortunately, the hospital is brand new and> hasn't even opened its doors yet..They were not expecting this last minute> opportunity (once WI. cancelled) and do not have the funds for business> class airfare in their budget. This last minute monkey wrench has put ISOP> approx. $3000 short for airfare cost and this will probably be Dr. M's last> ET Tutorial. This CO. conf is essential in helping children on the west> coast..The region needing properly ET trained docs the most! ISOP cant let> $ be the downfall of this conf.! We only need $3000 to help more children> on the west coast..Which will in turn help children everywhere. > > Can anyone out there help? ISOP will take anything you can spare $10, $20,> $50, $100, $1000! Remember, all donations are tax deductible and are going> straight towards airfare.. > > Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure> to give sponsorship credit to the parents on this group. Lets show the> medical community exactly what Parent Demand is! > > If you have any ideas on how to help ISOP make this happen, please call me> direct.> > Thanks gang!> > HRH> > (303) 507 2485> The New Busy is not the too busy. Combine all your e-mail accounts with Hotmail. Get busy. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 25, 2010 Report Share Posted May 25, 2010 Ide buy a case of Jenns energy....and I hope its contagious! HRH > Jenn, > > Just checked out the pics, boy, that is SO cute! Who could resist an > adorable boy in a brace and his cute pregnant Mommy? If you could bottle > your energy, I would buy a few cups! : ) Let us know how it goes! >  Heidi, Bexon's Mommy, (2 and a half years old, in 7th cast from Salt > Lake City Shriners, currently down from 62 degrees to 19.7 in cast) > > > > > ________________________________ > From: genericallyloud <jennifer.leggett@...> > infantile scoliosis treatment > Sent: Mon, May 24, 2010 1:23:00 PM > Subject: Re: ALL CAST Members > >  > Ok I have the website up about how we are doing out lemonade stand. I am > still finishing up the stand and will update the pictures when It is > complete. > http://web.me.com/jennifer.leggett/Site/Coles_Lemonade_Stand.html > > Also here is the youtube video our family made. > > > Any questions, just let us know! > > Jenn > Mommy to Cole, 2.5 years old, 1st brace from Rochester, 2 degrees laying > down out of brace, down from 47, after 10 months and 5 casts. > > >> >> Heidi, >> You are so good with writing stuff up why don't you make up an email we >> can all forward to family and friends >> Including the mailing address to mail in a check. If you have any >> free time. You just have a way with words. >> >> , I will get something in the mail this week. When is all >> this needed by? >>  Tasha >> Mommy of 5 year old twin boys- and >> Fort Worth, Texas >> is treated at Texas ish Rite Hospital in Dallas, Texas >> Series of 6 casts for 14 months followed by bracing since September 2007 >> You can read 's story at.... >> http://www.infantilescoliosis.org/stories.html >> >> >> >> >> >> >> >> >> ________________________________ >> From: NIck Guthe <nickguthe@...> >> infantile scoliosis treatment >> Sent: Mon, May 24, 2010 12:44:36 PM >> Subject: Re: ALL CAST Members >> >>  >> >> and Everyone, >> >> I know everybody is strapped for money these days, we all feel it, but >> we will donate what we can! It all adds up! Dr. Mehta's hands on, >> vast wealth of experience and knowledge is SO precious, and we >> would have been lost without her and ISOP!!! She is now in her 80's, >> right? This is crucial to get her here, at least this one last time! >> >> Does ISOP get all of the money through the Facebook causes donations? If >> not, please let me know, and we won't use it, we'll mail a check >> directly. >> >> I am trying to think of fundraising ideas, too. Bexon and we are >> eternally grateful to Min Mehta. >> Heidi, Bexon's Mommy, (2 and a half years old, in 7th cast from Salt >> Lake City Shriners, currently down from 62 degrees to 19.7 in cast) >> >> >> >> >> ________________________________ >> From: Hyatt <heather@infantilesc oliosis.org> >> infantile scoliosis treatment @groups. com >> Sent: Mon, May 24, 2010 9:13:22 AM >> Subject: [infantile_scoliosi s] ALL CAST Members >> >>  >> ISOP needs your help. ISOP found out last wk. that we are now >> responsible for 2/3 of the business class airfare cost to fly Dr. M (the >> pioneer of ET) to the U.S. This was not the original plan as we were >> hoping to have more help from the CO Hospital…Unfortunately, the >> hospital is brand new and hasn’t even opened its doors >> yet….They were not expecting this last minute opportunity (once >> WI. cancelled) and do not have the funds for business class airfare in >> their budget. This last minute monkey wrench has put ISOP approx. >> $3000 short for airfare cost and this will probably be Dr. M’s >> last ET Tutorial. This CO. conf is essential in helping children on >> the west coast….The region needing properly ET trained docs the >> most! ISOP cant let $ be the downfall of this conf.! We only >> need $3000 to help more children on the west coast……Which >> will in turn help children everywhere. >> Can anyone out there help? ISOP will take anything you can spare >> $10, $20, $50, $100, $1000! Remember, all donations are tax >> deductible and are going straight towards airfare…. >> Lets mobilize the CAST Support Group to raise this $ and ISOP will be >> sure to give sponsorship credit to the parents on this group. Lets >> show the medical community exactly what Parent Demand is! >> If you have any ideas on how to help ISOP make this happen, please call >> me direct. >> Thanks gang! >> HRH >> (303) 507 2485 >> >> >> Reply to sender | Reply to group | Reply via web post | Start a New >> Topic Messages in this topic (2) >> Recent Activity: * New Photos 1 >> Visit Your Group >> MARKETPLACE >> Stay on top of your group activity without leaving the page you're on - >> Get the Toolbar now. >> >> ________________________________ >> >> Get great advice about dogs and cats. Visit the Dog & Cat Answers >> Center. >> >> ________________________________ >> >> Get real-time World Cup coverage on the Toolbar. Download now to >> win a signed team jersey! >> >> Switch to: Text-Only, Daily Digest • Unsubscribe • Terms of >> Use >> . >> > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 25, 2010 Report Share Posted May 25, 2010 Thanks for posting this, ... I completely forgot that June is National Scoli Awareness month! I wonder how we may capitalize on this to raise more $? My wheels are a turnin....And, thank you for doing this! HRH > Just some more ideas... > > > > June is National Scoliosis Awareness Month. Last June I sold ISOP > bracelets as a fundraiser. This year we're holding a garage sale June 3-5 > with a portion of the proceeds benefiting ISOP. > > > > ~ > Noah 4 1/2 years old > 9 months of casting in SLC; Currently on 2 years of bracing at 6* in brace > And Mariella 15 months old - resolved Infantile Scoliosis > > > > > > > infantile scoliosis treatment > From: jennifer.leggett@... > Date: Mon, 24 May 2010 18:03:01 +0000 > Subject: Re: ALL CAST Members > > > > > > We are absolutely here to help you out ! > > We have decided to hold a lemonade stand in the center of town during the > annual Memorial Day Town Wide Tag Sale, this Saturday. Cole and I went and > got a slot donated for Saturday from 9-4. We built a Lemonade Stand (super > easy), and bought some lemonade, brownie mix, cups and napkins. We are > going to try to replicate this again during weekly concerts in the park > and I will try to solicit donations for these products. > > If you want to see what we did and how we did it check out our website > http://web.me.com/jennifer.leggett/Site/Coles_Lemonade_Stand.html (I know > it is blank now but I will post stuff when Cole goes down for a nap at > 3:00 EST). > > I hope we can raise some money to help out ISOP! > > Jenn > Mommy to Cole, 2.5 years old, 1st brace from Rochester, 2 degrees laying > down out of brace, down from 47, after 10 months and 5 casts. > > >> >> ISOP needs your help. ISOP found out last wk. that we are now >> responsible >> for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of >> ET) >> to the U.S. This was not the original plan as we were hoping to have >> more >> help from the CO Hospital.Unfortunately, the hospital is brand new and >> hasn't even opened its doors yet..They were not expecting this last >> minute >> opportunity (once WI. cancelled) and do not have the funds for business >> class airfare in their budget. This last minute monkey wrench has put >> ISOP >> approx. $3000 short for airfare cost and this will probably be Dr. M's >> last >> ET Tutorial. This CO. conf is essential in helping children on the west >> coast..The region needing properly ET trained docs the most! ISOP cant >> let >> $ be the downfall of this conf.! We only need $3000 to help more >> children >> on the west coast..Which will in turn help children everywhere. >> >> Can anyone out there help? ISOP will take anything you can spare $10, >> $20, >> $50, $100, $1000! Remember, all donations are tax deductible and are >> going >> straight towards airfare.. >> >> Lets mobilize the CAST Support Group to raise this $ and ISOP will be >> sure >> to give sponsorship credit to the parents on this group. Lets show the >> medical community exactly what Parent Demand is! >> >> If you have any ideas on how to help ISOP make this happen, please call >> me >> direct. >> >> Thanks gang! >> >> HRH >> >> (303) 507 2485 >> > > > > > > _________________________________________________________________ > The New Busy is not the too busy. Combine all your e-mail accounts with > Hotmail. > http://www.windowslive.com/campaign/thenewbusy?tile=multiaccount & ocid=PID28326::\ T:WLMTAGL:ON:WL:en-US:WM_HMP:042010_4 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 26, 2010 Report Share Posted May 26, 2010 , Count me in. Money is tight here (where ISN'T is tight, rigth?) but I will send you something. I also have some experience fundraising and working on various projects for Shriners, so let's chat soon and perhaps some of these ideas would also work for ISOP :-) Just this past February, we held a Chinese Auction that raised over $3,500 for the local transportation unit that drives kids to their appointments at the hospital. It was a lot of work, but it was also a lot of fun. > > ISOP needs your help. ISOP found out last wk. that we are now responsible > for 2/3 of the business class airfare cost to fly Dr. M (the pioneer of ET) > to the U.S. This was not the original plan as we were hoping to have more > help from the CO Hospital.Unfortunately, the hospital is brand new and > hasn't even opened its doors yet..They were not expecting this last minute > opportunity (once WI. cancelled) and do not have the funds for business > class airfare in their budget. This last minute monkey wrench has put ISOP > approx. $3000 short for airfare cost and this will probably be Dr. M's last > ET Tutorial. This CO. conf is essential in helping children on the west > coast..The region needing properly ET trained docs the most! ISOP cant let > $ be the downfall of this conf.! We only need $3000 to help more children > on the west coast..Which will in turn help children everywhere. > > Can anyone out there help? ISOP will take anything you can spare $10, $20, > $50, $100, $1000! Remember, all donations are tax deductible and are going > straight towards airfare.. > > Lets mobilize the CAST Support Group to raise this $ and ISOP will be sure > to give sponsorship credit to the parents on this group. Lets show the > medical community exactly what Parent Demand is! > > If you have any ideas on how to help ISOP make this happen, please call me > direct. > > Thanks gang! > > HRH > > (303) 507 2485 > Quote Link to comment Share on other sites More sharing options...
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