Hope for Hannah

Hi! Thanks for visiting our Hope for Hannah page. As many of you know Hannah was diagnosed with POTS Syndrome more than two years ago and sick for two years before receiving her diagnosis. It has been a very hard, long four years for Hannah and her family. At this point, Hannah's symptoms are progressing and becoming more debilitating so we are looking to take further action as she has not found proper answers/solutions within the local medical field. There are a few options for Hannah, all are quite costly, minimum of $10,000. We know so many of you have been praying for Hannah and supporting her in many ways and thought this was an excellent opportunity for all who know and love her to show her our love and support in a greater way... help her get treatment! There are a few POTS treatment centers around the country who deal directly with the autonomic nervous system (the center/root of the problem). They are all finding good results through their treatment plans. Until now we have found that doctors locally are only prescribing medicine to treat the symptoms, but not looking to address the source. There is very little knowledge or research that has been done, so therefore very few answers. We feel good about sending Hannah to any one of these centers and hope you can partner with us in this! Thank you ahead of time for your love and support. Hannah is currently on several waiting lists, some are more than a 10 month wait, others a few months. We are hoping she will be moved up on the list and be able to get there sooner!