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'''Externally Led Patient Focused Drug Development Meeting - Experiences from Groups''' 

*''Friedreich’s Ataxia Research Alliance''

FARA has hosted an ELPFDD as a stand alone meeting, held a reception the night prior and a board meeting following the ELPFDD.  FARA leadership felt the merit of the ELPFDD was important and sufficient to stand on its own.  A great deal of time and attention was given to identify appropriate panelists and in preparing panelists for their role in this meeting. Preparation was also provided to members of the audience who wished to make statements. The meeting was described by Ron Bartek as monumental in building relationships with the FDA and in providing insights about Friedreich's ataxia from the patient's perspective. The group hired a consultant.  Participation was not restricted to US residents. Anyone from anywhere was included. Many members of the community joined remotely. All responses provided via cell phone were tallied together and responses feedback to all regardless of whether the participant was attending the face-to-face meeting or joining online.

*''Genetic Alliance''

Genetic Alliance led ELPFDD for 3 diseases using the Platform for Engaging Everyone Responsibly (PEER) system. Some communities use PEER for registries, some for campaigns and some for trials.  The six disease groups (including three orgs representing sickle cell disease) developed videos and copy placed on GA portal. Tablets were used by volunteers in infusion clinics to get people’s preferences. These three groups were selected to be included in the first phase of the FDA Patient Focused Drug Development.  

*''Tuberous Sclerosis Alliance ''
Hosted a ELPFDD, see resources provided below.

*''Organic Acidemia Association'' and ''XLH Network'' are currently planning a ELPFDD meeting.

== Resources ==
[https://www.fda.gov/ForIndustry/UserFees/PrescriptionDrugUserFee/ucm453856.htm FDA]

[http://www.example.com link title]



Global Genes

https://globalgenes.org/fdaworkshop

Amyloidosis

http://www.arci.org/fda-page/

Myotonic Dystrophy

http://www.myotonic.org/developing-therapies-brain-related-dm-symptoms-add-your-voice

Acute Porphyrias

http://www.porphyriafoundation.com/content/fda-meeting-acute-porphyrias-march-1st-0

Osteoarthritis

https://www.arthritis.org/Documents/Sections/Advocate/Regulatory-Letters/AF-Comments-FDA-PDUFA-VI-Comittment-Letter.pdf

Spinal Muscular Atrophy

http://www.curesma.org/news/sma-voice-of-the-patient.html?referrer=https://www.google.com/

Friedreich's Ataxia (FA)

http://www.curefa.org/pdf/research/CoverPage-VOP-Report.pdf

http://www.curefa.org/news/friedreich-s-ataxia-voice-of-the-patient-report

Tuberous Sclerosis 

http://www.tsalliance.org/individuals-families/patient-focused-drug-development/

CG3, National Kidney Foundation

https://www.kidney.org/sites/default/files/C3G-PFDD-Agenda_FINAL.pdf

Lupus

https://lupuspfdd.org/

Hyperhidrosis

https://www.sweathelp.org/taking-action/patient-focused-drug-development.html