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This document serves as a disclaimer and informed consent for services provided by healers Magedelaine \'Sage\' Jessup and Elizabeth \'Willow\' Otto. It clarifies the nature of the healing services, their limitations, and the non-substitutive role of these services in relation to licensed medical treatment. Clients acknowledge understanding of the risks and agree to release healers from liability.
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01
Title the document clearly as 'Disclaimer and Informed Consent'.
02
Provide a brief introduction explaining the purpose of the document.
03
Clearly outline the risks involved in the activity or procedure.
04
Include a section detailing the rights of the participant.
05
Provide information about the benefits of participation.
06
Ensure there are sections for participant agreement and signature.
07
Include a statement confirming that the participant has had the opportunity to ask questions.
08
Date the document and obtain the necessary signatures.

Who needs disclaimer and informed consent?

01
Individuals participating in research studies.
02
Patients undergoing medical procedures.
03
Participants in clinical trials.
04
Clients receiving therapeutic services.
05
Users of software or online platforms requiring user consent.
06
Organizations providing services that involve inherent risks.
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A disclaimer is a statement that limits the liability of the party providing information. Informed consent is a process by which a participant is informed about the key facts regarding a procedure or intervention, allowing them to make an educated decision about their participation.
Researchers conducting studies involving human participants, medical professionals performing procedures, and any entity seeking to share information that may implicate liability are typically required to file disclaimers and obtain informed consent.
To fill out a disclaimer and informed consent form, ensure that all required information is accurate, including the purpose of the study, risks, benefits, and the participant’s rights. Sign and date the document where indicated and ensure the participant also signs to confirm understanding.
The purpose of a disclaimer is to protect the provider from legal liability, while informed consent aims to ensure that participants are fully informed about the risks and benefits of their involvement in a study or procedure, leading to ethical and voluntary participation.
The disclaimer and informed consent must include the purpose of the research, potential risks and benefits, confidentiality assurances, the right to withdraw, and contact information for questions or concerns.
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