jdbgrowing
Member
I posted this on the MMMA site and didn't get much of a response.
I am newly appointed primary caregiver for 1 patient. I am not currently a patient myself, but plan to apply in the near future. I will be taking new patients over the next couple months. While I understand that due to the nature of this process the entire community continues to fall into areas of gray. With that said I have a few questions I hope to get answered here.
1) What documentation, if any, do you require your patients to sign if they designate you as their primary caregiver? I was looking at this more from a safety standpoint. If I have a patient that does not take their 2.5 ounces of usable meds and they put me in an overage situation time after time can I remove them as a patient? Would a document signed at the beginning of the relationship stating that either of us can "opt out" of the relationship at any time with appropriate notice be acceptable? If anyone has a template for this would you be willing to share it?
2) I plan to log each patients plants, their strains, a log of when and how much medicine they were given. They will get bags or pill bottles with a label showing their name, patient id #, amount enclosed and a not for resale statement listed on each package. Should I consider anything else here?
3) What, if anything, is listed in the laws about caregivers "testing" meds for quality? This is a serious question and I could not really find any information on the topic. This is a case where I am not a patient yet?
4) Has anyone informed DTE that they are registered caregiver to avoid questions about increased usage? I have read that DTE has a policy where you can inform them you are a registered caregiver to avoid any potential "red flagging" issues.
Thank you in advance for any help!
JD
I am newly appointed primary caregiver for 1 patient. I am not currently a patient myself, but plan to apply in the near future. I will be taking new patients over the next couple months. While I understand that due to the nature of this process the entire community continues to fall into areas of gray. With that said I have a few questions I hope to get answered here.
1) What documentation, if any, do you require your patients to sign if they designate you as their primary caregiver? I was looking at this more from a safety standpoint. If I have a patient that does not take their 2.5 ounces of usable meds and they put me in an overage situation time after time can I remove them as a patient? Would a document signed at the beginning of the relationship stating that either of us can "opt out" of the relationship at any time with appropriate notice be acceptable? If anyone has a template for this would you be willing to share it?
2) I plan to log each patients plants, their strains, a log of when and how much medicine they were given. They will get bags or pill bottles with a label showing their name, patient id #, amount enclosed and a not for resale statement listed on each package. Should I consider anything else here?
3) What, if anything, is listed in the laws about caregivers "testing" meds for quality? This is a serious question and I could not really find any information on the topic. This is a case where I am not a patient yet?
4) Has anyone informed DTE that they are registered caregiver to avoid questions about increased usage? I have read that DTE has a policy where you can inform them you are a registered caregiver to avoid any potential "red flagging" issues.
Thank you in advance for any help!
JD