I wanted to share this with everyone and ask for your support.

As you know I am very passionate about my health, and advocating for adrenal insufficiency.

I was recently approached by RARE PATIENT VOICE. RPV brings the gap between patients and researchers. Patients have voice by being giving the opportunity to participate in research. RPV gives you, the patient the opportunity and you can choose if it is right for you. No obligation. No pressure. Your choice. Always.

This can be as simple as a survey to clinical trials. It is all up to the individual and many opportunities you get paid up to $125 US/hour.

Please join me. Register here:https://www.rarepatientvoice.com/rp/thepicklejar

It is pretty amazing and open to anyone with a diagnosed illness.

You simply register. Takes about 3 minutes. RPV reaches out if there is an opportunity. You decided if you choose to participate.

If you want change. If you want progress. You need to register and give yourself to oppoutniry to have your voice heard.

Again this is open to anyone with a diagsnosed illness.

ADRENAL INSUFFICIENCY patients desaparetly needed.

Only 366 registered in US.

Only 18 registered in Candaa

Only 44 registered in the UK.

All patients deserve to have a voice.

Please join me. Register here:https://www.rarepatientvoice.com/rp/thepicklejar

Please share this information and link with anyone you know who has an illness/diagnosis and give them the oppotunity to be part of change.

This is very important to me so I truly hope you considering join me.

Jill ❤️