hi. you don't know me, but my name is Eris. I've gotten increasingly more ill in the past 5 years, to the point that I am now bedbound and cannot work or drive. I'm asking for help.
if you can spare a minute of your time, I would love for you to share this with your friends and family. it would mean the world to me. thank you 🫶
i dont have energy for pictures this time, i tested positive for MS, an incurable degenerative disease. i am taking pain and nausea medication every day to stay functioning. i spend most of my time in bed
please help any way you can
Hi, my name is Eris. I have been disabled since childhood. But in the year 2020, things too… Eris Wicker needs your support for Help Eris Fi
hi. you don't know me, but my name is Eris. I've gotten increasingly more ill in the past 5 years, to the point that I am now bedbound and cannot work or drive. I'm asking for help.
if you can spare a minute of your time, I would love for you to share this with your friends and family. it would mean the world to me. thank you 🫶
hey if you guys wanna help share I only have about 300 left of this fund bc we're easily dropping 100-200 per appointment and I have multiple of them a month (sometimes per week
I have a heart condition and suspected MS so that is why 🫶
Hi, my name is Eris. I have been disabled since childhood. But in the year 2020, things too… Eris Wicker needs your support for Help Eris Fi
hello everyone
it has been over two months since I made my last update. the truth is, I haven't known what to say. so much has happened so close together that I felt like I could never stop and take a breath long enough to catch up.
so let's try and play catch up
the laparoscopy I received ruled out endometriosis on my ovaries and abdominal cavity. they were able to successfully remove the cyst
I was able to see a urogynecologist and we discussed treatment options. I have bladder surgery scheduled for this upcoming Monday, which will hopefully provide some answers and some relief
I was hospitalized for diverticulitis, bowel perforation, and colitis due to medical neglect. thankfully I have since made a full recovery
I was FINALLY able to see a neurologist. sadly, they have no idea what's wrong with me. so I am currently in the process of undergoing various tests and procedures to try and determine what's wrong. I was prescribed migraine medication, which I am struggling to get covered my insurance
I was also able to see a gastroenterologist, who prescribed me some medication and scheduled four different diagnostic procedures
I have upcoming appointments with opthalmology and cardiology. The former will investigate why I am losing my vision, and the latter specializes in POTS. I am optimistic that I will FINALLY be medicated after five years with this diagnosis
some tests I received brought back some concerning results, indicating that I am at risk for auto-immune deficiency and possibly cancer. we will be investigating that soon
that is all of the medical news that's occurred for me over the course of the last two months. the GOOD news is, I was able to use the funds from this campaign to purchase a smart watch, which helps monitor my heart rate.
the BEST news is that a local EDS clinic is FINALLY opening up in my state come July. this is huge, as it means I don't have to wait for Mayo clinic to have availability, or pay over 5k out of pocket to be treated. my family and I are so hopeful that this might give us some answers and change my life
I am leaving the goal as is, because as I said earlier, I am getting countless procedures done. each one, if covered by insurance, has a copay of 190 dollars. I'm just the last two months alone, we have already racked up nearly 2k in bills for procedures.
our out of pocket for insurance is 9k. meaning the remaining 6k of this fund would go towards travel costs, things not covered my insurance, and next year's medical needs
thanks for sticking around to read this. I have continued to get sicker - it's funny how the more you need help, the less you are able to ask for it. but as more and more costs keep piling up, I have to fight through the pain and fatigue to ask you once again; please share, please donate, please tell a friend. we need you
thank you so so much to everyone who donated today! a reminder I have PayPal, venmo, and cashapp all under erisphant
any donations received there will go directly to the medical fund, unless you specify you want it to go into the food and toiletries fund!! many thanks 🫶
got the MRI. they found signs of multiple sclerosis. further testing will likely be necessary to determine if it is that or some other demyelinating disease
graphic attached for educational purposes. please share
Hi, my name is Eris. I have been disabled since childhood. But in the year 2020, things too… Eris Wicker needs your support for Help Eris Fi
hello everyone
it has been over two months since I made my last update. the truth is, I haven't known what to say. so much has happened so close together that I felt like I could never stop and take a breath long enough to catch up.
so let's try and play catch up
the laparoscopy I received ruled out endometriosis on my ovaries and abdominal cavity. they were able to successfully remove the cyst
I was able to see a urogynecologist and we discussed treatment options. I have bladder surgery scheduled for this upcoming Monday, which will hopefully provide some answers and some relief
I was hospitalized for diverticulitis, bowel perforation, and colitis due to medical neglect. thankfully I have since made a full recovery
I was FINALLY able to see a neurologist. sadly, they have no idea what's wrong with me. so I am currently in the process of undergoing various tests and procedures to try and determine what's wrong. I was prescribed migraine medication, which I am struggling to get covered my insurance
I was also able to see a gastroenterologist, who prescribed me some medication and scheduled four different diagnostic procedures
I have upcoming appointments with opthalmology and cardiology. The former will investigate why I am losing my vision, and the latter specializes in POTS. I am optimistic that I will FINALLY be medicated after five years with this diagnosis
some tests I received brought back some concerning results, indicating that I am at risk for auto-immune deficiency and possibly cancer. we will be investigating that soon
that is all of the medical news that's occurred for me over the course of the last two months. the GOOD news is, I was able to use the funds from this campaign to purchase a smart watch, which helps monitor my heart rate.
the BEST news is that a local EDS clinic is FINALLY opening up in my state come July. this is huge, as it means I don't have to wait for Mayo clinic to have availability, or pay over 5k out of pocket to be treated. my family and I are so hopeful that this might give us some answers and change my life
I am leaving the goal as is, because as I said earlier, I am getting countless procedures done. each one, if covered by insurance, has a copay of 190 dollars. I'm just the last two months alone, we have already racked up nearly 2k in bills for procedures.
our out of pocket for insurance is 9k. meaning the remaining 6k of this fund would go towards travel costs, things not covered my insurance, and next year's medical needs
thanks for sticking around to read this. I have continued to get sicker - it's funny how the more you need help, the less you are able to ask for it. but as more and more costs keep piling up, I have to fight through the pain and fatigue to ask you once again; please share, please donate, please tell a friend. we need you
thank you so so much to everyone who donated today! a reminder I have PayPal, venmo, and cashapp all under erisphant
any donations received there will go directly to the medical fund, unless you specify you want it to go into the food and toiletries fund!! many thanks 🫶
got the MRI. they found signs of multiple sclerosis. further testing will likely be necessary to determine if it is that or some other demyelinating disease
graphic attached for educational purposes. please share
Hi, my name is Eris. I have been disabled since childhood. But in the year 2020, things too… Eris Wicker needs your support for Help Eris Fi
hello everyone
it has been over two months since I made my last update. the truth is, I haven't known what to say. so much has happened so close together that I felt like I could never stop and take a breath long enough to catch up.
so let's try and play catch up
the laparoscopy I received ruled out endometriosis on my ovaries and abdominal cavity. they were able to successfully remove the cyst
I was able to see a urogynecologist and we discussed treatment options. I have bladder surgery scheduled for this upcoming Monday, which will hopefully provide some answers and some relief
I was hospitalized for diverticulitis, bowel perforation, and colitis due to medical neglect. thankfully I have since made a full recovery
I was FINALLY able to see a neurologist. sadly, they have no idea what's wrong with me. so I am currently in the process of undergoing various tests and procedures to try and determine what's wrong. I was prescribed migraine medication, which I am struggling to get covered my insurance
I was also able to see a gastroenterologist, who prescribed me some medication and scheduled four different diagnostic procedures
I have upcoming appointments with opthalmology and cardiology. The former will investigate why I am losing my vision, and the latter specializes in POTS. I am optimistic that I will FINALLY be medicated after five years with this diagnosis
some tests I received brought back some concerning results, indicating that I am at risk for auto-immune deficiency and possibly cancer. we will be investigating that soon
that is all of the medical news that's occurred for me over the course of the last two months. the GOOD news is, I was able to use the funds from this campaign to purchase a smart watch, which helps monitor my heart rate.
the BEST news is that a local EDS clinic is FINALLY opening up in my state come July. this is huge, as it means I don't have to wait for Mayo clinic to have availability, or pay over 5k out of pocket to be treated. my family and I are so hopeful that this might give us some answers and change my life
I am leaving the goal as is, because as I said earlier, I am getting countless procedures done. each one, if covered by insurance, has a copay of 190 dollars. I'm just the last two months alone, we have already racked up nearly 2k in bills for procedures.
our out of pocket for insurance is 9k. meaning the remaining 6k of this fund would go towards travel costs, things not covered my insurance, and next year's medical needs
thanks for sticking around to read this. I have continued to get sicker - it's funny how the more you need help, the less you are able to ask for it. but as more and more costs keep piling up, I have to fight through the pain and fatigue to ask you once again; please share, please donate, please tell a friend. we need you
thank you so so much to everyone who donated today! a reminder I have PayPal, venmo, and cashapp all under erisphant
any donations received there will go directly to the medical fund, unless you specify you want it to go into the food and toiletries fund!! many thanks 🫶
Hi, my name is Eris. I have been disabled since childhood. But in the year 2020, things too… Eris Wicker needs your support for Help Eris Fi
hello everyone
it has been over two months since I made my last update. the truth is, I haven't known what to say. so much has happened so close together that I felt like I could never stop and take a breath long enough to catch up.
so let's try and play catch up
the laparoscopy I received ruled out endometriosis on my ovaries and abdominal cavity. they were able to successfully remove the cyst
I was able to see a urogynecologist and we discussed treatment options. I have bladder surgery scheduled for this upcoming Monday, which will hopefully provide some answers and some relief
I was hospitalized for diverticulitis, bowel perforation, and colitis due to medical neglect. thankfully I have since made a full recovery
I was FINALLY able to see a neurologist. sadly, they have no idea what's wrong with me. so I am currently in the process of undergoing various tests and procedures to try and determine what's wrong. I was prescribed migraine medication, which I am struggling to get covered my insurance
I was also able to see a gastroenterologist, who prescribed me some medication and scheduled four different diagnostic procedures
I have upcoming appointments with opthalmology and cardiology. The former will investigate why I am losing my vision, and the latter specializes in POTS. I am optimistic that I will FINALLY be medicated after five years with this diagnosis
some tests I received brought back some concerning results, indicating that I am at risk for auto-immune deficiency and possibly cancer. we will be investigating that soon
that is all of the medical news that's occurred for me over the course of the last two months. the GOOD news is, I was able to use the funds from this campaign to purchase a smart watch, which helps monitor my heart rate.
the BEST news is that a local EDS clinic is FINALLY opening up in my state come July. this is huge, as it means I don't have to wait for Mayo clinic to have availability, or pay over 5k out of pocket to be treated. my family and I are so hopeful that this might give us some answers and change my life
I am leaving the goal as is, because as I said earlier, I am getting countless procedures done. each one, if covered by insurance, has a copay of 190 dollars. I'm just the last two months alone, we have already racked up nearly 2k in bills for procedures.
our out of pocket for insurance is 9k. meaning the remaining 6k of this fund would go towards travel costs, things not covered my insurance, and next year's medical needs
thanks for sticking around to read this. I have continued to get sicker - it's funny how the more you need help, the less you are able to ask for it. but as more and more costs keep piling up, I have to fight through the pain and fatigue to ask you once again; please share, please donate, please tell a friend. we need you
update apparently I am having surgery complications and my surgeon is squeezing me in today. also a different doctor suggested I go to the emergency room
Hi, my name is Eris. I have been disabled since childhood. But in the year 2020, things too… Eris Wicker needs your support for Help Eris Fi
hello everyone
it has been over two months since I made my last update. the truth is, I haven't known what to say. so much has happened so close together that I felt like I could never stop and take a breath long enough to catch up.
so let's try and play catch up
the laparoscopy I received ruled out endometriosis on my ovaries and abdominal cavity. they were able to successfully remove the cyst
I was able to see a urogynecologist and we discussed treatment options. I have bladder surgery scheduled for this upcoming Monday, which will hopefully provide some answers and some relief
I was hospitalized for diverticulitis, bowel perforation, and colitis due to medical neglect. thankfully I have since made a full recovery
I was FINALLY able to see a neurologist. sadly, they have no idea what's wrong with me. so I am currently in the process of undergoing various tests and procedures to try and determine what's wrong. I was prescribed migraine medication, which I am struggling to get covered my insurance
I was also able to see a gastroenterologist, who prescribed me some medication and scheduled four different diagnostic procedures
I have upcoming appointments with opthalmology and cardiology. The former will investigate why I am losing my vision, and the latter specializes in POTS. I am optimistic that I will FINALLY be medicated after five years with this diagnosis
some tests I received brought back some concerning results, indicating that I am at risk for auto-immune deficiency and possibly cancer. we will be investigating that soon
that is all of the medical news that's occurred for me over the course of the last two months. the GOOD news is, I was able to use the funds from this campaign to purchase a smart watch, which helps monitor my heart rate.
the BEST news is that a local EDS clinic is FINALLY opening up in my state come July. this is huge, as it means I don't have to wait for Mayo clinic to have availability, or pay over 5k out of pocket to be treated. my family and I are so hopeful that this might give us some answers and change my life
I am leaving the goal as is, because as I said earlier, I am getting countless procedures done. each one, if covered by insurance, has a copay of 190 dollars. I'm just the last two months alone, we have already racked up nearly 2k in bills for procedures.
our out of pocket for insurance is 9k. meaning the remaining 6k of this fund would go towards travel costs, things not covered my insurance, and next year's medical needs
thanks for sticking around to read this. I have continued to get sicker - it's funny how the more you need help, the less you are able to ask for it. but as more and more costs keep piling up, I have to fight through the pain and fatigue to ask you once again; please share, please donate, please tell a friend. we need you
Hi, my name is Eris. I have been disabled since childhood. But in the year 2020, things too… Eris Wicker needs your support for Help Eris Fi
hello everyone
it has been over two months since I made my last update. the truth is, I haven't known what to say. so much has happened so close together that I felt like I could never stop and take a breath long enough to catch up.
so let's try and play catch up
the laparoscopy I received ruled out endometriosis on my ovaries and abdominal cavity. they were able to successfully remove the cyst
I was able to see a urogynecologist and we discussed treatment options. I have bladder surgery scheduled for this upcoming Monday, which will hopefully provide some answers and some relief
I was hospitalized for diverticulitis, bowel perforation, and colitis due to medical neglect. thankfully I have since made a full recovery
I was FINALLY able to see a neurologist. sadly, they have no idea what's wrong with me. so I am currently in the process of undergoing various tests and procedures to try and determine what's wrong. I was prescribed migraine medication, which I am struggling to get covered my insurance
I was also able to see a gastroenterologist, who prescribed me some medication and scheduled four different diagnostic procedures
I have upcoming appointments with opthalmology and cardiology. The former will investigate why I am losing my vision, and the latter specializes in POTS. I am optimistic that I will FINALLY be medicated after five years with this diagnosis
some tests I received brought back some concerning results, indicating that I am at risk for auto-immune deficiency and possibly cancer. we will be investigating that soon
that is all of the medical news that's occurred for me over the course of the last two months. the GOOD news is, I was able to use the funds from this campaign to purchase a smart watch, which helps monitor my heart rate.
the BEST news is that a local EDS clinic is FINALLY opening up in my state come July. this is huge, as it means I don't have to wait for Mayo clinic to have availability, or pay over 5k out of pocket to be treated. my family and I are so hopeful that this might give us some answers and change my life
I am leaving the goal as is, because as I said earlier, I am getting countless procedures done. each one, if covered by insurance, has a copay of 190 dollars. I'm just the last two months alone, we have already racked up nearly 2k in bills for procedures.
our out of pocket for insurance is 9k. meaning the remaining 6k of this fund would go towards travel costs, things not covered my insurance, and next year's medical needs
thanks for sticking around to read this. I have continued to get sicker - it's funny how the more you need help, the less you are able to ask for it. but as more and more costs keep piling up, I have to fight through the pain and fatigue to ask you once again; please share, please donate, please tell a friend. we need you