Jennifer J
Senior Member
- Messages
- 997
- Location
- Southern California
@Kati
Thank you. I like Patient in training under your name I agree saying that, in the way @SOC wrote to talk with my doctor's office is the best idea. And you're right, I do get PEM walking back and forth to the front door. Thank you for welcoming me to PR. I'm so glad all of you are here, and we can support and help each other through this.
Thank you, @Dreambirdie. I agree, @SOC, , and I like your name. too.
Hi, @minkeygirl,. I smile every time I see your cat picture. I know, it is starting to sound like insurance might be playing a role in what happened the other day with me. I'll know more when I talk to my doctor's office. I'm hoping to straighten it out Monday since I haven't had enough energy to verbally communicate or do much the past few days.
I do need to scan google some more when I can. All these things literally takes years due to limited energy and trying to survive. I did call a few food delivery places and I didn't fit their criteria. There's one for cancer or AIDS patients, that might do housebound patients. I need a social worker for them and I need to get my doctors notes fixed. The past few times I was there, in spite of me saying I was too tired to go over much, I was laying down, etc. My notes she marked patient isn't fatigued and no mention of anything that is going on with me.
I did phone some religious groups, too, a few years ago. They needed me to be or have been an attending member in their church or organization. They said unfortunately there is more need than what they are able to assist with in their own community.
I'll keep looking. I have all kinds of ideas how to make things happen. I just don't have enough ability. Years and years go by as I keep searching. Maybe, perhaps, hopefully, that will change with appropriate treatment/s or better housing and more substantial food.
Thank you for encouraging me and the ideas. I will also check out again the Americans with disabilities act. I did several years ago and it didn't seem to have anything that pertained to my situation. I need to be careful, I can't afford to lose my housing which could be easy to do. I've been looking for years trying to move out of here. I have an angiodema reaction to most scents which has complicated being able to find a place to live, as well as finances and being mainly bed and housebound.
I hope you were able to get Section 8. Sorry 5 and more years is so long to wait for it.
Thank you. I like Patient in training under your name I agree saying that, in the way @SOC wrote to talk with my doctor's office is the best idea. And you're right, I do get PEM walking back and forth to the front door. Thank you for welcoming me to PR. I'm so glad all of you are here, and we can support and help each other through this.
Thank you, @Dreambirdie. I agree, @SOC, , and I like your name. too.
Hi, @minkeygirl,. I smile every time I see your cat picture. I know, it is starting to sound like insurance might be playing a role in what happened the other day with me. I'll know more when I talk to my doctor's office. I'm hoping to straighten it out Monday since I haven't had enough energy to verbally communicate or do much the past few days.
I do need to scan google some more when I can. All these things literally takes years due to limited energy and trying to survive. I did call a few food delivery places and I didn't fit their criteria. There's one for cancer or AIDS patients, that might do housebound patients. I need a social worker for them and I need to get my doctors notes fixed. The past few times I was there, in spite of me saying I was too tired to go over much, I was laying down, etc. My notes she marked patient isn't fatigued and no mention of anything that is going on with me.
I did phone some religious groups, too, a few years ago. They needed me to be or have been an attending member in their church or organization. They said unfortunately there is more need than what they are able to assist with in their own community.
I'll keep looking. I have all kinds of ideas how to make things happen. I just don't have enough ability. Years and years go by as I keep searching. Maybe, perhaps, hopefully, that will change with appropriate treatment/s or better housing and more substantial food.
Thank you for encouraging me and the ideas. I will also check out again the Americans with disabilities act. I did several years ago and it didn't seem to have anything that pertained to my situation. I need to be careful, I can't afford to lose my housing which could be easy to do. I've been looking for years trying to move out of here. I have an angiodema reaction to most scents which has complicated being able to find a place to live, as well as finances and being mainly bed and housebound.
I hope you were able to get Section 8. Sorry 5 and more years is so long to wait for it.