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My father's kidney function is down to only 15% (borderline end stage). Has anyone had experience with this. If so how long did they live and did they ever hear about or try any "alternative" treatments
How old is your dad and what stage is his dementia in? Does he have a living will? Has his doctor discussed the options? I would suspect that his options would be confined to dialysis.
With his dementia, can he tolerate this treatment, that is likely to be several days per week. I don't know much about this treatment, but maybe others here do.
he's 84 yrs. old- diabetic/heart issues, etc. but at this point no symptoms. Was actually told by the specialist (at his age) dialysis doesn't prolong life..............just wondering about the "future"
I work in home healthcare and I have a patient with ESRD. She has 20% kidney function in one kidney. The other kidney is kaput. And while she's on hospice she's doing pretty well. She has a suprapubic catheter and stays in bed all the time but she still has quality of life. She visits with her grown children, listens as her husband reads aloud to her, she smiles and laughs. My staff and I keep a sharp eye out for UTI's but considering her health status she's doing as well if not better than can be expected.
I'm not aware of any alternative treatments at her stage. She has a large, supportive family who were reluctant to call in hospice. If there was something out there that could help their mom I think they would have come up with it.
She's been living with ESRD for months and months. More than 6 months at least.
Don't expect anything much to happen, especially not after one result. Has your father's kidney function being going downhill over time, perhaps a result of his heart condition? I'm just wondering what they were checking his renal function for if he's asymptomatic.
Dialysis is not fun, his heart issues could also contraindicate it, and I wouldn't push for it. But assuming your father is mentally fine this clinical decision should be his to make - not that I'd suggest he goes against medical advice. How does he feel about what the doctor is explaining to him?
By proceeding, I agree that I understand the following disclosures:
I. How We Work in Washington.
Based on your preferences, we provide you with information about one or more of our contracted senior living providers ("Participating Communities") and provide your Senior Living Care Information to Participating Communities. The Participating Communities may contact you directly regarding their services.
APFM does not endorse or recommend any provider. It is your sole responsibility to select the appropriate care for yourself or your loved one. We work with both you and the Participating Communities in your search. We do not permit our Advisors to have an ownership interest in Participating Communities.
II. How We Are Paid.
We do not charge you any fee – we are paid by the Participating Communities. Some Participating Communities pay us a percentage of the first month's standard rate for the rent and care services you select. We invoice these fees after the senior moves in.
III. When We Tour.
APFM tours certain Participating Communities in Washington (typically more in metropolitan areas than in rural areas.) During the 12 month period prior to December 31, 2017, we toured 86.2% of Participating Communities with capacity for 20 or more residents.
IV. No Obligation or Commitment.
You have no obligation to use or to continue to use our services. Because you pay no fee to us, you will never need to ask for a refund.
V. Complaints.
Please contact our Family Feedback Line at (866) 584-7340 or ConsumerFeedback@aplaceformom.com to report any complaint. Consumers have many avenues to address a dispute with any referral service company, including the right to file a complaint with the Attorney General's office at: Consumer Protection Division, 800 5th Avenue, Ste. 2000, Seattle, 98104 or 800-551-4636.
VI. No Waiver of Your Rights.
APFM does not (and may not) require or even ask consumers seeking senior housing or care services in Washington State to sign waivers of liability for losses of personal property or injury or to sign waivers of any rights established under law.
I agree that:
A.
I authorize A Place For Mom ("APFM") to collect certain personal and contact detail information, as well as relevant health care information about me or from me about the senior family member or relative I am assisting ("Senior Living Care Information").
B.
APFM may provide information to me electronically. My electronic signature on agreements and documents has the same effect as if I signed them in ink.
C.
APFM may send all communications to me electronically via e-mail or by access to an APFM web site.
D.
If I want a paper copy, I can print a copy of the Disclosures or download the Disclosures for my records.
E.
This E-Sign Acknowledgement and Authorization applies to these Disclosures and all future Disclosures related to APFM's services, unless I revoke my authorization. You may revoke this authorization in writing at any time (except where we have already disclosed information before receiving your revocation.) This authorization will expire after one year.
F.
You consent to APFM's reaching out to you using a phone system than can auto-dial numbers (we miss rotary phones, too!), but this consent is not required to use our service.
Does he have a living will?
Has his doctor discussed the options? I would suspect that his options would be confined to dialysis.
With his dementia, can he tolerate this treatment, that is likely to be several days per week. I don't know much about this treatment, but maybe others here do.
kidneyfailureweb/esrd/385.html
I'm not aware of any alternative treatments at her stage. She has a large, supportive family who were reluctant to call in hospice. If there was something out there that could help their mom I think they would have come up with it.
She's been living with ESRD for months and months. More than 6 months at least.
Dialysis is not fun, his heart issues could also contraindicate it, and I wouldn't push for it. But assuming your father is mentally fine this clinical decision should be his to make - not that I'd suggest he goes against medical advice. How does he feel about what the doctor is explaining to him?