Newly Diagnosed CKD Stage 3
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I had open heart surgery (full sternotomy) on 8/21/15. I'm 100% pacemaker dependent. A year later I'm now dealing with newly diagnosed "moderate" CKD Stage 3a. My urologist referred me to a nephrologist. My GP is now conferring with the urologist, the nephrologist, my endocrinologist and my cardiologist to figure out a course of treatment. Cardiologist agreed to stop my Coreg and double up the Losartan. Endo decided to stop the metFormin for my T2 Diabetes. I'm anemic and so tired. My kidneys ache pretty much all the time. Two weeks ago I had a Ureteroscopy to blast a kidney stone blocking my left ureter and several (of about 10) stones in the left kidney. My right kidney has shrunk. Neph say's I'm about 50% (eGFR is 53 & creatinine is 1.46, but my UR protein is super high at 314). I'm overwhelmed at this point with this new health challenge. Depression is a normal part of recovering from OHS, but it's gotten much worse in the past 2 months. I guess I need some assurance that, after surviving open heart surgery and 3 pacemaker surgeries (the last one on New Year's Eve), I can adjust and deal with this.
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helen54849 FLPatriot59
Posted
Hi,
I have CKD stage 5 6% GFR, have been on dialysis for two years and have my live doner transplant next week. You have summed it up yourself I think, you have been through so much and have been able to get through it. A serious heart op and other surgeries. Remember GFR is only an indication and not a deffinate science, your figures are recorded differently that they are hear in the UK also. Mediciation can effect you GFR also, all your medics seem to be talking to each other and this is a good thing it means that you will be put on suitable meds for all conditions where possible. A lot remain at stage 3 for years so ensure your blood pressure is kept within the limits, avoid salt and low salt, if you are over weight lose weight and avoid junk food. By doing all these things you can help protect your GFR for longer. There are no promises but if you do all you can to protect it fingers crossed it wont drop. Take each day at a time and don't stress about things you dont have control over o with it, it really is more pleseant. Is it easy no but you can do you know you can. Keep us posted
kathi70354 FLPatriot59
Posted
sonia68053 FLPatriot59
Posted
At one point I felt as if I was falling apart at the seams. Open heart surgery, kidney failure - dialysis, spine injury, osteo- arthritis leading to hip replacements (which now keep dislocating), fibromyalgia and emphysemia.
Then I began to be AMAZED. What medicine can do for a battered body! How wonderful is that. There are so many people out there who need encouragement to live their lives to the full, to believe in themselves and that they matter in this world. We who have lived long enough to learn coping methods and ways to prioritise need to be there to give them a boost.
At 76 I do not have the physical energy to get stuck in to making the world a better place but I have the life experience to help others play their role. The easiest way is to be involved with groups of people doing things like ... fund raising for the local church or hospital... do yoga or Tai Chi or some sort of group exercise/dance/game. These are places where you meet people you can support/give a lift to. It increases your opportunity to learn to be optimistic/positive.
Good luck. There is a wonderful world out there beyond the limits of our illnesses that we can be part of and enjoy.
kathi70354 sonia68053
Posted