Polycystic Kidney Disease (PKD) Support Group
Polycystic kidney disease (PKD) is a progressive, genetic disorder of the kidneys. It occurs in humans and other organisms. PKD is characterised by the presence of multiple cysts (polycystic) in both kidneys. The disease can also damage the liver, pancreas and rarely the heart and brain.
rogerjd
I apologise now for any typos because I ahve already taken sleeping meds and am a bit drowsy. Had my double nephrectomy on 2nd November due to problems experienced from size of kidneys and also suspicion of cancer. I am cancer free- tumors are not cancerous! Also I have plenty room now to eat (which I have not done for 2 years - i.e managed on milkshakes) and also I cna lie flat without my breathing being restricted so my life feels so optimistic at the moment and I can't wait for each and every improvement in my abulities every day.
The operation went really well- The surgeoins had told me they expected it to take 7-8 hours but it took between 4-5 hours and they also conducted a bladder cystoscopy and gave me all clear on that too. Gallbladder that seemed to be troubling me was examined and it was fine. They have advised that my liver is extremely large and much bigger than my kidneys and the spasmodic pain I have been having in my rib cage has been coming from this. I am unable to tell whether the pain has completely subsided so only time will tell. They have alsp mentioned that I need to be monitored for my liver as it may now grow faster now there is room- noty worrying about this yet though.
I had a general anaesthetic and also an epidural fitted so that they could feed it to me for first 3 days. During the op I obviously had plenty fluids and a couple of blood transfusions including the pain killing medication and anything else they gave me. For a couple of days the pain was pretty much well controlled until I tried to move. So lying in bed all day was pretty uncomfortable. My back seemed to be very sensitive probably due to large space left and was in too much pain t adjust my position. Unfortunately after a couple of days I still had not had any dialysis and wasn;t eating or sleeping. The wprst thing happened- I began having very realistic hallucinations- I can laugh about it now but for about 3 days I ws convinced they were trying to kill me and became very frightened and stressed whioch began to have an impact on my health and recovery. I tried to rip my tubes out and call the police- I was so scared and thought my life was over. I was so convincing with my stories that they embarked on a full investigation around the claims I was making (I thought they were taking photos of me) I convinced my whole family that I was in danger. I completely remember everything that happened and now know it was all hallucinatory and would hate for anyone to have to go through that. I ended up in a very critical state and was moved to ICU from the surgical high dependency ward. They prescribedme drugs for hallucinations which added to the toxins and they started to wean me off the epidural as they felt this was causing my hallucinations. It worked and I came to my normal senses but the pain was extremely significant and I couldn't do anything. I couldn't sleep, talk, read-m the pain was too much . I begged them for more but they explained that they had to balance my medication with the hallucinatory effects. After about a week I wa still in bad pain- My hemoglobin had a drastic drop and I had to have a couple of back to back transfusions as I fell unconscious. After that I began to get better so they moved me to renal high dependancy which felt very similar- I had my own nurse in my bay all day but they were specialised in renal. Immediately they wanted ot help me with the pain- what a difference- within a few hours after a few good doses of morphine and standard pain killers I became more alert and ready to start some exercise. My nurse worked really closely with me escortuing me to shower every day and chrcking on me every hour during night ensuring that my pain relief did not disappear. It was he mose fabulous care ever. They also put me on hemofiltraton for a couple of days. I understand that this is 24 hour dalysis but it only removes fluid it does not clean your blood. I had bloated so much that the balls of my feet were like golf balls and I couldn't bend my legs so my physio sessions had to be cancelled as I could not walk. They they started hemodialysis sessions. Unofrtunately first couple of sessions they struggled getting needles in and only managed 1 which didn't give me good dialysis or any significant fluid removal. I became very breathless so they got their best dialysis nurse in the hospital to do the needling on me becuase my fistula is so small most cannot needle it. They did a mammoth session and took off quite a lot of fluid- they advised that this was the most they could take without it affecting my health. In the last twenty minutes I passed out so they had to get me off in an emergency. I had daily dialysis daily for 2-3 days following this during which I got sick but fluid was definitely coming off. Tuesday this week had a really good session and they reached the weight they were aiming for even though they know there is still excess fluid there. They advised me that my hemaglobin has dropped quite drastically and so are prescribing 3 lots of EPO in my next dialysis on Thursday. They then let me home. It's absolutley amazing being home and being hungry eating more or less what I want as my potassium and phosphate are pretty low at the moment. Fluid restriction of 500 mils is a real challenge but I am managing it for now. I sip all day from a 500mil water bottle(only filled to 480 mil) and try to save as much as possible and at 9.00 at night I put vimto in and leave in fridge for an hour so then at 10.00 I can enjoy a good gupling from my bottle of vimto. I am obviously restricting fluid in my food aswell. As some of you my have read before I have been having 'trouble' woth my husband andit all came to a head on Tuesdy when I came out of hospital. I never felt so unwelcome in my own house in all my life. We have had a few cinfontations on this ans I asked for a separation. I will update on this another day because this update has gone on long enough for now. I am at home struggling getting about (3 story house) and missing handrails and bed rails to help me manouvre but other than that all is good and every day somehitn else becomes easier. Today I crossed my legs for the first time since operation- I have been trying to do this for a while and not been able to so improvements are small and slow but they are still there and keep me motivated and optimistic. And being with my daughters again is fantastic. Hospital photographer took photos of kidneys but I have to officially complete a form to receive a copy. I understand that this has to be legally approved so not put wheels in motion for this yet but as soon as I have photos I will post on here. further update to follow in next couple of days
The operation went really well- The surgeoins had told me they expected it to take 7-8 hours but it took between 4-5 hours and they also conducted a bladder cystoscopy and gave me all clear on that too. Gallbladder that seemed to be troubling me was examined and it was fine. They have advised that my liver is extremely large and much bigger than my kidneys and the spasmodic pain I have been having in my rib cage has been coming from this. I am unable to tell whether the pain has completely subsided so only time will tell. They have alsp mentioned that I need to be monitored for my liver as it may now grow faster now there is room- noty worrying about this yet though.
I had a general anaesthetic and also an epidural fitted so that they could feed it to me for first 3 days. During the op I obviously had plenty fluids and a couple of blood transfusions including the pain killing medication and anything else they gave me. For a couple of days the pain was pretty much well controlled until I tried to move. So lying in bed all day was pretty uncomfortable. My back seemed to be very sensitive probably due to large space left and was in too much pain t adjust my position. Unfortunately after a couple of days I still had not had any dialysis and wasn;t eating or sleeping. The wprst thing happened- I began having very realistic hallucinations- I can laugh about it now but for about 3 days I ws convinced they were trying to kill me and became very frightened and stressed whioch began to have an impact on my health and recovery. I tried to rip my tubes out and call the police- I was so scared and thought my life was over. I was so convincing with my stories that they embarked on a full investigation around the claims I was making (I thought they were taking photos of me) I convinced my whole family that I was in danger. I completely remember everything that happened and now know it was all hallucinatory and would hate for anyone to have to go through that. I ended up in a very critical state and was moved to ICU from the surgical high dependency ward. They prescribedme drugs for hallucinations which added to the toxins and they started to wean me off the epidural as they felt this was causing my hallucinations. It worked and I came to my normal senses but the pain was extremely significant and I couldn't do anything. I couldn't sleep, talk, read-m the pain was too much . I begged them for more but they explained that they had to balance my medication with the hallucinatory effects. After about a week I wa still in bad pain- My hemoglobin had a drastic drop and I had to have a couple of back to back transfusions as I fell unconscious. After that I began to get better so they moved me to renal high dependancy which felt very similar- I had my own nurse in my bay all day but they were specialised in renal. Immediately they wanted ot help me with the pain- what a difference- within a few hours after a few good doses of morphine and standard pain killers I became more alert and ready to start some exercise. My nurse worked really closely with me escortuing me to shower every day and chrcking on me every hour during night ensuring that my pain relief did not disappear. It was he mose fabulous care ever. They also put me on hemofiltraton for a couple of days. I understand that this is 24 hour dalysis but it only removes fluid it does not clean your blood. I had bloated so much that the balls of my feet were like golf balls and I couldn't bend my legs so my physio sessions had to be cancelled as I could not walk. They they started hemodialysis sessions. Unofrtunately first couple of sessions they struggled getting needles in and only managed 1 which didn't give me good dialysis or any significant fluid removal. I became very breathless so they got their best dialysis nurse in the hospital to do the needling on me becuase my fistula is so small most cannot needle it. They did a mammoth session and took off quite a lot of fluid- they advised that this was the most they could take without it affecting my health. In the last twenty minutes I passed out so they had to get me off in an emergency. I had daily dialysis daily for 2-3 days following this during which I got sick but fluid was definitely coming off. Tuesday this week had a really good session and they reached the weight they were aiming for even though they know there is still excess fluid there. They advised me that my hemaglobin has dropped quite drastically and so are prescribing 3 lots of EPO in my next dialysis on Thursday. They then let me home. It's absolutley amazing being home and being hungry eating more or less what I want as my potassium and phosphate are pretty low at the moment. Fluid restriction of 500 mils is a real challenge but I am managing it for now. I sip all day from a 500mil water bottle(only filled to 480 mil) and try to save as much as possible and at 9.00 at night I put vimto in and leave in fridge for an hour so then at 10.00 I can enjoy a good gupling from my bottle of vimto. I am obviously restricting fluid in my food aswell. As some of you my have read before I have been having 'trouble' woth my husband andit all came to a head on Tuesdy when I came out of hospital. I never felt so unwelcome in my own house in all my life. We have had a few cinfontations on this ans I asked for a separation. I will update on this another day because this update has gone on long enough for now. I am at home struggling getting about (3 story house) and missing handrails and bed rails to help me manouvre but other than that all is good and every day somehitn else becomes easier. Today I crossed my legs for the first time since operation- I have been trying to do this for a while and not been able to so improvements are small and slow but they are still there and keep me motivated and optimistic. And being with my daughters again is fantastic. Hospital photographer took photos of kidneys but I have to officially complete a form to receive a copy. I understand that this has to be legally approved so not put wheels in motion for this yet but as soon as I have photos I will post on here. further update to follow in next couple of days
The first time you will be able to enjoy a full meal will be a great experience I'm sure :) I wish you a full and speedy recovery. Maybe once things settle down with your health your relationship with your husband will improve as well? I know my husband does not function well under stress.
I look forward to seeing your pictures once they are posted. In the meantime take care of yourself. Hugs Kelley
Thanks Julie x
as your fistula matures it will be easier on you and the person doing the cannulation.
despite all you have been through you seem to have a very positive attitude and that will go a long way in your recovery.
keep up the good work and keep us informed of your progress.
btw, what is vimto?
You're going through a rough part of the road right now. It seems, though, that you'll make it through.
Consider yourself a tough woman!
Your persistence and toughness will carry you through!
BTW, what's "vimto?"
Peace and Blessings!
CoachRichie
Please keep us updated. you'll be in my thoughts as you recover.
I'm so glad your back to posting and seem to be recovering well. Keep it up. Wow, what an ordeal you have been through. I looked every day after your surgery to see if you were posting yet and finally you were. What a relief. I was so concerned about you.
You do have a great positive attitude and are an inspiration to me!
Love and hugs,
Jessica
Julie, so glad to see you are home recovering after quite the experience. I am thankful you have found some relief and are able to eat again and breathe :)
Are you able to use your health insurance to get a home health nurse for a few weeks?
Jennyd36 - this is the UK - no health insurance and no home help nurse on the NHS!
Julie, I know that your husband might not be there for you, so you must accept any offers of help from family and friends. If the offers don't come, ASK. I'm sure people will be happy to help if they know you need it. Sometimes if you seem self sufficient, others assume you don't need anything. Hopefully your daughters are supporting you well.
Enjoy the vimto!
Love Chewitt
Hope this is a bit helpful. Ask your doctor first of course.
What Foods & Supplements Are Good for Raising Hemoglobin Levels?
1 Comments
Jul 2, 2011 | By Lisa Porter
Lisa Porter began writing professionally in 2009. She writes for various websites and has a Bachelor of Arts in English literature.
What Foods & Supplements Are Good for Raising Hemoglobin Levels? Photo Credit Comstock Images/Comstock/Getty Images
Anemia can cause low levels of healthy red blood cells and hemoglobin, a protein in red blood cells that transports oxygen throughout the body. Deficiencies in iron, vitamin B-12, vitamin B-6 and folate may contribute to anemia and low hemoglobin levels, causing symptoms of fatigue and weakness. Eating plenty of foods rich in these nutrients can help prevent and treat anemia. Dietary supplements can provide additional sources of those nutrients.
Iron
The body needs iron to make hemoglobin. Animal-based iron sources contain heme iron, a type of iron derived from hemoglobin. The body absorbs heme iron more easily than nonheme iron, the type of iron found in plant-based foods and supplements. Sources of heme iron include chicken liver, oysters, beef, clams, turkey, chicken, tuna, halibut, crab, pork and shrimp. Sources of nonheme iron include fortified breakfast cereals and oatmeal, soybeans, lentils, tofu, spinach, raisins, whole-wheat bread and kidney, lima, navy, black and pinto beans.
Vitamin B-12
Vitamin B-12 plays an important role in red blood cell formation. Vitamin B-12 exists naturally in animal products such as meats, poultry, seafood and dairy products. Sources of B-12 include beef liver, salmon, trout, clams, haddock, tuna, turkey, chicken, eggs, milk and yogurt. Many fortified breakfast cereals contain added vitamin B-12.
Vitamin B-6
Vitamin B-6 plays a role in hemoglobin formation, and it also boosts the amount of oxygen hemoglobin carries, says the National Institutes of Health Office of Dietary Supplements. Many foods contain vitamin B-6, including fortified cereals, potatoes, oatmeal, bananas, garbanzo beans, chicken, pork, beef, trout, sunflower seeds, spinach, avocados, wheat bran, walnuts, peanut butter and tomato juice.
Folate
Folate also plays an essential role in red blood cell formation. Sources of folate include beef liver, spinach, great northern beans, asparagus, spinach, green peas, broccoli, avocado, peanuts, tomato juice, orange juice, turnip greens, cantaloupe, papaya and banana. Dietary supplements and fortified cereals, rice, breads and egg noodles provide folic acid, a synthetic form of folate.
References
* National Institutes of Health Office of Dietary Supplements: Iron
Read more: http://www.livestrong.com/article/483533-what-foods-supplements-are-good-for-raising-hemoglobin-levels/#ixzz1eHFEw828
All the best,
Jessica
Also I wanted to tell you that I had NO IDEA I would ever get some one to offer a kidney for me. I am very isolated, have no family that pays any attention or has any compassion, except my daughter who is on the other side of Alaska, and has PKD as well, and my husband is about as clueless as yours seems to be. So was I ever surprised when a woman half way across the country asked me if she could give me a kidney!!!! That was the last thing I expected. So, the whole world is open to you, and yet it is a good thing to rest in the stage that you are presently in. Right now is enough to deal with.
I have to say, I am very proud of you for standing up for yourself. VERY much. You rock!!!!
One question I wanted to ask (and I do so with fear and trembling because I am not sure if I could answer it myself) is have you been able to show your husband how much you have been hurt by his inaction and lack of care? I wonder if that would help? It sounds as if he feels intimidated by your strength and his lack of it. I could be way off..... but it's a thought.
Again, I just think that you are one gutsy gal, and I am amazed at what you have been through.
Lots of love,
Norma...
Jessica- I am going to the doctors with my daughter Sophie tomorrow as she is still having blood pressure issues even though she is on a good dose of medication so I will print off this extract that you have shared and discuss with my GP. I will also take it to renal with me when I go for dialysis on Tuesday and see if I can come up with a menu to improve my red blood count- this would be a much better option than transfusion - I am willing to try anything.
Heather- so nice to hear from you and sorry that you seem to be having trouble with your resident kidney but it does not surpsrise me. After my operation the surgeon has told me that my liver is much bigger than any of my kidneys and now there is space he thinks the liver will start to grow faster- I'm not thinking about that right now though- just want to get over this first and then see how I stand. Hope I haven't scared you with my updates. I suppose the ultimate solution is to have it removed and continue with your transplanted kidney but I'm sure you have plenty time left yet.
Norma- Lovely to hear from you- I hope you are well and fully recovered from your nasty operation and I hope your arthritis is not causing you too much pain. The operation has been the best thing I have ever done and I hope I can still say that next year. I am not that strong when we talk about my relationship - I just have really high morals and no matter how much I love Nigel I cannot accept a second rate relationship so he has a lot to prove over the coming weeks- I want to believe him so much but I am definitely on my guard. Over last couple of days though he has been making a really big effort -I think he is still in shock. And in response to what you have said Heather about letting him know how much he has hurt me. During all our exchanges over last few days I have been very emotional and explained how isolated and alone I have felt for a long time and how he can hurt me more when I am so fragile after the operation to me is someone who does not give a damn. He was very emotional when I said this and to be honest I think he has just focused on caring about his self without giving me a second thought. Hopefully our relationship will continue to improve as my health improves providing nothing sneaks out of the woodwork! Thanks again for all your words of wisdom and I will certainly take them all on board.