Question on the frequency of phlebotomies.
Posted , 10 users are following.
Hello,
I have the homozygous c282y gene and I have HH. I've had 3 phlebs in since June 20th of this year - about once every 8 weeks per my doctors orders. My iron level has come down from 218 to 164 (the healthy range Ive been told is 50-150) so I am close there. Iron saturation is 53% so I'm almost in range on that as well. Only 3% off from normal.
My ferritin however was 597 and rose to 602 as of September this year.
I saw a Hematologist today and she reccomended that I change to weekly phlebs and that what I am doing now won't be able to solve the problem (high ferritin levels with phlebs done every 8 weeks won't get the number into range.) The doctor wants me at 50 and then we start maintenance.
I'm not crazy about needles or blood but I am willing to do what it takes. All of my 3 phlebs so far I'm ok during - just some anxiety when its happening but not much more. Afterwards sometimes I have felt incredible the days following, sometimes I feel blah but it gets better.
For those of you who have done weekly phlebs - can you tell me your experience? How did you feel during? How did your weekly recovery go? What kind of diet did you eat? Anything you can share that can help me get a better understanding of what the doctor is looking for will be helpful. Weekly phlebs sounds like a lot of blood to give in short periods of time so I need more information on what to expect physically mentally emotionally.
Thank you.
1 like, 30 replies
Barb1028 abookreader
Posted
chorleyboy abookreader
Posted
Hi, my situation is that I have a high ferritin level, 2000 or so, and because the level would not show steady improvement whilst I was giving blood fortnightly, for some 15 months,, I decided, to just give blood once a month. However, the Consultant wrote to me almost straight away and said, no that won't work, you have to give blood weekly and I have been doing so for the last 12 weeks and this week, my ferritin level increased by 300+ so I just wonder when, and if, it is ever going to show a steady reduction and, no-one has answered the question. Giving 500ml of blood weekly, what affect does that have on the body generally. My diet is very good, so say the heath professionals, avoiding all the food and drinks that are not good for people with HH but that doesn't seem to be doing the trick either. Weeklty blood lets can be draining but you just have to persevere and hope that things improve and watch your diet, no greens, shelfish and there is list of avoidable foods online and the Haeomchromatosis Society are excellent if you have a query, you can ask them by email and they will reply swiftly. Regards Glyn
philx chorleyboy
Posted
Hi Glyn
I'm really sorry for your plight it must be soul destroying to be
Going up with levels more that some people are asking questions
about,but as you say we have to take things as they come,
Very best wishes for your future treatments and I hope they find
An answer somewhere
Cheers philx
chorleyboy philx
Posted
philx chorleyboy
Posted
Hi Glyn
If you are under the hospital, and having venesections there I cannot
Understand, why you don't have regular reviews, especially with the
Way your levels are,hospitals must differ.
At queen Elizabeth hospital Birmingham (England)
My initial appointment was 1.7.16 follow up appointment 14.10.16
And another one due 115.1.17 ,there is something drastically wrong
With you treatment, be more insistant demand to see your consultant
Don't take no for an answer.
Cheers Phil x
chorleyboy philx
Posted
sheryl37154 chorleyboy
Posted
Do they tell you why they cannot give you an appointment? Surely, even on a waiting list? Then you can phone and annoy them every now and then to see if you can fit in earlier.
What medical level is your Consultant, i.e. is he/she a haemotologist?
What is your gp doing about it? Also, what is the dr treating your inflamed eosophagus doing for you? This may be the cause of your high ferritin. I think I read that medications like Nexium can increase ferritin levels too. Check it out and go armed with information.
chorleyboy sheryl37154
Posted
Hi Sheryl, thank you for your message. At every blood let I ask to see or arrange an appointment with the Consultant, who is a Consultant Haemotologist. I am always told he is busy on the wards but at the first opporunity the nurse will mention my request. In April 2015 my ferritin level was 5265 and I was put on fortnightly phlebs. Because I had a tumour on the liver, I had a liver ablation carried out at St James's Leeds. and still continuing with the phlebs. My ferritin level has never been below 2000 and is always up and down. Last Wednesday it went up 300+ and when I go this Wednesday I will ask again to see the Consultant. I did try telephoning the Consultant's secretary who had my details up on screen and said, yes, I will speak to the Consultant, but never heard anything more. This was four months ago, and I then decided to go monthly to give blood but soon received a letter from the Consultant saying, no, that won't work, you must give blood weekly. So, for the last 12 weeks I have been doing that but there is no gradual reduction in the ferritin level. The esophagus I thought may be causing a high ferritin level but no-one has said anything other than take the tablets, omeprazole, which at my last GP visit, I explained that these tablets can cause possible liver damage and so he changed them to esomazole, and after reading the pamphlet inside, it said, possible kidney damage. I have a small lesion on my windpipe and was told that unless it increases in size or changes direction, then it would be left for now. Back at hospital this Wednesday giving blood and I will try again to see the Consultant. If and when I do, I have a list of questions. Regards Glyn
philx chorleyboy
Posted
Hi Glyn
Don't you think it's about time you enlisted outside help????
Contact your local pm or even the newspapers, it's your right to have
regular consultations with a consultant hemotologist,yours is a serious
Predicament and they are playing with your life???
Please don't delay with this,
Cheers philx
philx
Posted
Should be MP member of parliament, they appear to be giving you
No option, I think if you consultant gets a letter from your MP
You will very quickly get an appointment, it reflects badly not only
On the consultant but also the hospital.
Also maybe worth talking to pals at the hospital that is there job
To liaise between patients and hospital protocol.
Cheers philx
chorleyboy philx
Posted
sheryl37154 chorleyboy
Posted
Apart from Philx suggestion, or in accord with it, is there another haemotologist at the hospital? Ask to see another one, and say, as this one is not looking after me properly.
You are not likely to get to see one on demand when you turn up for your venesection. However, ask them for an appointment in advance while you are standing there and not leaving until you know the time/date.
And Glyn, eat your greens, they are good for you - they are NOT high in iron. Some other vegetables which you are probably eating all the time have much higher levels of iron.
chorleyboy sheryl37154
Posted