Home         Forums  

Go Back   Marrowforums > Bone Marrow Failure Diseases > Bone Marrow Failure
Register FAQ Search Today's Posts Mark Forums Read

Bone Marrow Failure Causes, treatment approaches, terminology, related diseases

Reply
 
Thread Tools Search this Thread
  #1  
Old Sun Feb 1, 2015, 07:42 PM
Shazza Shazza is offline
Member
 
Join Date: Jul 2013
Location: United Kingdom
Posts: 22
Neutropenia & Skin Rashes

Following the recent bad press in the UK connecting Antihistamine & Dementure, I have stopped taking anti itch pills.
So now I'm itching like mad. My neck, shoulders & arms, ankles & wrists seem to be most affected. My skin comes up in big red wheals when I scratch although I try my hardest not to.
I understand this could be related to my low neutrophils (currently 0.8).
Does anyone else have neutropenia & skin rashes?
Can somebody suggest an effective natural treatment please.
__________________
Neutrophils fluctuating between 0.8 & 1.7 since 2000.
Hypoplastic bone marrow (10-15% cellularity).
No cytogenetic abnormalities.
Reply With Quote
  #2  
Old Sun Feb 1, 2015, 09:51 PM
Cheryl C Cheryl C is offline
Member
 
Join Date: Dec 2011
Location: Lake Macquarie, Australia
Posts: 843
Hi Shazza

I've had neutropenia for around 10 years. I had itches like hives but only when I had excess blasts.
__________________
Dx MDS RAEB 10% blasts + hypogammaglobulinemia, Sep 2011. Jan 2012 BMB - blasts down to 2% w/out treatment so BMT cancelled. Re-diagnosis RCMD. Watch and wait from Feb 2012. IVIg 5-weekly. New diagnosis Oct 2019 AML 23% blasts in marrow, 10% blasts in peripheral blood.
Reply With Quote
  #3  
Old Mon Feb 2, 2015, 11:27 AM
Marlene Marlene is offline
Member
 
Join Date: Oct 2006
Location: Springfield, VA
Posts: 1,412
John would get hives from the cold and friction which was a result of low platelets for him. Once his platelets improved, so did the hives. But he's still prone to hives from time to time. One will pop up for no reason. He had isolated cases as a child but it really showed up with a vengeance when he got transfusions..mostly platelets. He had one platelet bag that gave him serious head to toe hives. And from then on, until his platelets improved, he got hives very easily in the winter when we went for walks.

I ended up getting him long underwear and made up an essential oil blend that he would apply prior to walking to prevent a breakout.

I think the blood vessels were more permeable because of low platelets and histamines would be released causing a reaction. Anything that relaxed his blood vessels too much could trigger a reaction.

You may try looking into supplements/food that lower histamines levels. Or look into foods that may increase histamine reactions and eliminate them from your diet.

Since homeopathy is popular in the UK, have you considered consulting with one?

Also consider trying a gluten free diet for a while.
__________________
Marlene, wife to John DX w/SAA April 2002, Stable partial remission; Treated with High Dose Cytoxan, Johns Hopkins, June 2002. Final phlebotomy 11/2016. As of July 2021 HGB 12.0, WBC 4.70/ANC 3.85, Plts 110K.
Reply With Quote
  #4  
Old Mon Feb 2, 2015, 01:22 PM
curlygirl curlygirl is offline
Member
 
Join Date: Jun 2013
Posts: 151
Not sure if this article is the study you're referencing: http://www.sciencedaily.com/releases...0126124721.htm

If so it said that anticholinergic medications, including Benadryl & other diphenhydramine drugs, were linked with developing dementia BUT it also says that second-generation antihistamine like loratadine (Claritin) for allergies are safe. Maybe Claritin would help instead?
Reply With Quote
  #5  
Old Wed Feb 4, 2015, 05:29 AM
Shazza Shazza is offline
Member
 
Join Date: Jul 2013
Location: United Kingdom
Posts: 22
Thank you for your replies.

I've been avoiding gluten for the past 6 months Marlene but that doesn't seem to have made any difference to the itching - I don't seem to ache quite as much though!
I hadn't thought about homeopathy so might give it a whirl - I'll let you know how I get on.

Thank you Curlygirl for the link. If I'm honest, it was a bit of a knee jerk reaction giving up the pills after reading just one article. However, I must've been taking a lot as I'm shocked to find how much I itch without them.
I'd prefer to get to the bottom of the problem & avoid pills altogether but it's good to know that Claritin is an option.
__________________
Neutrophils fluctuating between 0.8 & 1.7 since 2000.
Hypoplastic bone marrow (10-15% cellularity).
No cytogenetic abnormalities.
Reply With Quote
Reply


Thread Tools Search this Thread
Search this Thread:

Advanced Search

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

vB code is On
Smilies are On
[IMG] code is On
HTML code is Off
Forum Jump

Similar Threads
Thread Thread Starter Forum Replies Last Post
NOBODY with Bone Marrow Failure is that hurt. Barbara Anne Heinen Tell Your Story 11 Wed Feb 24, 2016 01:17 PM
Skin issues post BMT ecb220 Transplants 1 Tue Oct 7, 2014 05:18 PM
Acute GVHD if the skin MDSPerth Transplants 7 Sun Feb 9, 2014 11:57 PM
Chronic GVHD Skin suggestions? BrianFlaigmore Transplants 4 Tue Jul 2, 2013 05:17 PM
Dad has MDS, has anyone experienced this skin problem? Donna E MDS 16 Sat Aug 9, 2008 11:22 AM


All times are GMT -4. The time now is 11:35 AM.


Powered by vBulletin® Version 3.6.7
Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.
Forum sites may contain non-authoritative and unverified information.
Medical decisions should be made in consultation with qualified medical professionals.
Site contents exclusive of member posts Copyright © 2006-2020 Marrowforums.org