Myelodysplastic syndrome (MDS) and skin itching
what can be done for extreme itching from myelodysplasia
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what can be done for extreme itching from myelodysplasia
Interested in more discussions like this? Go to the Blood Cancers & Disorders Support Group.
@twitt1949, I moved your question about MDS and skin itching to this existing discussion where you can connect with others.
- Myelodysplastic syndrome (MDS) and skin itching
https://connect.mayoclinic.org/discussion/myelodysplasia-and-skin-itching/
Hi! Nancy here in Virginia.
Re: MDS AND ITCHING
i am on Inqovi every month, having transfusions mostly twice a week, and have MDS. All three cause itching and doctor can’t say which is causing mine. The only things I have found that helps are low dose of gabapentin 3x a day and 25 mg of hydroxyzine at nite which also helps at night. Anyone have anything better?
Antihistamines are fine if you don’t also have dry mouth, which I do.. nancy
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1 ReactionTry gabapentin and/ hydroxyzine which also helps with insomnia. With your doctor’s approval of course
@nancytrudeau. You’re so right, antihistamines can dry up more than a runny nose or relieve itching. Sorry to see you suffer from a dry mouth along with the itching from your MDS.
Dry mouth can be caused by underlying illnesses but also medications. While not permanent fixes there are a number of products on the market that can relieve the worst of the symptoms. There are a bunch of discussions in the forum regarding the remedies for dry mouth. Here is one link to get you started. Below that I posted a link to the full search.
Dry Mouth Remedies
https://connect.mayoclinic.org/discussion/dry-mouth-remedies/
~The search results for Dry Mouth Remedies. https://connect.mayoclinic.org/search/
Since you’re new to Connect let me welcome you to the forum. We have a very active and supportive MDS support group with members sharing their experiences.
This link will show the MDS discussions where you can feel free to jump into any conversation.
https://connect.mayoclinic.org/search/
How long ago were you diagnosed with MDS?