Oral Iron Therepy

Here you can share your experiences with substances that are ingested, inhaled, or otherwise consumed for the purpose of relieving RLS, other than prescription medications. For example, herbal remedies, nutritional supplements, diet, kratom, and marijuana (for now) should be discussed here. Tell others of successes, failures, side effects, and any known research on these substances. [Posts on these subjects created prior to 2009 are in the Physical Treatments forum.]

Important: Posts and information in this section are based on personal experiences and recommendations; they should not be considered a substitute for the advice of a healthcare provider.
Post Reply
RLS113
Posts: 11
Joined: Fri Oct 14, 2022 9:13 pm
Location: New Hampshire

Oral Iron Therepy

Post by RLS113 »

Hi folks
For those that oral iron supplements worked, how long after beginning oral therapy did it take to notice a difference??

Polar Bear
Moderator
Posts: 8823
Joined: Tue Dec 26, 2006 4:34 pm
Location: United Kingdom

Re: Oral Iron Therepy

Post by Polar Bear »

I did take oral iron for a while but stopped because of constipation.
However I understand it takes several months to show an increase and may take a lot longer to increase enough to show benefit. Sometimes oral iron cannot be increased sufficiently to show benefit.
Betty
https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation

Rustsmith
Moderator
Posts: 6515
Joined: Sat Sep 28, 2013 9:31 pm
Location: Colorado Springs, Colorado

Re: Oral Iron Therepy

Post by Rustsmith »

When I was first diagnosed, my ferritin was 46. After several months of taking oral iron two or three times a day, it was up to 90 but had no effect on my RLS. I continued taking it once a day for several years and eventually hit 650 and it never helped my RLS.

The Johns Hopkins data shows that only about 65% benefit from increased ferritin levels. For the rest of us, the theory is that there is a genetic issue that limits iron transport from the blood into the brain. For my group, infusions and oral iron don't help.
Steve

https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.

SquirmingSusan
Posts: 3028
Joined: Sun Nov 12, 2006 4:08 am
Location: Minnesota
Contact:

Re: Oral Iron Therepy

Post by SquirmingSusan »

You might find this website helpful. Caitlyn is releasing a book soon, and also has the whole "Iron Protocol" up in a Facebook group. https://theironprotocol.com/our-story/
Susan

TimG
Posts: 113
Joined: Wed Nov 23, 2011 2:26 pm

Re: Oral Iron Therepy

Post by TimG »

My ferritin level was 19 mg/dL when my PCP first measured it several years ago. After taking oral iron, 65 mg, daily it eventually got past 50 mg/dL in several months. It took about a year, but ferritin levels eventually reached 100 mg/dL. I only occasionally get RLS nowadays, and take 0.125 mg pramipexole when I do. I started taking pramipexole about a decade ago and have never augmented and never raised the dosage.

golfer904
Posts: 7
Joined: Sat Jun 12, 2021 11:00 am

Re: Oral Iron Therepy

Post by golfer904 »

My ferritin was 33 in March of 2022, I began taking 325 mgs of ferrous sulfate with 100 mgs of vitamin C every evening. After one year my ferritin measured 161, and my RLS symptoms have diminished a lot. I still take monthly B 12 injections as I was deficient in 2021. I believe the entire experience is related to the fact that I was diagnosed with atrophic gastritis in 2021 as well.

Rustsmith
Moderator
Posts: 6515
Joined: Sat Sep 28, 2013 9:31 pm
Location: Colorado Springs, Colorado

Re: Oral Iron Therepy

Post by Rustsmith »

Gastritis can certainly interfere with iron adsorption and thereby lead to low ferritin levels. It is great that you have been able to increase your ferritin to 161 after a year of oral iron and that it has helped with your RLS. Some doctors might say that you need to reduce the oral iron at this point, but Dr Earley at Hopkins believes that a ferritin level of 300 is the target for some people.
Steve

https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.

golfer904
Posts: 7
Joined: Sat Jun 12, 2021 11:00 am

Re: Oral Iron Therepy

Post by golfer904 »

Thanks for the reply Steve, I stopped taking the iron pills as they were causing digestive distress, and heartburn. I still have symptoms, but they are minor compared to what they were.

Rustsmith
Moderator
Posts: 6515
Joined: Sat Sep 28, 2013 9:31 pm
Location: Colorado Springs, Colorado

Re: Oral Iron Therepy

Post by Rustsmith »

There is a different iron product that is not iron sulfate that is supposed to be easier on the stomach. Often it goes by a name like "gentle iron". Often these are either iron gluconate or iron glycinate. It is more expensive than iron sulfate and you may need to take more than one pill in order to get the 65mg equivalents of iron. But it might be worth a try since iron sulfate helped other than the stomach distress.
Steve

https://www.mayoclinicproceedings.org/a ... 0/fulltext
Opinions presented by Discussion Board Moderators are personal in nature and do not, in any way, represent the opinion of the RLS Foundation, and are not medical advice.

Frunobulax
Posts: 438
Joined: Mon Jun 02, 2014 7:41 pm

Re: Oral Iron Therepy

Post by Frunobulax »

Rustsmith wrote:
Mon Dec 05, 2022 5:34 pm
When I was first diagnosed, my ferritin was 46. After several months of taking oral iron two or three times a day, it was up to 90 but had no effect on my RLS. I continued taking it once a day for several years and eventually hit 650 and it never helped my RLS.

The Johns Hopkins data shows that only about 65% benefit from increased ferritin levels. For the rest of us, the theory is that there is a genetic issue that limits iron transport from the blood into the brain. For my group, infusions and oral iron don't help.
I'm not a big fan of "genetic", because a lot of times it's used as substitute for "something that we don't have biomarkers yet, but it ruddy well needs a cause so let's say it's genetic".

Iron transport can be impaired due to nutritional or environmental factors. For example, oxalates (which we eat in large quantities in modern nutrition, much more than or hunter-and-gatherer predecessors) blocks iron transport. Iron release time is delayed by a factor between 20 to 500 (https://www.sciencedirect.com/science/a ... 3604003523).

Post Reply