LDN side effects: tingling, pain, numbn... - LDN Research Trust

LDN Research Trust

1,423 members1,520 posts

LDN side effects: tingling, pain, numbness ?

ilyfunnybunny profile image
5 Replies

Hello!

I'm a 26-year-old female with a history of thyroid cancer, and I just started taking LDN 4 weeks ago, working up to the current dose of 3mg. Over the past week or so I've noticed random tingling, numbness, and pain throughout my arms, legs, and neck. I wasn't experiencing any of these symptoms before—I'm taking LDN for cancer prevention and immune regulation after a prolonged case of mono, not MS or any diagnosed autoimmune disease.

I've read a couple of horror stories online where people have experienced an onset of MS-like symptoms by taking LDN, which did not resolve upon quitting the drug, and I'm concerned that I may have made a mis-step in trying this generally benign treatment.

I'm wondering if anyone here has experienced similar side effects, or has any insight into the issue.

Thank you!

Written by
ilyfunnybunny profile image
ilyfunnybunny
To view profiles and participate in discussions please or .
5 Replies
roskaspi profile image
roskaspi

I also wrote a question on this chat about the increased numbness I was experiencing in my feet going up my shins after staring LDN. I do not have the same illness you do, but from what I understand from reading extensively, this medication takes time. sometimes as much as 4 - 6 months. I have been taking LDN now for 2 months but reached 4.5 mg about 3 weeks ago. I put a lot of faith in this treatment and decided that I would give it time and wait patiently for the medication to "adjust" and for my body to "adjust". I hope this helps you with your decision.

ilyfunnybunny profile image
ilyfunnybunny in reply toroskaspi

Hi there!

Thanks for your reply. I've been trying to be patient as well, and allow for a period of adjustment. And I definitely love the anti-depressant effects of LDN—I haven't feel this emotionally level in at least a year.

I hope you get what you need from the medication, and feel free to let me know how things go for you. :)

aredtigress profile image
aredtigressAdministrator

The random tingling & pain is not a typical response to LDN, however with Thyroid issues those can happen. Are you also on Thyroid medications? I'm not a medical professional, so don't have a good understanding of the protocol for Thyroid cancer. As an admin here and on the Trust's Facebook page, I've seen many people have to adjust thyroid medications after staring LDN.

Roskaspi is correct, it can take up to 6 months to see benefits, some people report seeing new benefits after the 1 year mark as well. LDN is a journey, it takes *Patience - Tolerance - Positivity - Willingness to make adjustments*

as we each respond differently.

Have you listened to the testimonials about cancer on the Trust's website? Here's the link: ldnresearchtrust.org/ldn-vi...

Hope this helps!

Michelle

ilyfunnybunny profile image
ilyfunnybunny in reply toaredtigress

Hi tigress,

Could you tell me more about thyroid medication adjustments that people have had to make after starting LDN? I'm curious if they've had to increase or decrease their dosage.

Also, while proper thyroid hormone replacement is something I have struggled with for a couple of years, I've never experienced neurologic symptoms before. The onset of tingling, numbness, etc. directly corresponded with the most recent increase in my LDN dosage, and the sheer coincidence made me wonder about a potentially causal relationship between the symptoms and the drug.

While perhaps uncommon, it seems like people still ought to be aware of such reported side effects before embarking on the therapy, especially since LDN is still an experimental medication.

aredtigress profile image
aredtigressAdministrator

Most of the changes I read about are to lower dosages - but that is done with a doctor's knowledge. It's not my area of knowledge, there are a number of great interviews with doctors and papers accessible on the Trust's website. I highly encourage you to continue your research there.

Since these are new symptoms, please contact your doctor. There can be many reasons for neurologic symptoms, and she/he would be your best resource for guidance. If your doctor isn't able to help, there is a form at the bottom of the home page on the Trust's website to submit medical questions, it's a good resource.

Michelle

Not what you're looking for?

You may also like...

LDN and insomnia

Has anyone had insomnia from LDN? I just started taking it last night and only slept for about 20...
KristinCC profile image

LDN and thyroid

I'm currently taking 4.5 mg LDN morning and night. Besides Fibromyalgia, I'm also hypothyroid and...
ratoncita profile image

LDN Dosage for Ovarian Cancer

Hi I'm lookin for this information for my mother, basically just been informed she has months to...
MOLLYPOPPY profile image

Help with LDN

Hi. I have hashimotos and osteoartritis so was hoping ldn would help. I have been taking ldn for...
AKatieD profile image

Taking Tramadol with LDN for ME/ CFS and Fibromyalgia.

Morning All! I just started on 0.5 LDN this week. I have ME/ CFS, Fibromyalgia and I'm Hypothyroid...
Abi-Abster profile image

Moderation team

Shewulf profile image
ShewulfAdministrator
aredtigress profile image
aredtigressAdministrator
LDNRT profile image
LDNRTPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.