Experiences with

Complex regional pain syndrome

Been diagnosed with crps. An

It's Complex regional pain syndrome. ( Predictive text!!).

hello just wondering if anyone has heard of or received this treatment for CRPS..or any other type of pain…this would be for the lower extremities..

hello I am rather new here … I am wondering if anyone here has had this type of problem and any advise..my daughter has CRPS and her husband is divorcing her because of it becoming worse..just wondering if anyone has had a divorce due to this or any other type of pain disorder if so are there lawyers

I have been using oestrogel for over a year now and swapped to hrt patches about 2 months ago.I never tested for oestrogen or prog levels though.i am 52.I have been taking elvanse for adhd for over a year also...again didn't take any bloods. I am now in thos last week upping 150to 175 levothyroxine and

Hello All So I have blood tests coming up and I have been taking ferritin/iron tablets 210mg for the last 10 weeks. I have my blood test in 2 weeks. These are all the ones I currently take can someone help which to stop and the times to stop. Ferritin 210mg Vit c effervescent Complex B complex all 8

I started the B1 therapy in October 2023 (was diagnosed with YOPD in February 2023) following the protocol written on the book “Parkinson’s and the B1 Therapy” by Daphne Bryan. For the past 10 months, it has been helping me controlling symptoms such as extreme tiredness, lack of balance, dystonia, rigidity

On 8th April 2024 I had a blood test as I was feeling tired and generally under par, tested my TSH 3.7 ( 0.27-4.2) T4 12.6 (12-22) so my dr increased my Levothyroxin to 75mcg. I felt a little bit better but had another blood test on 5th June and my result was TSH 3.01 and my T4 13.7 I'm feeling tired

Hi everyone! Sharing my last test results!My levels all seem to be better, Antibodies are still high though, do you think is still worth keeping a GF and DF diet? I had the idea that removing gluten and dairy would magically reduce antibodies 😅 My symptoms have improved a bit, but I cannot say I'm

Regional Pain Syndrome and I have to have a specialist team doing the operation.

Hello everyone,I would really appreciate any advice regarding my latest fasting blood tests, done before taking my Levothyroxine tablet. I am still on 75mcg Levothyroxine since diagnosed with Hashimoto's in 2010. After my latest post, around Nov 2022, I followed the advice I was given and started taking

So now I walk with a limp and I have developed Complex Regional Pain Syndrome. Which I cannot take any pain killers due to being allergic to them, only paracetamol which is a waste of time.

I have tried steroid injection and it didn't do anything to relieve my pain and I've even worn braces and take an anti-inflammatories and it didn't relieve any pain. What complicates this further is that I have complex regional pain syndrome CRPS also known as RSD.

Lately I feel tired all the time, from when I wake up to when I go to bed in the evening, despite the fact that I sleep more than 8 hours per night. I take a lot of supplements (calcium, D3, folate, complex B, magnesium glycinate, heme iron), the only value that was low was ferritin but I do take

Hello againI just wondered if anyone who us suffering or suffered from this had swelling which went up and down, temperature changes and skin colour changes and if so how is this treated please? Also has anyone tried either low level or high level laser treatment and what was the outcome? Thanks

I have been taking shot of Prolia and shot of methotrexate every Tuesday.i have no pain but have tender spots on my head and if does not hurt to touch. I only seem to have it in my temple are and top and back of head.. I had a mri of my head a few years ago. I have had a couple of bad concussions 2

Let me start by saying that I have full body complex regional pain syndrome CRPS otherwise known as reflex sympathetic dystrophy RSD. So that is what is complicating this whole thing because it is most likely a flare of this neurological nerve pain disorder.

Has anyone in our group tried the antispasmodic Spasfon? Generic name is Phloroglucinol. It is approved and is an over the counter medication in France, Spain and I believe in a few other countries but not in the U.S. The research studies that I reviewed shows promise for IBS-D related pain and

I wanted to ask if anyone had to contemplate FET cycle that falls over Christmas? I had failed FET in January it took 12 months to reach this point because I decided to go attend RIF clinic but all the waiting time then treatment to hopefully deal with implant failure has meant my next cycle can start

Part of AI's response to "acetyl-l-leucine anxiety" Elevated lactate levels in the brain can occur with several neurological disorders, including anxiety, major depressive disorder, and Parkinson's disease. High levels of lactate can lower the brain's pH, which can affect neuronal activity and the