FAQ/Help |
Calendar |
Search |
Today's Posts |
![]() |
#7 | ||
|
|||
Junior Member
|
Quote:
I understand what you mean about self-medicating, I guess I have just been a bit desperate, especially having to wait to see a specialist. I'm not going to self medicate again, but was wondering if an immuno-suppressant like prednisone is worth asking the Neuro about, in case this is a result of some sort of immune system problem? being that my colitis is auto immune, could there be other auto immune problems going on? I hate taking pednisone for my colitis which I do short courses now and again (10-14 days) to control flares, but if it could help with this burning at all, I would do anything. The adrenal support caps I have been taking, but not since this started were: Vitamin B5 (calcium pantothenate) 150mg Vitamin B6 (pyridoxine hydrochloride) 50mg Vitamin C (ascorbic acid) 150mg Copper (copper glutamate) 500mcg Magnesium (aspartate) 50mg Potassium (citrate) 50mg L-Tyrosine 100mg Zinc 7.5mg Acanthopanax senticosus (Siberian Ginseng) root ext. 50mg Centella asiatica (gotu kola) herb 6:1 ext. 50mg Glycyrrhiza glabra (licorice root) ext. 100mg Rehmannia glutinose (shu di huang) root 5:1 ext. 100mg Withania somnifera (Indian ginseng) root 125mg Ginger Root 50mg and the Pentasa I have stopped as I said, as my renal function was slightly impaired. I just have to hope and pray a little that my Colitis stays under control without the pentasa for now, until I can speak to my gastro about my renal function and any alternatives to Pentasa in case this is causing the issues. As it can be toxic on the Kidney. The Neurologist was of the opinion that I do not have PN, as it was not presenting in the typical fashion. All vibration, skin prick, reflex, hot/cold sensation and muscle strength were fine. Which is why I tried to bring attention to the pubmed article on the dorsal ganglia, but it seems that he either didn't want to be shown something "from the internet" or maybe he just doesn't have enough experience with these sorts of Neuronopathies to recognise the symptoms. As even the article said those sorts of SFG's were not well recognised, So I'm guessing, in a country of 4 million down here, it's not often diagnosed. Your advice on this is very much appreciated. |
||
![]() |
![]() |
|
|
![]() |
||||
Thread | Forum | |||
We Search… | Creative Corner | |||
Burning back.... | Peripheral Neuropathy | |||
The search for WHY!? | Survivors of Suicide | |||
Burning pain at mid-back | Multiple Sclerosis | |||
Back to no answers | Gluten Sensitivity / Celiac Disease |