My operation was fine, no hitches but I won’t know for four months exactly how successful it’s been.
I thought it would be Dr Martin, I’m sure he will keep an eye on your levels and I’m also sure that you have to take them for years and years before you get problems with kidney stones …I’m told you need to drink masses of water, which I do now, to stop any thing like kidney stones.
Miserable day here in Herefordshire , hope it’s better in Stroud?
Hi All, Very interesting thread! My son Ben has just been told he has MS. I was wonder where is the best place to start to get a blood test to check vitiman levels. He has RRMS and is 21. Thanks
Firstly welcome to the forum to you and your son, lots of lovely people here always willing to listen and offer advice where they can.
You can ask your GP, ms nurse or neurologist for a blood test for vitamin d, also ask for B12 at the same time, as both can be low in ms. If he hasn’t yet been allocated a ms nurse, your GP can refer him to one, as there are now some very good drugs that help, and they can advise him.
Its a scary time to be told you have ms, although also a relief to have a name for the symptoms he is experiencing, but please tell him to give himself time to get his head round it, take one day at a time, as there is a very worthwhile life to be had even with ms.
Any other questions you or he may have, please ask.
I have been taking Adcal-D3 caplets along with Alendronic Acid tablets for a few years now… for Osteoporosis…!!! Just a reminder, Vitamin D is needed to help bones absorb Calcium.
I’m wondering whether anyone else has Osteoporosis along with a Vitamin D deficiency…?