Morning, just to give you an update on my immunity, I have heard from my Gp who has told me that I am going to be seen at a specialist Hospital for immune disorders
I have also been booked in for a covid booster 4th and I am only 64
I would have been more worried if I hadn’t started on vit D 3 as it has seemed to have improved my muscles and muscle spasms and I haven’t had a cough since, I also don’t need any help to get off the floor after playing with my grandson
Thank you Mary for giving information on Vit d3
Because I have Hughes Syndrome plus other conditions that have been caused by it, I have just accepted things mainly as I am fed up with local hospitals Gp etc
Although I must say I have had excellent care fromSt Thomas’s
Anyway, if anyone has symptoms don’t assume it’s caused by Hughes syndrome, keep fighting
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daisyd
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Hiya, well done with your progress, I too felt better on B12 and D3, plus Thyroid treatment once I got to the bottom of things. It is not unusual with Hughes/APS and Lupus etc to have deficiencies, which make us feel worse, my iron is also better than it was. MaryF
Thanks daisyd! You’ve been on my mind ever since your last post re you immunoglobulins levels. Glad to have your good news. Hope you’ll continue to keep us posted!
My University Hospital specialist Immunology dept looks after immune disorders & has been giving me great care for years now due to my below normal reference range Immunoglobulins G, A, M (panhypogammaglobulinaemia, a Primary Immunodeficiency Disease aka Antibody Deficiency Disease). thanks to them, I have been doing much better generally health-wise. So, my feeling is your specialist team will too
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