Dating someone with cvid
Your story definitely takes me back to my early ivIg days, 14 years ago. I just wanted to thank you so much for this article, I am currently pregnant with my first, so I am a little emotional, but I started crying with relief to see that there is someone out there with the exact same story as myself.
If you like my blog please nominate me …
There was an article describing a prevalent strain of pneumonia and I recognised all my symptoms. You can find the forum here: The only thing that kept me going through the infusions was the knowledge that it was a short-term measure, and that as soon as the babies were born I could go back to my beloved subcutaneous infusions!
This made it easy for IV antibiotics to be dating someone with cvid twice a day, and it was arranged for district nurses to come and administer this for me. I am delighted to hear that you will, at last, be starting IgG replacement therapy soon.
In June he proposed to me, and the following March we got married. We are still hoping we can go through just one winter without an infection. A very moving and touching story of fortitude and determination. They were perfect, beautiful, and most importantly, healthy. Any suggestions for advise or contacts with similar experience is greatly appreciated. I love him so much, and am so scared of this big unknown for our future.
By this time I was still seeing the private GP regularly and he was concerned that I was not making the progress I should, and so he referred me to a private chest physician in Harley Street.
Having children has been something I am not sure I can cope with and reading that you have twins, well gives me some comfort. Best std dating site really enjoyed reading your story.
After some months on subcutaneous immunoglobulin it became apparent that, not only were my infusions infinitely more bearable, but my health was improving significantly.
I consider myself very fortunate that my parents were able to afford the huge cost of the x-rays and frequent trips to the GP, and slowly I began to feel a little better. I had bronchitis, I had asthma, I had allergies … and after each visit I was sent away with the prescription that would improve my life. And then plan how you will celebrate your first week of feeling well. Oddly enough, my answers came from 10 minutes away.
Your support has been amazing over the last few months xx. A more loving and coping mother would be difficult to find and the dating someone with cvid that you are able to entertain so many people just makes you a more fantastic person.
Diagnosis day was the first day of the rest of your life! When I was 17 I went on holiday without my parents for the first time — I went with six girls from school to Mallorca. Things went reasonably well for a while, and on the day that the results for my degree were due I phoned the course tutor who had been so supportive over the past few months.
I longed to have the energy levels my friends did. She had pulled in whatever favors she had and managed to have me worked in as an emergency.
Luckily I had taken my aunt to the immunology clinic with me, who had made notes and asked questions, and on the Tube journey home I gradually began to absorb what we had been told.
And in the meantime there are lots of people who have been through the same thing and can give you the moral support you need to get through each infusion.
I was delighted when I was offered a position in an organisation that provided play schemes for children with special needs. I completed my dissertation and filled in a form saying I had mitigating circumstances affecting my studies.
My Mum came with me to the clinic for my first treatment, and tried to put on a brave face as she watched her baby being connected up to a drip.