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Ceftazidime intravenous infusion
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Mylo Fibrosis, et al
Hello. I'm new to this community and frankly new to social networking on health. My abbreviated story is that I transitioned to Mylo Fibrosis (MF) a few years ago, after dealing with Polycythemia Vera (PV) for 25+ years (I'm 66 years old). The PV regimen was inclusive of Phlebotomies, meds such as Agrilyn
Hello. I'm new to this community and frankly new to social networking on health. My abbreviated story is that I transitioned to Mylo Fibrosis (MF) a few years ago, after dealing with Polycythemia Vera (PV) for 25+ years (I'm 66 years old). The PV regimen was inclusive of Phlebotomies, meds such as Agrilyn
luvinretirement
in
MPN Voice
11 months ago
PIP Application form (Typing replies)
A little about me.I have been diagnosed with :- Lupus Rheumatoid Arthritis Fibromyalgia Underactive thyroid Hyperparathyrodism Carpal tunnel syndrome Osteoarthritis Depression Lower back spinal fusion Constant huge fatigue and brain fog I am planning on applying for PIP for the first time and
A little about me.I have been diagnosed with :- Lupus Rheumatoid Arthritis Fibromyalgia Underactive thyroid Hyperparathyrodism Carpal tunnel syndrome Osteoarthritis Depression Lower back spinal fusion Constant huge fatigue and brain fog I am planning on applying for PIP for the first time and
SLEepyhead123
in
NRAS
10 months ago
CAR-T Trial Update #3
Hello friends, I had planned on updating everyone much sooner, but life got in the way a bit. Last I wrote, I had received my T-cells back on June 5, 2023. The first few days were totally uneventful. I was walking the halls a lot, staying active, reading, and getting dressed in regular clothing every
Hello friends, I had planned on updating everyone much sooner, but life got in the way a bit. Last I wrote, I had received my T-cells back on June 5, 2023. The first few days were totally uneventful. I was walking the halls a lot, staying active, reading, and getting dressed in regular clothing every
nvp815
in
CLL Support
11 months ago
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Lori, NURSE
I worked in a homeless program where I worked 70-70 hours a week. I was in a BSN program full time. I caught meningitis from the homeless program. I went from a thriving healthy nurse who got the scholarship for school by being an exemplary Nurse. At first I thought it was a bad flu with light sensitivity
I worked in a homeless program where I worked 70-70 hours a week. I was in a BSN program full time. I caught meningitis from the homeless program. I went from a thriving healthy nurse who got the scholarship for school by being an exemplary Nurse. At first I thought it was a bad flu with light sensitivity
FeelingDesperate
in
Meningitis Now
11 months ago
alternative therapies
Hi, I was diagnosed in Feb2020, SLL, Unmutated, started treatment with FCR which gave me 18months before swollen nodes and spiking bloods showed the SLL was back. During my no treatment time I had a nasty case of Shingles which lasted 3 months then RSV which lasted 6 months. In September 22 I started
Hi, I was diagnosed in Feb2020, SLL, Unmutated, started treatment with FCR which gave me 18months before swollen nodes and spiking bloods showed the SLL was back. During my no treatment time I had a nasty case of Shingles which lasted 3 months then RSV which lasted 6 months. In September 22 I started
MareeM
in
CLL Support
1 year ago
Thrombocytopenia?
I have APS, Sjogren's, hypothyroidism and a host of other complaints. One of these is easy bruising and bleeding. So much so that I can no longer play with the dogs in case their claws catch me, I can't get to the outdoor tap because it's buried in the hedge that will attack me and wrench off a lump
I have APS, Sjogren's, hypothyroidism and a host of other complaints. One of these is easy bruising and bleeding. So much so that I can no longer play with the dogs in case their claws catch me, I can't get to the outdoor tap because it's buried in the hedge that will attack me and wrench off a lump
Coppernob
in
Hughes Syndrome APS Forum
1 year ago
Anxiety about all the immune based meds
HiIt looks like when I do an embryo transfer I will be on quite a large cocktail of medication. Recommendations for me are IVIG, steroids, clexane, asprin and intramuscular progesterone. I had an array of tests done which showed high NK cells and cytokines and an issue with the blood hence this medley
HiIt looks like when I do an embryo transfer I will be on quite a large cocktail of medication. Recommendations for me are IVIG, steroids, clexane, asprin and intramuscular progesterone. I had an array of tests done which showed high NK cells and cytokines and an issue with the blood hence this medley
Skittles11
in
Fertility Network UK
1 year ago
ivig advice and experiences
hi all I need to have IVIG for my frozen embryo transfer soon. We have been quoted 1.8k . …just wondering how much you paid and how many infusions of IVIG you needed? thanks!
hi all I need to have IVIG for my frozen embryo transfer soon. We have been quoted 1.8k . …just wondering how much you paid and how many infusions of IVIG you needed? thanks!
Poop84
in
Fertility Network UK
1 year ago
ERA results advice needed
Hi I have had my endo trio me test my Emma Alice and era results back. All is fine but I have elevated nk cell blood markers in particular cd19 ….I did a Google and it says it’s indicative of b lymphoma or an auto immune issue. Has anyone experienced this? I don’t want to worry but my consultant didn
Hi I have had my endo trio me test my Emma Alice and era results back. All is fine but I have elevated nk cell blood markers in particular cd19 ….I did a Google and it says it’s indicative of b lymphoma or an auto immune issue. Has anyone experienced this? I don’t want to worry but my consultant didn
Poop84
in
Fertility Network UK
1 year ago
Candida with Cellcept
I am being treated for primary ethromelalgia, Sjogrens, and Scleroderma. Has anyone had oral thrush associated with taking Cellcept? I have been on Cellcept for three months and IVIG for 14 months. Today, the inside of my lower lip exploded with white bumps. My research indicates that Candida is common
I am being treated for primary ethromelalgia, Sjogrens, and Scleroderma. Has anyone had oral thrush associated with taking Cellcept? I have been on Cellcept for three months and IVIG for 14 months. Today, the inside of my lower lip exploded with white bumps. My research indicates that Candida is common
HALNEUROPATHY
in
Scleroderma & Raynaud's UK (SRUK)
1 year ago
Zanubrutinib and water intake and sodium level
I am a 78 year old woman who has been on a very long watch and wait since 1999. I was diagnosed in 1998 and given a small amount of prednisone and chlorambucil and have received nothing since except ivig which started in June2021 due to infections. My watch and wait is over as I will be starting treatment
I am a 78 year old woman who has been on a very long watch and wait since 1999. I was diagnosed in 1998 and given a small amount of prednisone and chlorambucil and have received nothing since except ivig which started in June2021 due to infections. My watch and wait is over as I will be starting treatment
Bethsaida
in
CLL Support
1 year ago
When to give up.....?
So today I got a BFN on my latest round. Was my 7th in total but 5th failed transfer (nothing to transfer in the other 2). It was our 3rd transfer with donor eggs. I know I have some immune issues and they've tried various options to treat them- prednisole, tacrolimus, IVIG, granocyte. How do you decide
So today I got a BFN on my latest round. Was my 7th in total but 5th failed transfer (nothing to transfer in the other 2). It was our 3rd transfer with donor eggs. I know I have some immune issues and they've tried various options to treat them- prednisole, tacrolimus, IVIG, granocyte. How do you decide
river242
in
Fertility Network UK
1 year ago
Brain shrinking
My husband has had encephalitis for 16 months now and no treatment has worked so far. He has had steroids, IVIG, plasma exchange and rituximab and hes been deteriorating since the day he was diagnosed. Doctors have now said his brain is shrinking but I have not heard this from anyone else with encephalitis
My husband has had encephalitis for 16 months now and no treatment has worked so far. He has had steroids, IVIG, plasma exchange and rituximab and hes been deteriorating since the day he was diagnosed. Doctors have now said his brain is shrinking but I have not heard this from anyone else with encephalitis
Kw55
in
Encephalitis Society
1 year ago
update
i informed in my last post about my father advised to start acalabrutinib soon . but it was paused for some time as we admitted him in hospital last to last week due to sudden onset of fever and cough . after a 5 days course of amoxicillin followed by first IVIG the fever went down & it took 4-5 days
i informed in my last post about my father advised to start acalabrutinib soon . but it was paused for some time as we admitted him in hospital last to last week due to sudden onset of fever and cough . after a 5 days course of amoxicillin followed by first IVIG the fever went down & it took 4-5 days
Hidden
in
CLL Support
1 year ago
pseudomonas Again!
I had my last pseudomonas colonization around 20 days ago which included treatment with ceftazidime iv along woth ciprofloxacin for 14 days. 5 days ago things were settled until I got a low grade fever below 101 after that I visited my doc and he prescribed me levofloxacin and said it is not possible
I had my last pseudomonas colonization around 20 days ago which included treatment with ceftazidime iv along woth ciprofloxacin for 14 days. 5 days ago things were settled until I got a low grade fever below 101 after that I visited my doc and he prescribed me levofloxacin and said it is not possible
Warrior4104
in
Lung Conditions Community Forum
2 years ago
SI joint osteoarthritis
Anyone had successful si joint fusion?
Anyone had successful si joint fusion?
Jeaniem130
in
Cure Arthritis Community
1 year ago
PICSI or ZYMOT? also Intralipid or IVIG?
Good Morning everyone, I hope you are all well and having a good start to the week. I am hoping someone can add some valuable points or thoughts to help on our next and final round of ICSi. We have had 6 rounds of ICSI and the closest we got to a BFP, sadly ended up an ectopic on round 5. This round
Good Morning everyone, I hope you are all well and having a good start to the week. I am hoping someone can add some valuable points or thoughts to help on our next and final round of ICSi. We have had 6 rounds of ICSI and the closest we got to a BFP, sadly ended up an ectopic on round 5. This round
Annjali
in
Fertility Network UK
1 year ago
Finished the antibiotic course 15 days ago for pseudomonas colonization in lungs. Now fever has come up again
I was diagnosed with bronchiectasis around a month ago with pseudomonas. My doc had prescribed me ceftazidime IV along with ciprofloxacin for 14 days I got really better after completing the antibiotic course but from today I am getting a fever of about 100.3•Fahrenheit at 6 hours interval along with
I was diagnosed with bronchiectasis around a month ago with pseudomonas. My doc had prescribed me ceftazidime IV along with ciprofloxacin for 14 days I got really better after completing the antibiotic course but from today I am getting a fever of about 100.3•Fahrenheit at 6 hours interval along with
Warrior4104
in
Lung Conditions Community Forum
2 years ago
Low IgE...
I just got this result today... Even thouhh no lower limit shown, should I get worried for such a low IgE? Background: I am having monthly IVIG ingusion after 6 months of chemo due to low immunoglobulin levels... today gave blood sample ans waiting for the results..First time seeing IgE result...Previously
I just got this result today... Even thouhh no lower limit shown, should I get worried for such a low IgE? Background: I am having monthly IVIG ingusion after 6 months of chemo due to low immunoglobulin levels... today gave blood sample ans waiting for the results..First time seeing IgE result...Previously
eekibin
in
CLL Support
1 year ago
Further problems with allergy - what to do?
In February I wrote a post about an allergy crisis that I had just had, and many of you responded very kindly with good feedback and information. The situation has however developed and I am now feeling more at a loss than before and would certainly appreciate further comments and feedback. I will
In February I wrote a post about an allergy crisis that I had just had, and many of you responded very kindly with good feedback and information. The situation has however developed and I am now feeling more at a loss than before and would certainly appreciate further comments and feedback. I will
Provence
in
CLL Support
1 year ago
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