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Zenpep
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Need Relief
I have EPI for which I am prescribed PERT (
Zenpep
40K). I have also had a Celiac Plexis Nerve Block which provided some pain relief (~20%?). I am almost always in mild to moderate pain with severe flareups on occasion (every 4 weeks or so).
I have EPI for which I am prescribed PERT (
Zenpep
40K). I have also had a Celiac Plexis Nerve Block which provided some pain relief (~20%?). I am almost always in mild to moderate pain with severe flareups on occasion (every 4 weeks or so).
TVspike
in
Chronic Pancreatitis Support
10 days ago
terrible metalic taste in my mouth ALL the time!
I’m now into my second year of PMR, I’m on 5mgs of Prednisone and 20mgs of somac a day, 50mgs of Endep at night. I don’t think I have changed anything in my diet etc but I have a terrible metallic taste in my mouth constantly, nothing cuts through it, I’ve tried biting a lime and nothing, whatever
I’m now into my second year of PMR, I’m on 5mgs of Prednisone and 20mgs of somac a day, 50mgs of Endep at night. I don’t think I have changed anything in my diet etc but I have a terrible metallic taste in my mouth constantly, nothing cuts through it, I’ve tried biting a lime and nothing, whatever
Heidiypi1
in
PMRGCAuk
4 months ago
Hesitant to start Endep
I have severe rls and suffer augmentation. I am trying to slowly wean off sifrol and have been taking 400mg gabapentan.I take 30mg codeine in early hours of each morning(1-3am)to ease rls and help me go back tap sleep.I also have fibromyalgia.My sleep specialist wants me to start endep to help my sleep
I have severe rls and suffer augmentation. I am trying to slowly wean off sifrol and have been taking 400mg gabapentan.I take 30mg codeine in early hours of each morning(1-3am)to ease rls and help me go back tap sleep.I also have fibromyalgia.My sleep specialist wants me to start endep to help my sleep
Retiredlady
in
Restless Legs Syndrome
2 years ago
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enzmes help
my doctor only prescribed me zen pep and my insurance wont cover it, and i cant afford it is there anything else i can take to my enzmes that would help other than
zenpep
my doctor only prescribed me zen pep and my insurance wont cover it, and i cant afford it is there anything else i can take to my enzmes that would help other than
zenpep
tory2d
in
Chronic Pancreatitis Support
3 years ago
Getting the Right Enzyme Dose
If you're on pancreatic enzyme replacement therapy (PERT), whether you take Creon,
Zenpep
, or another brand of pancreatic enzymes, you should make sure your dose is right for you. In this 5 minute video, Dr. Steven Freedman explains how to dose pancreatic enzymes for adults.
If you're on pancreatic enzyme replacement therapy (PERT), whether you take Creon,
Zenpep
, or another brand of pancreatic enzymes, you should make sure your dose is right for you. In this 5 minute video, Dr. Steven Freedman explains how to dose pancreatic enzymes for adults.
Sofia_MC
Partner
in
Chronic Pancreatitis Support
3 years ago
Teenage daily migraines
First of all, sorry about my long-winded message. My 14 year old daughter has been getting daily “migraine-like” headaches that last from the moment she wakes up to the moment she goes to sleep. (This is the description the neurologist gives). She has had them now for 3 months & is unable to participate
First of all, sorry about my long-winded message. My 14 year old daughter has been getting daily “migraine-like” headaches that last from the moment she wakes up to the moment she goes to sleep. (This is the description the neurologist gives). She has had them now for 3 months & is unable to participate
Angebombange72
in
National Migraine Centre
3 years ago
Cervical cancer - 10 months on...
Hi everyone :) Thank you for accepting me into the group I'm pretty sure no one wants to be in! I was treated for stage 1b3 squamous cell cervical cancer late last year, so am almost a year post treatment (5 weeks of chemoradiation and 2 x brachytherapy.) I attended all my cervical screening appts,
Hi everyone :) Thank you for accepting me into the group I'm pretty sure no one wants to be in! I was treated for stage 1b3 squamous cell cervical cancer late last year, so am almost a year post treatment (5 weeks of chemoradiation and 2 x brachytherapy.) I attended all my cervical screening appts,
Ladyparts
in
Pelvic Radiation Disease Association
3 years ago
Nerve damage and endep
Does anybody else have nerve damage from surgery and have to go on endep? What are your stories? Thanks 😊😊
Does anybody else have nerve damage from surgery and have to go on endep? What are your stories? Thanks 😊😊
Vmvm
in
Endometriosis UK
3 years ago
Neuropathic pain everywhere!
Hi everyone, I haven't posted in a long time. 3.5 years ago i had chemotherapy and radiation treatments for cervical cancer and now for the last 18 months ive had nerve pain that seems to be spreading all over my body. Im taking 100mgs lyrica, 300mgs nupentin, 10mgs endep for nerve pain and I also have
Hi everyone, I haven't posted in a long time. 3.5 years ago i had chemotherapy and radiation treatments for cervical cancer and now for the last 18 months ive had nerve pain that seems to be spreading all over my body. Im taking 100mgs lyrica, 300mgs nupentin, 10mgs endep for nerve pain and I also have
Alwaysblue
in
Pain Concern
4 years ago
Restless Legs tonight
Has anyone took endep to wean them selves off pramipexole. I was prescribed it yesterday cause l have Augmented from been on Pramipexole 0.125 for 3 years February next month. I missed it tonight cause l havent been sleeping. So l can at least see if l sleep Thursday night Aust time. Its been a hell
Has anyone took endep to wean them selves off pramipexole. I was prescribed it yesterday cause l have Augmented from been on Pramipexole 0.125 for 3 years February next month. I missed it tonight cause l havent been sleeping. So l can at least see if l sleep Thursday night Aust time. Its been a hell
Boss15
in
Restless Legs Syndrome
4 years ago
Desperate
Buckle up for a long one. My mum is 57 and has suffered with RLS since she was a child but it got really bad when she was around 30 and pregnant. I think it settled down after my sister was born but has gradually gotten worse. I know probably over the last 2-3 years she has been really struggling and
Buckle up for a long one. My mum is 57 and has suffered with RLS since she was a child but it got really bad when she was around 30 and pregnant. I think it settled down after my sister was born but has gradually gotten worse. I know probably over the last 2-3 years she has been really struggling and
adeleoliver
in
Restless Legs Syndrome
5 years ago
Anyone else have chronic pain that has limited your ability to travel in a car or even leave the house for long period of time??
Question and long rant. I am struggling big time with chronic pain, mostly nerve pain but also ovary pain around ovulation and period weeks. I had my lap about 14 weeks ago that diagnosed and removed an extensive amount of endo and i have been on Visanne since then that has stopped my period bleeding
Question and long rant. I am struggling big time with chronic pain, mostly nerve pain but also ovary pain around ovulation and period weeks. I had my lap about 14 weeks ago that diagnosed and removed an extensive amount of endo and i have been on Visanne since then that has stopped my period bleeding
Lejay
in
Endometriosis UK
5 years ago
Meningoencephalitis Survivor
Hey everyone, I had Meningoencephalitis back in 2011, and have had a headache (usually a 5/10) everyday since (yup, 7 years worth). About once every two months i'll have a 'blow' out and have to go to hospital for stronger meds to bring the pain level back to 'my normal'. I have tried Sandomigran, Endep
Hey everyone, I had Meningoencephalitis back in 2011, and have had a headache (usually a 5/10) everyday since (yup, 7 years worth). About once every two months i'll have a 'blow' out and have to go to hospital for stronger meds to bring the pain level back to 'my normal'. I have tried Sandomigran, Endep
MeningoencephSur5ver
in
Meningitis Now
5 years ago
Newly diagnosed with Polymyalgia Rheumatica and more recently GCA
Hi everyone, I’m new here and have been reading lots of posts as I am in lots of pain and feeling pretty low. I have had Fibromyalgia since 2001 and have now been hit with another myalgia. Don’t know what I did to deserve this. Anyway, I am in my late 60s, usually pretty stoic and just get on with life
Hi everyone, I’m new here and have been reading lots of posts as I am in lots of pain and feeling pretty low. I have had Fibromyalgia since 2001 and have now been hit with another myalgia. Don’t know what I did to deserve this. Anyway, I am in my late 60s, usually pretty stoic and just get on with life
KrisAnne51
in
PMRGCAuk
5 years ago
Does anyone have any sleeping remedies or meds that work?
I was taking Endep (which gave me a full night's sleep) but my Neurologist changed me from Stalevo (which was giving me Dyskenesia) to Madopar + Xadago. But I had to cease the Endep as he said it could conflict with the Xadago, which is a fairly new drug that is still being trialled. He prescribed Paxam
I was taking Endep (which gave me a full night's sleep) but my Neurologist changed me from Stalevo (which was giving me Dyskenesia) to Madopar + Xadago. But I had to cease the Endep as he said it could conflict with the Xadago, which is a fairly new drug that is still being trialled. He prescribed Paxam
Hidden
in
Cure Parkinson's
5 years ago
IBS Cured
Just to update on my previous post: https://healthunlocked.com/theibsnetwork/posts/140191583/fybogel-not-effective-anymore For the past week I've been having normal bowel movements (every two days, at same time, normal consistency) without the use of fybogel or any supplements, medication etc. What
Just to update on my previous post: https://healthunlocked.com/theibsnetwork/posts/140191583/fybogel-not-effective-anymore For the past week I've been having normal bowel movements (every two days, at same time, normal consistency) without the use of fybogel or any supplements, medication etc. What
toffee1010
in
IBS Network
5 years ago
Life, diagnosis, drugs.... a bit of my life!
*long story sorry* After 10 years of severe pain and being told it was in my head... a lap finally diagnosed endo. After op, pain never totally went but improved, however this was only for a couple of months then it began building up again. Within 6 months it was back to it's usual full force. The gynae
*long story sorry* After 10 years of severe pain and being told it was in my head... a lap finally diagnosed endo. After op, pain never totally went but improved, however this was only for a couple of months then it began building up again. Within 6 months it was back to it's usual full force. The gynae
Butterflyblubum
in
Endometriosis UK
5 years ago
GP advised give up on anti depressant/anxiety medication ?
so I’ve tried setraline, pristiq, endep and now mirtazipine. all for at least 3 months each at the highest dose with no effect, most recently today I went into refill my mirtazipine which I take 60mg at night, and after telling doc I notice no difference in my depression/anxiety he suggests I continue
so I’ve tried setraline, pristiq, endep and now mirtazipine. all for at least 3 months each at the highest dose with no effect, most recently today I went into refill my mirtazipine which I take 60mg at night, and after telling doc I notice no difference in my depression/anxiety he suggests I continue
anxietypanic
in
Mental Health Support
5 years ago
Concussion symptom?
Has anyone ever experienced a period of hypersexuality after a concussion or with post-concussion syndrome? Don't have to go into detail it just appears that the correlation for this symptom is recognised with more serious or debilatating head injuries. Yet I had a concussion and pcs and have had this
Has anyone ever experienced a period of hypersexuality after a concussion or with post-concussion syndrome? Don't have to go into detail it just appears that the correlation for this symptom is recognised with more serious or debilatating head injuries. Yet I had a concussion and pcs and have had this
mereby
in
Headway
5 years ago
Shingles
Would be keen to hear from anyone with S.L.E. & Shingles. !st time I have had Shingles (S.L.E. 9yrs). A bit surprised at how painful it is & how low I feel. Left side under breast wraps around to spine. On Antivirals & Endep for pain (not making much of a difference) Dr said it may last 3 months. Yikes
Would be keen to hear from anyone with S.L.E. & Shingles. !st time I have had Shingles (S.L.E. 9yrs). A bit surprised at how painful it is & how low I feel. Left side under breast wraps around to spine. On Antivirals & Endep for pain (not making much of a difference) Dr said it may last 3 months. Yikes
Kazunlocked
in
LUPUS UK
5 years ago
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